PubRank

F Bernardi

Author PubWeight™ 167.82‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Complete sequence of pSC101. Nucleic Acids Res 1984 2.22
2 Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients. J Med Genet 2007 2.21
3 Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus. Nat Genet 1999 2.05
4 Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease. N Engl J Med 2000 1.94
5 Computational evidence in favor of a two-state, two-mode model of the retinal chromophore photoisomerization. Proc Natl Acad Sci U S A 2000 1.92
6 Potyvirus proteins: a wealth of functions. Virus Res 2001 1.85
7 Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998 1.71
8 Circulating levels of allopregnanolone in humans: gender, age, and endocrine influences. J Clin Endocrinol Metab 1998 1.63
9 Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma. Thromb Haemost 1996 1.51
10 Activated protein C resistance: a comparison between two clotting assays and their relationship to the presence of the factor V Leiden mutation. Br J Haematol 1996 1.39
11 Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis. Blood 1995 1.39
12 Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels? J Thromb Haemost 2005 1.38
13 Protein C deficiency: a database of mutations, 1995 update. On behalf of the Subcommittee on Plasma Coagulation Inhibitors of the Scientific and Standardization Committee of the ISTH. Thromb Haemost 1995 1.36
14 Two TaqI RFLPs in the human von Willebrand factor gene. Nucleic Acids Res 1987 1.33
15 Potyviral HC-Pro: a multifunctional protein. J Gen Virol 1996 1.26
16 PvuII RFLP inside the human estrogen receptor gene. Nucleic Acids Res 1987 1.22
17 Complete sequence of an IS element present in pSC101. Nucleic Acids Res 1981 1.22
18 Thyroid abnormalities during lithium treatment. Acta Psychiatr Scand 1991 1.18
19 Neonatal screening for congenital adrenal hyperplasia. Arch Dis Child 1983 1.17
20 Serum allopregnanolone levels in pregnant women: changes during pregnancy, at delivery, and in hypertensive patients. J Clin Endocrinol Metab 2000 1.16
21 Preferential maternal derivation in inv dup(15): analysis of eight new cases. Hum Genet 1981 1.08
22 Gene expression from viral RNA genomes. Plant Mol Biol 1996 1.05
23 Gene deletion in an Italian haemophilia B subject. J Med Genet 1985 1.05
24 A heminested polymerase chain reaction for the detection of Brazilian rabies isolates from vampire bats and herbivores. Mem Inst Oswaldo Cruz 2002 1.04
25 The frequency of oligonucleotides in mammalian genic regions. Comput Appl Biosci 1989 1.03
26 Allopregnanolone concentrations and premenstrual syndrome. Eur J Endocrinol 2000 0.99
27 Construction in vitro of hybrid plasmids carrying all the EcoRI fragments from lambdarifd18 DNA. Eur J Biochem 1979 0.99
28 Narcolepsy-cataplexy associated with precocious puberty. Neurology 2006 0.99
29 Combined surgery and chemotherapy for the treatment of primary gastrointestinal intermediate- or high-grade non-Hodgkin's lymphomas. Br J Cancer 1989 0.99
30 Influence of canine brain decomposition on laboratory diagnosis of rabies. Rev Soc Bras Med Trop 1999 0.98
31 Protein C deficiency: a database of mutations. For the Protein C & S Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1993 0.98
32 Co-localization of rare oligonucleotides and regulatory elements in mammalian upstream gene regions. J Mol Biol 1988 0.97
33 Enhanced superoxide production with no change of the antioxidant activity in gingival fluid of patients with chronic adult periodontitis. Free Radic Res Commun 1991 0.97
34 Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study. BMJ 2001 0.96
35 Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. J Med Genet 1993 0.95
36 Changes of serum allopregnanolone levels in the first 2 years of life and during pubertal development. Pediatr Res 1999 0.95
37 Esophageal leiomyomatosis in children: report of a case and review of the literature. Eur J Pediatr Surg 1998 0.94
38 Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet 1982 0.94
39 Self-preventive oral behavior in an Italian university student population. J Clin Periodontol 2001 0.94
40 Atypical deletions generated by mutated IS102 elements. Mol Gen Genet 1984 0.93
41 Clinical picture and management of congenital factor VII deficiency. Haemophilia 2004 0.93
42 Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII. J Thromb Haemost 2006 0.93
43 A new approach to DNA polymerase kinetics. J Mol Biol 1979 0.93
44 Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay. Thromb Haemost 1993 0.93
45 Protein S deficiency: a database of mutations--summary of the first update. Thromb Haemost 2000 0.92
46 Hyperhomocyst(e)inemia and a common methylenetetrahydrofolate reductase mutation (Ala223Val MTHFR) in patients with inherited thrombophilic coagulation defects. Arterioscler Thromb Vasc Biol 1997 0.92
47 Long-term low-dose dehydroepiandrosterone replacement therapy in aging males with partial androgen deficiency. Aging Male 2004 0.91
48 A double-blind study of L-sulpiride versus amitriptyline in lithium-maintained bipolar depressives. Acta Psychiatr Scand 1993 0.91
49 Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma. Leukemia 1995 0.91
50 Sublocalization of the human protein C gene on chromosome 2q13-q14. Hum Genet 1989 0.91
51 Neonatal screening for cystic fibrosis by dried blood spot trypsin assay. Results in 47 127 newborn infants from a homogeneous population. Acta Paediatr Scand 1984 0.90
52 Thrombosis in inherited factor VII deficiency. J Thromb Haemost 2003 0.90
53 Resistance to activated protein C in healthy women taking oral contraceptives. Br J Haematol 1995 0.89
54 Expression of the normal factor V allele modulates the APC resistance phenotype in heterozygous carriers of the factor V Leiden mutation. J Thromb Haemost 2005 0.89
55 Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene. Blood 1998 0.89
56 The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease. Arterioscler Thromb Vasc Biol 1997 0.89
57 D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Hum Genet 1993 0.89
58 Tibolone, transdermal estradiol or oral estrogen-progestin therapies: effects on circulating allopregnanolone, cortisol and dehydroepiandrosterone levels. Gynecol Endocrinol 2005 0.89
59 Luteinising hormone-releasing hormone nasal spray as therapy for undescended testicle. Arch Dis Child 1978 0.89
60 Site-specific deletions in the recombinant plasmid pSC101 containing the redB-ori region of phage lambda. Gene 1981 0.88
61 Molecular characteristics of a non-deletion alpha-thalassaemia of the Po River Delta. Eur J Biochem 1981 0.88
62 Relationships among the secretion of ACTH, GH, and cortisol during the insulin-induced hypoglycemia test in the normal and obese child. J Clin Endocrinol Metab 1975 0.88
63 Several cytogenetic subclones may be identified within plasma cells from patients with monoclonal gammopathy of undetermined significance, both at diagnosis and during the indolent course of this condition. Blood 1997 0.88
64 Hypophyso-gonadal function in the cryptorchid child: differences between unilateral and bilateral cryptorchids. Acta Endocrinol (Copenh) 1976 0.87
65 Hormonal replacement therapy affects calcitonin gene-related peptide and atrial natriuretic peptide secretion in postmenopausal women. Eur J Endocrinol 1997 0.87
66 RNA-based therapeutic approaches for coagulation factor deficiencies. J Thromb Haemost 2011 0.87
67 The use of dopamine agonists in the treatment of schizophrenia. Neuropharmacology 1981 0.87
68 Phenotypic homozygous activated protein C resistance associated with compound heterozygosity for Arg506Gln (factor V Leiden) and His1299Arg substitutions in factor V. Br J Haematol 1997 0.87
69 Displacement of T lymphocytes with the 'Helper/Inducer' phenotype from peripheral blood to lymphoid organs in untreated patients with Hodgkin's disease. Scand J Haematol 1983 0.87
70 Pulmonary function abnormalities in children with Henoch-Schönlein purpura. Eur Respir J 1999 0.87
71 The course of thyroid abnormalities during lithium treatment: a two-year follow-up study. Acta Psychiatr Scand 1992 0.86
72 Risk of venous thromboembolism and stroke associated with oral contraceptives. Role of congenital thrombophilias. Recenti Prog Med 1996 0.86
73 Potyvirus helper component-proteinase self-interaction in the yeast two-hybrid system and delineation of the interaction domain involved. Virology 1999 0.86
74 Menopause and the central nervous system: intervention options. Maturitas 1999 0.86
75 The accuracy of DNA replication. Biochimie 1978 0.86
76 Neuropeptides, neurotransmitters, neurosteroids, and the onset of puberty. Ann N Y Acad Sci 2000 0.85
77 Effect of long-term GH administration on pituitary-thyroid function in idiopathic hypopituitarism. Acta Paediatr Scand 1979 0.85
78 Combinations of 4 mutations (FV R506Q, FV H1299R, FV Y1702C, PT 20210G/A) affecting the prothrombinase complex in a thrombophilic family. Blood 2000 0.85
79 Effect of obesity on the hypothalamo-pituitary-gonadal function in childhood. Acta Paediatr Scand 1977 0.85
80 Protein A reactivity of IgM- and IgD-bearing lymphocytes from some patients with chronic lymphocytic leukemia. Clin Immunol Immunopathol 1981 0.85
81 A novel frame-shift deletion causing analbuminaemia in an Italian paediatric patient. Eur J Clin Invest 2010 0.84
82 An engineered U1 small nuclear RNA rescues splicing-defective coagulation F7 gene expression in mice. J Thromb Haemost 2014 0.84
83 [Comparison of the action of 3 non-steroidal anti-inflammatory agents in the control of post-operative pain. Effectiveness of NSAID against pain]. Attual Dent 1985 0.84
84 Neonatal screening for congenital adrenal hyperplasia using a microfilter paper method for 17-alpha-hydroxyprogesterone radioimmunoassay. Experience gained from the study of 22,233 cases. Horm Res 1982 0.84
85 Genealogical analyses of rabies virus strains from Brazil based on N gene alleles. Epidemiol Infect 2002 0.84
86 Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3. Am J Med Genet 1996 0.84
87 On the mechanism of nucleotide incorporation into DNA and RNA. FEBS Lett 1975 0.84
88 Enamel matrix proteins and guided tissue regeneration with titanium-reinforced expanded polytetrafluoroethylene membranes in the treatment of infrabony defects: a comparative controlled clinical trial. J Periodontol 2002 0.83
89 Venous thromboembolism, oral contraceptives and high prothrombin levels. J Thromb Haemost 2003 0.83
90 Hypothalamic amenorrhea with normal body weight: ACTH, allopregnanolone and cortisol responses to corticotropin-releasing hormone test. Eur J Endocrinol 2000 0.83
91 Nucleic acid-binding properties of a bacterially expressed potato virus Y helper component-proteinase. J Gen Virol 1996 0.83
92 Value of thyroid echography in the long-term follow-up of lithium-treated patients. Neuropsychobiology 1997 0.83
93 Adrenal response to adrenocorticotropic hormone stimulation in patients with premenstrual syndrome. Gynecol Endocrinol 2004 0.83
94 Protein S deficiency: a database of mutations. For the Plasma Coagulation Inhibitors Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1997 0.83
95 Reduced factor VII and factor VIII levels and prolonged thrombin-generation times during a healthy diet in middle-aged women with mild to moderate cardiovascular disease risk. J Thromb Haemost 2008 0.83
96 Opposite deletions/duplications of the X chromosome: two novel reciprocal rearrangements. Eur J Hum Genet 2000 0.83
97 Identification and functional analysis of the turnip yellow mosaic tymovirus subgenomic promoter. J Virol 2000 0.83
98 A new factor V gene polymorphism (His 1254 Arg) present in subjects of african origin mimics the R2 polymorphism (His 1299 Arg) Blood 1998 0.83
99 Role of the mechanical properties of tracheobronchial airways in determining the respiratory resistance time course. Ann Biomed Eng 2001 0.82
100 Relationship between paraoxonase Q192R gene polymorphism and on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention. J Thromb Haemost 2011 0.82
101 Bronchial reactivity and sex hormone: study in a Turner's population. Pediatr Pulmonol 1990 0.82
102 Bronchial reactivity in diabetic patients. Relationship to duration of diabetes and degree of glycemic control. Am J Dis Child 1988 0.82
103 Vitamin K-induced modification of coagulation phenotype in VKORC1 homozygous deficiency. J Thromb Haemost 2008 0.82
104 CD19 and immunophenotype of bone marrow plasma cells in monoclonal gammopathy of undetermined significance. J Clin Pathol 1995 0.81
105 Chromosomal localization of human p85 alpha, a subunit of phosphatidylinositol 3-kinase, and its homologue p85 beta. Oncogene 1992 0.81
106 Combined surgery and chemotherapy in primary gastric non-Hodgkin's lymphoma: a retrospective study in sixty-six patients. Leuk Lymphoma 1994 0.81
107 Venous thromboembolism in young women; role of thrombophilic mutations and oral contraceptive use. Eur Heart J 2002 0.81
108 Molecular bases of pseudo-homozygous APC resistance: the compound heterozygosity for FV R506Q and a FV null mutation results in the exclusive presence of FV Leiden molecules in plasma. Thromb Haemost 1998 0.81
109 DNA rearrangements in a hybrid plasmid carrying the redB imm region of coliphage lambda. Gene 1980 0.81
110 Deletion mapping of the potyviral helper component-proteinase reveals two regions involved in RNA binding. Virology 2000 0.81
111 Effect of estrogens on dopamine autoreceptors in male rats. Eur J Pharmacol 1983 0.81
112 Molecular and clinical aspects of factor VII deficiency. Blood Coagul Fibrinolysis 1998 0.81
113 Laparoscopic antireflux surgery in neurologically impaired children. Pediatr Surg Int 2004 0.80
114 Progesterone, progestagens and the central nervous system. Hum Reprod 2000 0.80
115 [Dynamic exploration of the antehypophysis in the child]. Minerva Pediatr 1975 0.80
116 Novel phenotype and γ-glutamyl carboxylase mutations in combined deficiency of vitamin K-dependent coagulation factors. Haemophilia 2011 0.80
117 Intramolecular transposition of IS102. Gene 1986 0.80
118 Organization of alpha-globin genes and mRNA translation in subjects carrying haemoglobin Hasharon (alpha 47 Asp replaced by His) from the Ferrara Region (Northern Italy). Eur J Biochem 1980 0.80
119 Detection of two missense mutations and characterization of a repeat polymorphism in the factor VII gene (F7). Hum Genet 1992 0.80
120 Functional properties of factor V and factor Va encoded by the R2-gene. Thromb Haemost 2001 0.80
121 c-myc oncogene alterations in human thyroid carcinomas. Cancer Detect Prev 1987 0.80
122 Effect of a booster-dose of rabies vaccine on the duration of virus neutralizing antibody titers in bovines. Rev Soc Bras Med Trop 1998 0.80
123 Gentamicin induces sub-therapeutic levels of coagulation factor VII in patients with nonsense mutations. J Thromb Haemost 2006 0.79
124 Human leukemic K562 cells: suppression of hemoglobin accumulation by a monoclonal antibody to human transferrin receptor. Biochim Biophys Acta 1986 0.79
125 RFLP analysis in families with sporadic hemophilia A. Estimate of the mutation ratio in male and female gametes. Hum Genet 1987 0.79
126 Disordered prolactin secretion in the obese child and adolescent. Arch Dis Child 1981 0.79
127 Cloning and characterization of the immunity region of phage phi 80. Mol Gen Genet 1987 0.79
128 Congenital hypopituitarism associated with neonatal hypoglycemia and microphallus: effect of GH therapy. Helv Paediatr Acta 1977 0.79
129 Modulation of factor VII levels by intron 7 polymorphisms: population and in vitro studies. Blood 2000 0.79
130 An analysis of Xq deletions. Hum Genet 1996 0.79
131 Mapping of human thyroglobulin gene on the long arm of chromosome 8 by in situ hybridization. Hum Genet 1985 0.79
132 Serum phospholipids are the main environmental determinants of activated factor VII in the most common FVII genotype. European Union Concerted Action "Clotart". Haematologica 1999 0.79
133 Six-month oral dehydroepiandrosterone supplementation in early and late postmenopause. Gynecol Endocrinol 2000 0.79
134 [Occupational exposure to blood and body fluids in a Department of Odontostomatologic Sciences: results of a ten-year surveillance study]. Med Lav 2010 0.78
135 A novel deletion of FVIII gene associated with variable levels of FVIII inhibitor. Eur J Haematol 1992 0.78
136 beta-Globin messenger RNA in Ferrara beta 0 thalassemia. Ann N Y Acad Sci 1980 0.78
137 Familial rates of affective illness in Sardinia with special reference to schizoaffective disorder. Eur Arch Psychiatry Clin Neurosci 1990 0.78
138 The rôle of time in reducing gingival overgrowth in heart-transplanted patients following cyclosporin therapy. J Clin Periodontol 2000 0.78
139 Neonatal screening programme for congenital adrenal hyperplasia in a homogeneous Caucasian population. J Inherit Metab Dis 1986 0.78
140 Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy. Blood 1995 0.78
141 A missense mutation (Y1702C) in the coagulation factor V gene is a frequent cause of factor V deficiency in the Italian population. Haematologica 2001 0.78
142 Sublocalization of von Willebrand factor pseudogene to 22q11.22-q11.23 by in situ hybridization in a 46,X,t(X;22)(pter;q11.21) translocation. Hum Genet 1989 0.78
143 Mutations in the R2 FV gene affect the ratio between the two FV isoforms in plasma. Thromb Haemost 2000 0.78
144 A double-blind study of minaprine versus amitriptyline in major depression. Neuropsychobiology 1992 0.78
145 Evaluation of the toxicity of the dopaminergic neurotoxins MPTP and MPP+ in PC12 pheochromocytoma cells: binding and biological studies. Neurosci Lett 1988 0.77
146 Human leukemia K562 cells: relationship between hemin-mediated erythroid induction, cell proliferation and expression of c-abl and c-myc oncogenes. Biochem Biophys Res Commun 1984 0.77
147 Plasma factor VII levels are influenced by a polymorphism in the promoter region of the FVII gene. Blood Coagul Fibrinolysis 1996 0.77
148 Hypophyso-gonadal function in the diabetic child. Acta Paediatr Scand 1978 0.77
149 Effect of mutations within the cys-rich region of potyvirus helper component-proteinase on self-interaction. J Gen Virol 1999 0.77
150 The heterozygous 20210 G/A genotype prevalence in patients affected by central and branch retinal vein occlusion: a pilot study. Graefes Arch Clin Exp Ophthalmol 2001 0.77
151 Clozapine in idiopathic Parkinson's disease. Neurology 1990 0.77
152 A global investigation of excited state surfaces within time-dependent density-functional response theory. J Chem Phys 2004 0.77
153 Modification of nonspecific bronchial reactivity in hypothyroid children under different regimens of substitutive opotherapy. Pediatr Pulmonol 1987 0.77
154 Molecular bases of type II protein S deficiency: the I203-D204 deletion in the EGF4 domain alters GLA domain function. J Thromb Haemost 2006 0.77
155 Primary conjunctival lymphoma: response to chemotherapy in 4 cases. Acta Haematol 1982 0.77
156 A polymorphism in the 5' region of coagulation factor VII gene (F7) caused by an inserted decanucleotide. Hum Genet 1993 0.77
157 [Alprazolam versus lorazepam in the treatment of anxiety: controlled clinical study]. Riv Patol Nerv Ment 1987 0.77
158 Properties of 3H-MPTP binding sites in human blood platelets. Life Sci 1986 0.77
159 A missense mutation (178Cys-->Tyr) and two neutral dimorphisms (115His and 333Ser) in the human coagulation factor VII gene. Hum Mol Genet 1993 0.77
160 Effect of acute corticotropin releasing factor on pituitary-adrenocortical responsiveness in elderly women and men. J Endocrinol Invest 1998 0.77
161 Reduced activation of the Gla19Ala FX variant via the extrinsic coagulation pathway results in symptomatic CRMred FX deficiency. Thromb Haemost 2002 0.77
162 Study of a protein S gene polymorphism at DNA and mRNA level in a family with symptomatic protein S deficiency. Br J Haematol 1993 0.76
163 A rare association of inlet patch with laryngospasm: a report of two children and literature review. Pediatr Pulmonol 2011 0.76
164 Effects of estradiol and raloxifene analog on brain, adrenal and serum allopregnanolone content in fertile and ovariectomized female rats. Neuroendocrinology 2000 0.76
165 Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype. Am J Ophthalmol 1999 0.76
166 Switches in the mode of transmission select for or against a poorly aphid-transmissible strain of potato virus Y with reduced helper component and virus accumulation. J Gen Virol 1996 0.76
167 Clinical manifestations, management, and molecular genetics in congenital factor VII deficiency: the International Registry on Congenital Factor VII Deficiency (IRF7) Blood 2000 0.76
168 PCR detection of a repeat polymorphism within the F7 gene. Nucleic Acids Res 1991 0.76
169 Characterization of a deleted Y chromosome in a male with Turner stigmata. Clin Genet 1993 0.76
170 Pharmacokinetic properties of recombinant FVIIa in inherited FVII deficiency account for a large volume of distribution at steady state and a prolonged pharmacodynamic effect. Thromb Haemost 2014 0.76
171 Image analysis in multiple myeloma at diagnosis. Correlation with cytogenetic study. Cancer Genet Cytogenet 1994 0.76
172 Monoclonal gammopathy of undetermined significance: chromosome changes are a common finding within bone marrow plasma cells. Br J Haematol 1995 0.76
173 High affinity binding sites for 1-methyl-4-phenyl-pyridinium ion (MPP+) are present in mouse brain. Eur J Pharmacol 1986 0.76
174 A new disease-causing mutation in the GAP-related domain of the NF1 gene. Hum Mol Genet 1993 0.76
175 beta (+)-Thalassaemia in the Po river delta region (northern Italy): genotype and beta globin synthesis. J Med Genet 1985 0.76
176 Assignment of human coagulation factor XII (fXII) to chromosome 5 by cDNA hybridization to DNA from somatic cell hybrids. Hum Genet 1988 0.76
177 Agenesis of the corpus callosum with mosaicism 46,XY/47,XY, extra ring chromosome. J Med Genet 1980 0.75
178 Methylation and expression of c-myc and c-abl oncogenes in human leukemic K562 cells before and after treatment with 5-azacytidine. Cancer Detect Prev 1986 0.75
179 Quantum mechanical analysis of oxygenated and deoxygenated states of hemocyanin: theoretical clues for a plausible allosteric model of oxygen binding. Protein Sci 1999 0.75
180 Factor XII gene alteration in Hageman trait detected by TaqI restriction enzyme. Blood 1987 0.75
181 Raloxifene analog LY 117018 effects on central and peripheral beta-endorphin. Gynecol Endocrinol 1999 0.75
182 Two additional TaqI RFLPs in von Willebrand factor gene (VWF) and pseudogene. Nucleic Acids Res 1989 0.75
183 Growth hormone release during sleep in growth-retarded children with normal response to pharmacological tests. Arch Dis Child 1978 0.75
184 Clinical implications of circulating neurosteroids. Int Rev Neurobiol 2001 0.75
185 New coagulation factor V gene polymorphisms define a single and infrequent haplotype underlying the factor V Leiden mutation in Mediterranean populations and Indians. Thromb Haemost 1997 0.75
186 Plasma ACTH values during the first seven days of life in infants of diabetic mothers. J Pediatr 1975 0.75
187 [Incidence of Mycoplasma pneumoniae infections in a general pediatric medical department]. Minerva Pediatr 1982 0.75
188 An engineered U1 small nuclear RNA rescues splicing defective coagulation F7 gene expression in mice. J Thromb Haemost 2014 0.75
189 [Therapeutic effects and tolerance of aztreonam in infections of the urinary tract in childhood]. G Ital Chemioter 1986 0.75
190 [Relationship between the secretion of ACTH, GH and cortisol during insulin hypoglycemia test in the normal and obese child]. Minerva Pediatr 1974 0.75
191 [Use of sulprostone in abortion induced during the first pregnancy trimester in women with previous cesarean section]. Minerva Ginecol 1990 0.75
192 [Clinical experience and histological investigation of periosteal stimulation on repositioned grafts]. Arch Stomatol (Napoli) 1983 0.75
193 [Aspirin and indomethacin therapy in 2 familial cases of Bartter's disease. Follow-up for growth and endocrine pattern]. Minerva Pediatr 1980 0.75
194 Epsilon-globin gene is undermethylated in K-562 cells: increased expression after treatment of the cells with 5-azacytidine. Cell Biol Int Rep 1984 0.75
195 The thyrotropin releasing hormone test in idiopathic pituitary dwarfism. Helv Paediatr Acta 1974 0.75
196 alpha-Thalassemia trait in the region of Ferrara. Haematologica 1981 0.75
197 [Cytogenetic evaluation of subgingival lesions: fibromatous, angiomatous, giant-cell and granular-cell (so-called epulis)]. Minerva Stomatol 1988 0.75
198 Sensitivity to exogenous insulin and release of endogenous insulin in hypopituitary non-hypoglycemic children treated with hGH. Acta Paediatr Scand 1981 0.75
199 [Sensitivity to exogenous insulin and the efficiency and release of endogenous insulin in subjects with non-hypoglycemic hypopituitarism treated with growth hormone]. Minerva Pediatr 1980 0.75
200 [Aspects of cardiorespiratory function in obese children]. Minerva Pediatr 1987 0.75
201 Association of membranous nephropathy with familial resistance to activated protein C. Nephrol Dial Transplant 1995 0.75
202 Neonatal screening for congenital adrenal hyperplasia. Lancet 1982 0.75
203 Deletion breakpoints in a 32 bp perfect repeat located 45.1 Kb apart in the human growth hormone gene cluster. Hum Mol Genet 1993 0.75
204 Symptomatic type II protein C deficiency caused by a missense mutation (Gly 381-->Ser) in the substrate-binding pocket. Br J Haematol 1993 0.75
205 Australia antigen in diabetic subjects. Acta Diabetol Lat 1977 0.75
206 De novo complex autosomal translocation involving chromosomes 8, 13 and 15 in a girl with a sporadic retinoblastoma. Hum Genet 1987 0.75
207 The brain as a new frontier for reproductive endocrinology. Curr Opin Obstet Gynecol 1999 0.75
208 [Behavior of corticotropinemia and cortisolemia in insulin-induced hypoglycemia. Evaluation of plasma ACTH with a radioimmunological method]. Minerva Pediatr 1973 0.75
209 Reduced levels of variant alpha-globins in beta-thalassaemia. Haematologica 1979 0.75
210 [Behavior of plasma ACTH and somatotropin during hypoglycemia due to insulin in subjects affected by congenital adrenogenital syndrome]. Minerva Pediatr 1976 0.75
211 Characterization of the pseudogenic and genic homologous regions of von Willebrand factor. Br J Haematol 1991 0.75
212 [Oral cavity angioma treatment by cryotherapy]. Minerva Stomatol 1981 0.75
213 [Cryotherapy of precancerous lesions of the oral cavity]. Minerva Stomatol 1981 0.75
214 Comparison among natural (Arg304Gln, Arg304Trp) and artificial (Arg290His, Arg290Lys) mutations in coagulation factor VII loops. J Thromb Haemost 2003 0.75
215 [So-called Castleman's benign lymphoma. Original case of hyalino-vascular histological type, including immunological tests]. Arch De Vecchi Anat Patol 1980 0.75
216 [Chromosome mapping by in situ hybridization of cloned human DNA sequences]. Boll Soc Ital Biol Sper 1985 0.75
217 TaqI polymorphism at the human coagulation factor XII locus (F12). Nucleic Acids Res 1986 0.75
218 Inhibition of viral aphid transmission by the N-terminus of the maize dwarf mosaic virus coat protein. Virology 1995 0.75
219 Cyclosporin A effects on extra oral connective tissue in heart transplanted patients. J Int Acad Periodontol 1999 0.75
220 [Relationships between hypophyso-gonadal function and development of the gonads and pubic hair]. Minerva Pediatr 1979 0.75
221 [Cases of endometrial hyperplasia diagnosed at a regional hospital in the Province of Pavia]. Minerva Ginecol 1991 0.75
222 [Occurrence of secretor and non-secretor phenotypes]. Ann Med Nav (Roma) 1971 0.75
223 [Cardiotocographic findings in the course of labor analgesia by association of diazepam-sodium 4 hydroxybutyrate]. Minerva Anestesiol 1969 0.75
224 [Fatal hemophagocytic syndrome following infectious mononucleosis in a non immunosuppressed subject]. Presse Med 1995 0.75
225 [Voluntary interruption of pregnancy using the Karman method and T-lymphocyte dependent immunity]. Minerva Ginecol 1989 0.75
226 A novel factor V null mutation detected in a thrombophilic patient with pseudo-homozygous APC resistance and in an asymptomatic unrelated subject. Blood 1998 0.75
227 [Neonatal screening for congenital hypothyroidism. Experience at a Regional Center]. Pediatr Med Chir 1985 0.75
228 [Conclusive considerations on the use of fibrin glue in periodontal surgery. Histological controls]. Minerva Stomatol 1986 0.75
229 Dehydroepiandrosterone as neurosteroid: neuroendocrine effects in post-menopausal women. J Endocrinol Invest 1999 0.75
230 [Candidiasis and leukoplakia of the oral cavity in the patient wearing complete dentures]. Minerva Stomatol 1989 0.75
231 [Response to treatment with HGH (human growth hormone) in 33 patients with idiopathic hypopituitarism]. Minerva Pediatr 1975 0.75
232 Recommendations for the diagnosis of pediatric tuberculosis. Eur J Clin Microbiol Infect Dis 2016 0.75
233 [LH-RH and TRH test in patients with congenital adrenogenital syndrome under various treatment]. Minerva Pediatr 1976 0.75
234 Human leukemic K562 cells: differential effects of 5-azacytidine on DNA methylation of epsilon-, gamma-globin and 7SL RNA genes. Boll Soc Ital Biol Sper 1984 0.75
235 [Alpha- and beta-thalassemia genotypes in the Po delta]. Minerva Med 1981 0.75
236 Do supra-antara paths really exist for 2 + 2 cycloaddition reactions? Analytical computation of the MC-SCF Hessians for transition states of ethylene with ethylene, singlet oxygen, and ketene. J Am Chem Soc 1988 0.75
237 [2:12 (p25;q21) translocation classed at first as 2/X]. Ann Genet 1975 0.75
238 Cyclosporin A upregulates phospholipase C beta1 in fibroblasts from gingival overgrowth. J Periodontol 2000 0.75
239 Neuropsychiatric implications of drugs acting on dopamine receptors: the effect of apomorphine. Prog Clin Biol Res 1980 0.75
240 [Nasolabial cysts, a rare disease. Clinical case]. Dent Cadmos 1988 0.75
241 [Diagnosis of gastro-esophageal reflux in children. Ultrasonography versus pH monitoring]. Radiol Med 1993 0.75
242 [Extralobar pulmonary sequestration in children: presentation of a case]. Pediatr Med Chir 1991 0.75
243 Neonatal screening program for congenital adrenal hyperplasia in a homogeneous Caucasian population. Ann N Y Acad Sci 1985 0.75
244 Treatment of large cell lymphoma with the Fi2 regimen (doxorubicin, vincristine, cyclophosphamide, bleomycin and prednisone): 25-year experience. Oncol Rep 2000 0.75
245 [Rebasing in prosthetic practice. II--Materials]. Stomatol Mediterr 1987 0.75
246 Identification of a c-myc oncogene lacking the exon 1 in the normal cells of a patient carrying a thyroid carcinoma. FEBS Lett 1986 0.75
247 Two cases of t(1;16)(p11;p11) in multiple myeloma: confirmation by chromosome painting. Cancer Genet Cytogenet 1994 0.75
248 [Extrauterine pregnancy. Critical review of the clinical diagnosis and early echography]. Minerva Ginecol 1990 0.75
249 [Histiocytosis X: contribution to the study of the eosinophilic granuloma in the jaws]. Arch Stomatol (Napoli) 1983 0.75
250 [Inhibition of heme biosynthesis in erythroid precursors (BFU-e) isolated from human peripheral blood: effects on globin synthesis]. Boll Soc Ital Biol Sper 1983 0.75
251 Two mutations causing complete androgen insensitivity: a frame-shift in the steroid binding domain and a Cys-->Phe substitution in the second zinc finger of the androgen receptor. Hum Mol Genet 1994 0.75
252 Involvement of peripheral blood cells in multiple myeloma: chromosome changes are the rule within circulating plasma cells but not within B lymphocytes. Leukemia 1997 0.75
253 Factor IX propeptide mutation and life threatening bleeding. Thromb Res 2011 0.75
254 [Plasmacytoma and a case localized in the mouth]. G Stomatol Ortognatodonzia 1985 0.75
255 [Use of sulprostone for cervical dilation in nulliparas during 1st trimester abortions]. Minerva Ginecol 1988 0.75
256 Estrogen effects on neuroendocrine function: the new challenge of pulsed therapy. Climacteric 2002 0.75
257 [Detection with the Holter method of asymptomatic arrhythmias and silent ischemias in myocardial infarct patients transferred from the coronary unit]. Boll Soc Ital Cardiol 1980 0.75
258 Ferrara beta o-thalassemia. Birth Defects Orig Artic Ser 1982 0.75
259 A novel mutation (Leu817Pro) causing type 2A von Willebrand disease. Br J Haematol 1996 0.75
260 [Antibacterial activity and blood levels of 2 tetracyclines]. Antibiotica 1969 0.75
261 Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization. Liver 1992 0.75
262 The factor V Glu1608Lys mutation is recurrent in familial thrombophilia. J Thromb Haemost 2005 0.75
263 Molecular bases of CRM+ factor X deficiency: a frequent mutation (Ser334Pro) in the catalytic domain and a substitution (Glu102Lys) in the second EGF-like domain. Br J Haematol 1995 0.75
264 A highly polymorphic microsatellite in the factor V gene is an informative tool for the study of factor V-related disorders. Br J Haematol 2001 0.75
265 An assessment of pocket depth in vitro with a computerized periodontal probe. Int J Periodontics Restorative Dent 1987 0.75
266 Effect of compliant intermediate airways on total respiratory resistance and elastance in mechanical ventilation. Med Eng Phys 2001 0.75
267 [Messenger RNA in cases of heterozygous beta and delta-beta Thalassemia. Biosynthetic and hybridization studies]. Boll Soc Ital Biol Sper 1980 0.75
268 Computerized periodontal probe with adjustable pressure. Int J Periodontics Restorative Dent 1987 0.75
269 Protein S mRNA in patients with protein S deficiency. Thromb Haemost 1995 0.75
270 Non-secretory multiple myeloma with multinucleated giant plasma cells. Leuk Lymphoma 1997 0.75
271 Direct detection of a missense mutation causing severe hemophilia A by PCR amplification and fluorescence scanning. Hematol Pathol 1990 0.75
272 [Alkaline phosphatase isoenzymes in a case of transient hyperphosphatasemia]. Pediatr Med Chir 1996 0.75
273 Use of 3'HVR genomic probe for presymptomatic diagnosis of adult polycystic kidney disease in northern Italy: comparison of DNA analysis and renal ultrasonographic data. Nephrol Dial Transplant 1988 0.75
274 [Polymorphonuclear neutrophilic granulocytes and the defense and damage of periodontal tissues]. Minerva Stomatol 1989 0.75
275 Fanconi's anaemia in adults: study of three families. Haematologica 1977 0.75
276 [Globin synthesis in erythroid cultures from normal and thalassemic subjects]. Boll Soc Ital Biol Sper 1980 0.75
277 [Pulmonary embolism disclosing activated protein C resistance]. Rev Mal Respir 1996 0.75
278 [Behavior of TSH, T4, free T4, T3, free T3 and reverse T3 in the first 15 days of life]. Minerva Pediatr 1980 0.75
279 [Construction of a genome library from a beta-0-thalassemic individual from Ferrara: characterization of clones containing beta globin genes]. Boll Soc Ital Biol Sper 1983 0.75
280 [Sturge-Weber syndrome]. Minerva Stomatol 1988 0.75
281 [HDL-cholesterol in coronary disease in the acute phase]. Boll Soc Ital Cardiol 1981 0.75
282 GH, ACTH, LH and FSH behaviour in the first seven days of life. Acta Paediatr Scand 1976 0.75
283 [Small supernumerary ring chromosome in a subject with agenesis of the corpus callosum]. Pathologica 1980 0.75
284 [Pulmonitis in childhood. Preliminary multicenter study 1980-1981]. Minerva Pediatr 1984 0.75
285 [Pituitary-gonadal function in obese children]. Minerva Pediatr 1977 0.75
286 [Case of odontogenic epithelial tumor with induced changes in the connective tissue]. Minerva Stomatol 1986 0.75
287 [Acute respiratory stridor in infancy]. Minerva Pediatr 2010 0.75
288 A new protocol (MiCEP) for the treatment of intermediate or high-grade non-Hodgkin's lymphoma in the elderly. Leuk Lymphoma 1996 0.75
289 Sertoli-Leydig cell androgens-estrogens secreting tumor of the ovary: ultra-conservative surgery. Eur J Obstet Gynecol Reprod Biol 2004 0.75
290 [Association of diazepam-sodium 4 hydroxybutyrate in labor analgesia]. Minerva Anestesiol 1969 0.75
291 MPTP fails to induce lipid peroxidation in vivo. Biochem Pharmacol 1987 0.75
292 Decreased prolactin secretion in obesity. J Pediatr 1986 0.75
293 Characterization and mapping of the 5' portion of von Willebrand factor pseudogene. Hum Genet 1992 0.75
294 The Ser460Pro substitution of the protein S (PS) gene in rare in Italian patients with type IIa PS deficiency. Blood 1996 0.75
295 [Relations between pituitary-gonadal function and testicular histological pattern in cryptorchidism in boys]. Minerva Pediatr 1977 0.75
296 Hypopyso-gonadal and hypophyso-adrenal function in boys with discordance between pubic hair and genital development. Eur J Pediatr 1981 0.75
297 Decay of beta-globin synthesis in heterozygous beta (0) Ferrara thalassaemia. Haematologica 1982 0.75
298 [The karyotype in couples with spontaneous abortion]. Minerva Ginecol 1984 0.75
299 [Non-stress test. Evaluation of a new scheme for reading the results]. Minerva Ginecol 1989 0.75
300 [Periodontal disease and crevicular neutrophils. Role of superoxide radicals]. Dent Cadmos 1989 0.75
301 [In vivo antibacterial activity of an antibiotic association and its components]. Antibiotica 1969 0.75
302 [The use of the mucotome in the free gingival grafts]. G Stomatol Ortognatodonzia 1984 0.75
303 [TRH (Thyrotropin Releasing Hormone) test in normal children and in children with various forms of thyroid diseases]. Minerva Pediatr 1975 0.75
304 Involvement of monoamine oxidase enzymes in the action of 1-methyl-4-phenyl-1,2,5,6-tetrahydropyridine, a selective neurotoxin, in the squirrel monkey: binding and biochemical studies. Brain Res 1986 0.75
305 GH, ACTH, TSH, LH, and FSH reserve in pre pubertal girls with congenital adrenal hyperplasia. J Clin Endocrinol Metab 1976 0.75
306 [Double-blind comparative study of alprazolam (Xanax) and amitriptyline in the treatment of anxiety associated with depression]. Minerva Psichiatr 1989 0.75
307 [Behavior of plasma gonadotropins (FSH-LH) after stimulation with LH-RH in prepuberal eucrinic children and in patients with idiopathic hypopituitarism]. Minerva Pediatr 1974 0.75
308 Beta-endorphin response to oral glucose tolerance test in obese and non-obese pre- and postmenopausal women. Gynecol Endocrinol 1998 0.75
309 Oral contraceptives highlight the genotype-specific association between serum phospholipids and activated factor VII. Arterioscler Thromb Vasc Biol 1999 0.75
310 [Efficiency and secretion of insulin in obese children. Study using a mathemetical model]. Minerva Pediatr 1978 0.75
311 Reproductive failure and parental chromosome abnormalities. Hum Reprod 1986 0.75
312 Phenotype and genotype expression in pseudohomozygous factor VLEIDEN : the need for phenotype analysis. Arterioscler Thromb Vasc Biol 1999 0.75
313 [Preliminary notes on the use of a human fibrin glue in periodontal surgery]. Minerva Stomatol 1983 0.75
314 Resistance to activated protein C, associated with oral contraceptives use; effect of formulations, duration of assumption, and doses of oestro-progestins. Contraception 1996 0.75
315 Management of kidney transplantation in a factor VII-deficient patient: case report. Transplant Proc 2012 0.75
316 [Problems and results in the diagnosis and therapy of hyposomia with growth hormone deficiency]. Minerva Pediatr 1974 0.75
317 The parental origin of hydatidiform moles and blighted ova: molecular probing with hypervariable DNA polymorphisms. Mol Cell Probes 1993 0.75
318 Cyclosporin-A-induced gingival overgrowth in heart transplant patients. A cross-sectional study. J Clin Periodontol 1996 0.75
319 MPTP-induced parkinsonism. Recent studies on the mechanism of toxicity. Funct Neurol 1989 0.75
320 Phenotype and genotype expression in pseudohomozygous R2 factor V. Blood 2001 0.75