Published in Boll Soc Ital Biol Sper on June 15, 1980
Comparison of classic and molecular approaches for the identification of untypeable enteroviruses. J Clin Microbiol (2000) 3.99
The Conconi test: methodology after 12 years of application. Int J Sports Med (1996) 2.39
Complete sequence of pSC101. Nucleic Acids Res (1984) 2.22
Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients. J Med Genet (2007) 2.21
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus. Nat Genet (1999) 2.05
Plasma renin concentration as a predictor of outcome in a medical intensive care setting: a retrospective pilot study. Minerva Anestesiol (2012) 1.97
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
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
Potyvirus proteins: a wealth of functions. Virus Res (2001) 1.85
Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost (1998) 1.71
Molecular epidemiology study of exogenous reinfection in an area with a low incidence of tuberculosis. J Clin Microbiol (2001) 1.66
Circulating levels of allopregnanolone in humans: gender, age, and endocrine influences. J Clin Endocrinol Metab (1998) 1.63
Does fluvastatin favour HCV replication in vivo? A pilot study on HIV-HCV coinfected patients. J Viral Hepat (2009) 1.62
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma. Thromb Haemost (1996) 1.51
Cutaneous infection caused by Mycobacterium gordonae in a human immunodeficiency virus-infected patient receiving antimycobacterial treatment. Clin Infect Dis (1997) 1.46
Determination of the anaerobic threshold by a noninvasive field test in runners. J Appl Physiol Respir Environ Exerc Physiol (1982) 1.40
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
Improved cytogenetics in multiple myeloma: a study of 151 patients including 117 patients at diagnosis. Blood (1995) 1.39
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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
Two TaqI RFLPs in the human von Willebrand factor gene. Nucleic Acids Res (1987) 1.33
Monitoring of transmission of tuberculosis between wild boars and cattle: genotypical analysis of strains by molecular epidemiology techniques. J Clin Microbiol (1999) 1.29
Potyviral HC-Pro: a multifunctional protein. J Gen Virol (1996) 1.26
Complete sequence of an IS element present in pSC101. Nucleic Acids Res (1981) 1.22
PvuII RFLP inside the human estrogen receptor gene. Nucleic Acids Res (1987) 1.22
Physiological characterization of 'stay green' mutants in durum wheat. J Exp Bot (2003) 1.20
Thyroid abnormalities during lithium treatment. Acta Psychiatr Scand (1991) 1.18
Neonatal screening for congenital adrenal hyperplasia. Arch Dis Child (1983) 1.17
Serum allopregnanolone levels in pregnant women: changes during pregnancy, at delivery, and in hypertensive patients. J Clin Endocrinol Metab (2000) 1.16
Analysis of the trinucleotide repeat expansion in Italian families affected with Huntington disease. Hum Mol Genet (1994) 1.13
A PCR-colorimetric microwell plate hybridization assay for detection of Mycobacterium tuberculosis and M. avium from culture samples and Ziehl-Neelsen-positive smears. J Clin Microbiol (2000) 1.10
Preferential maternal derivation in inv dup(15): analysis of eight new cases. Hum Genet (1981) 1.08
Detection of T cell receptor circles (TRECs) as biomarkers for de novo T cell synthesis using a quantitative polymerase chain reaction-enzyme linked immunosorbent assay (PCR-ELISA). J Immunol Methods (2000) 1.08
Induction of -globin synthesis in the -thalassaemia of Ferrara. Nat New Biol (1972) 1.08
Lethal midline granuloma: a case of Ki-1 lymphoma. Rev Laryngol Otol Rhinol (Bord) (1993) 1.07
Gene deletion in an Italian haemophilia B subject. J Med Genet (1985) 1.05
Gene expression from viral RNA genomes. Plant Mol Biol (1996) 1.05
A heminested polymerase chain reaction for the detection of Brazilian rabies isolates from vampire bats and herbivores. Mem Inst Oswaldo Cruz (2002) 1.04
Parotid sialography and minor salivary gland biopsy in the diagnosis of Sjögren's syndrome. A comparative study of 84 patients. J Rheumatol (1988) 1.03
The frequency of oligonucleotides in mammalian genic regions. Comput Appl Biosci (1989) 1.03
Direct demonstration of beta-globin mRNA in homozygous Ferrara betaO-thalassaemia patients. Nature (1977) 1.02
KSHV/HHV-8 associated lymph node based lymphomas in HIV seronegative subjects. Report of two cases with anaplastic large cell morphology and plasmablastic immunophenotype. J Clin Pathol (2005) 1.02
Appearance of beta globin synthesis in erythroid cells of Ferrara beta -o-thalassaemic patients following blood transfusion. Nature (1975) 1.00
Allopregnanolone concentrations and premenstrual syndrome. Eur J Endocrinol (2000) 0.99
Construction in vitro of hybrid plasmids carrying all the EcoRI fragments from lambdarifd18 DNA. Eur J Biochem (1979) 0.99
Narcolepsy-cataplexy associated with precocious puberty. Neurology (2006) 0.99
Combined surgery and chemotherapy for the treatment of primary gastrointestinal intermediate- or high-grade non-Hodgkin's lymphomas. Br J Cancer (1989) 0.99
Influence of canine brain decomposition on laboratory diagnosis of rabies. Rev Soc Bras Med Trop (1999) 0.98
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
Co-localization of rare oligonucleotides and regulatory elements in mammalian upstream gene regions. J Mol Biol (1988) 0.97
A HindIII RFLP and a gene lesion in the coagulation factor VIII gene. Hum Genet (1988) 0.97
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
Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study. BMJ (2001) 0.96
Nested polymerase chain reaction for Mycobacterium tuberculosis IS6110 sequence on formalin-fixed paraffin-embedded tissues with granulomatous diseases for rapid diagnosis of tuberculosis. Am J Clin Pathol (1998) 0.96
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. J Med Genet (1993) 0.95
Absence of beta-globin synthesis and excess of gamma-globin synthesis in homozygous beta-thalassaemic subjects from the Ferrara region. Nature (1968) 0.95
Absence of beta-globin synthesis and excess of alpha-globin synthesis in homozygous beta-thalassemia. Eur J Biochem (1967) 0.95
An enzyme-linked immunosorbent assay that measures protective antibody levels to Newcastle disease virus in chickens. Avian Dis (1985) 0.95
Changes of serum allopregnanolone levels in the first 2 years of life and during pubertal development. Pediatr Res (1999) 0.95
Esophageal leiomyomatosis in children: report of a case and review of the literature. Eur J Pediatr Surg (1998) 0.94
Cloning and characterization of the hsp 18.55 gene, a new member of the small heat shock gene family isolated from wine Lactobacillus plantarum. Res Microbiol (2004) 0.94
Self-preventive oral behavior in an Italian university student population. J Clin Periodontol (2001) 0.94
Duplication of the short arm of chromosome 9. Analysis of five cases. Hum Genet (1982) 0.94
Exposure to myelotoxic agents and myelodysplasia: case-control study and correlation with clinicobiological findings. Br J Haematol (1998) 0.93
Atypical deletions generated by mutated IS102 elements. Mol Gen Genet (1984) 0.93
Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay. Thromb Haemost (1993) 0.93
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII. J Thromb Haemost (2006) 0.93
A new approach to DNA polymerase kinetics. J Mol Biol (1979) 0.93
Clinical picture and management of congenital factor VII deficiency. Haemophilia (2004) 0.93
Protein S deficiency: a database of mutations--summary of the first update. Thromb Haemost (2000) 0.92
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
Sublocalization of the human protein C gene on chromosome 2q13-q14. Hum Genet (1989) 0.91
A double-blind study of L-sulpiride versus amitriptyline in lithium-maintained bipolar depressives. Acta Psychiatr Scand (1993) 0.91
Long-term low-dose dehydroepiandrosterone replacement therapy in aging males with partial androgen deficiency. Aging Male (2004) 0.91
Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma. Leukemia (1995) 0.91
Nosocomial bacterial pneumonia in HIV-infected patients: risk factors for adverse outcome and implications for rational empiric antibiotic therapy. Infection (2006) 0.91
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
Clinical outcome from mechanical intermittent cervical traction for the treatment of cervical radiculopathy: a case series. J Orthop Sports Phys Ther (2001) 0.90
Thrombosis in inherited factor VII deficiency. J Thromb Haemost (2003) 0.90
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma. Arterioscler Thromb Vasc Biol (1996) 0.89
Circadian rhythms, athletic performance, and jet lag. Br J Sports Med (1998) 0.89
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Hum Genet (1993) 0.89
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
Resistance to activated protein C in healthy women taking oral contraceptives. Br J Haematol (1995) 0.89
Tibolone, transdermal estradiol or oral estrogen-progestin therapies: effects on circulating allopregnanolone, cortisol and dehydroepiandrosterone levels. Gynecol Endocrinol (2005) 0.89
Cyclic GMP-dependent inhibition of acid sphingomyelinase by nitric oxide: an early step in protection against apoptosis. Cell Death Differ (2002) 0.89
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
Molecular mechanisms of FVII deficiency: expression of mutations clustered in the IVS7 donor splice site of factor VII gene. Blood (1998) 0.89