Published in Acta Endocrinol (Copenh) on September 01, 1976
Luteinising hormone-releasing hormone nasal spray as therapy for undescended testicle. Arch Dis Child (1978) 0.89
Hormonal regulation of testicular descent. Eur J Pediatr (1987) 0.75
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). J Endocrinol Invest (2006) 3.17
Complement functional tests for monitoring eculizumab treatment in patients with atypical hemolytic uremic syndrome. J Thromb Haemost (2014) 2.38
Complete sequence of pSC101. Nucleic Acids Res (1984) 2.22
Cohort study of association of risk of breast cancer with cyst type in women with gross cystic disease of the breast. BMJ (1997) 2.21
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
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
Hypertension-associated point mutations in the adducin alpha and beta subunits affect actin cytoskeleton and ion transport. J Clin Invest (1996) 1.83
Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost (1998) 1.71
Circulating levels of allopregnanolone in humans: gender, age, and endocrine influences. J Clin Endocrinol Metab (1998) 1.63
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma. Thromb Haemost (1996) 1.51
Younger age at diagnosis of type 1 diabetes mellitus in children of immigrated families born in Italy. J Endocrinol Invest (2004) 1.49
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
Does factor V Asp79His (409 G/C) polymorphism influence factor V and APC resistance levels? J Thromb Haemost (2005) 1.38
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
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
Thyroid abnormalities during lithium treatment. Acta Psychiatr Scand (1991) 1.18
Two point mutations within the adducin genes are involved in blood pressure variation. Proc Natl Acad Sci U S A (1994) 1.17
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
Can antigliadin antibody detect symptomless coeliac disease in children with short stature? Lancet (1985) 1.14
Evidence for an interaction between adducin and Na(+)-K(+)-ATPase: relation to genetic hypertension. Am J Physiol (1999) 1.08
Preferential maternal derivation in inv dup(15): analysis of eight new cases. Hum Genet (1981) 1.08
Pelvic organs in premenarcheal girls: real-time ultrasonography. Radiology (1984) 1.08
Blood alcohol concentration and management of road trauma patients in the emergency department. J Trauma (2001) 1.07
Empty sella in children and adolescents with possible hypothalamic-pituitary disorders. J Clin Endocrinol Metab (1994) 1.06
Gene expression from viral RNA genomes. Plant Mol Biol (1996) 1.05
Gene deletion in an Italian haemophilia B subject. J Med Genet (1985) 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
Congenital adrenal hyperplasia: neonatal mass screening compared with clinical diagnosis only in the Emilia-Romagna region of Italy, 1980-1995. Pediatrics (1996) 1.03
The frequency of oligonucleotides in mammalian genic regions. Comput Appl Biosci (1989) 1.03
Serum immunoglobulins and lymphocyte subpopulations derangement in Turner's syndrome. J Immunogenet (1981) 1.03
Gene dosage imbalances in patients with 46,XY gonadal DSD detected by an in-house-designed synthetic probe set for multiplex ligation-dependent probe amplification analysis. Clin Genet (2008) 1.02
Allopregnanolone concentrations and premenstrual syndrome. Eur J Endocrinol (2000) 0.99
Narcolepsy-cataplexy associated with precocious puberty. Neurology (2006) 0.99
Construction in vitro of hybrid plasmids carrying all the EcoRI fragments from lambdarifd18 DNA. Eur J Biochem (1979) 0.99
Measurement of body fat in healthy elderly men: a comparison of methods. J Gerontol A Biol Sci Med Sci (1999) 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
Pelvic ultrasonography in premenarcheal girls: relation to puberty and sex hormone concentrations. Arch Dis Child (1985) 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
Co-localization of rare oligonucleotides and regulatory elements in mammalian upstream gene regions. J Mol Biol (1988) 0.97
Plasma testosterone and estradiol concentration in prepubertal boys with cryptorchidism before and after dexamethasone and after human chorionic gonadotropin administration. Helv Paediatr Acta (1974) 0.96
Abnormal insulin response to glucose following treatment for Wilms' tumor in childhood. Eur J Pediatr (1997) 0.96
Value of family history in identifying women at risk of venous thromboembolism during oral contraception: observational study. BMJ (2001) 0.96
Types, stability, and phenotypic consequences of chromosome rearrangements leading to interstitial telomeric sequences. J Med Genet (1993) 0.95
Pelvic ultrasonography in girls with precocious puberty, congenital adrenal hyperplasia, obesity, or hirsutism. J Pediatr (1988) 0.95
Value and limits of pharmacological and physiological tests to diagnose growth hormone (GH) deficiency and predict therapy response: first and second retesting during replacement therapy of patients defined as GH deficient. J Clin Endocrinol Metab (1994) 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
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
Atypical deletions generated by mutated IS102 elements. Mol Gen Genet (1984) 0.93
Clinical picture and management of congenital factor VII deficiency. Haemophilia (2004) 0.93
Short stature and celiac disease: a relationship to consider even in patients with no gastrointestinal tract symptoms. J Pediatr (1983) 0.93
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII. J Thromb Haemost (2006) 0.93
Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay. Thromb Haemost (1993) 0.93
A new approach to DNA polymerase kinetics. J Mol Biol (1979) 0.93
Protein S deficiency: a database of mutations--summary of the first update. Thromb Haemost (2000) 0.92
Gonadal function and pubertal development after treatment of a childhood malignancy. J Pediatr Endocrinol Metab (2003) 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
Molecular cloning of an adducin-like protein: evidence of a polymorphism in the normotensive and hypertensive rats of the Milan strain. Biochem Biophys Res Commun (1991) 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
Sublocalization of the human protein C gene on chromosome 2q13-q14. Hum Genet (1989) 0.91
Interphase fluorescence in situ hybridization (FISH) as a powerful tool for the detection of aneuploidy in multiple myeloma. Leukemia (1995) 0.91
Renal Na,K-ATPase in genetic hypertension. Hypertension (1996) 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
Final height of patients treated for isolated GH deficiency: examination of 83 patients. Eur J Endocrinol (1997) 0.90
Thrombosis in inherited factor VII deficiency. J Thromb Haemost (2003) 0.90
D8S7 is consistently deleted in inverted duplications of the short arm of chromosome 8 (inv dup 8p). Hum Genet (1993) 0.89