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Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Helicobacter pylori infection and cytotoxic antigen associated gene "A" status in short childrenE Cacciari, M Menegatti, S Salardi, et al.European Journal of Histochemistry : EJH|June 20, 2001
Lymphocyte dysmetabolism: an immunocytochemical comparative approach in IDDM and control subjectsA Pugnaloni, G Sgarbi, M Tesei, et al.Pediatric Pulmonology|April 5, 2011
A rare association of inlet patch with laryngospasm: a report of two children and literature reviewE di Palmo, S Cazzato, S Tursini, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 1, 2001
Unresolved problems in optimal therapy of pubertal disorders in oncological and bone marrow transplanted patientsM Bozzola, A Albanese, G E Butler, et al.Journal of Endocrinological Investigation|June 6, 2009
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescenceS Bertelloni, A Balsamo, L Giordani, et al.Hormone Research|December 5, 1998
Androgens and fetal growthF de Zegher, I Francois, A L Boehmer, et al.Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.Pageof 16