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European Journal of Endocrinology|April 8, 2011
AME position statement on adrenal incidentalomaM Terzolo, A Stigliano, I Chiodini, et al.
Human Mutation|October 26, 1999
Jagged-1 mutation analysis in Italian Alagille syndrome patientsG Pilia, M Uda, D Macis, et al.
Transplantation Proceedings|December 31, 2003
Liver transplantation for the management of hepatoblastomaU Cillo, F A Ciarleglio, M Bassanello, 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 13, 2003
Diagnosis and complications of Cushing's syndrome: a consensus statementG Arnaldi, A Angeli, A B Atkinson, 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.
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