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Bernardo Liberman

Bernardo Liberman, Jewish Brazilian endocrinologist (193? –



DESCRIBED NEW SYNDROMES & GENETIC MUTATIONS CAUSING DISEASES

With R.A. Toledo, D.M. Lourenço Jr, F.L. Coutinho, S.P.A. Toledo, M.C.C. Machado et al. Novel MEN 1 germline mutations in Brazilian families with multiple endocrine neoplasia Type I. Clin. Endocr. 67(3):377-84, 2007

With J.L. Rocha, A. Moreira, F. Friedman, B.C. Silva & L. Marco. A novel polymorphism in the coding region of the vasopressin type 2 receptor gene. Braz. J. Med. Biol. Res. 30(4):443-5, 1997

With G. Medeiros Neto, C. Nogueira & C.K. Leite. Familial panhypopituitarism in a consanguineous family in Brazil: a novel type of genetic defect (1996) 

With M. Pinheiro, N. Freire-Maia, E. Chautard-Freire-Maia & L. Araujo AREDYLD: a syndrome combining an acrorenal field defect, ectodermal dysplasia, lipoatrophic diabetes, and other manifestations. Am J Med Genet. 16 (1): 29-33, 1983

With F.J. Modesto, C. Ventrella, S.D. Giannini, B.L. Wajchenberg & G. Hoxter. Lipoatrophic diabetes: a new variant characterized by tapeto-retinal degeneration, late onset, generalized lipoatrophy, insulin-resistant hyperglycemia and hyperlipidemia. Israel J. Med. Sciences 8(6):793, 1972