Zobrazeno 1 - 10
of 18
pro vyhledávání: '"JAYME GOLDMAN"'
Autor:
MARCELO MIRANDA, LUCIANA BARROS, MIRTA KNOPFELMACHER, ELIANA C. AUGUSTO, ANGELO JACOMOSSI, ARTHUR CUKIERT, LUIS R. SALGADO, MARCIA NERY, JAYME GOLDMAN, BERNARDO LIBERMAN
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 56, Iss 3A, Pp 449-452 (1998)
A apoplexia pituitária é evento raro e a ocorrência de remissão endócrina em pacientes portadores de tumores secretores é ainda mais incomum. O presente estudo relata os casos de dois pacientes portadores de macroadenomas (um com doença de Cus
Externí odkaz:
https://doaj.org/article/01de136c99ab4e5a9c2e4a14d6dd6637
Autor:
MARCELO MAIA PINHEIRO, BERNARDO LIBERMAN, LUIS ROBERTO SALGADO, JAYME GOLDMAN, MARCIA NERY, ARTHUR CUKIERT
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 57, Iss 3A, Pp 686-688 (1999)
A doença de Cushing é rara em crianças e sua ocorrência em gêmeos é ainda mais rara. O presente estudo relata a ocorrência de gêmeas idênticas discordantes quanto à doença de Cushing. Uma das gêmeas, desenvolveu síndrome de Cushing aos 1
Externí odkaz:
https://doaj.org/article/0f4a24fcbede48aeb699253c9f7f766c
Autor:
Luis R. Salgado, Arthur Cukiert, Jayme Goldman, Fernando Pimentel, Marcelo de Medeiros Pinheiro, Bernardo Liberman, Marcia Nery
Publikováno v:
Arquivos de Neuro-Psiquiatria v.57 n.1 1999
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 57, Iss 1, Pp 74-77 (1999)
Arquivos de Neuro-Psiquiatria, Volume: 57, Issue: 1, Pages: 74-77, Published: MAR 1999
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 57, Iss 1, Pp 74-77 (1999)
Arquivos de Neuro-Psiquiatria, Volume: 57, Issue: 1, Pages: 74-77, Published: MAR 1999
Apoplexia pituitária aguda é fenômeno relativamente raro, mesmo em macroadenomas. No entanto, a presença de áreas necro-hemorrágicas intratumorais nestes tumores que não se relacionam a qualquer sintomatologia aguda parece ser bem mais frequen
Autor:
Bernardo Liberman, Angelo Jacomossi, Mirta Knopfelmacher, Jayme Goldman, Luciana Barros, Eliana C. Augusto, Luis R. Salgado, Arthur Cukiert, Marcia Nery, Marcelo Miranda
Publikováno v:
Arquivos de Neuro-Psiquiatria v.56 n.3A 1998
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 56, Issue: 3A, Pages: 449-452, Published: SEP 1998
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Volume: 56, Issue: 3A, Pages: 449-452, Published: SEP 1998
A apoplexia pituitária é evento raro e a ocorrência de remissão endócrina em pacientes portadores de tumores secretores é ainda mais incomum. O presente estudo relata os casos de dois pacientes portadores de macroadenomas (um com doença de Cus
Autor:
Bernardo Liberman, Jayme Goldman, A. A. Bosco, A. C. Lerario, Bernardo Leo Wajchenberg, S. Levin, M. M. Marone, Marcia Nery, Manoel de Souza Rocha
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 80:2791-2794
Body composition determined by dual energy x-ray absorptiometry and the abdominal visceral fat component determined by computed tomographic scanning were examined in women with Cushing's disease and compared with those in obese women with the same an
Autor:
Jayme Goldman, Luiz Roberto Salgado, Bernardo Léo Wajchenberg, Mirta Knoepfelmacher, M Semer, Bernardo Liberman, Ana Maria Crous Tsanaclis, Berenice B. Mendonca
Publikováno v:
Endocrine Pathology. 6:57-66
Nodular corticotrope hyperplasia is a rare pathology causing Cushing's syndrome owing to a primary pituitary disease or ectopic CRH production. In this study, we evaluated the laboratory and pathological findings and results of transsphenoidal pituit
Autor:
Ana Teresa Santomauro, Brock A. Beamer, Soren Snitker, Chung-Jen Yen, Bernardo Leo Wajchenberg, Jayme Goldman, Rasa Kazlauskaite, Kristi D. Silver, Alan R. Shuldiner
Publikováno v:
Clinical Endocrinology. 54:412-414
Sirs, Congenital generalized lipodystrophy (CGL) is an autosomal recessive disorder, characterized by severe metabolic derangement associated with the absence of subcutaneous adipose tissue. The exact genetic defect is unknown, and systematic studies
Autor:
Bernardo Liberman, Marcelo Maia Pinheiro, Arthur Cukiert, Jayme Goldman, Luis R. Salgado, Marcia Nery
Publikováno v:
Arquivos de Neuro-Psiquiatria. 57:686-688
Cushing's disease is rare in children and its ocurrence in identical twins is extremely rare. This paper reports on identical twins discordant for Cushing's disease. One of them first presented with a cushingoid phenotype by the age of 10. Her evalua
Autor:
Arthur Cukiert, Bernardo Liberman, Mirta Knoepfelmacher, Luis R. Salgado, Mario Sergio Duarte Andrioli, Fernando Pimentel, Jayme Goldman, Marcia Nery
Publikováno v:
Arquivos de Neuro-Psiquiatria, Volume: 56, Issue: 1, Pages: 107-110, Published: MAR 1998
Arquivos de Neuro-Psiquiatria, Vol 56, Iss 1, Pp 107-110 (1998)
Arquivos de Neuro-Psiquiatria v.56 n.1 1998
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
Arquivos de Neuro-Psiquiatria, Vol 56, Iss 1, Pp 107-110 (1998)
Arquivos de Neuro-Psiquiatria v.56 n.1 1998
Arquivos de neuro-psiquiatria
Academia Brasileira de Neurologia
instacron:ABNEURO
The classical imaging gold-standard for this diagnosis is the presence of tumor lateral to the carotid artery. Seventeen patients with pituitary macroadenomas with intraoperative confirmation of cavernous sinus invasion were studied with MRI. Only 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::906d07c35f835dc22edc49765d20700f
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1998000100017&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-282X1998000100017&lng=en&tlng=en
Autor:
S. S. Achando, Bernardo Léo Wajchenberg, Jayme Goldman, Y. L. Thomsen, S. S. Lima, T. S. Kyan
Publikováno v:
Clinical Endocrinology. 13:401-404
SUMMARY Four patients with untreated congenital virilizing adrenal hyper-plasia (partial 21-hydroxylase deficiency) were studied by bilateral adrenal vein catheterization. Simultaneous right and left adrenal and peripheral blood samples were collecte