Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Catarina B d'Alva"'
Autor:
Camila R. Muniz, Gabriela A. M. Bezerra, Viviane C. da Silva, Priscilla M. F. Aguiar, Gunter Gerson, Catarina B. D’Alva, André A. A. Nunes
Publikováno v:
Journal of Medical Case Reports, Vol 15, Iss 1, Pp 1-5 (2021)
Abstract Background Glomangioma is a benign tumor of mesenchymal origin, derived from the glomus body. It is responsible for the thermal regulation of the dermis. The occurrence of oncogenic osteomalacia related to glomangioma is rare. Only two cases
Externí odkaz:
https://doaj.org/article/20be530cd5bf4cc6a19cab66be0ba844
Autor:
Jérôme Bertherat, Lionel Groussin, Vivian Viallon, Gwenaelle Abiven-Lepage, Marie Annick Dugué, Catarina B d'Alva, Xavier Bertagna
Publikováno v:
European Journal of Endocrinology. 159:641-647
ObjectiveAdrenocortical tumors (ACT) account for no more than 0.2% of the causes of androgen excess (AE). Conversely, these rare tumors have a very poor prognosis. It is difficult and important to exclude this diagnosis whenever there is AE.DesignRet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b00c524de0e89b132a793491ff94cf4
https://doi.org/10.1530/eje-08-0324
https://doi.org/10.1530/eje-08-0324
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia. 46:593-600
A ocorrencia de hipoglicemia associada a hipopituitarismo e evento raro em pacientes adultos e um pouco mais frequente em criancas portadoras de disfuncao pituitaria semelhante. Nos pacientes portadores de insuficiencia adrenal, a hipoglicemia e mais
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::892c9c4aaa399089667573f869bcd839
https://doi.org/10.1590/s0004-27302002000500014
https://doi.org/10.1590/s0004-27302002000500014
Autor:
Catarina B. D’Alva, Filomena Marino Carvalho, Heloísa Marcelina da Cunha Palhares, Ivo J.P. Arnhold, Vinicius Nahime Brito, Berenice B. Mendonca, Ana Claudia Latronico
Publikováno v:
Clinical Endocrinology. 65:408-410
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32f6e016c270b2e78dce8945553bc83a
https://doi.org/10.1111/j.1365-2265.2006.02596.x
https://doi.org/10.1111/j.1365-2265.2006.02596.x
Autor:
Eitan Friedman, Juliana C. Sarubi, Daniela R. Faria, Catarina B. D’Alva, Luiz De Marco, Bernardo Léo Wajchenberg, W. L. Boson
Publikováno v:
Clinical Endocrinology. 58:108-110
Familial neurohypophysial diabetes insipidus (FNDI) is a rare autosomal dominant syndrome stemming from the absence of arginine vasopressin (AVP). More than thirty-five different germline mutations in the arginine vasopressin-neurophysin II gene have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0aa524490ebd1f12fb2810d2af86c446
https://doi.org/10.1046/j.1365-2265.2003.01667.x
https://doi.org/10.1046/j.1365-2265.2003.01667.x
Autor:
Wolfanga L, Boson, Juliana C, Sarubi, Catarina B, d'Alva, Eitan, Friedman, Daniela, Faria, Luiz, De Marco, Bernardo, Wajchenberg
Publikováno v:
Clinical endocrinology. 58(1)
Familial neurohypophysial diabetes insipidus (FNDI) is a rare autosomal dominant syndrome stemming from the absence of arginine vasopressin (AVP). More than thirty-five different germline mutations in the arginine vasopressin-neurophysin II gene have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3851fb7eb2ef7ba360473c0548b4f33a
https://pubmed.ncbi.nlm.nih.gov/12519420
https://pubmed.ncbi.nlm.nih.gov/12519420
Autor:
Berenice B. Mendonca, Ana Elisa C. Billerbeck, Catarina B. D’Alva, Ivo J.P. Arnhold, Ana Claudia Latronico, Emilia M. Pinto
Publikováno v:
Clinical Endocrinology. 59:533-534
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee128410a1d329ee0c8b36ed6e2f803d
https://doi.org/10.1046/j.1365-2265.2003.01810.x
https://doi.org/10.1046/j.1365-2265.2003.01810.x