Zobrazeno 1 - 8 of 8 pro vyhledávání: '"M C L Ezabella"'
1
Sporadic Medullary Thyroid Carcinoma: Clinical Data From A University Hospital
Autor: Joya E. M. Correia-Deur, M C L Ezabella, Delmar M. Lourenço, Sergio P. A. Toledo, Rodrigo A. Toledo, Alice Takimoto Imazawa, Marcos Tavares
Publikováno v: Clinics, Vol 64, Iss 5, Pp 379-386 (2009)
Clinics; v. 64 n. 5 (2009); 379-386
Clinics; Vol. 64 Núm. 5 (2009); 379-386
Clinics; Vol. 64 No. 5 (2009); 379-386
Clinics
Universidade de São Paulo (USP)
instacron:USP
Clinics, Volume: 64, Issue: 5, Pages: 379-386, Published: MAY 2009
Clinics (Sao Paulo, Brazil)
INTRODUCTION: Medullary thyroid carcinoma may occur in a sporadic (s-medullary thyroid carcinoma, 75%) or in a multiple endocrine neoplasia type 2 form (MEN2, 25%). These clinical forms differ in many ways, as s-medullary thyroid carcinoma cases are
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b14f6a030c9cc42cbaa28ebd58130d9c
https://doi.org/10.1590/s1807-59322009000500002
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2
Rastreamento gênico da neoplasia endócrina múltipla tipo 2: experiência da Unidade de Endocrinologia Genética da USP
Autor: Delmar Muniz Lourenço Junior, C Y Hayashida, Marcelo dos Santos, N M A Abelin, Sergio P. A. Toledo, M C L Ezabella, Ivone Izabel Mackowiak da Fonseca, Rodrigo A. Toledo, Adriana Bezerra Nunes
Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia. 50:7-16
A neoplasia endócrina múltipla tipo 2 (NEM-2) é uma síndrome tumoral hereditária que compreende: carcinoma medular de tireóide, hiperparatiroidismo primário, feocromocitoma e outras doenças não-endócrinas. Desde a identificação das primei
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cc75b915d6ed21c245e7b4159dd8bd5e
https://doi.org/10.1590/s0004-27302006000100003
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3
Abordagem clínica e laboratorial do bócio uninodular sólido: vantagens da determinação da calcitonina sérica por métodos distintos no rastreamento do carcinoma medular de tireóide, forma esporádica
Autor: Maria Tereza Ivanoff, Sergio P. A. Toledo, M C L Ezabella, N M A Abelin, C Y Hayashida, Susimeire Gomes
Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia. 43:104-113
A apresentação clínica mais freqüente da forma esporádica do carcinoma medular da tireóide (CMT) é o bócio uninodular sólido (BUS), apresentação esta semelhante aos demais tumores que afetam a glândula. O estabelecimento da freqüência d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c0406fdd9385ab468a8abca323a0cb24
https://doi.org/10.1590/s0004-27301999000200006
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4
Carcinoma medular da tireóide
Autor: C Y Hayashida, Sergio P. A. Toledo, M C L Ezabella, N M A Abelin
Publikováno v: Arquivos Brasileiros de Endocrinologia & Metabologia. 42:310-322
CARCINOMA MEDULAR DA TIREOIDE (CMT), identificado inicialmentecomo entidade clinico-patologica, em 1959, por Hazard e cols.(l)deriva das celulas C, produtoras de calcitonina. Tem caracteristicas especi-ficas como presenca de material amiloide, alta i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::69c4d82f085c5e49a845d86ac5088e39
https://doi.org/10.1590/s0004-27301998000400013
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5
A novel Val648Ile substitution in RET protooncogene observed in a Cys634Arg multiple endocrine neoplasia type 2A kindred presenting with an adrenocorticotropin-producing pheochromocytoma
Autor: M C L Ezabella, José Eduardo Krieger, Alexandre C. Pereira, Sergio P. A. Toledo, Adriana Bezerra Nunes
Publikováno v: The Journal of clinical endocrinology and metabolism. 87(12)
Multiple endocrine neoplasia type 2 (MEN 2) comprises a heterogeneous group of neoplasic disorders that most commonly have a single missense substitution of the RET protooncogene (RET) involving exons 10 and 11. It was previously reported a MEN 2A ki
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::262752e82b6b5cf7bc7711482b0e7f7c
https://pubmed.ncbi.nlm.nih.gov/12466368
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6
A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia: correlation between receptor activity and phenotype
Autor: M C L Ezabella, N M A Abelin, John W.M. Martens, Sergio P. A. Toledo, Han G. Brunner, Axel P. N. Themmen, Miriam Verhoef-Post
Publikováno v: Molecular endocrinology (Baltimore, Md.). 12(6)
Leydig cell hypoplasia (LCH) is characterized by a decreased response of the Leydig cells to LH. As a result, patients with this syndrome display aberrant male development ranging from complete pseudohermaphroditism to males with micropenis but with
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d03f90c0673e30028681bf0b20345941
https://pubmed.ncbi.nlm.nih.gov/9626653
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