Zobrazeno 1 - 10
of 93
pro vyhledávání: '"Knobel,Meyer"'
Autor:
Duarte, Glaucia C., Tomimori, Eduardo K., Camargo, Rosalinda Y.A., Rubio, Ileana G.S., Wajngarten, Mauricio, Rodrigues, Amanda G., Knobel, Meyer, Medeiros-Neto, Geraldo *
Publikováno v:
In Clinics February 2009 64(2):135-142
Publikováno v:
In Clinics August 2007 62(4):411-418
Autor:
Camargo, Rosalinda Y.A., Tomimori, Eduarto K., Neves, Solange C., Knobel, Meyer, Medeiros-Neto, Geraldo
Publikováno v:
In Clinics 2006 61(4):307-312
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Neves, Solange Caires, Mezalira, Paola Rossi, Dias, Vera M. A., Chagas, Antonio J., Viana, Maria, Targovnik, Hector, Knobel, Meyer, Medeiros-Neto, Geraldo, Rubio, Ileana G. S.
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.54 n.8 2010
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 54, Issue: 8, Pages: 732-737, Published: NOV 2010
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 54, Issue: 8, Pages: 732-737, Published: NOV 2010
The aim of this study was to identify the genetic defect of a patient with dyshormonogenetic congenital hypothyroidisms (CH) with total iodide organification defect (TIOD). A male child diagnosed with CH during neonatal screening. Laboratory tests co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::76b999603e3f503625d26a51f6f07588
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302010000800012
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302010000800012
Autor:
Rubio, Ileana G. S., Galrao, Ana Luiza, Pardo, Viviane, Knobel, Meyer, Possato, Roberta F., Camargo, Rosalinda R. Y., Ferreira, Marcelo A., Kanamura, Cristina T., Gomes, Simone A., Medeiros-Neto, Geraldo
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 52, Issue: 8, Pages: 1337-1344, Published: NOV 2008
OBJECTIVE: To extend the molecular analysis of the IVS30+1G>T intronic thyroglobulin (TG) mutation, and to report the eleven year follow-up of the affected patients. METHOSD: Two siblings with severe congenital hypothyroidism with fetal and neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::ad9912334c7a23675a2c6dc83712537f
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302008000800022&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302008000800022&lng=en&tlng=en
Autor:
Rubio,Ileana G. S., Galrao,Ana Luiza, Pardo,Viviane, Knobel,Meyer, Possato,Roberta F., Camargo,Rosalinda R. Y., Ferreira,Marcelo A., Kanamura,Cristina T., Gomes,Simone A., Medeiros-Neto,Geraldo
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia v.52 n.8 2008
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
Arquivos Brasileiros de Endocrinologia & Metabologia
Sociedade Brasileira de Endocrinologia e Metabologia (SBEM)
instacron:SBEM
OBJECTIVE: To extend the molecular analysis of the IVS30+1G>T intronic thyroglobulin (TG) mutation, and to report the eleven year follow-up of the affected patients. METHOSD: Two siblings with severe congenital hypothyroidism with fetal and neonatal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::ad9912334c7a23675a2c6dc83712537f
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302008000800022
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302008000800022
Autor:
Knobel, Meyer
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::7a2e6549c8d5e19212f4c5ba7e5a34a8
http://www.springerlink.com/content/35181362741j042u/fulltext.pdf
http://www.springerlink.com/content/35181362741j042u/fulltext.pdf
Autor:
Knobel, Meyer, Medeiros-Neto, Geraldo
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 51, Issue: 5, Pages: 701-712, Published: JUL 2007
Iodine is a trace element that is essential for the synthesis of thyroid hormone. Both chronic iodine deficiency and iodine excess have been associated with hypertrophy and hyperplasia of follicular cells, attributed to excessive secretion of TSH. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::9a1c662d52d4dae3d87f5947186bbc42
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302007000500007&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302007000500007&lng=en&tlng=en
Autor:
Lima, Nicolau, Knobel, Meyer, Camargo, Rosalinda Y., Tomimori, Eduardo, Medeiros-Neto, Geraldo
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia, Volume: 49, Issue: 4, Pages: 575-583, Published: AUG 2005
O objetivo do presente estudo foi avaliar esquema terapêutico medicamentoso para aumentar a aderência ao tratamento da moléstia de Graves-Basedow (MGB) em Hospital Público Universitário. Os pacientes foram selecionados segundo critérios rigoros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______608::5c7644d5aadff5434d2579b0cdfc8af8
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000400017&lng=en&tlng=en
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27302005000400017&lng=en&tlng=en