Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Andreina, Cattani"'
Autor:
Andreina Cattani Ortega
Publikováno v:
ARS Medica, Vol 20, Iss 3, Pp 174-178 (2017)
Sin resumen
Externí odkaz:
https://doaj.org/article/8c0cd2d6795a467cacd7ff0f6f1e56ee
Autor:
Andreina Cattani Ortega
Publikováno v:
ARS Medica, Vol 20, Iss 3, Pp 201-207 (2017)
Sin resumen
Externí odkaz:
https://doaj.org/article/e33a454b334d46b0a3b2fe764f598638
Autor:
Andreina Cattani Ortega
Publikováno v:
ARS Medica, Vol 20, Iss 3, Pp 182-187 (2017)
Sin resumen
Externí odkaz:
https://doaj.org/article/4aa6aa14619141a8b04acd349a5db609
Autor:
Andreina Cattani Ortega
Publikováno v:
ARS Medica, Vol 20, Iss 3, Pp 164-165 (2017)
Sin resumen
Externí odkaz:
https://doaj.org/article/da04d7b0ee5745d5a42efea8e4f9f37a
Autor:
Daniela Quiroga, María José Bruera, Josefa Vidaurre, Jaime Cerda, Andreina Cattani, Hernán García
Publikováno v:
Andes Pediatrica. 93:214
La pubertad precoz central consiste en una activación prematura del eje hipotálamo-hipófisis-gonadal, lo que produce una fusión temprana del cartílago de crecimiento y, en muchos casos, una talla inferior al objetivo genético. Un adecuado pron
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::194a5f0f31876567ca237d1253844c4e
https://doi.org/10.32641/andespediatr.v93i2.3503
https://doi.org/10.32641/andespediatr.v93i2.3503
Autor:
Daniela, Quiroga, María José, Bruera, Josefa, Vidaurre, Jaime, Cerda, Andreina, Cattani, Hernán, García
Publikováno v:
Andes pediatrica : revista Chilena de pediatria. 93(2)
Central precocious puberty is the premature activation of the hypothalamic-pituitary-gonadal axis, leading to an early epiphyseal fusion and, in many cases, heights below the genetic target. Therefore, a proper adult stature prediction is essential f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b5e8da92d73726d66c89ef53c77fb977
https://pubmed.ncbi.nlm.nih.gov/35735300
https://pubmed.ncbi.nlm.nih.gov/35735300
Autor:
Marcela Lagos, Andreina Cattani, Reyes L, Alejandro Martinez-Aguayo, Arriaza M, Hernan Garcia, Mariana Aracena, Cecilia Mellado, Vera A, H Rumié, Lacourt P, Teresa Aravena, Helena Poggi, Avalos C, Mericq, Godoy C
Publikováno v:
Hormone Research in Paediatrics. 84:254-257
Background: Deletions in the SHOX gene are the most frequent genetic cause of Leri-Weill syndrome and Langer mesomelic dysplasia, which are also present in idiopathic short stature. Aim: To describe the molecular and clinical findings observed in 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ef4e036fc58c16da63d0f790a76b2b8f
https://doi.org/10.1159/000439109
https://doi.org/10.1159/000439109
Autor:
Berenice B. Mendonca, Pedro Henrique Silveira Corrêa, Andreina Cattani, Mariana Tenorio Antunes Reis, Regina Matsunaga Martin
Publikováno v:
Arquivos Brasileiros de Endocrinologia & Metabologia. 54:728-731
The objective of this study was to describe a new mutation in GNAS in a family with pseudohypoparathyroidism type Ia (PHP Ia), a rare osteometabolic disease. An 8-month-old boy was seen by an Endocrinologist due to obesity and low growth velocity. No
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32af109ba7e13704b6a2151f9a66a096
https://doi.org/10.1590/s0004-27302010000800011
https://doi.org/10.1590/s0004-27302010000800011
Autor:
Ana Rocha, N. Rojas, Marcela Lagos, Helena Poggi, C. García, L. Valdivia, R. Parra, Andreina Cattani, Alejandro Martinez-Aguayo
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 92:4583-4589
Context: Infertility observed in adult males with congenital adrenal hyperplasia (CAH) has been associated with testicular adrenal rest tumors (TART) that may originate during childhood. Objective: Our objective was to describe the prevalence of TART
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7455b7343c276c1ad96e631d0bd63bac
https://doi.org/10.1210/jc.2007-0383
https://doi.org/10.1210/jc.2007-0383
Autor:
Helena, Poggi, Alejandra, Vera, Carolina, Avalos, Marcela, Lagos, Cecilia, Mellado, Mariana, Aracena, Teresa, Aravena, Hernan, Garcia, Claudia, Godoy, Andreina, Cattani, Loreto, Reyes, Patricia, Lacourt, Hana, Rumie, Veronica, Mericq, Marta, Arriaza, Alejandro, Martinez-Aguayo
Publikováno v:
Hormone research in paediatrics. 84(4)
Deletions in the SHOX gene are the most frequent genetic cause of Leri-Weill syndrome and Langer mesomelic dysplasia, which are also present in idiopathic short stature.To describe the molecular and clinical findings observed in 23 of 45 non-consangu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::592f42c9258b530c18895fb318ca8ec4
https://pubmed.ncbi.nlm.nih.gov/26337568
https://pubmed.ncbi.nlm.nih.gov/26337568