Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Barbara Iwaniszewska"'
Autor:
Aleksandra Rojek, Maciej R. Krawczynski, Aleksander Jamsheer, Anna Sowinska-Seidler, Barbara Iwaniszewska, Ewa Malunowicz, Marek Niedziela
Publikováno v:
International Journal of Endocrinology, Vol 2016 (2016)
X-linked Adrenal Hypoplasia Congenita (AHC) is caused by deletions or point mutations in the NR0B1 (DAX1) gene. We present a boy with AHC who came at the age of 25 days in a severe state due to prolonged vomiting and progressive dehydration. Laborato
Externí odkaz:
https://doaj.org/article/5396c66c2ffc447b80f4aeb6bbc066ce
Autor:
Ewa Malunowicz, Barbara Iwaniszewska, Maciej R Krawczyński, Aleksander Jamsheer, Marek Niedziela, Aleksandra Rojek, Anna Sowińska-Seidler
Publikováno v:
International Journal of Endocrinology, Vol 2016 (2016)
International Journal of Endocrinology
International Journal of Endocrinology
X-linked Adrenal Hypoplasia Congenita (AHC) is caused by deletions or point mutations in theNR0B1 (DAX1)gene. We present a boy with AHC who came at the age of 25 days in a severe state due to prolonged vomiting and progressive dehydration. Laboratory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfb494f6dd7e29144e44a0cdeb8ebe9d
https://doaj.org/article/5396c66c2ffc447b80f4aeb6bbc066ce
https://doaj.org/article/5396c66c2ffc447b80f4aeb6bbc066ce
Autor:
Magdalena, Zbikowska-Bojko, Anna, Szaflarska-Popławska, Olgierd, Pilecki, Dorota, Charemska, Barbara, Iwaniszewska, Irena, Nowak, Mieczysława, Czerwionka-Szaflarska
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 20(117)
Modern serological tests and changed clinical appearance are the causes of more frequent occurrence of celiac disease (CD) in general population, also in risk groups for instance in patients suffering from diabetes mellitus type 1 (DM t. 1). The aim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8d29a15ed880a55d3a3d0cf1d26643ca
https://pubmed.ncbi.nlm.nih.gov/16780266
https://pubmed.ncbi.nlm.nih.gov/16780266