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pro vyhledávání: '"Najada Abdul"'
Autor:
Hazza Issa, Najada Abdul
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 10, Iss 2, Pp 171-174 (1999)
Galloway-Mowat Syndrome (GMS) has a wide variety of clinical manifestations and histologic findings. All reported cases had developed nephrotic syndrome in the first two years of life. We report a case of 12 years old boy with microcephaly, mental re
Externí odkaz:
https://doaj.org/article/3c6c861917824d9a89bd9a203cd74b00
Autor:
Khriesat, Imad1 imad-k@lycos.com, Najada, Abdul Hameed2
Publikováno v:
European Journal of Pediatrics. 2003, Vol. 162 Issue 12, p868-871. 4p.
Publikováno v:
Saudi Journal of Kidney Diseases and Transplantation, Vol 11, Iss 1, Pp 53-58 (2000)
Wolfram′s syndrome is usually considered as an autosomal recessive condition, with wide phenotypic variation. The syndrome is commonly called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy and deafness), although some patients have a
Externí odkaz:
https://doaj.org/article/f7d96c937bf44b1584e722b689a46817