Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Adel A. Kareem"'
Autor:
Adel A. Kareem
Publikováno v:
مجله كليه طب الكندي, Vol 13, Iss 1 (2019)
Background:Amino acid disorders are a major group of inborn error metabolism (IEM) with variable clinical presentation; its diagnosis constitutes a real challenge in a community with high consanguinity rate and no systematic newborn screening. Obj
Externí odkaz:
https://doaj.org/article/d59e92997f174460a282a14a507b505d
Publikováno v:
Journal of Contemporary Medical Sciences, Vol 2, Iss 7, Pp 107-110 (2016)
Background Maple syrup urine disease (MSUD) is a rare inborn error of metabolism, caused by a deficiency in the activity of the branched chain alpha-keto acid dehydrogenase impairing the degradation of the branched chain amino acids (leucine, isoleuc
Externí odkaz:
https://doaj.org/article/05396d690a2b45ae88498741d7f7ab75
Autor:
Adel Abdel-Kareem Badawy, Tarek Mohamed El Saba, Mohammad Abdel -Hakeem Seleem, Sara Salah Gaffer
Publikováno v:
International Neuropsychiatric Disease Journal. :17-28
Aims: To evaluate SD in depressed married premenopausal women and to study mood in married women with primary sexual complain. Study Design: Cross-sectional case control research. Place and Duration of Study: Neuropsychiatry and Obstetrics and Gyneco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a493b01ce918f52992ca57814ec9df9
https://doi.org/10.9734/indj/2022/v17i330202
https://doi.org/10.9734/indj/2022/v17i330202
Publikováno v:
AL-Kindy College Medical Journal. 13:39-45
Background:Amino acid disorders are a major group of inborn error metabolism (IEM) with variable clinical presentation; its diagnosis constitutes a real challenge in a community with high consanguinity rate and no systematic newborn screening. Object
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7852b5c27c85c58977e608215559291
https://doi.org/10.47723/kcmj.v13i1.121
https://doi.org/10.47723/kcmj.v13i1.121
Autor:
Franz Grill, Ali Al Kaissi, Rudolf Ganger, Polina Ochirova, S. O. Ryabykh, Vladimir Kenis, Susanne Gerit Kircher, Adel A Kareem
Publikováno v:
Minerva pediatrica.
Background Maroteaux-Lamy disease (MPS Type VI) is an autosomal recessive lysosomal storage disorder. Skeletal abnormalities are vast. Early recognition may facilitate timely diagnosis and intervention, leading to improved patient outcomes. The most
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::030cd364b5ae820c10cef9533878baec
https://pubmed.ncbi.nlm.nih.gov/32748606
https://pubmed.ncbi.nlm.nih.gov/32748606
Autor:
Adel A. Kareem
Publikováno v:
Cerebral Palsy-Clinical and Therapeutic Aspects
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29eea46ae73f5eb4f4b486c7bdbb5388
http://www.intechopen.com/articles/show/title/use-of-botulinum-toxin-a-in-cerebral-palsy
http://www.intechopen.com/articles/show/title/use-of-botulinum-toxin-a-in-cerebral-palsy
