Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Omer S M, Suliman"'
Autor:
Omer S M, Suliman, Mustafa A M, Salih, Zein A, Karrar, Abdelrahim O, Mohammed, Chrestover, Helsing
Publikováno v:
Sudanese journal of paediatrics. 11(1)
The pre-dietary rehabilitation levels of acute phase proteins (APP) namely, alpha-1-antitrypsin (AAT), orosomucoid (ORO), haptoglobin (HAP), fibrinogen (FIB) and C-reactive protein (CRP) in the plasma of Sudanese children with severe protein energy m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::589468eca8334210c0300171c4cdd07a
https://pubmed.ncbi.nlm.nih.gov/27493306
https://pubmed.ncbi.nlm.nih.gov/27493306
Autor:
Omer S M, Suliman, Mustafa A M, Salih, Zein A, Karrar, Abdelrahim O, Mohammed, Chrestover, Helsing
Publikováno v:
Sudanese journal of paediatrics. 11(2)
A hospital-based case control study was carried out to determine the pattern of infections and immunoblobulin levels in Sudanese children with severe protein energy malnutrition (PEM). The pre-dietary rehabilitation levels of the three major immunogl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::22a22bbe2f80f2d7467a7869bdfdb17c
https://pubmed.ncbi.nlm.nih.gov/27493317
https://pubmed.ncbi.nlm.nih.gov/27493317
Autor:
Wim Van Hul, Adel H Suhaibani, Salah A. Elmalik, Thomas M. Bosley, Ibrahim A. Alorainy, Hattan Khiari, Bram Perdu, Liesbeth Van Wesenbeeck, Abdulmajeed AlDrees, Khaled K. Abu-Amero, M Zahidul Islam, Omer S M Suliman, Mustafa A. Salih, Sigri Beckers, Salem Al Malki, Darren T. Oystreck
Publikováno v:
Brain
Carbonic anhydrase type II deficiency syndrome is an uncommon autosomal recessive disease with cardinal features including osteopetrosis, renal tubular acidosis and brain calcifications. We describe the neurological, neuro-ophthalmological and neuror
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be31a3904e500a6c6beb62858767cfcf
https://pubmed.ncbi.nlm.nih.gov/22120147
https://pubmed.ncbi.nlm.nih.gov/22120147