Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mustafa S. Al-Kahlout"'
Autor:
Mohammad E. Shubair, Mahmoud M. Sirdah, N. Scott Reading, Jamal M. Al-Tayeb, Mustafa S. Al-Kahlout, Josef T. Prchal
Publikováno v:
Hematology. 22:370-374
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked inherited enzymopathic disorder affecting more than 500 million people worldwide. It has so far been linked to 2...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d535a70d99a957fce317ba7230f3eee
https://doi.org/10.1080/10245332.2016.1276117
https://doi.org/10.1080/10245332.2016.1276117
Publikováno v:
Clinical Genetics. 90:191-198
Congenital genetic disorders affecting neonates or young children can have serious clinical consequences if undiagnosed and left untreated. Early detection and an accurate diagnosis are, therefore, of major importance for preventing negative patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8be3d0e845b19a84adc5e1279162cbaf
https://doi.org/10.1111/cge.12786
https://doi.org/10.1111/cge.12786
Autor:
Mahmoud M, Sirdah, Mohammad E, Shubair, Mustafa S, Al-Kahlout, Jamal M, Al-Tayeb, Josef T, Prchal, N Scott, Reading
Publikováno v:
Hematology (Amsterdam, Netherlands). 22(6)
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X-linked inherited enzymopathic disorder affecting more than 500 million people worldwide. It has so far been linked to 217 distinct genetic variants in the exons and exon-intron boundar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db23546e6c50af5582563c7e586ec532
https://pubmed.ncbi.nlm.nih.gov/28059001
https://pubmed.ncbi.nlm.nih.gov/28059001
Autor:
Lina N. Aboud, N. Scott Reading, Maysaa Abu Shaban, Lucio Luzzatto, Josef T. Prchal, Jamal M. Al-Tayeb, Benjamin W. Nelson, Mohammad E. Shubair, Mustafa S. Al-Kahlout, Mahmoud M. Sirdah
Publikováno v:
Blood cells, moleculesdiseases. 60
Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common genetic abnormality known to predispose to acute hemolytic anemia (AHA), which can be triggered by certain drugs or infection. However, the commonest trigger is fava beans (Vicia faba) i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3ac8b95f1d8b63bf60faa40940c1533
https://pubmed.ncbi.nlm.nih.gov/27519946
https://pubmed.ncbi.nlm.nih.gov/27519946