Literature DB >> 24030929

Sanfilippo syndrome, glucose-6-phosphate dehydrogenase deficiency and sickle cell/β+ thalassemia in a child: the burden of consanguinity.

Sarar Mohamed1.   

Abstract

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Year:  2013        PMID： 24030929     DOI： 10.1002/ajmg.a.36180

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN： 1552-4825            Impact factor:   2.802


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  3 in total

1.  Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients.

Authors:  Sarar Mohamed; Muddathir H Hamad; Khaled K Abu-Amero
Journal:  Saudi Med J       Date:  2015-09       Impact factor: 1.484

2.  Glucose-6-phosphate dehydrogenase deficiency among Yemeni children residing in malaria-endemic areas of Hodeidah governorate and evaluation of a rapid diagnostic test for its detection.

Authors:  Rashad Abdul-Ghani; Mohammed A K Mahdy; Reyadh Saif-Ali; Sameer A Alkubati; Abdulhabib R Alqubaty; Abdullah A Al-Mikhlafy; Samira M Al-Eryani; Abdusalam M Al-Mekhlafi; Ali Alhaj
Journal:  Malar J       Date:  2016-06-21       Impact factor: 2.979

3.  Glutaric aciduria type 1 as a cause of dystonic cerebral palsy.

Authors:  Sarar Mohamed; Muddathir H Hamad; Hamdy H Hassan; Mustafa A Salih
Journal:  Saudi Med J       Date:  2015-11       Impact factor: 1.484
  3 in total

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