Browsing by Author Dweikat, Imad$AAUP$Palestinian



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Showing results 1 to 5 of 5
Issue DateTitleAuthor(s)
2022-11-24CLINICAL HETEROGENEITY OF HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME IN THIRTEEN PALESTINIAN PATIENTS AND REPORT OF A NOVEL VARIANT IN THE SLC25A15 GENEDweikat, Imad$AAUP$Palestinian
2022-11-24Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 geneDweikat, Imad$AAUP$Palestinian; Khalaf-Nazzal, Reham$AAUP$Palestinian
2024-11-04Genetic, Clinical, and Biochemical Characterization of a Large Cohort of Palestinian Patients With Fanconi-Bickel SyndromeDweikat, Imad$AAUP$Palestinian; Hodrob, Tamer$AAUP$Palestinian; Abusalameh; Ismail, Ibrahim$AAUP$Palestinian; Abu Rmeilah, Sarah$AAUP$Palestinian; Sultan, Mutaz$AAUP$Palestinian; Abu Libdeh, Bassam$AAUP$Palestinian; Abu Libdeh; Shweiki, Shaher$AAUP$Palestinian; Damseh
2021-09-17Niemann–Pick disease type C in Palestine: genotype and phenotype of sixteen patients and report of a novel mutation in the NPC1 geneDweikat, Imad$AAUP$Palestinian
2024-03-04TECPR2-related hereditary sensory and autonomic neuropathy in two siblings from PalestineKhalaf-nazzal, Reham$AAUP$Palestinian; Dweikat, Imad$AAUP$Palestinian; Al-Hijawi, Fida'$Other$Palestinian; Baker, Wisam$Other$Palestinian; Alawneh, Maysa'$Other$Palestinian; Sawafta, Reem$Other$Palestinian; Maree, Mosab$Other$Palestinian; Turnpenny, Peter$Other$Other; Baple, Emma$Other$Other; Crosby, Andrew$Other$Other; Fasham, James$Other$Other; Ubeyratna, Nishanka$Other$Other; Gunning, Adam$Other$Other; Voutsina, Nikol$Other$Other; McGavin, Lucy$Other$Other; Rawlin, Lettie$Other$Other