Imad Dweikat - Department of Pediatrics, Makassed Islamic Hospital

基本信息

Career Trajectory

Bio

Imad Dweikat currently works at the Arab American University - Palestine. Imad does research in Metabolic diseases and Pediatrics . Their current project is 'Cyclin and CBS domain divalent metal cation transport mediators (CNNMs) and their cellular partners'.

Research Interests

Papers共 29 篇Author StatisticsCo-AuthorSimilar Experts

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Genetic, Clinical, and Biochemical Characterization of a Large Cohort of Palestinian Patients with Fanconi-Bickel Syndrome

Tamer Hodrob, Alaaeddin Abusalameh, Ibrahim Ismail,Imad Dweikat, Sarah Abu Rmeilah,Mutaz Sultan,Bassam Abu Libdeh, Abd-Al-Salam Abu Libdeh, Shaher Shweiki,Nadirah Damseh

Clinical genetics（2024）

Cited0Views0WOSBibtex

Reham Khalaf-Nazzal,Imad Dweikat,Nishanka Ubeyratna,James Fasham,Maysa Alawneh,Joseph Leslie,Mosab Maree,Adam Gunning, Deyala Z. Zayed,Nikol Voutsina,Lucy McGavin,Reem Sawafta,Martina Owens,Wisam Baker,Peter Turnpenny,Fida' Al-Hijawi,Emma L. Baple,Andrew H. Crosby,Lettie E. Rawlins

American Journal of Medical Genetics Part Ano. 7 (2024)

Cited1Views0WOSBibtex

Late Onset Hyperornithinemia, Hyperammonemia, and Homocitrullinuria Syndrome, Presenting As Recurrent Metabolic Encephalopathy, A Case Report

Fajr M. A. Sarhan,Afnan W. M. Jobran, Ali Fayyad,Zaid Ghanim,Imad Dweikat, Shireen Elewie, Ala Mustafa Habboub

Annals of Medicine and Surgery (2022)

Cited1Views0WOSBibtex

Clinical Heterogeneity of Hyperornithinemia-Hyperammonemia-homocitrullinuria Syndrome in Thirteen Palestinian Patients and Report of a Novel Variant in the SLC25A15 Gene

Imad Dweikat,Reham Khalaf-Nazzal

Frontiers in Genetics（2022）

Cited4Views0WOSBibtex

Prevalent MLC1 Mutation Causing Autosomal Recessive Megalencephalic Leukoencephalopathy in Consanguineous Palestinian Families

Reham Khalaf-Nazzal,Imad Dweikat,Mosab Maree,Maysa Alawneh, Myassar Barahmeh, Rasha T. Doulani, Mohammad Qrareya,Mohammad Qadi,Anwar Dudin

Brain and Development（2022）

Cited2Views0WOSBibtex

Niemann–Pick Disease Type C in Palestine: Genotype and Phenotype of Sixteen Patients and Report of a Novel Mutation in the NPC1 Gene

Dweikat Imad, Thaher Othman, Abosleem Abdulrahman,Zeer Almotazbellah, Mokh Ameer Abo

BMC Medical Genomics（2021）

Cited3Views0WOSBibtex

Phenotype, Genotype, and Outcome of 25 Palestinian Patients with Hereditary Tyrosinemia Type 1

Imad Dweikat,Nada Qawasmi, Aysha Najeeb,Mohammad Radwan

Metabolism open (2021): 100083-100083

Cited2Views0WOSBibtex

PNC2 (SLC25A36) Deficiency Associated with the Hyperinsulinism/Hyperammonemia Syndrome

Maher A. Shahrour,Francesco M. Lasorsa,Vito Porcelli,Imad Dweikat,Maria Antonietta Di Noia,Michal Gur,Giulia Agostino,Avraham Shaag,Teresa Rinaldi,Giuseppe Gasparre,Flora Guerra,Alessandra Castegna,Simona Todisco,Bassam Abu-Libdeh,Orly Elpeleg,Luigi Palmieri

The Journal of clinical endocrinology and metabolism/Journal of clinical endocrinology & metabolis...（2021）

Cited8Views0WOSBibtex

Genotype and clinical phenotype in four patients with glutathione synthetase deficiency

Firas Alqarajeh,Sadi A. Abukhalaf, Bara Hmeidat, Jacklyn O. Omorodion,Imad M. Dweikat

Meta Gene（2020）

Cited2Views0Bibtex

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