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Imad Dweikat

Observed names: Dweikat Imad, Imad M. Dweikat, Imad Mohammad Dweikat, ImadMohammad Dweikat
ORCID: 0000-0002-2993-9957
Observed ORCID: 0000-0002-2993-9957
OpenAlex ID: A5079713554
Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathy
2010 · Carlo Viscomi, Alberto B Burlina, et al. · Nature Medicine · 155
Glutaric aciduria type 1: Clinical, biochemical and molecular findings in patients from Israel
2007 · Stanley H. Korman, Cornelis Jakobs, et al. · European Journal of Paediatric Neurology · 39
Mitochondrial PITRM1 peptidase loss-of-function in childhood cerebellar atrophy
2018 · Yeshaya Langer, Adi Aran, et al. · Journal of Medical Genetics · 38
A novel SLC25A20 splicing mutation in patients of different ethnic origin with neonatally lethal carnitine-acylcarnitine translocase (CACT) deficiency
2006 · Stanley H. Korman, James J. Pitt, et al. · Molecular Genetics and Metabolism · 23
Propionic acidemia mimicking diabetic ketoacidosis
2010 · Imad M. Dweikat, Enas N. Naser, et al. · Brain and Development · 22
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission
2023 · James Fasham, Antje K Huebner, et al. · Brain · 20
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Tricho‐hepato‐enteric syndrome: A case of hemochromatosis with intractable diarrhea, dysmorphic features, and hair abnormality
2007 · Imad Dweikat, Mutaz Sultan, et al. · American Journal of Medical Genetics Part A · 20
PNC2 (SLC25A36) Deficiency Associated With the Hyperinsulinism/Hyperammonemia Syndrome
2021 · Maher A Shahroor, Francesco M Lasorsa, et al. · The Journal of Clinical Endocrinology & Metabolism · 13
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Ethylmalonic encephalopathy associated with crescentic glomerulonephritis
2012 · Imad Dweikat, Enas Naser, et al. · Metabolic Brain Disease · 13
Fanconi-Bickel syndrome in two Palestinian children: marked phenotypic variability with identical mutation
2016 · Imad Mohammad Dweikat, Issa Shaher Alawneh, et al. · BMC Research Notes · 12
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MEGDEL Syndrome in a Child From Palestine: Report of a Novel Mutation in SERAC1 Gene
2014 · Imad M. Dweikat, Samer Abdelrazeq, et al. · Journal of Child Neurology · 11
Gm1 Gangliosidosis Associated With Neonatal-onset of Diffuse Ecchymoses and Mongolian Spots
2011 · Imad Dweikat, Bassam Abu Libdeh, et al. · Indian Journal of Dermatology · 11
TECPR2 ‐related hereditary sensory and autonomic neuropathy in two siblings from Palestine
2024 · Reham Khalaf‐Nazzal, Imad Dweikat, et al. · American Journal of Medical Genetics Part A · 7
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Severe persistent unremitting dermatitis, chronic diarrhea and hypoalbuminemia in a child; Hartnup disease in setting of celiac disease
2014 · Thomas Ciecierega, Imad Dweikat, et al. · BMC Pediatrics · 7
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Clinical heterogeneity of hyperornithinemia-hyperammonemia-homocitrullinuria syndrome in thirteen palestinian patients and report of a novel variant in the SLC25A15 gene
2022 · Imad Dweikat, Reham Khalaf-Nazzal · Frontiers in Genetics · 6
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Phenotype, genotype, and outcome of 25 Palestinian patients with hereditary tyrosinemia type 1
2021 · Imad Dweikat, Nada Qawasmi, et al. · Metabolism Open · 5
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Clinical heterogeneity of glycine encephalopathy in three Palestinian siblings: A novel mutation in the glycine decarboxylase ( GLDC ) gene
2017 · Waseem Khraim, Bassam Abu-Libdeh, et al. · Brain and Development · 5
Genotype and clinical phenotype in four patients with glutathione synthetase deficiency
2020 · Firas Alqarajeh, Sadi A. Abukhalaf, et al. · Meta Gene · 4
Prevalent MLC1 mutation causing autosomal recessive megalencephalic leukoencephalopathy in consanguineous Palestinian families
2022 · Reham Khalaf-Nazzal, Imad Dweikat, et al. · Brain and Development · 3
Niemann–Pick disease type C in Palestine: genotype and phenotype of sixteen patients and report of a novel mutation in the NPC1 gene
2021 · Imad Dweikat, Othman Thaher, et al. · BMC Medical Genomics · 3
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Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathy
2011 · Carlo Viscomi⁎, Alberto Burlina, et al. · Mitochondrion · 3
Late onset hyperornithinemia, hyperammonemia, and homocitrullinuria syndrome, presenting as recurrent metabolic encephalopathy, A case report
2022 · Fajr M A Sarhan, Afnan W.M. Jobran, et al. · Annals of Medicine and Surgery · 2
Whole exome sequencing reveals complex inheritance patterns and identifies two gene mutations implicated in the development of Autism and Intellectual Disability in a consanguineous Palestinian family
2016 · Khalaf-Nazzal Reham, Dweikat Imad, et al. · Frontiers in Neuroscience · 2
A distinct phenotype of childhood leukodystrophy presenting as absence seizure
2014 · ImadMohammad Dweikat, Nadera Damsah, et al. · Journal of Pediatric Neurosciences · 2
Molecular characterization, clinical phenotype, and neurological outcome of twelve Palestinian children with beta-ketothiolase deficiency: report of two novel variants in the ACAT1 gene
2025 · Imad M. Dweikat, Hamza A. Abdul-Hafez, et al. · BMC Medical Genomics · 1
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Works count: 38
Citation count: 428
H-index: 11
I10-index: 12
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