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Motaz Altamimi

Observed names: Mu'taz Altamimi, Mutaz Altamimi, Mu’taz Altamimi
Institution: Hebron University
ORCID: 0009-0004-8811-3559
Observed ORCID: 0009-0004-8811-3559
OpenAlex ID: A5116717072
Congenital glucose‐galactose malabsorption: A case report with a novel SLC5A1 mutation
2018 · Manar Al‐lawama, Jumana Albaramki, et al. · Clinical Case Reports · 7
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Knowledge and attitudes toward urinary incontinence among healthcare students in palestine: a cross-sectional study
2026 · Maaweya Jabareen, Wasef Alhroub, et al. · BMC Medical Education
Case Report of Dual Variants in SLC1A4 and APOE : A Possible Link Between Amino Acid and Lipid Metabolism
2026 · Mohammed Qaisiya, Kenana Altell, et al. · Clinical Case Reports
Hereditary Myopathy With Early Respiratory Failure Associated With an Incidental COL4A5 Variant: A Case Report
2026 · Ursula Abu Nahla, Rahaf Bleibel, et al. · Case Reports in Genetics
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Severe Multisystem Dysfunction in Ank3-Related Intellectual Disability: A Case Report of a Novel Nonsense Mutation
2025 · Mai Arafeh, Ursula Abu Nahla, et al. · SSRN Electronic Journal
Works count: 5
Citation count: 7
H-index: 1
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