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Zahra Alsahlawi

Observed names: Al-Sahlawi, Zahra, Z. Alsahlawi, Zahra Al Sahlawi, Zahra Al sahlawi, Zahra Al-Sahlawi, Zahra Al-sahlawi, Zahra AlSahlawi
Observed institutions: Royal College of Surgeons in Ireland, Salmaniya Medical Complex, King Faisal Specialist Hospital & Research Centre, King Hamad University Hospital, Sultan Qaboos University Hospital, Government Hospitals, Arabian Gulf University
ORCID: 0000-0003-1231-1132
Observed ORCID: 0000-0003-1231-1132
OpenAlex ID: A5078914763
Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature
2015 · Ola Khalifa, Zahra Al-Sahlawi, et al. · European Journal of Medical Genetics · 53
A Case of DeSanto-Shinawi Syndrome in Bahrain with a Novel Mutation
2020 · Zahra Alsahlawi, Mohamed Jailani, et al. · Case Reports in Pediatrics · 14
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HIDEA syndrome is caused by biallelic, pathogenic, rare or founder P4HTM variants impacting the active site or the overall stability of the P4H‐TM protein
2022 · Minna Kraatari‐Tiri, Leila Soikkonen, et al. · Clinical Genetics · 9
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Optic neuropathy in classical methylmalonic acidemia
2019 · Mohammed AlOwain, Ola Ali Khalifa, et al. · Ophthalmic Genetics · 7
Clinical spectrum and outcome of nine patients with a novel genetic variant of galactosialidosis in the Kingdom of Bahrain
2022 · Zahra Alsahlawi, Emtithal Aljishi, et al. · JIMD Reports · 6
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Poretti-Boltshauser Syndrome: A Report of Two Cases From Bahrain With a Novel Mutation and Literature Review
2025 · Zahra Alsahlawi, Ameera M Barni, et al. · Cureus · 3
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Meningoencephalitis in a novel mutation in MNGIE (mitochondrial neurogastrointestinal encephalomyopathy) ending a familial diagnostic odyssey: A case series report
2024 · Noor Redha, Zahra Al-Sahlawi, et al. · Journal of Central Nervous System Disease · 3
Variable manifestations in lysinuric protein intolerance: a report of two novel mutations from Bahrain
2020 · Emtithal Aljishi, Zahra Alsahlawi, et al. · Journal of Biochemical and Clinical Genetics · 3
Galactosialidosis: A Report of Three Cases Diagnosed With a Founder Genetic Mutation in the Bahraini Population
2025 · Zahra Alsahlawi, Zahraa J Alhadi, et al. · Cureus · 2
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Vanishing White Matter Disease in Children: An Unusual Association, a Novel Mutation, and a Literature Review
2024 · Zahra Alsahlawi, Hasan M Isa, et al. · Cureus · 2
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Infantile systemic hyalinosis: report of a case from Bahrain and review of literature
2020 · Zahra Alsahlawi, Fatema Naser Alfayez, et al. · Journal of Biochemical and Clinical Genetics · 2
Clinical variability in cerebral tendinous xanthomatosis (CTX): Insights from 16 cases across Gulf Cooperation Council’s (GCC’s) high consanguineous population
2025 · Mohammed A. Almuqbil, Mashael M. ALQuaimi, et al. · Journal of clinical lipidology · 1
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Alkaptonuria: Clinical Spectrum of a Diagnosed Case in Bahrain With a Literature Review
2025 · Zahra Alsahlawi, Layla I Salman, et al. · Cureus · 1
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A Case of Carnitine Palmitoyltransferase II Deficiency in Bahrain With a Novel Mutation
2022 · Zahra Alsahlawi, Zainab Fadhul, et al. · Cureus · 1
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Expert Delphi consensus on the diagnosis and management of Hypophosphatasia in the Gulf Cooperation Council region
2026 · Majid Alfadhel, M. Zulf Mughal, et al. · Orphanet Journal of Rare Diseases
Elevated Creatine Kinase in Mucolipidosis Type IV: Investigating an Atypical Manifestation and Its Clinical Complications
2026 · Zahra Alsahlawi, Hasan M Isa, et al. · Cureus
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High Incidence of Neonatal Inborn Errors of Metabolism in Bahrain Revealed by Tandem Mass Spectrometry
2025 · Abdelaziz Elamin, Diab E. Diab, et al. · Research Square
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Aseptic Pleocytosis Can Only be Classified as a Phenotypic Manifestation of MNGIE After Exclusion of all Differential Causes
2025 · Zahra Al-sahlawi, Noor Abdulla Redha, et al. · Journal of Central Nervous System Disease
Characterization of 3-Hydroxyisobutyryl-Coa Hydrolase (HIBCH) Deficiency in Bahrain: A Retrospective Cohort Study
2024 · Emtithal Al jishi, Zahra Al sahlawi, et al. · Journal of Biochemical and Clinical Genetics
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The Impact of the COVID-19 Pandemic on Educational and Academic Activities of Healthcare Professionals in Bahrain
2023 · Khadija Ali, Hasan M Isa, et al. · Cureus
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Carbamoyl phosphate synthetase 1 deficiency: First report of this rare metabolic disorder in Kingdom of Bahrain with novel mutation
2018 · Z. Alsahlawi, E. Aljishi, et al. · Case Reports International
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Erlenmeyer Flask Bone Deformity in a Child with Polyarthritis: Could This be a Distinct Disorder?
2015 · Intisar Albuhairan, Khalid Alismail, et al. · Annals of Paediatric Rheumatology
Works count: 24
Citation count: 107
H-index: 5
I10-index: 2
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