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Ramzi H. Mujahed

Observed names: Ramzi H Mujahed, Ramzi Hmedan Mujahed, Ramzi Mujahed
Observed institution: Palestine Polytechnic University
ORCID: 0009-0006-9010-0129
Observed ORCID: 0009-0006-9010-0129
OpenAlex ID: A5114623672
De Novo KCNJ11 Mutation in an Infant With Neonatal Diabetes Mellitus Presenting as Diabetic Ketoacidosis: A Case Report and Literature Review
2025 · Ramzi H. Mujahed, Amal M. Shawabka, et al. · Journal of Investigative Medicine High Impact Case Reports · 2
Surviving trisomy 18: A case report of a 5-year-old girl
2025 · Mohamad A. Banat, Ramzi Mujahed, et al. · Medicine · 1
First reported case of de Novo claes-jensen syndrome (CJS) in Palestine: diagnostic challenges and genetic insights
2025 · Manal M. Shaheen, Ramzi H. Mujahed, et al. · BMC Pediatrics · 1
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Early-onset pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: the first genetically confirmed case from Palestine
2026 · Bushra Kh. Pujee, Ramzi Mujahed, et al. · Annals of Medicine and Surgery
Expanding the Phenotypic Spectrum of SLC1A4 -Related Spastic Tetraplegia: A Case With Novel Multisystem Features
2026 · Ramzi H. Mujahed, Leyana Alawawdeh, et al. · Journal of Investigative Medicine High Impact Case Reports
A Rare NPHS2 Mutation (E130K) in Hereditary Steroid‐Resistant Nephrotic Syndrome: A Case Report
2026 · Ramzi Hmedan Mujahed, Omar Hammam Salloum, et al. · Case Reports in Nephrology
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Mature Testicular Teratoma Mimicking Hydrocele in a 3-Year-Old Boy: Case Report and Literature Review
2025 · Rahaf W. Thabaineh, Ramzi H. Mujahed, et al. · Journal of Investigative Medicine High Impact Case Reports
A rare early-onset bilateral renal cysts, focal seizures in a 1-year-old male with tuberous sclerosis and No mutation identified
2025 · Dana Salahat, Ramzi Mujahed, et al. · Oxford Medical Case Reports
Hypomyelination Leukodystrophy Type 11 (HLD11) Presenting with Diabetes: A Case Report and Literature Review
2025 · Qusai A. Alsalah, Donya Y. Alqam, et al. · Sage Open Pediatrics
Secretory Diarrhea Caused by Activating GUCY2C Mutation in a Patient With Atypical Kawasaki Disease: A Rare Case Report
2025 · Ramzi Mujahed, Mohamad A. Banat, et al. · Sage Open Pediatrics
Congenital hiatal hernia with vermis hypoplasia, dysmorphic features and negative genetic study: A case report
2024 · Ramzi H Mujahed, Manal M Shaheen, et al. · SAGE Open Medical Case Reports
Works count: 11
Citation count: 4
H-index: 1
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