Ramzi H. Mujahed
Hebron, WBK, Palestine
Last Updated: 09/26/2026
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Found 11 publications
Expanding the Phenotypic Spectrum of SLC1A4-Related Spastic Tetraplegia: A Case With Novel Multisystem Features.
Journal: Journal of investigative medicine high impact case reports
Published: April 04, 2026
Mature Testicular Teratoma Mimicking Hydrocele in a 3-Year-Old Boy: Case Report and Literature Review.
Journal: Journal of investigative medicine high impact case reports
Published: December 23, 2025
Early-onset pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: the first genetically confirmed case from Palestine.
Journal: Annals of medicine and surgery (2012)
Published: November 07, 2025
De Novo KCNJ11 Mutation in an Infant With Neonatal Diabetes Mellitus Presenting as Diabetic Ketoacidosis: A Case Report and Literature Review.
Journal: Journal of investigative medicine high impact case reports
Published: August 22, 2025
A Rare NPHS2 Mutation (E130K) in Hereditary Steroid-Resistant Nephrotic Syndrome: A Case Report.
Journal: Case reports in nephrology
Published: August 15, 2025
A rare early-onset bilateral renal cysts, focal seizures in a 1-year-old male with tuberous sclerosis and No mutation identified.
Journal: Oxford medical case reports
Published: May 09, 2025
Surviving trisomy 18: A case report of a 5-year-old girl.
Journal: Medicine
Published: February 18, 2025
Congenital hiatal hernia with vermis hypoplasia, dysmorphic features and negative genetic study: A case report.
Journal: SAGE open medical case reports
Published: June 10, 2024
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Last Updated: 09/26/2026