Hamdy H. Hassan
Riyadh, Saudi Arabia
Last Updated: 09/26/2026
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Found 12 publications
JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.
Journal: The New England journal of medicine
Published: January 16, 2020
Pediatric intracranial hypertension. Experience from 2 Tertiary Centers.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: December 25, 2019
Aggressive surgical management of recurrent intracranial juvenile xanthogranuloma: case report and review of the literature.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: April 11, 2019
Idiopathic intracranial hypertension in children: Diagnostic and management approach.
Journal: Sudanese journal of paediatrics
Published: January 18, 2017
Glutaric aciduria type 1 as a cause of dystonic cerebral palsy.
Journal: Saudi medical journal
Published: November 24, 2015
ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita.
Journal: Human genetics
Published: February 27, 2015
The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.
Journal: Sudanese journal of paediatrics
Published: January 01, 2014
Radiological predictors of neurological compromise in adults with filum terminale lipoma.
Journal: Neurosciences (Riyadh, Saudi Arabia)
Published: April 03, 2013
NPHP4 mutation is linked to cerebello-oculo-renal syndrome and male infertility.
Journal: Clinical genetics
Published: January 17, 2013
Weaver syndrome and defective cortical development: a rare association.
Journal: American journal of medical genetics. Part A
Published: May 08, 2012
Showing 1-12 of 12
Last Updated: 09/26/2026