H. Hassan

发表

The many faces of KIF7

F. Alkuraya, Duna H. Barakeh, E. Faqeih, 2015, Human Genome Variation.

Pediatric intracranial hypertension

H. Hassan, M. Salih, F. Bashiri, 2019, Neurosciences.

Agenesis of the corpus callosum associated with spinal open neural tube defect

H. Hassan, M. Salih, S. Elwatidy, 2014, Saudi medical journal.

Moyamoya syndrome as a risk factor for stroke in Saudi children. Novel and usual associations.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Hematologic risk factors for stroke in Saudi children.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita

F. Alkuraya, H. Hassan, F. Bashiri, 2015, Human Genetics.

Glutaric aciduria type 1 as a cause of dystonic cerebral palsy

H. Hassan, M. Salih, Sarar H Mohamed, 2015, Saudi medical journal.

A newly recognized autosomal recessive syndrome affecting neurologic function and vision

T. Wienker, H. Hassan, A. Tzschach, 2013, American journal of medical genetics. Part A.

Congenital and genetic cerebrovascular anomalies as risk factors for stroke in Saudi children.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Stroke from systemic vascular disorders in Saudi children. The devastating role of hypernatremic dehydration.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Ophthalmic features of PLA2G6-related paediatric neurodegeneration with brain iron accumulation

M. Koenig, G. Stevanin, H. Hassan, 2014, British Journal of Ophthalmology.

Cardiac diseases as a risk factor for stroke in Saudi children.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Weaver syndrome and defective cortical development: A rare association

F. Alkuraya, H. Hassan, A. Alazami, 2013, American journal of medical genetics. Part A.

Infectious and inflammatory disorders of the circulatory system as risk factors for stroke in Saudi children.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

NPHP4 mutation is linked to cerebello‐oculo‐renal syndrome and male infertility

H. Hassan, A. Alazami, M. Baig, 2014, Clinical genetics.

Stroke from cervicocephalic arterial dissection in Saudi children.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Primary retroperitoneal synovial sarcoma in CT and MRI

H. Hassan, M. El-sharkawy, Abdulmajeed R. Alhazzani, 2010, Urology annals.

A Study on Herpes Simplex Encephalitis in 18 Children, Including 3 Relapses

H. Hassan, M. Salih, M. Al-Nasser, 2009 .

The neurologic aspects of hypomelanosis of Ito: Case report and review of the literature.

H. Hassan, M. Hamad, A. Kentab, 2014, Sudanese journal of paediatrics.

Idiopathic intracranial hypertension in children: Diagnostic and management approach.

Taim A. Muayqil, H. Hassan, M. Salih, 2016, Sudanese journal of paediatrics.

Cystic hygroma of the neck with multiple bone lymphangiomas

H. Hassan, M. El-Essawy, 2011 .

Stroke due to mitochondrial disorders in Saudi children.

M. Zeviani, H. Hassan, M. Salih, 2006, Saudi medical journal.

Fluid-fluid level in Langerhans cell histiocytosis of the skull.

F. Albadr, H. Hassan, I. Alorainy, 2006, Neurosciences.

JAK Inhibitor Therapy in a Child with Inherited USP18 Deficiency.

J. Casanova, A. Al-Eyadhy, M. Temsah, 2020, The New England journal of medicine.

Aggressive surgical management of recurrent intracranial juvenile xanthogranuloma: case report and review of the literature

H. Hassan, S. Elwatidy, K. Aljerian, 2019, Child's Nervous System.

Perinatal stroke in Saudi children. Clinical features and risk factors.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Stroke in Saudi children. Epidemiology, clinical features and risk factors.

H. Hassan, M. Salih, I. Alorainy, 2006, Saudi medical journal.

Epidemiology, clinical features and risk factors

H. Hassan, M. Salih, I. Alorainy, 2006 .

Pellagra‐like condition is xeroderma pigmentosum/Cockayne syndrome complex and niacin confers clinical benefit

H. Hassan, M. Mukhtar, H. Hijazi, 2015, Clinical genetics.

Split cord malformation associated with spinal open neural tube defect

H. Hassan, M. Salih, S. Elwatidy, 2014, Saudi medical journal.

Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

I. Katona, M. Koenig, R. Rodenburg, 2013, PLoS ONE.

New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations

I. Katona, M. Koenig, R. Rodenburg, 2013, PloS one.

Effect of Implementing Evidence Based Nursing Guidelines on Nurses’ Performance Regarding Care Provided for Children Undergoing Hemodialysis

H. Hassan, R. Bahgat, R. Kafl, 2020 .

Structural and Functional Involvement of Pituitary Gland in Wegener’s Granulomatosis

H. Hassan, A. Bilal, N. Barlas, 2011, Clinical Neuroradiology.

Cerebral Iron Accumulation Is Not a Major Feature of FA2H/SPG35

N. Drouot, M. Koenig, H. Hassan, 2015, Movement disorders clinical practice.

Idiopathic intracranial hypertension in children: Diagnostic and management approach.

Taim A. Muayqil, H. Hassan, M. Salih, 2016, Sudanese journal of paediatrics.