Infundibular buckling as an adjunctive sign of pituitary adenoma

Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly.

Saudi journal of biological sciences·2020

Parental perceptions of dental health and need for treatment in children with epilepsy: a multicenter cross-sectional study.

Pediatric health, medicine and therapeutics·2018

Treatment of infantile spasms in Saudi Arabia.

Neurosciences (Riyadh, Saudi Arabia)·2018

Publications pattern of clinical epilepsy research in Saudi Arabia.

Neurosciences (Riyadh, Saudi Arabia)·2017

Public awareness of autism spectrum disorder.

Neurosciences (Riyadh, Saudi Arabia)·2017

A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family.

Journal of the neurological sciences·2016

Knowledge, Practice and Perceived Barriers of Healthcare Provider Adherence to the Notifiable Disease Surveillance System (NDSS) in Government Hospitals and Primary Healthcare Centers in Jazan, Saudi Arabia: A Cross-Sectional Study.

Saudi medical journal·2026

Potential Drug-Drug Interactions in Patients Undergoing Hemodialysis: A Retrospective Observational Study.

Saudi medical journal·2026

Advancing Impact: A National Approach to Knowledge Translation in Saudi Arabia-The Saudi National Institute of Health Experience.

Saudi medical journal·2026

From Bench to Bedside: Evolving Definitions of Translational Research.

Saudi medical journal·2026

Cranial MRI in Girls With Central Precocious Puberty: Clinical Characteristics and Predictors of Abnormal Findings.

Saudi medical journal·2026

Quality, Patient Experience, and Service Gaps in Home Healthcare in Saudi Arabia: A Systematic Review Aligned with Vision 2030.

Saudi medical journal·2026

Human Umbilical Cord Mesenchymal Stem Cells Alleviate Autoimmune POI Associated With Downregulated UBE2N-Mediated Ovarian Inflammation.

International journal of rheumatic diseases·2026

The Role of S100A8/A9 in Autoimmune Eye Diseases: From Pathogenesis to Targeted Therapy.

Investigative ophthalmology & visual science·2026

Exploratory analysis of IFN-α-high and CXCL9-high cytokine distributions in systemic lupus erythematosus-associated macrophage activation syndrome.

Immunological medicine·2026

Safety and efficacy of zetomipzomib in relapsed or insufficiently responding autoimmune hepatitis: Results from the randomized, double-blind, placebo-controlled, phase 2a PORTOLA study and open-label extension.

Hepatology (Baltimore, Md.)·2026

Low-grade appendiceal mucinous neoplasm in an uncomplicated Amyand's hernia: a case report.

Journal of surgical case reports·2026

A Rare Case of Gastritis with Prominent IgG4-Positive Plasmacytosis Mimicking IgG4-Related Gastrointestinal Disease.

Inflammatory intestinal diseases·2026

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Infundibular buckling as an adjunctive sign of pituitary adenoma

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Next generation sequencing reveals novel homozygous frameshift in PUS7 and splice acceptor variants in AASS gene leading to intellectual disability, developmental delay, dysmorphic feature and microcephaly.

Parental perceptions of dental health and need for treatment in children with epilepsy: a multicenter cross-sectional study.

Treatment of infantile spasms in Saudi Arabia.

Publications pattern of clinical epilepsy research in Saudi Arabia.

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A novel mutation in PGAP2 gene causes developmental delay, intellectual disability, epilepsy and microcephaly in consanguineous Saudi family.

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Infundibular buckling as an adjunctive sign of pituitary adenoma

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