Abdelilah Radi

Rabat, Morocco

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 10 publications

Deep Vein Thrombosis in an 11-Year-Old Child With Pulmonary Tuberculosis: A Case Report.

Deep Vein Thrombosis in an 11-Year-Old Child With Pulmonary Tuberculosis: A Case Report.

Journal: Cureus

Published: July 14, 2026

Pulmonary hemosiderosis revealing class II HLA deficiency in a 9-month-old infant: a case report

Pulmonary hemosiderosis revealing class II HLA deficiency in a 9-month-old infant: a case report

Journal: The Pan African medical journal

Published: December 10, 2025

Griscelli Syndrome Type 2 Revealed by Macrophage Activation Syndrome: Two Cases From the Same Family.

Griscelli Syndrome Type 2 Revealed by Macrophage Activation Syndrome: Two Cases From the Same Family.

Journal: Cureus

Published: September 25, 2025

Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping.

Novel ANKRD11 Mutation in KBG Syndrome: A diagnostic triad of hearing loss, radiological macrodontia and artificial intelligence-assisted facial phenotyping.

Journal: Sultan Qaboos University medical journal

Published: August 19, 2025

Novel MCT8 mutation: diagnostic value of T3/T4 ratio.

Novel MCT8 mutation: diagnostic value of T3/T4 ratio.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: August 09, 2025

Type 3 Von Willebrand disease: two clinical cases of a rare disorder.

Type 3 Von Willebrand disease: two clinical cases of a rare disorder.

Journal: Oxford medical case reports

Published: June 29, 2025

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region.

Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay with Early-Onset Epilepsy and Novel Clinical Features: A rare entity from Morocco in the Middle East and North Africa region.

Journal: Sultan Qaboos University medical journal

Published: February 11, 2025

Severe congenital hyperinsulinism with progressive neurological deterioration due to novel HADH-GHSR digenic mutations: the first case report.

Severe congenital hyperinsulinism with progressive neurological deterioration due to novel HADH-GHSR digenic mutations: the first case report.

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: January 01, 2025

From growth hormone deficiency to Kleefstra-2 syndrome: diagnostic reassessment of treatment-refractory short stature.

From growth hormone deficiency to Kleefstra-2 syndrome: diagnostic reassessment of treatment-refractory short stature.

Journal: Pediatric endocrinology, diabetes, and metabolism

Published: January 01, 2025

Multifocal tuberculosis revealed by a sternal swelling in an immunocompetent child.

Multifocal tuberculosis revealed by a sternal swelling in an immunocompetent child.

Journal: Access microbiology

Published: February 19, 2024

Showing 1-10 of 10

Last Updated: 09/26/2026