Rachid Abilkassem

Rabat, Morocco

Last Updated: 09/26/2026

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Found 47 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

Scurvy Masquerading as Malignancy: A Diagnostic Challenge in a Child With Severe Selective Eating.

Scurvy Masquerading as Malignancy: A Diagnostic Challenge in a Child With Severe Selective Eating.

Journal: Cureus
Published: July 01, 2026

X-linked Hypophosphatemic Rickets Revealed by Exome Sequencing: A Pediatric Case Report of a PHEX Pathogenic Variant.

X-linked Hypophosphatemic Rickets Revealed by Exome Sequencing: A Pediatric Case Report of a PHEX Pathogenic Variant.

Journal: Cureus
Published: May 25, 2026

Diffuse Infantile Hepatic Hemangiomatosis: A Rare Cause of Consumptive Hypothyroidism.

Diffuse Infantile Hepatic Hemangiomatosis: A Rare Cause of Consumptive Hypothyroidism.

Journal: Cureus
Published: May 01, 2026

Neonatal right ventricular rhabdomyoma: Imaging findings and spontaneous regression.

Neonatal right ventricular rhabdomyoma: Imaging findings and spontaneous regression.

Journal: Radiology case reports
Published: April 19, 2026

Fatal Hemorrhagic Rupture of a Cystic Hepatic Hemangioma in a 27-Week Preterm Neonate.

Fatal Hemorrhagic Rupture of a Cystic Hepatic Hemangioma in a 27-Week Preterm Neonate.

Journal: Cureus
Published: March 12, 2026

Hepatocellular carcinoma in a child with hereditary tyrosinemia type I despite early NTBC therapy: When should we suspect it?

Hepatocellular carcinoma in a child with hereditary tyrosinemia type I despite early NTBC therapy: When should we suspect it?

Journal: Radiology case reports
Published: January 24, 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

Neonatal osteogenesis imperfecta revealed by antenatal fractures: A case report.

Neonatal osteogenesis imperfecta revealed by antenatal fractures: A case report.

Journal: Radiology case reports
Published: November 06, 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
Showing 1-12 of 47

Last Updated: 09/26/2026