Abdelouahed Belmalih

Bron, France

Last Updated: 09/26/2026

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Found 16 publications

Performance of Relative Exchangeable Copper for the Diagnosis of Wilson Disease in Acute Liver Failure.

Performance of Relative Exchangeable Copper for the Diagnosis of Wilson Disease in Acute Liver Failure.

Journal: Journal of inherited metabolic disease

Published: December 14, 2024

Evaluation of vitamin B6 supplementation in Wilson's disease patients treated with D-penicillamine.

Evaluation of vitamin B6 supplementation in Wilson's disease patients treated with D-penicillamine.

Journal: BMJ open gastroenterology

Published: July 10, 2023

Phenotype and molecular characterization of Wilson's disease in Morocco.

Phenotype and molecular characterization of Wilson's disease in Morocco.

Journal: Clinics and research in hepatology and gastroenterology

Published: August 01, 2022

Long-Term Urinary Copper Excretion and Exchangeable Copper in Children With Wilson Disease Under Chelation Therapy.

Long-Term Urinary Copper Excretion and Exchangeable Copper in Children With Wilson Disease Under Chelation Therapy.

Journal: Journal of pediatric gastroenterology and nutrition

Published: June 16, 2022

Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305].

Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64 (10) (October 2021) 104305].

Journal: European journal of medical genetics

Published: February 20, 2022

Maintenance therapy simplification using a single daily dose: A preliminary real-life feasibility study in patients with Wilson disease.

Maintenance therapy simplification using a single daily dose: A preliminary real-life feasibility study in patients with Wilson disease.

Journal: Clinics and research in hepatology and gastroenterology

Published: February 08, 2022

Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64(10) (2021) 104305].

Corrigendum to "ATP7B variant spectrum in a French pediatric Wilson disease cohort" [Eur. J. Med. Genet. 64(10) (2021) 104305].

Journal: European journal of medical genetics

Published: September 21, 2021

Pediatric Wilson's Disease: Phenotypic, Genetic Characterization and Outcome of 182 Children in France.

Pediatric Wilson's Disease: Phenotypic, Genetic Characterization and Outcome of 182 Children in France.

Journal: Journal of pediatric gastroenterology and nutrition

Published: June 06, 2021

Epidemiology, clinical features, and mortality rate of Wilson disease in Moroccan children: A pediatric case series.

Epidemiology, clinical features, and mortality rate of Wilson disease in Moroccan children: A pediatric case series.

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: May 24, 2021

A Particular SORL1 Micro-haplotype May Prevent Severe Liver Disease in a French Cohort of Alpha 1-Antitrypsin-deficient Children.

A Particular SORL1 Micro-haplotype May Prevent Severe Liver Disease in a French Cohort of Alpha 1-Antitrypsin-deficient Children.

Journal: Journal of pediatric gastroenterology and nutrition

Published: March 15, 2021

ATP7B variant spectrum in a French pediatric Wilson disease cohort.

ATP7B variant spectrum in a French pediatric Wilson disease cohort.

Journal: European journal of medical genetics

Published: December 30, 2020

The blood copper isotopic composition is a prognostic indicator of the hepatic injury in Wilson disease.

The blood copper isotopic composition is a prognostic indicator of the hepatic injury in Wilson disease.

Journal: Metallomics : integrated biometal science

Published: October 15, 2020

Showing 1-12 of 16

Last Updated: 09/26/2026