Idiopathic haemochromatosis: an autosomal recessive disease

Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

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The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

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The presymptomatic phase of Huntington disease.

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[Critical approach to clinical trials: difficulties of such research in Lebanon].

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A one year prevalence study of schizophrenia on Reunion Island.

European psychiatry : the journal of the Association of European Psychiatrists·2009

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

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Recurrent Sterile Polyserositis Reveals an Underrecognized Autoinflammatory Phenotype in MECP2 Duplication Syndrome.

Clinical genetics·2026

Identification of Copy Number Variants as a Suspected Cause of Cerebral Small Vessel Disease.

Clinical genetics·2026

Uncovering the Genetic Landscape of Pediatric Hearing Loss Along the Texas-Mexico Border.

Clinical genetics·2026

Knowledge on the Haemophilia Care Among Healthcare Providers in Tanzania: A Multicenter Cross-Sectional Study.

Journal of blood medicine·2026

Rapid spontaneous regression of a massive post-thrombolysis intracerebral hemorrhage: A case report.

Surgical neurology international·2026

Human leukocyte antigen genotype modulates cytomegalovirus- and Epstein-Barr virus-specific T-cell response in healthy donors for optimized virus-specific T-cell donor selection.

Frontiers in immunology·2026

Persistent Gingival Bleeding After Scaling: A Diagnostic Clue to von Willebrand Disease.

Clinical case reports·2026

Development and Validation of a Checklist for Safe Blood Transfusion in Anesthesia: A Methodological Study.

Health science reports·2026

Efficacy and safety comparison of hetrombopag and eltrombopag in children with cancer therapy-induced thrombocytopenia: a single-center retrospective study.

Frontiers in medicine·2026

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Idiopathic haemochromatosis: an autosomal recessive disease

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Guidelines for presymptomatic testing for Huntington's disease: past, present and future in France.

The involvement of the trans-generational effect in the high incidence of the hydatidiform mole in Africa.

The presymptomatic phase of Huntington disease.

[Critical approach to clinical trials: difficulties of such research in Lebanon].

A one year prevalence study of schizophrenia on Reunion Island.

Homozygous mutation of the PHOX2B gene in congenital central hypoventilation syndrome (Ondine's Curse).

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