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Familial epilepsy in Algeria: Clinical features and inheritance profiles

Type de record:

paper
Créateur:
AmiAïcMicMoh
Éditeur:
Elsevier BV
Hôte:

Visit

doi.org

Licenses

https://www.elsevier.com/tdm/userlicense/1.0/https://www.elsevier.com/legal/tdmrep-licensehttp://www.elsevier.com/open-access/userlicense/1.0/

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Clinical features, proximate causes, and consequences of active convulsive epilepsy in Africa

Purpose

Epilepsy is common in sub-Saharan Africa (SSA), but the clinical

Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria

Abstract Introduction The incidence of afibrinogenemia had not been previously reported in Algeri

Differential mutational profiles of familial Mediterranean fever in North Africa

Abstract Familial Mediterranean fever (FMF) is a recessive autoinflammatory disease, mainly occurri

Familial form of typical childhood absence epilepsy in a consanguineous context

Summary Causative genes for childhood absence epilepsy (CAE) are unknown partly because families ar

Determination of Familial Inheritance of Human External Ear Pattern Among the Urhobos in Delta State, Nigeria.

Aim: This study determined the familial inheritance of the external ear pattern among the Urhobos in

Epidemiological features of epilepsy in the countries of the African continent

This review is devoted to the analysis of the published results of studies conducted in Africa, whic