[Towards the discovery of genes predisposing to multiple sclerosis]

Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtel.

American journal of human genetics·2000

Linkage analysis of candidate myelin genes in familial multiple sclerosis.

Neurogenetics·1999

Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31.

American journal of human genetics·1998

Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene.

Genomics·1997

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.

Nature genetics·1996

Genetics of demyelinating diseases.

Brain pathology (Zurich, Switzerland)·1996

Antibacterial and antibiofilm activities of Laurus nobilis L. essential oil against Staphylococcus aureus strains associated with oral infections.

Pathologie-biologie·2015

Oxidative damage and histopathological changes in lung of rat chronically exposed to nicotine alone or associated to ethanol.

Pathologie-biologie·2015

Biological diagnosis of diabetes mellitus.

Pathologie-biologie·2015

Association of CagPAI integrity with severeness of Helicobacter pylori infection in patients with gastritis.

Pathologie-biologie·2015

[Diagnostic performance of graphical anomalies in the detection of large platelets and platelet clumps].

Pathologie-biologie·2015

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

Pathologie-biologie·2015

QTL mapping.

Genetics·2026

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Case reports in ophthalmological medicine·2026

Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.

Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

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[Towards the discovery of genes predisposing to multiple sclerosis]

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Vacuoliting megalencephalic leukoencephalopathy with subcortical cysts, mapped to chromosome 22qtel.

Linkage analysis of candidate myelin genes in familial multiple sclerosis.

Vocal cord and pharyngeal weakness with autosomal dominant distal myopathy: clinical description and gene localization to 5q31.

Gene sequence, localization, and evolutionary conservation of DAZLA, a candidate male sterility gene.

A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group.

Genetics of demyelinating diseases.

Antibacterial and antibiofilm activities of Laurus nobilis L. essential oil against Staphylococcus aureus strains associated with oral infections.

Oxidative damage and histopathological changes in lung of rat chronically exposed to nicotine alone or associated to ethanol.

Biological diagnosis of diabetes mellitus.

Association of CagPAI integrity with severeness of Helicobacter pylori infection in patients with gastritis.

[Diagnostic performance of graphical anomalies in the detection of large platelets and platelet clumps].

Association analysis of APOA5 rs662799 and rs3135506 polymorphisms with obesity in Moroccan patients.

QTL mapping.

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian-Azeri Family.

Altered thalamo-prefrontal synchrony dynamics during spatial working memory task performance in a SETD1A loss-of-function mouse model of schizophrenia predisposition.

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

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