[Leber's disease. A family 10 years later]

Duck production systems and highly pathogenic avian influenza H5N8 in France, 2016-2017.

Scientific reports·2019

Spread rate of lumpy skin disease in the Balkans, 2015-2016.

Transboundary and emerging diseases·2017

Syndromic surveillance of abortions in beef cattle based on the prospective analysis of spatio-temporal variations of calvings.

Scientific reports·2015

Preventive vaccination contributes to control classical swine fever in wild boar (Sus scrofa sp.).

Veterinary microbiology·2009

[Bone densitometry in inflammatory rheumatic diseases : Characteristics of the measurement site and disease-specific factors].

Zeitschrift fur Rheumatologie·2009

Associations with subregional BMD-measurements in patients with rheumatoid arthritis.

Rheumatology international·2008

[Keratomycoses: practical aspects].

Bulletin des societes d'ophtalmologie de France·1990

[Magnetic resonance imaging in the evaluation of malignant melanoma of the choroid and ciliary body].

Bulletin des societes d'ophtalmologie de France·1990

[Fuchs' cyclitis: etiologic and clinical aspects].

Bulletin des societes d'ophtalmologie de France·1990

[Risk factors of non-proliferating retinopathy in insulin-dependent diabetes].

Bulletin des societes d'ophtalmologie de France·1990

[Retinal detachment caused by giant tears: recent clinical results].

Bulletin des societes d'ophtalmologie de France·1990

[Basedow's disease and atypical ophthalmologic signs].

Bulletin des societes d'ophtalmologie de France·1990

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

[Leber's disease. A family 10 years later]

Related Concept Videos

Duck production systems and highly pathogenic avian influenza H5N8 in France, 2016-2017.

Spread rate of lumpy skin disease in the Balkans, 2015-2016.

Syndromic surveillance of abortions in beef cattle based on the prospective analysis of spatio-temporal variations of calvings.

Preventive vaccination contributes to control classical swine fever in wild boar (Sus scrofa sp.).

[Bone densitometry in inflammatory rheumatic diseases : Characteristics of the measurement site and disease-specific factors].

Associations with subregional BMD-measurements in patients with rheumatoid arthritis.

[Keratomycoses: practical aspects].

[Magnetic resonance imaging in the evaluation of malignant melanoma of the choroid and ciliary body].

[Fuchs' cyclitis: etiologic and clinical aspects].

[Risk factors of non-proliferating retinopathy in insulin-dependent diabetes].

[Retinal detachment caused by giant tears: recent clinical results].

[Basedow's disease and atypical ophthalmologic signs].

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

[Leber's disease. A family 10 years later]

Related Concept Videos

Related Articles