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Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3

Human molecular genetics, 2006-03, Vol.15 (5), p.767-776

2006

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Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

Human molecular genetics, 2004-10, Vol.13 (20), p.2473-2482

2004

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Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

Human molecular genetics, 2003-09, Vol.12 (18), p.2369-2378

2003

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PARTIDOS Y SISTEMA DE PARTIDOS EN LAS ELECCIONES MEXICANAS DE 2018

Foro internacional, 2020-04, Vol.60 (2 (240)), p.397-450

Prud’homme, Jean-François

2020

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Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome

Human molecular genetics, 2003-04, Vol.12 (8), p.925-935

2003

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l-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1

Human molecular genetics, 2004-11, Vol.13 (22), p.2803-2811

2004

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

Nature genetics, 1999-11, Vol.23 (3), p.296-303

1999

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An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin Disorders

Journal of investigative dermatology, 2009-11, Vol.129 (11), p.2637-2645

2009

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Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31

Annals of neurology, 2001-06, Vol.49 (6), p.786-792

2001

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LA INSATISFACCIÓN CON LA DEMOCRACIA EN EL MÉXICO ACTUAL

Foro internacional, 2015-01, Vol.55 (1 (219)), p.302-341

Prud'homme, Jean-François

2015

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A locus for simple pure febrile seizures maps to chromosome 6q22–q24

Brain (London, England : 1878), 2002-12, Vol.125 (12), p.2668-2680

2002

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First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

Nature genetics, 2001-05, Vol.28 (1), p.46-48

2001

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Novel Mutations in the Gene Encoding Secreted Lymphocyte Antigen-6/Urokinase-type Plasminogen Activator Receptor-related Protein-1 (SLURP-1) and Description of Five Ancestral Haplotypes in Patients with Mal de Meleda

Journal of investigative dermatology, 2003-03, Vol.120 (3), p.351-355

2003

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Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Human molecular genetics, 2002, Vol.11 (1), p.107-113

2002

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Rafael Rojas, Historia minima de la Revolucion Cubana.(Resena de libro)

Historia mexicana, 2017-01, Vol.66 (3), p.1659

Francois Prud'homme, Jean

2017

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Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Human molecular genetics, 2002-01, Vol.11 (1), p.107-113

2002

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Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity

American journal of human genetics, 2000-03, Vol.66 (3), p.904-913

2000

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New Susceptibility Locus for Rheumatoid Arthritis Suggested by a Genome-Wide Linkage Study

Proceedings of the National Academy of Sciences - PNAS, 1998-09, Vol.95 (18), p.10746-10750

1998

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Del populismo de los antiguos al populismo de los modernos

1, 2001

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Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

American journal of human genetics, 2001-11, Vol.69 (5), p.1002-1012

2001

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Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome

Journal of investigative dermatology, 2001-12, Vol.117 (6), p.1657-1661

2001

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A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33

American journal of human genetics, 1999-10, Vol.65 (4), p.1078-1085

1999

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ADAM33, a new candidate for psoriasis susceptibility

PloS one, 2007-09, Vol.2 (9), p.e906-e906

2007

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A Radiation Hybrid Map of the Human Genome

Human molecular genetics, 1996-03, Vol.5 (3), p.339-346

1996

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Mutations in a new cytochrome P450 gene in lamellar ichthyosis type 3

Mutations in ichthyin a new gene on chromosome 5q33 in a new form of autosomal recessive congenital ichthyosis

Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2

PARTIDOS Y SISTEMA DE PARTIDOS EN LAS ELECCIONES MEXICANAS DE 2018

Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome

l-2-Hydroxyglutaric aciduria: identification of a mutant gene C14orf160, localized on chromosome 14q22.1

Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

An Association Study of 22 Candidate Genes in Psoriasis Families Reveals Shared Genetic Factors with Other Autoimmune and Skin Disorders

Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31

LA INSATISFACCIÓN CON LA DEMOCRACIA EN EL MÉXICO ACTUAL

A locus for simple pure febrile seizures maps to chromosome 6q22–q24

First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene

Linkage Analysis and Disease Models in Benign Familial Infantile Seizures: A Study of 16 Families

Novel Mutations in the Gene Encoding Secreted Lymphocyte Antigen-6/Urokinase-type Plasminogen Activator Receptor-related Protein-1 (SLURP-1) and Description of Five Ancestral Haplotypes in Patients with Mal de Meleda

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Rafael Rojas, Historia minima de la Revolucion Cubana.(Resena de libro)

Lipoxygenase-3 (ALOXE3) and 12(R)-lipoxygenase (ALOX12B) are mutated in non-bullous congenital ichthyosiform erythroderma (NCIE) linked to chromosome 17p13.1

Two New Loci for Autosomal Recessive Ichthyosis on Chromosomes 3p21 and 19p12-q12 and Evidence for Further Genetic Heterogeneity

New Susceptibility Locus for Rheumatoid Arthritis Suggested by a Genome-Wide Linkage Study

Del populismo de los antiguos al populismo de los modernos

Mutations in CGI-58, the Gene Encoding a New Protein of the Esterase/Lipase/Thioesterase Subfamily, in Chanarin-Dorfman Syndrome

Novel Point Mutations, Deletions, and Polymorphisms in the Cathepsin C Gene in Nine Families from Europe and North Africa with Papillon–Lefèvre Syndrome

A Second Locus for Familial Generalized Epilepsy with Febrile Seizures Plus Maps to Chromosome 2q21-q33

ADAM33, a new candidate for psoriasis susceptibility

A Radiation Hybrid Map of the Human Genome

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