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A marker for Stevens-Johnson syndrome ...: ethnicity matters

The pharmacogenomics journal, 2006-07, Vol.6 (4), p.265-268

2006

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A marker for Stevens-Johnson syndrome ...: ethnicity matters

The pharmacogenomics journal, 2006-07, Vol.6 (4), p.265-268

2006

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Concentrations plasmatiques et intra-prostatiques d’ertapénème après administration préopératoire : expérience prospective monocentrique – étude ERTAPRO

Progrès en urologie (Paris), 2015-11, Vol.25 (13), p.775-775

2015

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Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy

Neurology, 1998-11, Vol.51 (5), p.1454-1456

1998

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Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: Evidence for genetic heterogeneity

Arthritis & rheumatology (Hoboken, N.J.), 2002-08, Vol.46 (8), p.2039-2044

2002

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Not Available

Progrès en urologie (Paris), 2015-11, Vol.25 (13), p.775-775

2015

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[278] ASSOCIATION OF CYP1B1 GERMLINE MUTATIONS WITH HNF1a MUTATED HEPATOCELLULAR ADENOMA

Journal of hepatology, 2007, Vol.46, p.S111-S111

2007

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Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

Journal of medical genetics, 1997-06, Vol.34 (6), p.470-475

1997

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A Human Genome Diversity Cell Line Panel

Science (American Association for the Advancement of Science), 2002-04, Vol.296 (5566), p.261-262

2002

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Biological and clinical significance of concurrent p53 gene alterations, MDR1 gene expression, and S-phase fraction analyses in breast cancer patients treated with primary chemotherapy or radiotherapy

Clinical cancer research, 1997-12, Vol.3 (12), p.2471-2478

1997

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A 3.9-Centimorgan-Resolution Human Single-Nucleotide Polymorphism Linkage Map and Screening Set

American journal of human genetics, 2003-08, Vol.73 (2), p.271-284

2003

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Significant linkage to spondyloarthropathy on 9q31–34

Human molecular genetics, 2004-08, Vol.13 (15), p.1641-1648

2004

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From adhalinopathies to alpha-sarcoglycanopathies: An overview

Neuromuscular disorders : NMD, 1996-12, Vol.6 (6), p.463-465

1996

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A national DNA bank in The Gambia, West Africa, and genomic research in developing countries

Nature genetics, 2004-08, Vol.36 (8), p.785-786

2004

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Synthesis and pharmacological evaluation of new indole derivatives structurally related to thymoxamine

European journal of medicinal chemistry, 1994, Vol.29 (7), p.551-559

1994

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A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Annals of neurology, 1997-08, Vol.42 (2), p.222-229

1997

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Research progress on catalytic pyrolysis and reuse of waste plastics and petroleum sludge

ES Materials & Manufacturing, 2021-03

2021

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Adrenomedullin Levels are High in Primary Aldosteronism due to Adenoma and Decline after Surgical Cure

Blood pressure, 1998, Vol.7 (1), p.19-23

1998

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Contributions of Matrilineal and Patrilineal Kin Alloparental Effort to the Development of Life History Strategies and Patriarchal Values: A Cross-Cultural Life History Approach

Journal of cross-cultural psychology, 2014-05, Vol.45 (4), p.534-554

2014

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Penetrance of the FSHD mutation differs according to the D4Z4 repeat number

Neuromuscular disorders : NMD, 1997-09, Vol.7 (6), p.444-444

1997

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Device and Method for Measuring Volume in Receptacles for Storing Wine

Journal of Physics & Optics Sciences, 2021-06, p.1-4

L, Castañeda

2021

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Is the del521T mutation in the gamma-sarcoglycan gene a founder mutation in Mediterranean countries?

Neuromuscular disorders : NMD, 1997-09, Vol.7 (6), p.441-441

1997

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Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan)

Neuromuscular disorders : NMD, 1996-03, Vol.6 (2), p.S8-S8

1996

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Fungal persister cells: The basis for recalcitrant infections?

PLoS pathogens, 2018-10, Vol.14 (10), p.e1007301-e1007301

2018

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Archaeometric study of Roman tesserae from Salamanca (Spain). Archaeology and geochemical analysis

Interdisciplinaria archaeologica, 2018-11, Vol.IX (1), p.31-42

2018

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A marker for Stevens-Johnson syndrome ...: ethnicity matters

A marker for Stevens-Johnson syndrome ...: ethnicity matters

Concentrations plasmatiques et intra-prostatiques d’ertapénème après administration préopératoire : expérience prospective monocentrique – étude ERTAPRO

Cardiac involvement in genetically confirmed facioscapulohumeral muscular dystrophy

Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: Evidence for genetic heterogeneity

Not Available

[278] ASSOCIATION OF CYP1B1 GERMLINE MUTATIONS WITH HNF1a MUTATED HEPATOCELLULAR ADENOMA

Mutational diversity and hot spots in the alpha-sarcoglycan gene in autosomal recessive muscular dystrophy (LGMD2D)

A Human Genome Diversity Cell Line Panel

Biological and clinical significance of concurrent p53 gene alterations, MDR1 gene expression, and S-phase fraction analyses in breast cancer patients treated with primary chemotherapy or radiotherapy

A 3.9-Centimorgan-Resolution Human Single-Nucleotide Polymorphism Linkage Map and Screening Set

Significant linkage to spondyloarthropathy on 9q31–34

From adhalinopathies to alpha-sarcoglycanopathies: An overview

A national DNA bank in The Gambia, West Africa, and genomic research in developing countries

Synthesis and pharmacological evaluation of new indole derivatives structurally related to thymoxamine

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

Research progress on catalytic pyrolysis and reuse of waste plastics and petroleum sludge

Adrenomedullin Levels are High in Primary Aldosteronism due to Adenoma and Decline after Surgical Cure

Contributions of Matrilineal and Patrilineal Kin Alloparental Effort to the Development of Life History Strategies and Patriarchal Values: A Cross-Cultural Life History Approach

Penetrance of the FSHD mutation differs according to the D4Z4 repeat number

Device and Method for Measuring Volume in Receptacles for Storing Wine

Is the del521T mutation in the gamma-sarcoglycan gene a founder mutation in Mediterranean countries?

Genetic, allelic and phenotypic heterogeneity of muscular dystrophies with primary and secondary involvement of adhalin (alpha-sarcoglycan)

Fungal persister cells: The basis for recalcitrant infections?

Archaeometric study of Roman tesserae from Salamanca (Spain). Archaeology and geochemical analysis

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