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Relationships between Cholesterol, Apolipoprotein E Polymorphism and Dementia: A Cross-Sectional Analysis from the PAQUID Study

Neuroepidemiology, 2000-05, Vol.19 (3), p.141-148

2000

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Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport

American journal of respiratory and critical care medicine, 2010-10, Vol.182 (7), p.929-936

2010

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CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders

Journal of medical genetics, 2013-04, Vol.50 (4), p.220-227

2013

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The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible

Clinical case reports, 2017-05, Vol.5 (5), p.658-663

2017

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Renal impairment in children with cystic fibrosis

Journal of cystic fibrosis, 2010-07, Vol.9 (4), p.263-268

2010

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p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study

European journal of human genetics : EJHG, 2011-01, Vol.19 (1), p.36-42

2011

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Analysis of the effect of aluminum in drinking water and transferrin C2 allele on Alzheimer's disease

European journal of neurology, 2006-09, Vol.13 (9), p.1022-1025

2006

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Influence of the Duplication of CFTR Exon 9 and Its Flanking Sequences on Diagnosis of Cystic Fibrosis Mutations

The Journal of molecular diagnostics : JMD, 2009-09, Vol.11 (5), p.488-493

2009

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p.Ser1235Arg should no longer be considered as a Cystic Fibrosis mutation: results from a large collaborative study: p.Ser1235Arg is not associated with CF disease

European journal of human genetics : EJHG, 2010-08

2010

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CFTR genotypes in patients with normal or borderline sweat chloride levels

Human mutation, 2003-10, Vol.22 (4), p.340-340

2003

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French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-09, Vol.17 (9), p.1349-1358

2010

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Rapid and accurate detection of the CFTR gene mutation 1811+1.6 kbA>G by real-time fluorescence resonance energy transfer PCR

Molecular and cellular probes, 2005-10, Vol.19 (5), p.358-362

2005

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CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening

Genetic testing, 2008-03, Vol.12 (1), p.25

2008

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Rapid and accurate detection of the CFTR gene mutation 1811+1.6kbA>G by real-time fluorescence resonance energy transfer PCR

Molecular and cellular probes, 2005-10, Vol.19 (5), p.358-362

2005

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Improved methods for genotype determination of human alcohol dehydrogenase (ADH) at ADH 2 and ADH 3 loci by using polymerase chain reaction-directed mutagenesis

Clinical chemistry (Baltimore, Md.), 1990-10, Vol.36 (10), p.1765

1990

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Common and rare genotypes of human apolipoprotein E determined by specific restriction profiles of polymerase chain reaction-amplified DNA

Clinical chemistry (Baltimore, Md.), 1994-01, Vol.40 (1), p.24

1994

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Decreased acute hepatotoxicity of carbon tetrachloride and bromobenzene by cholestyramine in the rat

Gastroenterology (New York, N.Y. 1943), 1981-09, Vol.81 (3), p.520-526

1981

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Glutathione S-transferase class μ in French alcoholic cirrhotic patients

Human genetics, 1991-09, Vol.87 (5), p.628-630

1991

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GENOTYPING STUDY OF ALCOHOL DEHYDROGENASE CLASS I POLYMORPHISM IN FRENCH PATIENTS WITH ALCOHOLIC CIRRHOSIS

Alcohol and alcoholism (Oxford), 1990, Vol.25 (6), p.623-626

1990

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Compound heterozygote for both rare apolipoprotein E1 (Gly127-->Asp, Arg158-->Cys) and E3(Cys112-->Arg, Arg251-->Gly) alleles in a multigeneration pedigree with hyperlipoproteinaemia

Clinical science (1979), 1997-07, Vol.93 (1), p.89

1997

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The importance of functional tests to assess the effect of a new CFTR variant when genotype-phenotype correlation is not possible

Clinical case reports, 2017, Vol.5 (5), p.658-663

2017

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Identification of a new apolipoprotein E variant (E 2 Arg 142 → Leu) in type III hyperlipidemia

Atherosclerosis, 1995-01, Vol.112 (1), p.19-28

1995

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Glutathione S-transferase class ? in French alcoholic cirrhotic patients

Human genetics, 1991-09, Vol.87 (5)

1991

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Relationships between Cholesterol, Apolipoprotein E Polymorphism and Dementia: A Cross-Sectional Analysis from the PAQUID Study

Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport

Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis

CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders

Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France

The importance of functional tests to assess the effect of a new CFTR variant when genotype–phenotype correlation is not possible

Renal impairment in children with cystic fibrosis

p.Ser1235Arg should no longer be considered as a cystic fibrosis mutation: results from a large collaborative study

Analysis of the effect of aluminum in drinking water and transferrin C2 allele on Alzheimer's disease

Influence of the Duplication of CFTR Exon 9 and Its Flanking Sequences on Diagnosis of Cystic Fibrosis Mutations

p.Ser1235Arg should no longer be considered as a Cystic Fibrosis mutation: results from a large collaborative study: p.Ser1235Arg is not associated with CF disease

CFTR genotypes in patients with normal or borderline sweat chloride levels

French guidelines for sweat test practice and interpretation for cystic fibrosis neonatal screening

Rapid and accurate detection of the CFTR gene mutation 1811+1.6 kbA>G by real-time fluorescence resonance energy transfer PCR

CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening

Rapid and accurate detection of the CFTR gene mutation 1811+1.6kbA>G by real-time fluorescence resonance energy transfer PCR

Improved methods for genotype determination of human alcohol dehydrogenase (ADH) at ADH 2 and ADH 3 loci by using polymerase chain reaction-directed mutagenesis

Common and rare genotypes of human apolipoprotein E determined by specific restriction profiles of polymerase chain reaction-amplified DNA

Decreased acute hepatotoxicity of carbon tetrachloride and bromobenzene by cholestyramine in the rat

Glutathione S-transferase class μ in French alcoholic cirrhotic patients

GENOTYPING STUDY OF ALCOHOL DEHYDROGENASE CLASS I POLYMORPHISM IN FRENCH PATIENTS WITH ALCOHOLIC CIRRHOSIS

Compound heterozygote for both rare apolipoprotein E1 (Gly127-->Asp, Arg158-->Cys) and E3(Cys112-->Arg, Arg251-->Gly) alleles in a multigeneration pedigree with hyperlipoproteinaemia

The importance of functional tests to assess the effect of a new CFTR variant when genotype-phenotype correlation is not possible

Identification of a new apolipoprotein E variant (E 2 Arg 142 → Leu) in type III hyperlipidemia

Glutathione S-transferase class ? in French alcoholic cirrhotic patients

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