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Drying Mechanisms in Plasticized Latex Films: Role of Horizontal Drying Fronts

The journal of physical chemistry. B, 2016-07, Vol.120 (27), p.6791-6802

2016

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Influence of formulation on friction properties of latex films

Progress in organic coatings, 2017-12, Vol.113, p.189-199

2017

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Fetomaternal hemorrhage: practitioner's point of view

Journal de gynécologie, obstétrique et biologie de la reproduction, 2009-06, Vol.38 (4), p.286-297

2009

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Hémorragie fœtomaternelle : le point de vue du clinicien

Journal de gynécologie, obstétrique et biologie de la reproduction, 2009-06, Vol.38 (4), p.286-297

2009

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Fracture Characterization and Modeling of a Tight-Carbonate Reservoir

Journal of petroleum technology, 2005-10, Vol.57 (10), p.61-64

Denney, Dennis

2005

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Additive effect of APOE rare variants on the phenotype of familial hypercholesterolemia

Atherosclerosis, 2023-08, Vol.379, p.S26

2023

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Combined liver-kidney transplantation in primary hyperoxaluria type 1

European journal of pediatrics, 1999-12, Vol.158 Suppl 2 (S2), p.S75-S080

1999

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Identification of a Mutation Cluster in Mevalonate Kinase Deficiency, Including a New Mutation in a Patient of Mennonite Ancestry

American journal of human genetics, 1999-08, Vol.65 (2), p.327-335

1999

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N-acetylaspartylglutamate in Canavan disease : an adverse effector?

European journal of pediatrics, 1999-05, Vol.158 (5), p.406-409

1999

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A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)

American journal of human genetics, 1993-09, Vol.53 (3), p.730-739

1993

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N‐Acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophy

Journal of inherited metabolic disease, 1988-09, Vol.11 (3), p.307-308

1988

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L'acidurie N-acétylaspartique: une nouvelle forme d'encéphalopathie démyélinisante

La Presse médicale (1983), 1988-01, Vol.17 (3)

1988

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Thiamin-responsive megaloblastic anaemia: a disorder of thiamin transport?

Journal of inherited metabolic disease, 1984, Vol.7 (2), p.153-154

1984

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The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene

Human genetics, 1991-08, Vol.87 (4), p.425-428

1991

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N-acetylaspartic aciduria: a new form of demyelinating encephalopathy

La Presse médicale (1983), 1988-01, Vol.17 (3), p.126-126

1988

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The antenatal diagnosis and aid to the management of hereditary tyrosinaemia by use of a specific and sensitive GC-MS assay for succinylacetone

Journal of inherited metabolic disease, 1984, Vol.7 (2), p.135-136

1984

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Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine

Clinica chimica acta, 1983-05, Vol.130 (2), p.231-238

1983

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An evaluation of urine lactate for detection of inborn errors of metabolism

Journal of inherited metabolic disease, 1984, Vol.7 (2), p.111-112

1984

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UNE MALADIE FAMILIALE CARACTÉRISÉE PAR UNE ANGIOMATOSE DIFFUSE CORTICO-MÉNINGÉE NON CALCIFIANTE ET UNE DÉMYÉLINISATION PROGRESSIVE DE LA SUBSTANCE BLANCHE

Journal of neurology, neurosurgery and psychiatry, 1946-04, Vol.9 (2), p.41-54

1946

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N-acetylaspartic aciduria. Clinical, biological and physiopathological study

Archives françaises de pediatrie, 1991-06, Vol.48 (6), p.409

1991

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Painful and transient spasm of the cardioesophageal sphincter (author's transl)

Journal de radiologie, d'electrologie, et de medecine nucleaire, 1977-04, Vol.58 (4), p.261

1977

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Intravenous duodenography: a routine investigation (author's transl)

Journal de radiologie, d'electrologie, et de medecine nucleaire, 1975-12, Vol.56 (12), p.861

1975

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INTRAMEDULLARY CAVERNOUS ANGIOMA OF THE CERVICAL PROTUBERANCE AND AMYOTROPHIC LATERAL PSEUDOSCLEROSIS

Acta neurologica et psychiatrica Belgica, 1963-07, Vol.63, p.527

1963

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Trickling mucography under high pressure and with moderate contrast. First phase of gastroduodenal examinations (author's transl)

Journal de radiologie, d'electrologie, et de medecine nucleaire, 1978-04, Vol.59 (4), p.239

1978

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Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency

Pédiatrie (Paris ), 1984-12, Vol.39 (8), p.661

1984

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Drying Mechanisms in Plasticized Latex Films: Role of Horizontal Drying Fronts

Influence of formulation on friction properties of latex films

Fetomaternal hemorrhage: practitioner's point of view

Hémorragie fœtomaternelle : le point de vue du clinicien

Fracture Characterization and Modeling of a Tight-Carbonate Reservoir

Additive effect of APOE rare variants on the phenotype of familial hypercholesterolemia

Combined liver-kidney transplantation in primary hyperoxaluria type 1

Identification of a Mutation Cluster in Mevalonate Kinase Deficiency, Including a New Mutation in a Patient of Mennonite Ancestry

N-acetylaspartylglutamate in Canavan disease : an adverse effector?

A rare disease-associated mutation in the medium-chain acyl-CoA dehydrogenase (MCAD) gene changes a conserved arginine, previously shown to be functionally essential in short-chain acyl-CoA dehydrogenase (SCAD)

N‐Acetylaspartic aciduria: report of three new cases in children with a neurological syndrome associating macrocephaly and leukodystrophy

L'acidurie N-acétylaspartique: une nouvelle forme d'encéphalopathie démyélinisante

Thiamin-responsive megaloblastic anaemia: a disorder of thiamin transport?

The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene

N-acetylaspartic aciduria: a new form of demyelinating encephalopathy

The antenatal diagnosis and aid to the management of hereditary tyrosinaemia by use of a specific and sensitive GC-MS assay for succinylacetone

Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine

An evaluation of urine lactate for detection of inborn errors of metabolism

UNE MALADIE FAMILIALE CARACTÉRISÉE PAR UNE ANGIOMATOSE DIFFUSE CORTICO-MÉNINGÉE NON CALCIFIANTE ET UNE DÉMYÉLINISATION PROGRESSIVE DE LA SUBSTANCE BLANCHE

N-acetylaspartic aciduria. Clinical, biological and physiopathological study

Painful and transient spasm of the cardioesophageal sphincter (author's transl)

Intravenous duodenography: a routine investigation (author's transl)

INTRAMEDULLARY CAVERNOUS ANGIOMA OF THE CERVICAL PROTUBERANCE AND AMYOTROPHIC LATERAL PSEUDOSCLEROSIS

Trickling mucography under high pressure and with moderate contrast. First phase of gastroduodenal examinations (author's transl)

Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency

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