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1

2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: Report of a new case

N. Guffon, C. Lopez-Mediavilla, R. Dumoulin, B. Mousson, C. Godinot, H. Carrier, J. M. Collombet, P. Divry, M. Mathieu, P. Guibaud

Journal:

Journal of Inherited Metabolic Disease

Year:

1993

Language:

english

File:

PDF, 562 KB

english, 1993

2

The Fracture Characterization and Fracture Modeling of a Tight Carbonate Reservoir—The Najmah-Sargelu of West Kuwait

Fonta, Olivier, Al-Ajmi, Hamad, Verma, Naveen, Matar, Saad, Divry, Vincent, Al-Qallaf, Hanadi

Journal:

SPE Reservoir Evaluation & Engineering

Year:

2007

Language:

english

File:

PDF, 6.07 MB

english, 2007

3

Routine gas chromatographic/mass spectrometric analysis of urinary organic acids. Results over a three-year period

P. Divry, C. Vianey-Liaud, J. Cotte

Journal:

Biological Mass Spectrometry = Journal of Mass Spectrometry (Wiley)

Year:

1987

Language:

english

File:

PDF, 465 KB

english, 1987

4

l-2-Hydroxyglutaric aciduria: Two further cases

P. Divry, C. Jakobs, C. Vianey-Saban, K. M. Gibson, H. Michelakakis, A. Papadimitriou, R. Divari, B. Chabrol, M. A. Cournelle, M. O. Livet

Journal:

Journal of Inherited Metabolic Disease

Year:

1993

Language:

english

File:

PDF, 180 KB

english, 1993

5

The mutational spectrum in very long-chain acyl-CoA dehydrogenase deficiency

B. S. Andresen, C. Vianey-Saban, P. Bross, P. Divry, C. R. Roe, M. A. Nada, I. Knudsen, N. Gregersen

Journal:

Journal of Inherited Metabolic Disease

Year:

1996

Language:

english

File:

PDF, 283 KB

english, 1996

6

Seventeen novel mutations that cause profound biotinidase deficiency

B Wolf, K Jensen, G Hüner, M Demirkol, T Baykal, P Divry, M.-O Rolland, C Perez-Cerdá, M Ugarte, R Straussberg, L Basel-Vanagaite, E.R Baumgartner, T Suormala, S Scholl, A.M Das, S Schweitzer, E Proni

Journal:

Molecular Genetics and Metabolism

Year:

2002

Language:

english

File:

PDF, 79 KB

english, 2002

7

THE INFLUENCE OF CHEMICAL COMPOSITION ON THE CRYSTALLIZATION AND THE HEAT TRANSFER OF SYNTHETIC MOULD FLUXES

VERMEULEN, Y., DIVRY, E., RIGAUD, M.

Journal:

Canadian Metallurgical Quarterly

Year:

2004

Language:

english

File:

PDF, 719 KB

english, 2004

8

[Society of Petroleum Engineers SPE Middle East Oil and Gas Show and Conference - Kingdom of Bahrain (2005-03-12)] SPE Middle East Oil and Gas Show and Conference - The fracture characterization and fracture modeling of a tight carbonate reservoir: the Najmah Sargelu of West Kuwait

Fonta, Olivier, Matar, Saad Awad, Divry, Vincent Eric, Verma, Naveen Kumar, Al-Shamali, Adnan Aiesh, Al-Qallaf, Hanadi, Morice, Pierre

Language:

english

File:

PDF, 2.75 MB

english

9

Indications Du Traitement Chirurgical De L’Hypertension Artérielle Essentielle:

Dumont, Leon, Divry, A.

Journal:

Acta Clinica Belgica

Year:

1948

File:

PDF, 4.13 MB

1948

10

Influence of formulation on friction properties of latex films

Divry, V., Jacomine, L., Le Houérou, V., Collin, D., Gauthier, C., Holl, Y.

Journal:

Progress in Organic Coatings (Elsevier)

Year:

2017

Language:

english

File:

PDF, 1.08 MB

english, 2017

11

Novel OCTN2 mutations: No genotype–phenotype correlations: Early carnitine therapy prevents cardiomyopathy

Anne-Marie Lamhonwah, Simon E. Olpin, Rodney J. Pollitt, Christine Vianey-Saban, Priscille Divry, Nathalie Guffon, Guy T. N. Besley, Russell Onizuka, Linda J. De Meirleir, Ljerka Cvitanovic-Sojat, Ivo

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 321 KB

english, 2002

12

Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease

P. Divry, M. Mathieu

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 64 KB

english, 1989

13

Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake

Dr. Charles A. Stanley, Susan DeLeeuw, Paul M. Coates, Christine Vianey-Liaud, Priscille Divry, Jean-Paul Bonnefont, Jean-Marie Saudubray, Morey Haymond, Friedrich K. Trefz, Galen N. Breningstall, Reb

Journal:

Annals of Neurology

Year:

1991

Language:

english

File:

PDF, 734 KB

english, 1991

14

3-Methylglutaconic aciduria in “optic atrophy plus”

Dr. Hanan Costeff, Orly Elpeleg, Naomi Apter, Priscille Divry, Natan Gadoth

Journal:

Annals of Neurology

Year:

1993

Language:

english

File:

PDF, 226 KB

english, 1993

15

A 13-bp deletion (1952 del 13) in the methylmalonyl CoA mutase gene of an affected patient

Renaud-Laurian Touraine, Marie-Odile Rolland, Priscille Divry, Monique Mathieu, Pierre Guibaud, Dominique Bozon

Journal:

Year:

1995

Language:

english

File:

PDF, 284 KB

english, 1995

16

A new case of prenatal diagnosis of isovaleric acidaemia

R. Dumoulin, P. Divry, G. Mandon, M. Mathieu

Journal:

Prenatal Diagnosis

Year:

1991

Language:

english

File:

PDF, 158 KB

english, 1991

17

Prenatal diagnosis of combined methylmalonic aciduria and homocystinuria (cobalamin CblC or CblD mutant)

B. Chadefaux-Vekemans, M. O. Rolland, S. Lyonnet, D. Rabier, P. Divry, P. Kamoun

Journal:

Prenatal Diagnosis

Year:

1994

Language:

english

File:

PDF, 136 KB

english, 1994

18

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

Steen Kølvraa, Niels Gregersen, Alexandra I. F. Blakemore, Anne K. Schneidermann, Vibeke Winter, Brage S. Andresen, Diana Curtis, Paul C. Engel, Divry Pricille, William Rhead, Lars Bolund

Journal:

Year:

1991

Language:

english

File:

PDF, 395 KB

english, 1991

19

3-Methylglutaconic aciduria: a phenotype in which activity of 3-methylglutaconyl-coenzyme A hydratase is normal

K. M. Gibson, W. L. Nyhan, L. Sweetman, K. Narisawa, W. Lehnert, P. Divry, B. H. Robinson, K. S. Roth, F. A. Beemer, F. J. Sprang, M. Duran, S. K. Wadman, B. Cartigny

Journal:

European Journal of Pediatrics

Year:

1988

Language:

english

File:

PDF, 816 KB

english, 1988

20

Serum orosomucoid concentration in newborn infants

L. Sann, J. Bienvenu, C. Lahet, P. Divry, J. Cotte, M. Bethenod

Journal:

European Journal of Pediatrics

Year:

1981

Language:

english

File:

PDF, 368 KB

english, 1981

21

Prenatal diagnosis of hereditary tyrosinaemia type I by determination of fumarylacetoacetase in chorionic villus material

E. A. Kvittingen, Pr. P. Guibaud, P. Divry, G. Mandon, M. O. Rolland, Y. Domenichini, C. Jakobs, E. Christensen

Journal:

European Journal of Pediatrics

Year:

1986

Language:

english

File:

PDF, 219 KB

english, 1986

22

Defective succinic semialdehyde dehydrogenase activity in 4-hydroxybutyric aciduria

K. M. Gibson, L. Sweetman, W. L. Nyhan, G. Lenon, P. Divry

Journal:

European Journal of Pediatrics

Year:

1984

Language:

english

File:

PDF, 308 KB

english, 1984

23

Infantile form of carnitine palmitoyltransferase II deficiency in a girl with rapid fatal onset

C. Vianey-Saban, N. Stremler, O. Paut, T. Buttin, P. Divry, M. T. Zabot, J. Camboulives, M. Mathieu, B. Mousson

Journal:

Journal of Inherited Metabolic Disease

Year:

1995

Language:

english

File:

PDF, 137 KB

english, 1995

24

First-trimester prenatal diagnosis of Canavan disease

M. O. Rolland, P. Divry, G. Mandon, J. M. Thoulon, A. Fiumara, M. Mathieu

Journal:

Journal of Inherited Metabolic Disease

Year:

1993

Language:

english

File:

PDF, 138 KB

english, 1993

25

Reliable prenatal diagnosis of Canavan disease (aspartoacylase deficiency): Comparison of enzymatic and metabolite analysis

M. J. Bennett, K. M. Gibson, W. G. Sherwood, P. Divry, M. O. Rolland, O. N. Elpeleg, P. Rinaldo, C. Jakobs

Journal:

Journal of Inherited Metabolic Disease

Year:

1993

Language:

english

File:

PDF, 377 KB

english, 1993

26

Lethal dilated cardiomyopathy due to long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

E. Martins, A. Costa, E. Silva, M. Medina, M. L. Cardoso, C. Vianey-Saban, P. Divry, L. Vilarinho

Journal:

Journal of Inherited Metabolic Disease

Year:

1996

Language:

english

File:

PDF, 161 KB

english, 1996

27

Sudden infant death syndrome: Organic acid profiles in cerebrospinal fluid from 47 children and the occurrence ofN-acetylaspartic acid

P. Divry, C. Vianey-Liaud, C. Jakobs, H. J. Ten-Brink, J. Dutruge, R. Gilly

Journal:

Journal of Inherited Metabolic Disease

Year:

1990

Language:

english

File:

PDF, 210 KB

english, 1990

28

Early prenatal diagnosis of propionic acidaemia with simultaneous sampling of chorionic villus and amniotic fluid

M. O. Rolland, P. Divry, G. Mandon, P. Guibaud, M. Mathieu, G. Sournies, J. M. Thoulon

Journal:

Journal of Inherited Metabolic Disease

Year:

1990

Language:

english

File:

PDF, 237 KB

english, 1990

29

A new case of hyperlysinaemia with saccharopinuria

C. Vianey-Liaud, M. O. Rolland, P. Divry, G. Puthet, M. T. Zabot, J. Cotte

Journal:

Journal of Inherited Metabolic Disease

Year:

1986

Language:

english

File:

PDF, 288 KB

english, 1986

30

GC-MS identification of urinary succinylacetone in two cases of hereditary tyrosinaemia

P. Divry, M. O. Rolland, J. Tessier, M. Desage, J. Cotte

Journal:

Journal of Inherited Metabolic Disease

Year:

1982

Language:

english

File:

PDF, 258 KB

english, 1982

31

Stable-isotope selected-ion monitoring quantification of methylmalonic acid in dried filter-paper urine samples

J. M. Parnet, P. Divry, C. Vianey-Saban, M. Mathieu

Journal:

Journal of Inherited Metabolic Disease

Year:

1996

Language:

english

File:

PDF, 184 KB

english, 1996

32

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

P. Divry, C. Vianey-Liaud, C. Gay, V. Macabeo, F. Rapin, B. Echenne

Journal:

Journal of Inherited Metabolic Disease

Year:

1988

Language:

english

File:

PDF, 156 KB

english, 1988

33

A new case of isolated sulphite oxidase deficiency with rapid fatal outcome

C. Vianey-Liaud, P. Desjacques, J. Gaulme, C. Dorche, P. Vanlieferinghen, P. Dechelotte, P. Divry

Journal:

Journal of Inherited Metabolic Disease

Year:

1988

Language:

english

File:

PDF, 189 KB

english, 1988

34

A new case of methylmalonic aciduria with unexplained negative urinary methylmalonic colorimetric test

C. Charpentier, M. Coude, J-L. Perignon, A. Lombes, J-M. Saudubray, P. Divry

Journal:

Journal of Inherited Metabolic Disease

Year:

1986

Language:

english

File:

PDF, 123 KB

english, 1986

35

Canavan disease: findings in four new cases

H. Michelakakis, S. Giouroukos, P. Divry, E. Katsarou, M. O. Rolland, A. Skardoutsou

Journal:

Journal of Inherited Metabolic Disease

Year:

1991

Language:

english

File:

PDF, 174 KB

english, 1991

36

Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

B. T. Poll-The, J. P. Bonnefont, H. Ogier, C. Charpentier, A. Pelet, J. M. Le Fur, C. Jakobs, R. M. Kok, M. Duran, P. Divry, J. Scotto, J. M. Saudubray

Journal:

Journal of Inherited Metabolic Disease

Year:

1988

Language:

english

File:

PDF, 210 KB

english, 1988

37

Propionyl-CoA-carboxylase determination: Study of enzyme parameters in cultured skin fibroblasts from enzyme-deficient and normal subjects

P. Divry, M. O. Rolland, N. Dingeon, M. Mathieu, J. Cotte, P. Guibaud

Journal:

Journal of Inherited Metabolic Disease

Year:

1978

Language:

english

File:

PDF, 467 KB

english, 1978

38

3-Methylglutaconic aciduria: Familial neonatal form with fatal onset

P. Divry, C. Vianey-Liaud, O. Mory, J. J. Ravussin

Journal:

Journal of Inherited Metabolic Disease

Year:

1987

Language:

english

File:

PDF, 278 KB

english, 1987

39

Combined deficiency of xanthine oxidase and sulphite oxidase: Diagnosis of a new case followed by an antenatal diagnosis

P. Desjacques, B. Mousson, C. Vianey-Liaud, R. Boulieu, C. Bory, P. Baltassat, P. Divry, M. T. Zabot, J. Cotte, P. Lagier, N. Philip

Journal:

Journal of Inherited Metabolic Disease

Year:

1985

Language:

english

File:

PDF, 276 KB

english, 1985

40

α-Aminoadipic andα-ketoadipic aciduria: Detection of a new case by a screening program using two-dimensional thin layer chromatography of amino acids

C. Vianey-Liaud, P. Divry, J. Cotte, G. Teyssier

Journal:

Journal of Inherited Metabolic Disease

Year:

1985

Language:

english

File:

PDF, 255 KB

english, 1985

41

5-Oxoprolinuria (glutathione synthetase deficiency): a case with neonatal presentation and rapid fatal outcome

P. Divry, F. Roulaud-Parrot, C. Dorche, M. T. Zabot, B. Contraire, L. Hagenfeldt, A. Larsson

Journal:

Journal of Inherited Metabolic Disease

Year:

1991

Language:

english

File:

PDF, 225 KB

english, 1991

42

The inborn errors of mitochondrial fatty acid oxidation

C. Vianey-Liaud, P. Divry, N. Gregersen, M. Mathieu

Journal:

Journal of Inherited Metabolic Disease

Year:

1987

Language:

english

File:

PDF, 2.63 MB

english, 1987

43

Carnitine palmitoyl transferase I deficiency presenting as a Reye-like syndrome without hypoglycaemia

C. Vianey-Saban, B. Mousson, C. Bertrand, D. Stamm, R. Dumoulin, M. T. Zabot, P. Divry, D. Floret, M. Mathieu

Journal:

European Journal of Pediatrics

Year:

1993

Language:

english

File:

PDF, 426 KB

english, 1993

44

Prenatal diagnosis of Canavan disease

C. Jakobs, H. J. ten Brink, P. Divry, M. O. Rolland

Journal:

European Journal of Pediatrics

Year:

1992

Language:

english

File:

PDF, 125 KB

english, 1992

45

Stroke, hemiparesis and deficient mitochondrial β-oxidation

Louis Vallée, Monique Fontaine, Jean-Pierre Nuyts, Guy Ricart, Ivan Krivosic, Priscille Divry, Christine Vianey-Saban, Michel Lhermitte, Joseph Vamecq

Journal:

European Journal of Pediatrics

Year:

1994

Language:

english

File:

PDF, 1.27 MB

english, 1994

46

Biochemical study of four cases of propionic acidaemia: GC/MS study of urinary metabolites

P. Divry, R. Boulieu, J. Cotte, M. Desage, R. Guilluy

Journal:

Journal of Inherited Metabolic Disease

Year:

1981

Language:

english

File:

PDF, 159 KB

english, 1981

47

3-Hydroxy-3-methylglutaric aciduria combined with 3-methylglutaconic aciduria: A new case

P. Divry, M. O. Rolland, J. Teyssier, J. Cotte, M. C. Formosinho Fernandes, I. Tavares de Almeida, C. da Silveira

Journal:

Journal of Inherited Metabolic Disease

Year:

1981

Language:

english

File:

PDF, 199 KB

english, 1981

48

4-Hydroxybutyric aciduria: A new inborn error of metabolism. III. Enzymology and inheritance

K. M. Gibson, I. Jansen, L. Sweetman, W. L. Nyhan, D. Rating, C. Jakobs, P. Divry

Journal:

Journal of Inherited Metabolic Disease

Year:

1984

Language:

english

File:

PDF, 206 KB

english, 1984

49

4-Hydroxybutyric aciduria: A new inborn error of metabolism. I. Clinical review

D. Rating, F. Hanefeld, H. Siemes, J. Kneer, C. Jakobs, M. Hermier, P. Divry

Journal:

Journal of Inherited Metabolic Disease

Year:

1984

Language:

english

File:

PDF, 323 KB

english, 1984

50

4-Hydroxybutyric aciduria: A new inborn error of metabolism. II. Biochemical findings

C. Jakobs, J. Kneer, D. Rating, F. Hanefeld, P. Divry, M. Hermier

Journal:

Journal of Inherited Metabolic Disease

Year:

1984

Language:

english

File:

PDF, 253 KB

english, 1984