DIVRY, Priscille: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

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

2

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

3

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

4

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

5

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

6

Two Missense Point Mutations in Different Alleles in the 3-Hydroxy-3-methylglutaryl Coenzyme A Lyase Gene Produce 3-Hydroxy-3-methylglutaric Aciduria in a French Patient

Núria Zapater, Juan Pié, Jorge Lloberas, Marie-Odile Rolland, Bernard Leroux, Michel Vidailhet, Priscille Divry, Fausto G. Hegardt, Núria Casals

Journal:

Archives of Biochemistry and Biophysics

Year:

1998

Language:

english

File:

PDF, 480 KB

english, 1998

7

Hypoxanthine and xanthine concentrations determined by high performance liquid chromatography in biological fluids from patients with xanthinuria

Roselyne Boulieu, Claude Bory, Pierre Baltassat, Priscille Divry

Journal:

Clinica Chimica Acta

Year:

1984

Language:

english

File:

PDF, 405 KB

english, 1984

8

Purification of electron transfer flavoprotein from pig liver mitochondria and its application to the diagnosis of deficiencies of acyl-CoA dehydrogenases in human fibroblasts

Catherine Bertrand, Renée Dumoulin, Priscille Divry, Monique Mathieu, Christine Vianey-Saban

Journal:

Clinica Chimica Acta

Year:

1992

Language:

english

File:

PDF, 1.30 MB

english, 1992

9

Acylcarnitine removal in a patient with acyl-CoA β-oxidation deficiency disorder: effect of l-carnitine therapy and starvation

Monique Fontaine, Gilbert Briand, Louis Vallée, Guy Ricart, Pierre Degand, Priscille Divry, Christine Vianey-Saban, Joseph Vamecq

Journal:

Clinica Chimica Acta

Year:

1996

Language:

english

File:

PDF, 726 KB

english, 1996

10

Mitochondrial very-long-chain acyl-coenzyme A dehydrogenase deficiency: clinical characteristics and diagnostic considerations in 30 patients

Christine Vianey-Saban, Priscille Divry, Michèle Brivet, Mohamed Nada, Marie-Thérèse Zabot, Monique Mathieu, Charles Roe

Journal:

Clinica Chimica Acta

Year:

1998

Language:

english

File:

PDF, 163 KB

english, 1998

11

Metabolic studies in a patient with severe carnitine palmitoyltransferase type II deficiency

Monique Fontaine, Gilbert Briand, Claude Largillière, Pierre Degand, Priscille Divry, Christine Vianey-Saban, Bénédicte Mousson, Joseph Vamecq

Journal:

Clinica Chimica Acta

Year:

1998

Language:

english

File:

PDF, 125 KB

english, 1998

12

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

Debra D. Hinson, Richard M. Ross, Skaidrite Krisans, Joanne L. Shaw, Viktor Kozich, Marie-Odile Rolland, Priscille Divry, Josette Mancini, Georg F. Hoffmann, K. Michael Gibson

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 373 KB

english, 1999

13

Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency

Jean-Paul Harpey, Christiane Charpentier, Marie Coudé, Priscille Divry, Marion Paturneau-Jouas

Journal:

The Journal of Pediatrics

Year:

1987

Language:

english

File:

PDF, 327 KB

english, 1987

14

Mevalonic aciduria in 3 siblings: A new recognizable metabolic encephalopathy

Mancini, Josette, Philip, Nicole, Chabrol, Brigitte, Divry, Priscille, Rolland, Marie-Odile, Pinsard, Nicole

Journal:

Pediatric Neurology

Year:

1993

Language:

english

File:

PDF, 688 KB

english, 1993

15

LIVER TRANSPLANTATION IN PRIMARY HYPEROXALURIA TYPE 1

Cochat, Pierre, Louis Faure, Jean, Divry, Priscille, Danpure, ChristopherJ., Descos, Bruno, Wright, Catherine, Takvorian, Philippe, Floret, Daniel

Journal:

Year:

1989

Language:

english

File:

PDF, 348 KB

english, 1989

16

A nonsense mutation in the 3-hydroxy-3-methylglutaryl-CoA lyase gene produces exon skipping in two patients of different origin with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

PIÉ, Juan, CASALS, Núria, CASALE, Cesar H., BUESA, Carlos, MASCARÓ, Cristina, BARCELÓ, Anna, ROLLAND, Marie-Odile, ZABOT, Theresa, HARO, Diego, EYSKENS, François, DIVRY, Priscille, HEGARDT, Fausto G.

Journal:

Biochemical Journal

Year:

1997

Language:

english

File:

PDF, 458 KB

english, 1997

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@z-lib.do

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски