F Demaugre - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

F Demaugre

Showing results (41-50 of 46) with videos related to

Pageof 5

Sort By:

You have reached the last page of results.This site can display upto 46 results.

Progress in Clinical and Biological Research|January 1, 1992

Approach to the patient with a fatty acid oxidation disorderJ M Saudubray, G Mitchell, J P Bonnefont, et al.

The Journal of Pediatrics|October 1, 1992

Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite familyJ C Haworth, F Demaugre, F A Booth, et al.

Journal of Child Neurology|July 1, 1989

Deficiency of carnitine palmitoyltransferase IJ P Bonnefont, R Haas, J Wolff, et al.

Neuromuscular Disorders : NMD|March 29, 2000

Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patientL Thuillier, C Sevin, F Demaugre, et al.

Molecular Genetics and Metabolism|October 6, 1998

Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiencyB Z Yang, J H Ding, T Dewese, et al.

Molecular Genetics and Metabolism|May 15, 2001

Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.

Pageof 5

Search research articles

Showing results (41-50 of 46) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 46 results.

Progress in Clinical and Biological Research|January 1, 1992

Approach to the patient with a fatty acid oxidation disorderJ M Saudubray, G Mitchell, J P Bonnefont, et al.

The Journal of Pediatrics|October 1, 1992

Atypical features of the hepatic form of carnitine palmitoyltransferase deficiency in a Hutterite familyJ C Haworth, F Demaugre, F A Booth, et al.

Journal of Child Neurology|July 1, 1989

Deficiency of carnitine palmitoyltransferase IJ P Bonnefont, R Haas, J Wolff, et al.

Neuromuscular Disorders : NMD|March 29, 2000

Genotype/phenotype correlation in carnitine palmitoyl transferase II deficiency: lessons from a compound heterozygous patientL Thuillier, C Sevin, F Demaugre, et al.

Molecular Genetics and Metabolism|October 6, 1998

Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiencyB Z Yang, J H Ding, T Dewese, et al.

Molecular Genetics and Metabolism|May 15, 2001

Molecular and enzymatic characterization of a unique carnitine palmitoyltransferase 1A mutation in the Hutterite communityC Prip-Buus, L Thuillier, N Abadi, et al.

Pageof 5