E-LIB Suche - Ergebnisse für: Redonnet-Vernhet, Isabelle

1

Preventing hyperhomocysteinemia using vitamin B6 supplement..:

Redonnet-Vernhet, Isabelle ; Mercié, Patrick ; Lebreton, Louis...
Molecular Genetics and Metabolism Reports. 39 (2024) - p. 101076 , 2024

Link: https://doi.org/10.1016/..

2

Amino acids and vitamins status during continuous renal rep..:

Schneider, Antoine G. ; Picard, Walter ; Honoré, Patrick M....
Anaesthesia Critical Care & Pain Medicine. 40 (2021) 2 - p. 100813 , 2021

Link: https://doi.org/10.1016/..

3

Energy Metabolism Rewiring Precedes UVB-Induced Primary Ski..:

Hosseini, Mohsen ; Dousset, Léa ; Mahfouf, Walid...
Cell Reports. 23 (2018) 12 - p. 3621-3634 , 2018

Link: https://doi.org/10.1016/..

4

Fluxomic evidence for impaired contribution of short-chain ..:

Dessein, Anne-Frédérique ; Fontaine, Monique ; Joncquel-Chevalier Curt, Marie...
Clinica Chimica Acta. 471 (2017) - p. 101-106 , 2017

Link: https://doi.org/10.1016/..

5

Coagulopathies frequency in aseptic osteonecrosis patients:

Mehsen, Nadia ; Barnetche, Thomas ; Redonnet-Vernhet, Isabelle...
Joint Bone Spine. 76 (2009) 2 - p. 166-169 , 2009

Link: https://doi.org/10.1016/..

6

Ostéonécrose aseptique : fréquence des coagulopathies:

Mehsen, Nadia ; Barnetche, Thomas ; Redonnet-Vernhet, Isabelle...
Revue du Rhumatisme. 76 (2009) 3 - p. 256-260 , 2009

Link: https://doi.org/10.1016/..

7

Maladie de Fabry: propositions d'ungroupe d'experts françai..:

Lidove, Olivier ; Bekri, Soumeya ; Goizet, Cyril...
La Presse Médicale. 36 (2007) 7-8 - p. 1084-1097 , 2007

Link: https://doi.org/10.1016/..

8

Statistical Analysis of Mitochondrial Pathologies in Childh..:

Letellier, Thierry ; Durrieu, Gilles ; Malgat, Monique...
Laboratory Investigation. 80 (2000) 7 - p. 1019-1030 , 2000

Link: https://doi.org/10.1038/..

9

Cholesteryl Ester Storage Disease: Relationship between Mol..:

Redonnet-Vernhet, Isabelle ; Chatelut, Martine ; Basile, Jean-Pierre..
Biochemical and Molecular Medicine. 62 (1997) 1 - p. 42-49 , 1997

Link: https://doi.org/10.1006/..

10

Significance of two point mutations present in each HEXB al..:

Redonnet-Vernhet, Isabelle ; Mahuran, Don J. ; Salvayre, Robert..
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1317 (1996) 2 - p. 127-133 , 1996

Link: https://doi.org/10.1016/..

11

Postauthorization safety study of betaine anhydrous:

Mütze, Ulrike ; Gleich, Florian ; Garbade, Sven F....
Journal of Inherited Metabolic Disease. 45 (2022) 4 - p. 719-733 , 2022

Link: https://doi.org/10.1002/..

12

Adult‐onset diagnosis of urea cycle disorders: Results of a..:

Toquet, Ségolène ; Spodenkiewicz, Marta ; Douillard, Claire...
Journal of Inherited Metabolic Disease. 44 (2021) 5 - p. 1199-1214 , 2021

Link: https://doi.org/10.1002/..

13

Downregulation of Glutamine Synthetase, not glutaminolysis,..:

Nguyen, Tra Ly ; Nokin, Marie‐Julie ; Terés, Silvia...
Molecular Oncology. 15 (2021) 5 - p. 1412-1431 , 2021

Link: https://doi.org/10.1002/..

14

Clinical and molecular characterization of adult patients w..:

Marelli, Cecilia ; Lavigne, Christian ; Stepien, Karolina M....
Journal of Inherited Metabolic Disease. 44 (2020) 3 - p. 777-786 , 2020

Link: https://doi.org/10.1002/..

15

Succinate‐CoA ligase deficiency due to mutations in SUCLA2 ..:

Carrozzo, Rosalba ; Verrigni, Daniela ; Rasmussen, Magnhild...
Journal of Inherited Metabolic Disease. 39 (2015) 2 - p. 243-252 , 2015

Link: https://doi.org/10.1007/..