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Annales De Biologie Clinique|April 9, 2008
[Biochemical exploration of energetic metabolism and oxidative stress in low grade gliomas: central and peripheral tumor tissue analysis]F Lamari, R La Schiazza, R Guillevin, et al.
The Journal of Clinical Endocrinology and Metabolism|September 22, 2000
Elevated levels of interleukin 6 are reduced in serum and subcutaneous adipose tissue of obese women after weight lossJ P Bastard, C Jardel, E Bruckert, et al.
Neurology|December 15, 2004
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysisS Vicart, D Sternberg, E Fournier, et al.
Cardiovascular Research|March 23, 2000
Novel mutations in KvLQT1 that affect Iks activation through interactions with IskC Chouabe, N Neyroud, P Richard, et al.
Journal of Molecular Biology|December 28, 1999
COOH-terminal truncated cardiac myosin-binding protein C mutants resulting from familial hypertrophic cardiomyopathy mutations exhibit altered expression and/or incorporation in fetal rat cardiomyocytesJ Flavigny, M Souchet, P Sébillon, et al.
Annales De Biologie Clinique|November 26, 2004
[Influence of pyridoxal phosphate in measuring aminotransferases activities in patients with viral hepatitis]G Férard, F Imbert-Bismut, D Messous, et al.
Nutrition, Metabolism, and Cardiovascular Diseases : NMCD|March 22, 2000
Modifications of alpha-tocopherol and fatty acid concentrations in blood and adipose tissue of obese patients during a weight loss programmeD Bonnefont-Rousselot, S Lepage, P Thérond, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2001
[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]J M Lupoglazoff, I Denjoy, M Berthet, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|March 7, 2000
Subcutaneous adipose tissue expression of plasminogen activator inhibitor-1 gene during very low calorie diet in obese subjectsJ P Bastard, H Vidal, C Jardel, et al.
Brain : a Journal of Neurology|May 17, 2001
Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4AD Sternberg, T Maisonobe, K Jurkat-Rott, et al.
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