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Systemic low-grade inflammation is related to both circulating and adipose tissue TNFα, leptin and IL-6 levels in obese womenMAACHI, M; PIERONI, L; BRUCKERT, E et al.International journal of obesity. 2004, Vol 28, Num 8, pp 993-997, issn 0307-0565, 5 p.Article

Interpretation of circulating C-reactive protein levels in adults: Body mass index and gender are a mustPIDRONI, L; BASTARD, J. P; PITON, A et al.Diabetes & metabolism. 2003, Vol 29, Num 2, pp 133-138, issn 1262-3636, 6 p., 1Article

Cure de diurèse : effets comparés de l'eau de Vittel grande source et d'une eau peu minéralisée sur 27 variables urinaires et sanguines chez 23 sujets sains = Diuresis cure. Biological comparison of the effect of a mineral water (Vittel Grande Source) and a low mineralised water on 23 healthy adults, analysed through 27 urinary and plasmatic variablesDELABROISE, A.-M; BARTHELEMY, C; LEGRAND, S et al.Médecine et nutrition. 1990, Vol 26, Num 1, pp 15-20, issn 0398-7604Article

Prélèvement du tissu adipeux : techniques, intérêt en recherche et en clinique = Adipose tissue biopsy : techniques, clinical relevance and research valueBASTARD, J.-P; JARDEL, C; HAINQUE, B et al.STV. Sang thrombose vaisseaux. 1996, Vol 8, Num 5, pp 323-325, issn 0999-7385Article

Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNAWAHBI, K; LARUE, S; JARDEL, C et al.Neurology. 2010, Vol 74, Num 8, pp 674-677, issn 0028-3878, 4 p.Article

Subcutaneous adipose tissue expression of plasminogen activator inhibitor-1 gene during very low calorie diet in obese subjectsBASTARD, J.-P; VIDAL, H; JARDEL, C et al.International journal of obesity. 2000, Vol 24, Num 1, pp 70-74, issn 0307-0565Article

Peroxisome proliferator activated receptor-γ, leptin and tumor necrosis factor-α mRNA expression during very low calorie diet in subcutaneous adipose tissue in obese womenBASTARD, J.-P; HAINQUE, B; LAVILLE, M et al.Diabetes/metabolism research and reviews (Print). 1999, Vol 15, Num 2, pp 92-98, issn 1520-7552Article

Antioxidant status of elderly chronic renal patients treated by continuous ambulatory peritoneal dialysisBONNEFONT-ROUSSELOT, D; JAUDON, M. C; ISSAD, B et al.Nephrology, dialysis, transplantation (Print). 1997, Vol 12, Num 7, pp 1399-1405, issn 0931-0509Article

The role of interleukin-6 in vitamin A deficiency during Plasmodium falciparum malaria and possible consequences for vitamin A supplementationTABONE, M. D; MUANZA, K; LYAGOUBI, M et al.Immunology (Oxford). 1992, Vol 75, Num 3, pp 553-554, issn 0019-2805Article

Adult cases of mitochondrial DNA depletion due to TK2 defect: An expanding spectrumBEHIN, A; JARDEL, C; CLAEYS, K. G et al.Neurology. 2012, Vol 78, Num 9, pp 644-648, issn 0028-3878, 5 p.Article

Anderson's disease (chylomicron retention disease) : a new mutation in the SARA2 gene associated with muscular and cardiac abnormalitiesSILVAIN, M; BLIGNY, D; WALKER, F et al.Clinical genetics. 2008, Vol 74, Num 6, pp 546-552, issn 0009-9163, 7 p.Article

Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutationBATAILLARD, M; CHATZOGLOU, E; RUMBACH, L et al.Neurology. 2001, Vol 56, Num 3, pp 405-407, issn 0028-3878Article

β2-Microglobuline : étude comparative et transférabilité des résultats obtenus à partir de différents analyseurs = β2-Microglobulin : a comparison of results obtained by several analyzersGLIKMANAS, G; HAMIDA, F; RAINTEAU, D et al.Immuno analyse & biologie spécialisée. 1997, Vol 12, Num 1, pp 29-35, issn 0923-2532Conference Paper

Protéines glyquées plasmatiques dans l'insuffisance rénale chronique = Glycated plasma proteins in patients with chronic renal failureBORDAS-FONDREDE, M; SAUSER, E; JARDEL, C et al.Annales de biologie clinique (Paris). 1990, Vol 48, Num 10, pp 717-721, issn 0003-3898Article

Le Champ Pagès = The Pagès CampGAUSSEN, J; JARDEL, C; MERLAUD, B et al.Paléo (Les Eyzies de Tayac-Sireuil). 1993, Num 5, pp 239-247, issn 1145-3370Article

Severe epilepsy as the major symptom of new mutations in the mitochondrial tRNAPhe geneZSURKA, G; HAMPEL, K. G; KUNZ, W. S et al.Neurology. 2010, Vol 74, Num 6, pp 507-512, issn 0028-3878, 6 p.Article

Kearns Sayre syndrome : an unusual form of mitochondrial diabetesLALOI-MICHELIN, M; VIRALLY, M; GUILLAUSSEAU, P. J et al.Diabetes & metabolism. 2006, Vol 32, Num 2, pp 182-186, issn 1262-3636, 5 p.Article

Subcutaneous adipose tissue expression of tumour necrosis factor-α is not associated with whole body insulin resistance in obese nondiabetic or in type-2 diabetic subjectsKOISTINEN, H. A; BASTARD, J.-P; HAINQUE, B et al.European journal of clinical investigation. 2000, Vol 30, Num 4, pp 302-310, issn 0014-2972Article

Evidence for a relationship between plasminogen activator inhibitor-1 and gamma glutamyl transferaseBASTARD, J.-P; BRUCKERT, E; PORQUET, D et al.Thrombosis research. 1996, Vol 81, Num 2, pp 271-275, issn 0049-3848Article

Are free fatty acids related to plasma plasminogen activator inhibitor 1 in android obesity ?BASTARD, J.-P; BRUCKERT, J.-J; ROBERT, J.-J et al.International journal of obesity. 1995, Vol 19, Num 11, pp 836-838, issn 0307-0565Article

Antimalarial activity of cedroninMORETTI, C; DEHARO, E; SAUVAIN, M et al.Journal of ethnopharmacology. 1994, Vol 43, Num 1, pp 57-61, issn 0378-8741Article

Déficit multiple en acyl-CoA déshydrogénases: une cause traitable de lipidose musculaire d'origine génétique = Multiple acyl-CoA dehydrogenase deficiency (MADD): A curable cause of genetic muscular lipidosisMAILLART, E; ACQUAVIVA-BOURDAIN, C; RIGAL, O et al.Revue neurologique (Paris). 2010, Vol 166, Num 3, pp 289-294, issn 0035-3787, 6 p.Article

Muscle coenzyme Q10 deficiencies in ataxia with oculomotor apraxia 1LE BER, I; DUBOURG, O; BENOIST, J.-F et al.Neurology. 2007, Vol 68, Num 4, pp 295-297, issn 0028-3878, 3 p.Article

Errance diagnostique dans les myopathies mitochondriales : étude de 12 patients thymectomisés = Misdiagnosis of mitochondrial myopathies : a study of 12 thymectomized patientsBEN YAOU, R; LAFORET, P; BECANE, H. M et al.Revue neurologique (Paris). 2006, Vol 162, Num 3, pp 339-346, issn 0035-3787, 8 p.Article

Myopathie-lipomatose par mutation A8344G de l'ADN mitochondrial = Myopathy-lipomatosis associated with a tRNAlys A8344G mitochondrial DNA mutationAURE, K; STERNBERG, D; MAISONOBE, T et al.Revue neurologique (Paris). 2003, Vol 159, Num 12, pp 1163-1168, issn 0035-3787, 6 p.Article

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