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C Vigouroux

Showing results (51-60 of 68) with videos related to

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Transplant International : Official Journal of the European Society for Organ Transplantation|December 1, 1988
One liver for two: an experimental study in primatesD Houssin, C Vigouroux, F Filipponi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 12, 2003
A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathyF Caux, E Dubosclard, O Lascols, et al.
Diabetes & Metabolism|August 31, 2018
Irisin levels in LMNA-associated partial lipodystrophiesF Bensmaïne, K Benomar, S Espiard, et al.
Clinical Endocrinology|May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronismM C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Diabetes & Metabolism|October 4, 2016
One-year metreleptin therapy decreases PCSK9 serum levels in diabetic patients with monogenic lipodystrophy syndromesC Vatier, L Arnaud, X Prieur, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2008
Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophyM C Vantyghem, D Vincent-Desplanques, F Defrance-Faivre, et al.
European Journal of Histochemistry : EJH|April 9, 2009
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
European Journal of Histochemistry : EJH|September 27, 2018
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Transplant International : Official Journal of the European Society for Organ Transplantation|December 1, 1988
One liver for two: an experimental study in primatesD Houssin, C Vigouroux, F Filipponi, et al.
The Journal of Clinical Endocrinology and Metabolism|March 12, 2003
A new clinical condition linked to a novel mutation in lamins A and C with generalized lipoatrophy, insulin-resistant diabetes, disseminated leukomelanodermic papules, liver steatosis, and cardiomyopathyF Caux, E Dubosclard, O Lascols, et al.
Diabetes & Metabolism|August 31, 2018
Irisin levels in LMNA-associated partial lipodystrophiesF Bensmaïne, K Benomar, S Espiard, et al.
Clinical Endocrinology|May 26, 2007
Familial partial lipodystrophy due to the LMNA R482W mutation with multinodular goitre, extrapyramidal syndrome and primary hyperaldosteronismM C Vantyghem, F Faivre-Defrance, S Marcelli-Tourvieille, et al.
Diabetes & Metabolism|October 4, 2016
One-year metreleptin therapy decreases PCSK9 serum levels in diabetic patients with monogenic lipodystrophy syndromesC Vatier, L Arnaud, X Prieur, et al.
The Journal of Clinical Endocrinology and Metabolism|November 9, 2004
Patients with familial partial lipodystrophy of the Dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalitiesM C Vantyghem, P Pigny, C A Maurage, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2008
Fertility and obstetrical complications in women with LMNA-related familial partial lipodystrophyM C Vantyghem, D Vincent-Desplanques, F Defrance-Faivre, et al.
European Journal of Histochemistry : EJH|April 9, 2009
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
European Journal of Histochemistry : EJH|September 27, 2018
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeriaS Dominici, V Fiori, M Magnani, et al.
Diabetes|November 15, 2000
Lamin A/C gene: sex-determined expression of mutations in Dunnigan-type familial partial lipodystrophy and absence of coding mutations in congenital and acquired generalized lipoatrophyC Vigouroux, J Magré, M C Vantyghem, et al.
Pageof 7