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Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study.
BMC Public Health. 2016 Sep 29;16(1):1021. doi: 10.1186/s12889-016-3690-9.
BMC Public Health. 2016.
PMID: 27682602
Free PMC article.
Familial Hypocalciuric Hypercalcemia Types 1 and 3 and Primary Hyperparathyroidism: Similarities and Differences.
Vargas-Poussou R, Mansour-Hendili L, Baron S, Bertocchio JP, Travers C, Simian C, Treard C, Baudouin V, Beltran S, Broux F, Camard O, Cloarec S, Cormier C, Debussche X, Dubosclard E, Eid C, Haymann JP, Kiando SR, Kuhn JM, Lefort G, Linglart A, Lucas-Pouliquen B, Macher MA, Maruani G, Ouzounian S, Polak M, Requeda E, Robier D, Silve C, Souberbielle JC, Tack I, Vezzosi D, Jeunemaitre X, Houillier P.
Vargas-Poussou R, et al. Among authors: dubosclard e.
J Clin Endocrinol Metab. 2016 May;101(5):2185-95. doi: 10.1210/jc.2015-3442. Epub 2016 Mar 10.
J Clin Endocrinol Metab. 2016.
PMID: 26963950
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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 cardiomyopathy.
Caux F, Dubosclard E, Lascols O, Buendia B, Chazouillères O, Cohen A, Courvalin JC, Laroche L, Capeau J, Vigouroux C, Christin-Maitre S.
Caux F, et al. Among authors: dubosclard e.
J Clin Endocrinol Metab. 2003 Mar;88(3):1006-13. doi: 10.1210/jc.2002-021506.
J Clin Endocrinol Metab. 2003.
PMID: 12629077
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[Diabetes and genetic and acquired lipodystrophy syndrome].
Capeau J, Magré J, Vigouroux C, Caron M, Maachi M, Dubosclard E, Lascols O, Bastard JP.
Capeau J, et al. Among authors: dubosclard e.
Journ Annu Diabetol Hotel Dieu. 2003:99-109.
Journ Annu Diabetol Hotel Dieu. 2003.
PMID: 12868305
Review.
French.
No abstract available.
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Nuclear envelope disorganization in fibroblasts from lipodystrophic patients with heterozygous R482Q/W mutations in the lamin A/C gene.
Vigouroux C, Auclair M, Dubosclard E, Pouchelet M, Capeau J, Courvalin JC, Buendia B.
Vigouroux C, et al. Among authors: dubosclard e.
J Cell Sci. 2001 Dec;114(Pt 24):4459-68. doi: 10.1242/jcs.114.24.4459.
J Cell Sci. 2001.
PMID: 11792811
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Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.
Favreau C, Dubosclard E, Ostlund C, Vigouroux C, Capeau J, Wehnert M, Higuet D, Worman HJ, Courvalin JC, Buendia B.
Favreau C, et al. Among authors: dubosclard e.
Exp Cell Res. 2003 Jan 1;282(1):14-23. doi: 10.1006/excr.2002.5669.
Exp Cell Res. 2003.
PMID: 12490190
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