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1
CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait
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CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait

Molin, A ; Baudoin, R ; Kaufmann, M ; Souberbielle, J. C ; Ryckewaert, A ; Vantyghem, M. C ; Eckart, P ; Bacchetta, J ; Deschenes, G ; Kesler-Roussey, G ; Coudray, N ; Richard, N ; Wraich, M ; Bonafiglia, Q ; Tiulpakov, A ; Jones, G ; Kottler, M.-L

The journal of clinical endocrinology and metabolism, 2015-10, Vol.100 (10), p.E1343-E1352 [Periódico revisado por pares]

United States: Endocrine Society

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2
Irisin levels in LMNA-associated partial lipodystrophies
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Artigo
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Irisin levels in LMNA-associated partial lipodystrophies

Bensmaïne, F. ; Benomar, K. ; Espiard, S. ; Vahe, C. ; Le Mapihan, K. ; Lion, G. ; Lemdani, M. ; Chazard, E. ; Ernst, O. ; Vigouroux, C. ; Pigny, P. ; Vantyghem, M.-C.

Diabetes & metabolism, 2019-01, Vol.45 (1), p.67-75 [Periódico revisado por pares]

France: Elsevier Masson SAS

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3
One-year metreleptin therapy decreases PCSK9 serum levels in diabetic patients with monogenic lipodystrophy syndromes
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Artigo
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One-year metreleptin therapy decreases PCSK9 serum levels in diabetic patients with monogenic lipodystrophy syndromes

Vatier, C ; Arnaud, L ; Prieur, X ; Guyomarch, B ; Le May, C ; Bigot, E ; Pichelin, M ; Daguenel, A ; Vantyghem, M.-C ; Gautier, J.-F ; Vigouroux, C ; Cariou, B

Diabetes & metabolism, 2017-06, Vol.43 (3), p.275-279 [Periódico revisado por pares]

France: Elsevier Masson SAS

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4
Multiple Endocrine Neoplasia Type 4: Novel CDNK1B variant and immune anomalies
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Artigo
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Multiple Endocrine Neoplasia Type 4: Novel CDNK1B variant and immune anomalies

Chevalier, B. ; Odou, M.-F. ; Demonchy, J. ; Cardot-Bauters, C. ; Vantyghem, M.-C.

Annales d'endocrinologie, 2020-06, Vol.81 (2-3), p.124-125 [Periódico revisado por pares]

France: Elsevier Masson SAS

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5
Islet Survival and Function Following Intramuscular Autotransplantation in the Minipig
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Artigo
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Islet Survival and Function Following Intramuscular Autotransplantation in the Minipig

Sterkers, A. ; Hubert, T. ; Gmyr, V. ; Torres, F. ; Baud, G. ; Delalleau, N. ; Vantyghem, M. C. ; Kerr‐Conte, J. ; Caiazzo, R. ; Pattou, F.

American journal of transplantation, 2013-04, Vol.13 (4), p.891-898 [Periódico revisado por pares]

Hoboken, NJ: Wiley

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6
Phenotype–genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome
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Artigo
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Phenotype–genotype correlation and follow-up in adult patients with hypokalaemia of renal origin suggesting Gitelman syndrome

Balavoine, A S ; Bataille, P ; Vanhille, P ; Azar, R ; Noël, C ; Asseman, P ; Soudan, B ; Wémeau, J L ; Vantyghem, M C

European journal of endocrinology, 2011-10, Vol.165 (4), p.665-673 [Periódico revisado por pares]

Bristol: BioScientifica

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7
Glycemic variability indices can be used to diagnose islet transplantation success in type 1 diabetic patients
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Artigo
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Glycemic variability indices can be used to diagnose islet transplantation success in type 1 diabetic patients

Jalbert, Manon ; Zheng, Fei ; Wojtusciszyn, Anne ; Forbes, Florence ; Bonnet, Stéphane ; Skaare, Kristina ; Benhamou, Pierre-Yves ; Lablanche, Sandrine

Acta diabetologica, 2020-03, Vol.57 (3), p.335-345 [Periódico revisado por pares]

Milan: Springer Milan

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8
Treating diabetes with islet transplantation: Lessons from the past decade in Lille
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Artigo
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Treating diabetes with islet transplantation: Lessons from the past decade in Lille

Vantyghem, M.-C ; Defrance, F ; Quintin, D ; Leroy, C ; Raverdi, V ; Prévost, G ; Caiazzo, R ; Kerr-Conte, J ; Glowacki, F ; Hazzan, M ; Noel, C ; Pattou, F

Diabetes & metabolism, 2014-04, Vol.40 (2), p.108-119 [Periódico revisado por pares]

Paris: Elsevier Masson SAS

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9
Fertility and Obstetrical Complications in Women with LMNA-Related Familial Partial Lipodystrophy
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Artigo
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Fertility and Obstetrical Complications in Women with LMNA-Related Familial Partial Lipodystrophy

Vantyghem, M. C ; Vincent-Desplanques, D ; Defrance-Faivre, F ; Capeau, J ; Fermon, C ; Valat, A. S ; Lascols, O ; Hecart, A. C ; Pigny, P ; Delemer, B ; Vigouroux, C ; Wemeau, J. L

The journal of clinical endocrinology and metabolism, 2008-06, Vol.93 (6), p.2223-2229 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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10
Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to a LMNA R482W Mutation Show Muscular and Cardiac Abnormalities
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Patients with Familial Partial Lipodystrophy of the Dunnigan Type Due to a LMNA R482W Mutation Show Muscular and Cardiac Abnormalities

Vantyghem, M. C ; Pigny, P ; Maurage, C. A ; Rouaix-Emery, N ; Stojkovic, T ; Cuisset, J. M ; Millaire, A ; Lascols, O ; Vermersch, P ; Wemeau, J. L ; Capeau, J ; Vigouroux, C

The journal of clinical endocrinology and metabolism, 2004-11, Vol.89 (11), p.5337-5346 [Periódico revisado por pares]

Bethesda, MD: Endocrine Society

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