Morphological Mosaicism of the Pancreatic Islets: A Novel Anatomopathological Form of Persistent Hyperinsulinemic Hypoglycemia of Infancy
Sempoux, C, Capito, C, Bellanné-Chantelot, C, Verkarre, V, de Lonlay, P, Aigrain, Y, Fekete, C, Guiot, Y, Rahier, J
Published in The journal of clinical endocrinology and metabolism (01.12.2011)
Published in The journal of clinical endocrinology and metabolism (01.12.2011)
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The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes
Laloi-Michelin, M., Meas, T., Ambonville, C., Bellanné-Chantelot, C., Beaufils, S., Massin, P., Vialettes, B., Gin, H., Timsit, J., Bauduceau, B., Bernard, L., Bertin, E., Blickle, J.-F., Cahen-Varsaux, J., Cailleba, A., Casanova, S., Cathebras, P., Charpentier, G., Chedin, P., Crea, T., Delemer, B, Dubois-Laforgue, D., Duchemin, F., Ducluzeau, P. H., Bouhanick, B., Dusselier, L., Gabreau, T., Grimaldi, A., Guerci, B., Jacquin, V., Kaloustian, E., Larger, E., Lecleire-Collet, A., Lorenzini, F., Louis, J., Mausset, J., Murat, A., Nadler-Fluteau, S., Olivier, F., Paquis-Flucklinger, V., Paris-Bockel, D., Raynaud, I., Reznik, Y., Riveline, J. P., Schneebeli, S., Sonnet, E., Sola-Gazagnes, A., Thomas, J. L., Trabulsi, B., Virally, M., Guillausseau, P. J.
Published in The journal of clinical endocrinology and metabolism (01.08.2009)
Published in The journal of clinical endocrinology and metabolism (01.08.2009)
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Journal Article
S162: SOMATIC GENETIC LANDSCAPE IN GATA2 DEFICIENCY PATIENTS
Largeaud, L., Collin, M., Monselet, N., Vergez, F., Larcher, L., Hirsch, P., Duployez, N., Bustamante, J., Bellanné‐Chantelot, C., Donadieu, J., Sicre de Fontbrune, F., Nolla, M., Fieschi, C., Delhommeau, F., Delabesse, E., Pasquet, M.
Published in HemaSphere (01.06.2022)
Published in HemaSphere (01.06.2022)
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Intellectual disability in patients with MODY due to hepatocyte nuclear factor 1B ( HNF1B ) molecular defects
Dubois-Laforgue, D, Bellanné-Chantelot, C, Charles, P, Jacquette, A, Larger, E, Ciangura, C, Saint-Martin, C, Rastel, C, Keren, B, Timsit, J
Published in Diabetes & metabolism (01.02.2017)
Published in Diabetes & metabolism (01.02.2017)
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Journal Article
Congenital hyperinsulinism and mosaic abnormalities of the ploidy
Giurgea, I, Sanlaville, D, Fournet, J-C, Sempoux, C, Bellanné-Chantelot, C, Touati, G, Hubert, L, Groos, M-S, Brunelle, F, Rahier, J, Henquin, J-C, Dunne, M J, Jaubert, F, Robert, J-J, Nihoul-Fékété, C, Vekemans, M, Junien, C, de Lonlay, P
Published in Journal of medical genetics (01.03.2006)
Published in Journal of medical genetics (01.03.2006)
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Efficacy of dupilumab for controlling severe atopic dermatitis with dominant‐negative CARD11 variant
Charvet, E., Bourrat, E., Hickman, G., Donadieu, J., Bellanné‐Chantelot, C., Jachiet, M., Bouaziz, J‐D., Bagot, M., Cassius, C.
Published in Clinical and experimental dermatology (01.10.2021)
Published in Clinical and experimental dermatology (01.10.2021)
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Journal Article
Identification of 14 new glucokinase mutations and description of the clinical profile of 42 MODY-2 families
VELHO, G, BLANCHE, H, MAROTTA, D, PILKIS, S. J, LIPKIND, G. M, BELL, G. I, FROGUEL, P, VAXILLAIRE, M, BELLANNE-CHANTELOT, C, PARDINI, V. C, TIMSIT, J, PASSA, P, DESCHAMPS, I, ROBERT, J.-J, WEBER, I. T
Published in Diabetologia (01.02.1997)
Published in Diabetologia (01.02.1997)
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The Gly482Ser polymorphism in the peroxisome proliferator-activated receptor-γ coactivator-1 gene is associated with hypertension in type 2 diabetic men
CHEURFA, N, REIS, A. F, DUBOIS-LAFORGUE, D, BELLANNE-CHANTELOT, C, TIMSIT, J, VELHO, G
Published in Diabetologia (01.11.2004)
Published in Diabetologia (01.11.2004)
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Monogenic diabetes in adults: A multi-ancestry study reveals strong disparities in diagnosis rates and clinical presentation
Mifsud, F., Saint-Martin, C., Dubois-Laforgue, D., Bouvet, D., Timsit, J., Bellanné-Chantelot, C.
Published in Diabetes research and clinical practice (01.06.2022)
Published in Diabetes research and clinical practice (01.06.2022)
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Journal Article
Dominantly inherited hyperinsulinaemic hypoglycaemia
De Lonlay, P., Giurgea, I., Sempoux, C., Touati, G., Jaubert, F., Rahier, J., Ribeiro, M., Brunelle, F., Nihoul‐Fékété, C., Robert, J.‐J., Saudubray, J.‐M., Stanley, C., Bellanné‐Chantelot, C.
Published in Journal of inherited metabolic disease (01.01.2005)
Published in Journal of inherited metabolic disease (01.01.2005)
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Mutation screening in 18 Caucasian families suggest the existence of other MODY genes
CHEVRE, J.-C, HANI, E. H, BECKERS, D, MAES, M, BELLANNE-CHANTELOT, C, VELHO, G, FROGUEL, P, BOUTIN, P, VAXILLAIRE, M, BLANCHE, H, VIONNET, N, PARDINI, V. C, TIMSIT, J, LARGER, E, CHARPENTIER, G
Published in Diabetologia (01.09.1998)
Published in Diabetologia (01.09.1998)
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Screening for G-CSF receptor mutations in patients with secondary myeloid or lymphoid transformation of severe congenital neutropenia. A report from the French neutropenia register
Cassinat, B, Bellanné-Chantelot, C, Notz-Carrère, A, Menot, M L, Vaury, C, Micheau, M, Bader-Meunier, B, Perel, Y, Leblanc, T, Donadieu, J, Chomienne, C
Published in Leukemia (01.09.2004)
Published in Leukemia (01.09.2004)
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Heterogeneity of diabetes phenotype in patients with 3243 bp mutation of mitochondrial DNA (Maternally Inherited Diabetes and Deafness or MIDD)
Guillausseau, PJ, Dubois-Laforgue, D, Massin, P, Laloi-Michelin, M, Bellanné-Chantelot, C, Gin, H, Bertin, E, Blickle, JF, Bauduceau, B, Bouhanick, B, Cahen-Varsaux, J, Casanova, S, Charpentier, G, Chedin, P, Derrien, C, Grimaldi, A, Guerci, B, Kaloustian, E, Lorenzini, F, Murat, A, Olivier, F, Paques, M, Paquis-Flucklinger, V, Tielmans, A, Vincenot, M, Vialettes, B, Timsit, J
Published in Diabetes & metabolism (01.04.2004)
Published in Diabetes & metabolism (01.04.2004)
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Genetic and clinical characterisation of maturity-onset diabetes of the young in Spanish families
Costa, A, Bescos, M, Velho, G, Chevre, J, Vidal, J, Sesmilo, G, Bellanne-Chantelot, C, Froguel, P, Casamitjana, R, Rivera-Fillat, F, Gomis, R, Conget, I
Published in European journal of endocrinology (01.04.2000)
Published in European journal of endocrinology (01.04.2000)
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Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism
Saint-Martin, C., Zhou, Q., Martin, G.M., Vaury, C., Leroy, G., Arnoux, J.-B., de Lonlay, P., Shyng, S.-L., Bellanné-Chantelot, C.
Published in Clinical genetics (01.05.2015)
Published in Clinical genetics (01.05.2015)
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Journal Article
ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism
Bellanné-Chantelot, C, Saint-Martin, C, Ribeiro, M-J, Vaury, C, Verkarre, V, Arnoux, J-B, Valayannopoulos, V, Gobrecht, S, Sempoux, C, Rahier, J, Fournet, J-C, Jaubert, F, Aigrain, Y, Nihoul-Fékété, C, de Lonlay, P
Published in Journal of medical genetics (01.11.2010)
Published in Journal of medical genetics (01.11.2010)
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To: Lindner T, Cockburn BN, Bell GI (1999). Molecular genetics of MODY in Germany. Diabetologia 42: 121-123
Ziemssen, F, Bellanné-Chantelot, C, Osterhoff, M, Schatz, H, Pfeiffer, A F H
Published in Diabetologia (01.02.2002)
Published in Diabetologia (01.02.2002)
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