Christine Bellanné : rechercher sur Z-Library

Le plus grand référentiel d'articles scientifiques au monde. 70,000,000+ d'articles gratuitement.

Don't use scam websites

Livres
Articles (71)
Les plus populaires
Liste
- Liste
- Tableau

51

ATG2B and GSKIP : two new genes predisposing to myeloid malignancies

Plo, Isabelle, Bellanné-Chantelot, Christine, Vainchenker, William

Journal:

Molecular & Cellular Oncology

Année:

2015

Langue:

english

Fichier:

PDF, 1.77 MB

english, 2015

52

Fertility in Women with Nonclassical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Bidet, Maud, Bellanné-Chantelot, Christine, Galand-Portier, Marie-Béatrice, Golmard, Jean-Louis, Tardy, Véronique, Morel, Yves, Clauin, Séverine, Coussieu, Christiane, Boudou, Philippe, Mowzowicz, Ire

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 31 KB

english, 2010

53

Hepatic Hemangioendothelioma in an Infant With Severe Congenital Neutropenia

Dinand, Veronique, Yadav, Satya Prakash, Bellanné-Chantelot, Christine, Jain, Sunila, Bhargava, Manorama, Sachdeva, Anupam

Journal:

Journal of Pediatric Hematology/Oncology

Année:

2012

Langue:

english

Fichier:

PDF, 148 KB

english, 2012

54

Neurofibromatosis type 1 with undescribed osseous abnormalities: new features?

Leruste, Amaury, Chateil, Jean-François, Ramirez, Stéphane, Bellanné, Christine, Vidaud, Dominique, Lacombe, Didier

Journal:

Clinical Dysmorphology

Année:

2009

Langue:

english

Fichier:

PDF, 212 KB

english, 2009

55

Clinical Spectrum Associated with Hepatocyte Nuclear Factor-1β Mutations

Bellanné-Chantelot, Christine

Journal:

Annals of Internal Medicine

Année:

2004

Langue:

english

Fichier:

PDF, 487 KB

english, 2004

56

Diabetes, Associated Clinical Spectrum, Long-term Prognosis and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1 B ( HNF1B ) Molecular Defects

Dubois-Laforgue, Danièle, Cornu, Erika, Saint-Martin, Cécile, Coste, Joël, Bellanné-Chantelot, Christine, Timsit, José

Journal:

Année:

2017

Langue:

english

Fichier:

PDF, 693 KB

english, 2017

57

Strengths and limitations of using 18 fluorine-fluorodihydroxyphenylalanine PET/CT for congenital hyperinsulinism

Montravers, Françoise, Arnoux, Jean-Baptiste, Ribeiro, Maria-Joao, Kerrou, Khaldoun, Nataf, Valérie, Galmiche, Louise, Aigrain, Yves, Bellanné-Chantelot, Christine, Saint-Martin, Cécile, Ohnona, Jessi

Journal:

Expert Review of Endocrinology & Metabolism

Année:

2014

Langue:

english

Fichier:

PDF, 757 KB

english, 2014

58

Lymphoid differentiation of hematopoietic stem cells requires efficient Cxcr4 desensitization

Freitas, Christelle, Wittner, Monika, Nguyen, Julie, Rondeau, Vincent, Biajoux, Vincent, Aknin, Marie-Laure, Gaudin, Françoise, Beaussant-Cohen, Sarah, Bertrand, Yves, Bellanné-Chantelot, Christine, D

Journal:

Journal of Experimental Medicine

Année:

2017

Langue:

english

Fichier:

PDF, 2.80 MB

english, 2017

59

Un piège de l’insulinome

Jannin, Arnaud, Douillard, Claire, Espiard, Stéphanie, Bellanné-Chantelot, Christine, Vantyghem, Marie-Christine

Journal:

Diabetes & Metabolism

Année:

2017

Langue:

french

Fichier:

PDF, 58 KB

french, 2017

60

How to differentiate congenital from noncongenital chronic neutropenia at the first medical examination? Proposal of score: A pilot study from the French Severe Chronic Neutropenia registry

Bejjani, Naim, Beaupain, Blandine, Bertrand, Yves, Bellanne-Chantelot, Christine, Donadieu, Jean

Journal:

Pediatric Blood & Cancer

Année:

2017

Langue:

english

Fichier:

PDF, 272 KB

english, 2017

61

Response to Comment on Dubois-Laforgue et al. Diabetes, Associated Clinical Spectrum, Long-term Prognosis, and Genotype/Phenotype Correlations in 201 Adult Patients With Hepatocyte Nuclear Factor 1B ( HNF1B ) Molecular Defects. Diabetes Care 2017;40:1436–1443

Dubois-Laforgue, Danièle, Cornu, Erika, Saint-Martin, Cécile, Coste, Joël, Bellanné-Chantelot, Christine, Timsit, José

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 524 KB

english, 2018

62

Hyperinsulinemic hypoglycemia without insulinoma: Think of activating glucokinase mutation

Jannin, Arnaud, Espiard, Stéphanie, Douillard, Claire, Pasquier, Florence, Bellanné-Chantelot, Christine, Vantyghem, Marie-Christine

Journal:

La Presse Médicale

Année:

2018

Langue:

english

Fichier:

PDF, 768 KB

english, 2018

63

New somatic BRAF splicing mutation in Langerhans cell histiocytosis

Héritier, Sébastien, Hélias-Rodzewicz, Zofia, Chakraborty, Rikhia, Sengal, Amel G., Bellanné-Chantelot, Christine, Thomas, Caroline, Moreau, Anne, Fraitag, Sylvie, Allen, Carl E., Donadieu, Jean, Emil

Journal:

Molecular Cancer

Année:

2017

Langue:

english

Fichier:

PDF, 2.10 MB

english, 2017

64

The Common HNF1A Variant I27L is a Modifier of Age at Diabetes Diagnosis in HNF1A-MODY Individuals

Locke, Jonathan M, Saint-Martin, Cécile, Laver, Thomas W, Patel, Kashyap A, Wood, Andrew R, Sharp, Seth A, Ellard, Sian, Bellanné-Chantelot, Christine, Hattersley, Andrew T, Harries, Lorna W, Weedon,

Journal:

Année:

2018

Langue:

english

Fichier:

PDF, 312 KB

english, 2018

65

Identification of MPL R102P Mutation in Hereditary Thrombocytosis

Bellanné-Chantelot, Christine, Mosca, Matthieu, Marty, Caroline, Favier, Rémi, Vainchenker, William, Plo, Isabelle

Journal:

Frontiers in Endocrinology

Année:

2017

Langue:

english

Fichier:

PDF, 363 KB

english, 2017

66

Genetic Alterations of the Thrombopoietin/MPL/JAK2 Axis Impacting Megakaryopoiesis

Plo, Isabelle, Bellanné-Chantelot, Christine, Mosca, Matthieu, Mazzi, Stefania, Marty, Caroline, Vainchenker, William

Journal:

Frontiers in Endocrinology

Année:

2017

Langue:

english

Fichier:

PDF, 539 KB

english, 2017

67

Severe Congenital Adrenal Hyperplasia Presenting as Bilateral Testicular Tumors and Azoospermia in the Third Decade of Life

Sarfati, Julie, Vatier, Camille, Keller, Isabelle, Guéchot, Jérome, Bellanné-Chantelot, Christine, Christin-Maitre, Sophie

Journal:

Journal of the Endocrine Society

Année:

2018

Langue:

english

Fichier:

PDF, 136 KB

english, 2018

68

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome

Bellanné-Chantelot, Christine, Schmaltz-Panneau, Barbara, Marty, Caroline, Fenneteau, Odile, Callebaut, Isabelle, Clauin, Séverine, Docet, Aurélie, Damaj, Gandhi-Laurent, Leblanc, Thierry, Pellier, Is

Journal:

Année:

2018

Fichier:

PDF, 3.50 MB

2018

69

Liver Adenomatosis in Patients with HNF1A ‐Mody Diabetes: Clinical, Radiological and Pathological Characteristics in a French Series

Haddouche, Aini, Bellanne‐Chantelot, Christine, Rod, Anne, Fournier, Luc, Chiche, Laurence, Gautier, Jean‐Francois, Timsit, Jose, Laboureau, Sandrine, Chaillous, Lucy, Valero, Rene, Larger, Etienne, J

Journal:

Journal of Diabetes

Année:

2019

Fichier:

PDF, 1.53 MB

2019

70

Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis

Donath, Xavier, Saint-Martin, Cécile, Dubois-Laforgue, Danièle, Rajasingham, Ramanan, Mifsud, François, Ciangura, Cécile, Timsit, José, Bellanné-Chantelot, Christine

Journal:

Année:

2019

Langue:

english

Fichier:

PDF, 917 KB

english, 2019

71

Next-generation sequencing identifies monogenic diabetes in 16% of patients with late adolescence/adult-onset diabetes selected on a clinical basis: a cross-sectional analysis

Donath, Xavier, Saint-Martin, Cécile, Dubois-Laforgue, Danièle, Rajasingham, Ramanan, Mifsud, François, Ciangura, Cécile, Timsit, José, Bellanné-Chantelot, Christine

Journal:

Année:

2019

Fichier:

PDF, 917 KB

2019