Publications by authors named "Matthieu Decamp"

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Efficacy and safety of azacitidine for VEXAS syndrome: a large-scale retrospective study from FRENVEX.
Vincent Jachiet, Olivier Kosmider, Maxime Beydon, Jérôme Hadjadj, Lin-Pierre Zhao, Matthieu Decamp

Blood· September 2025

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Involvement of the JAK-STAT pathway in the molecular landscape of tyrosine kinase fusion-negative hypereosinophilic syndromes: A nationwide CEREO study.
Matthieu Groh, Laurène Fenwarth, Mathilde Labro, Augustin Boudry, Elise Fournier, Matthieu Decamp

Am J Hematol· June 2024

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Cytogenetics in the management of myeloproliferative neoplasms, mastocytosis and myelodysplastic/myeloproliferative neoplasms: Guidelines from the Group Francophone de Cytogénétique Hématologique (GFCH).
Matthieu Decamp, Emilie Klein, Catherine Godon, Valentin Lestringant, Pauline Roynard

Curr Res Transl Med· December 2023

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Cytogenetics in the management of acute myeloid leukemia and histiocytic/dendritic cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Audrey Bidet, Julie Quessada, Wendy Cuccuini, Matthieu Decamp, Marina Lafage-Pochitaloff

Curr Res Transl Med· December 2023

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French guidelines for the etiological workup of eosinophilia and the management of hypereosinophilic syndromes.
Matthieu Groh, Julien Rohmer, Nicolas Etienne, Wadih Abou Chahla, Antoine Baudet, Matthieu Decamp

Orphanet J Rare Dis· April 2023

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USAID Associated with Myeloid Neoplasm and VEXAS Syndrome: Two Differential Diagnoses of Suspected Adult Onset Still's Disease in Elderly Patients.
Marion Delplanque, Achille Aouba, Pierre Hirsch, Pierre Fenaux, Julie Graveleau

J Clin Med· November 2021

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Myeloid malignancies with translocation t(4;12)(q11-13;p13): molecular landscape, clonal hierarchy and clinical outcomes.
Vincent Parinet, Elise Chapiro, Audrey Bidet, Baptiste Gaillard, Odile Maarek, Matthieu Decamp

J Cell Mol Med· October 2021

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Successful Imatinib therapy as a bridge to transplant in an atypical myeloproliferative neoplasm.
Thomas Hueso, Hyacinthe Johnson-Ansah, Matthieu Decamp, Elsa Maitre, Alexandra Henry

Curr Res Transl Med· November 2019

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High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B.
Cindy Colson, Matthieu Decamp, Nicolas Gruchy, Nadia Coudray, Céline Ballandonne

Bone· June 2019

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Growth hormone deficiency and pituitary malformation in a recurrent Cat-Eye syndrome: a family report.
Guillaume Jedraszak, Karine Braun, Aline Receveur, Matthieu Decamp, Joris Andrieux

Ann Endocrinol (Paris)· October 2015

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15q11.2 microdeletion (BP1-BP2) and developmental delay, behaviour issues, epilepsy and congenital heart disease: a series of 52 patients.
Clémence Vanlerberghe, Florence Petit, Valérie Malan, Catherine Vincent-Delorme, Sonia Bouquillon, Matthieu Decamp

Eur J Med Genet· March 2015

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The first familial case of inherited 2q37.3 interstitial deletion with isolated skeletal abnormalities including brachydactyly type E and short stature.
Nolwenn Jean-Marçais, Matthieu Decamp, Marion Gérard, Virginie Ribault, Joris Andrieux

Am J Med Genet A· January 2015

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21q21 deletion involving NCAM2: report of 3 cases with neurodevelopmental disorders.
Florence Petit, Ghislaine Plessis, Matthieu Decamp, Jean-Marie Cuisset, Moira Blyth

Eur J Med Genet· January 2015

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12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4.
Arnaud Molin, Guillaume Benoist, Corinne Jeanne-Pasquier, Nadia Elkartoufi, Julie Litzer, Matthieu Decamp

Eur J Med Genet· October 2013

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Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNA.
Nicolas Gruchy, Matthieu Decamp, Nicolas Richard, Corinne Jeanne-Pasquier, Guillaume Benoist

Prenat Diagn· April 2012

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