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Decamp, Matthieu
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1

Involvement of the JAK‐STAT pathway in the molecular landsc..:

Groh, Matthieu ; Fenwarth, Laurène ; Labro, Mathilde...
American Journal of Hematology.  99 (2024)  6 - p. 1108-1118 , 2024
Link: https://doi.org/10.1002/..
 
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2

French guidelines for the etiological workup of eosinophili..:

Groh, Matthieu ; Rohmer, Julien ; Etienne, Nicolas...
Orphanet Journal of Rare Diseases.  18 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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3

Cytogenetics in the management of myeloproliferative neopla..:

Decamp, Matthieu ; Klein, Emilie ; Godon, Catherine...
Current Research in Translational Medicine.  71 (2023)  4 - p. 103424 , 2023
Link: https://doi.org/10.1016/..
 
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4

Cytogenetics in the management of acute myeloid leukemia an..:

Bidet, Audrey ; Quessada, Julie ; Cuccuini, Wendy...
Current Research in Translational Medicine.  71 (2023)  4 - p. 103421 , 2023
Link: https://doi.org/10.1016/..
 
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5

Myeloid malignancies with translocation t(4;12)(q11‐13;p13)..:

Parinet, Vincent ; Chapiro, Elise ; Bidet, Audrey...
Journal of Cellular and Molecular Medicine.  25 (2021)  20 - p. 9557-9566 , 2021
Link: https://doi.org/10.1111/..
 
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6

USAID Associated with Myeloid Neoplasm and VEXAS Syndrome: ..:

Delplanque, Marion ; Aouba, Achille ; Hirsch, Pierre...
Journal of Clinical Medicine.  10 (2021)  23 - p. 5586 , 2021
Link: https://doi.org/10.3390/..
 
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7

Successful Imatinib therapy as a bridge to transplant in an..:

Hueso, Thomas ; Johnson-Ansah, Hyacinthe ; Decamp, Matthieu...
Current Research in Translational Medicine.  67 (2019)  4 - p. 149-151 , 2019
Link: https://doi.org/10.1016/..
 
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8

High frequency of paternal iso or heterodisomy at chromosom..:

Colson, Cindy ; Decamp, Matthieu ; Gruchy, Nicolas...
Bone.  123 (2019)  - p. 145-152 , 2019
Link: https://doi.org/10.1016/..
 
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9

Growth hormone deficiency and pituitary malformation in a r..:

Jedraszak, Guillaume ; Braun, Karine ; Receveur, Aline...
Annales d'Endocrinologie.  76 (2015)  5 - p. 629-634 , 2015
Link: https://doi.org/10.1016/..
 
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10

15q11.2 microdeletion (BP1–BP2) and developmental delay, be..:

Vanlerberghe, Clémence ; Petit, Florence ; Malan, Valérie...
European Journal of Medical Genetics.  58 (2015)  3 - p. 140-147 , 2015
Link: https://doi.org/10.1016/..
 
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11

21q21 deletion involving NCAM2: Report of 3 cases with neur..:

Petit, Florence ; Plessis, Ghislaine ; Decamp, Matthieu...
European Journal of Medical Genetics.  58 (2015)  1 - p. 44-46 , 2015
Link: https://doi.org/10.1016/..
 
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12

The first familial case of inherited 2q37.3 interstitial de..:

Jean‐Marçais, Nolwenn ; Decamp, Matthieu ; Gérard, Marion...
American Journal of Medical Genetics Part A.  167 (2014)  1 - p. 185-189 , 2014
Link: https://doi.org/10.1002/..
 
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13

12q21 Microdeletion in a fetus with Meckel syndrome involvi..:

Molin, Arnaud ; Benoist, Guillaume ; Jeanne-Pasquier, Corinne...
European Journal of Medical Genetics.  56 (2013)  10 - p. 580-583 , 2013
Link: https://doi.org/10.1016/..
 
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14

Array CGH analysis in high‐risk pregnancies: comparing DNA ..:

Gruchy, Nicolas ; Decamp, Matthieu ; Richard, Nicolas...
Prenatal Diagnosis.  32 (2011)  4 - p. 383-388 , 2011
Link: https://doi.org/10.1002/..
 
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15

French guidelines for the etiological workup of eosinophili..:

Groh, Matthieu ; Rohmer, Julien ; Etienne, Nicolas...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148979/.  , 2023
Link: http://www.ncbi.nlm.nih...
 
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