Isabelle Marie
Overview
Explore the profile of Isabelle Marie including associated specialties, affiliations and a list of published articles.
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Articles
119
Citations
2115
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Recent Articles
1.
Lebel N, Marie I, Grosjean J, Brevet P, Leclercq M, Dumont A, et al.
Clin Exp Rheumatol
. 2024 Mar;
42(8):1536-1540.
PMID: 38489323
Objectives: To analyse in routine practice the efficacy of targeted therapies on joint involvement of patients with rheumatoid arthritis/systemic sclerosis (RA/SSc) overlap syndrome. Methods: This was a retrospective analysis of...
2.
Da Costa L, Mohandas N, David-NGuyen L, Platon J, Marie I, ODonohue M, et al.
Blood Cells Mol Dis
. 2024 Feb;
106:102838.
PMID: 38413287
Diamond-Blackfan anemia (DBA) was the first ribosomopathy described in humans. DBA is a congenital hypoplastic anemia, characterized by macrocytic aregenerative anemia, manifesting by differentiation blockage between the BFU-e/CFU-e developmental erythroid...
3.
Lecornec N, Castex M, Reguerre Y, Moreau P, Marie I, Garcon L, et al.
Br J Haematol
. 2022 Jul;
199(2):285-288.
PMID: 35852515
No abstract available.
4.
Kessel C, Kone-Paut I, Tellier S, Belot A, Masjosthusmann K, Wittkowski H, et al.
J Clin Immunol
. 2022 Jun;
42(6):1330-1341.
PMID: 35699824
Purpose: A recent phase II open-label study of the interleukin 1 (IL-1) receptor antagonist (IL-1Ra) anakinra in treating IVIG-resistant Kawasaki disease (KD) patients reported promising results. Here, we aimed to...
5.
Rottenberg P, Brevet P, Leclercq M, Jouen F, Marie I, Levesque H, et al.
J Clin Rheumatol
. 2022 Mar;
28(8):e699-e702.
PMID: 35293888
Background: Rhupus syndrome is better characterized, but uncertainties remain, and therapeutic management must be defined. The objective was to analyze therapeutic procedures with a focus on biologic disease-modifying antirheumatic drugs...
6.
Da Costa L, Marie I, Leblanc T
Hematology Am Soc Hematol Educ Program
. 2021 Dec;
2021(1):353-360.
PMID: 34889440
Diamond-Blackfan anemia (DBA) is an inherited bone marrow failure syndrome, characterized as a rare congenital bone marrow erythroid hypoplasia (OMIM#105650). Erythroid defect in DBA results in erythroblastopenia in bone marrow...
7.
Sudrie-Arnaud B, Snanoudj S, Dabaj I, Dranguet H, Abily-Donval L, Lebas A, et al.
Diagnostics (Basel)
. 2021 Mar;
11(2).
PMID: 33673364
Diagnosis of lysosomal disorders (LDs) may be hampered by their clinical heterogeneity, phenotypic overlap, and variable age at onset. Conventional biological diagnostic procedures are based on a series of sequential...
8.
Zuelgaray E, Chevret S, Jachiet M, Cacoub P, Kahn J, Groh M, et al.
J Am Acad Dermatol
. 2020 Nov;
88(1):160-163.
PMID: 33188872
No abstract available.
9.
Kone-Paut I, Tellier S, Belot A, Brochard K, Guitton C, Marie I, et al.
Arthritis Rheumatol
. 2020 Aug;
73(1):151-161.
PMID: 32779863
Objective: Anakinra has been shown to be successful in preventing and treating cardiovascular lesions both in experimental murine models of Kawasaki disease (KD) and in several studies on intravenous immunoglobulin...
10.
Serratrice C, Cherin P, Lidove O, Noel E, Masseau A, Leguy-Seguin V, et al.
J Hematol
. 2020 Apr;
8(3):121-124.
PMID: 32300455
Background: Gaucher disease is a rare inborn error of lysosomal metabolism, characterized by lysosomal storage of the β-glucosylceramide. Bleedings observed in type-1 Gaucher disease (GD1) are commonly attributed to a...