Yigal Dror
Overview
Explore the profile of Yigal Dror including associated specialties, affiliations and a list of published articles.
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Articles
88
Citations
1405
Followers
0
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Recent Articles
1.
Ketharnathan S, Pokharel S, Prykhozhij S, Cordeiro-Santanach A, Ban K, Dogan S, et al.
Leukemia
. 2024 Aug;
38(10):2115-2126.
PMID: 39138265
Mutations in the DNAJC21 gene were recently described in Shwachman-Diamond syndrome (SDS), a bone marrow failure syndrome with high predisposition for myeloid malignancies. To study the underlying biology in hematopoiesis...
2.
Lagos-Monzon A, Ng S, Luca A, Li H, Sabanayagam M, Benicio M, et al.
Eur J Haematol
. 2024 Jul;
113(4):530-542.
PMID: 38967591
Shwachman-Diamond syndrome (SDS) is an inherited bone marrow failure disorder that often presents at infancy. Progress has been made in revealing causal mutated genes (SBDS and others), ribosome defects, and...
3.
Shimano K, Sasa G, Broglie L, Gloude N, Myers K, Nakano T, et al.
Pediatr Blood Cancer
. 2024 May;
71(8):e31075.
PMID: 38764170
Severe aplastic anemia (SAA) is a rare potentially fatal hematologic disorder. Although overall outcomes with treatment are excellent, there are variations in management approach, including differences in treatment between adult...
4.
Shimano K, Rothman J, Allen S, Castillo P, de Jong J, Dror Y, et al.
Pediatr Blood Cancer
. 2024 May;
71(8):e31070.
PMID: 38757488
Severe aplastic anemia (SAA) is a rare potentially fatal hematologic disorder. Although overall outcomes with treatment are excellent, there are variations in management approach, including differences in treatment between adult...
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Kowalczyk A, Chopra Y, Saleh M, Colaiacovo S, Dror Y, Leppington S, et al.
Pediatr Blood Cancer
. 2023 Feb;
70(6):e30253.
PMID: 36786374
No abstract available.
8.
Moshiri H, Cabrera Riofrio D, Lim Y, Lauhasurayotin S, Manisterski M, Elhasid R, et al.
Leukemia
. 2022 Jun;
36(8):2132-2135.
PMID: 35643866
No abstract available.
9.
Lim Y, Arbiv O, Kalbfleisch M, Klaassen R, Fernandez C, Rayar M, et al.
Eur J Haematol
. 2021 Dec;
108(4):278-287.
PMID: 34897809
Classification of inherited bone marrow failure syndromes (IBMFSs) according to clinical and genetic diagnoses enables proper adjustment of treatment. Unfortunately, 30% of patients enrolled in the Canadian Inherited Marrow Failure...
10.
Tsui M, Min W, Ng S, Dobbs K, Notarangelo L, Dror Y, et al.
Front Immunol
. 2021 Nov;
12:748519.
PMID: 34777360
Inherited defects that abrogate the function of the adenosine deaminase (ADA) enzyme and consequently lead to the accumulation of toxic purine metabolites cause profound lymphopenia and severe combined immune deficiency....