221 related articles for article (PubMed ID: 36115694)
21. Clinical utility of next-generation sequencing for inherited bone marrow failure syndromes.
Muramatsu H; Okuno Y; Yoshida K; Shiraishi Y; Doisaki S; Narita A; Sakaguchi H; Kawashima N; Wang X; Xu Y; Chiba K; Tanaka H; Hama A; Sanada M; Takahashi Y; Kanno H; Yamaguchi H; Ohga S; Manabe A; Harigae H; Kunishima S; Ishii E; Kobayashi M; Koike K; Watanabe K; Ito E; Takata M; Yabe M; Ogawa S; Miyano S; Kojima S
Genet Med; 2017 Jul; 19(7):796-802. PubMed ID: 28102861
[TBL] [Abstract][Full Text] [Related]
22. Monosomy 7/del (7q) in inherited bone marrow failure syndromes: A systematic review.
Pezeshki A; Podder S; Kamel R; Corey SJ
Pediatr Blood Cancer; 2017 Dec; 64(12):. PubMed ID: 28708320
[TBL] [Abstract][Full Text] [Related]
23. Somatic MECOM mosaicism in a patient with congenital bone marrow failure without a radial abnormality.
Osumi T; Tsujimoto SI; Nakabayashi K; Taniguchi M; Shirai R; Yoshida M; Uchiyama T; Nagasawa J; Goyama S; Yoshioka T; Tomizawa D; Kurokawa M; Matsubara Y; Kiyokawa N; Matsumoto K; Hata K; Kato M
Pediatr Blood Cancer; 2018 Jun; 65(6):e26959. PubMed ID: 29356389
[No Abstract] [Full Text] [Related]
24. Function and malfunction of hematopoietic stem cells in primary bone marrow failure syndromes.
Risitano AM; Maciejewski JP; Selleri C; Rotoli B
Curr Stem Cell Res Ther; 2007 Jan; 2(1):39-52. PubMed ID: 18220891
[TBL] [Abstract][Full Text] [Related]
25. Paroxysmal nocturnal hemoglobinuria clones are not infrequent in patients with inherited bone marrow failure syndromes.
Sreedharanunni S; Varma N; Sachdeva MUS; Naseem S; Malhotra P; Bansal D; Sood A; Bose P; Varma S
Eur J Haematol; 2017 Aug; 99(2):194-195. PubMed ID: 28452421
[No Abstract] [Full Text] [Related]
26. MECOM-associated syndrome: a heterogeneous inherited bone marrow failure syndrome with amegakaryocytic thrombocytopenia.
Germeshausen M; Ancliff P; Estrada J; Metzler M; Ponstingl E; Rütschle H; Schwabe D; Scott RH; Unal S; Wawer A; Zeller B; Ballmaier M
Blood Adv; 2018 Mar; 2(6):586-596. PubMed ID: 29540340
[TBL] [Abstract][Full Text] [Related]
27. Cytogenetics in the management of bone marrow failure syndromes: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Cuccuini W; Collonge-Rame MA; Auger N; Douet-Guilbert N; Coster L; Lafage-Pochitaloff M
Curr Res Transl Med; 2023; 71(4):103423. PubMed ID: 38016422
[TBL] [Abstract][Full Text] [Related]
28. The inherited bone marrow failure syndromes.
Chirnomas SD; Kupfer GM
Pediatr Clin North Am; 2013 Dec; 60(6):1291-310. PubMed ID: 24237972
[TBL] [Abstract][Full Text] [Related]
29. Refining the phenotype associated with biallelic DNAJC21 mutations.
D'Amours G; Lopes F; Gauthier J; Saillour V; Nassif C; Wynn R; Alos N; Leblanc T; Capri Y; Nizard S; Lemyre E; Michaud JL; Pelletier VA; Pastore YD; Soucy JF
Clin Genet; 2018 Aug; 94(2):252-258. PubMed ID: 29700810
[TBL] [Abstract][Full Text] [Related]
30. Inherited bone marrow failure syndromes: considerations pre- and posttransplant.
Alter BP
Blood; 2017 Nov; 130(21):2257-2264. PubMed ID: 29167174
[TBL] [Abstract][Full Text] [Related]
31. Acquired and Inherited Bone Marrow Failure Syndromes.
Sieff CA
Hematol Oncol Clin North Am; 2018 Aug; 32(4):xiii-xiv. PubMed ID: 30047424
[No Abstract] [Full Text] [Related]
32. When to consider inherited marrow failure syndromes in adults.
Gutierrez-Rodrigues F; Patel BA; Groarke EM
Hematology Am Soc Hematol Educ Program; 2023 Dec; 2023(1):548-555. PubMed ID: 38066926
[TBL] [Abstract][Full Text] [Related]
33. Congenital hypoplastic bone marrow failure associated with a de novo partial deletion of the MECOM gene at 3q26.2.
Kjeldsen E; Veigaard C; Aggerholm A; Hasle H
Gene; 2018 May; 656():86-94. PubMed ID: 29496554
[TBL] [Abstract][Full Text] [Related]
34. Cell senescence and malignant transformation in the inherited bone marrow failure syndromes: Overlapping pathophysiology with therapeutic implications.
Groarke EM; Calado RT; Liu JM
Semin Hematol; 2022 Jan; 59(1):30-37. PubMed ID: 35491056
[TBL] [Abstract][Full Text] [Related]
35. [Inherited bone marrow failure syndrome: management and diagnostic advances utilizing next-generation sequencing].
Muramatsu H
Rinsho Ketsueki; 2018; 59(6):716-722. PubMed ID: 29973450
[TBL] [Abstract][Full Text] [Related]
36. Bone mineral density in patients with inherited bone marrow failure syndromes.
Shankar RK; Giri N; Lodish MB; Sinaii N; Reynolds JC; Savage SA; Stratakis CA; Alter BP
Pediatr Res; 2017 Sep; 82(3):458-464. PubMed ID: 28486441
[TBL] [Abstract][Full Text] [Related]
37. Cell-Cycle-Specific Function of p53 in Fanconi Anemia Hematopoietic Stem and Progenitor Cell Proliferation.
Li X; Wilson AF; Du W; Pang Q
Stem Cell Reports; 2018 Feb; 10(2):339-346. PubMed ID: 29307578
[TBL] [Abstract][Full Text] [Related]
38. Clonal hematopoiesis in the inherited bone marrow failure syndromes.
Tsai FD; Lindsley RC
Blood; 2020 Oct; 136(14):1615-1622. PubMed ID: 32736377
[TBL] [Abstract][Full Text] [Related]
39. Clinical spectrum and clonal evolution in germline syndromes with predisposition to myeloid neoplasms.
Perez Botero J; Ho TP; Hogan WJ; Kenderian S; Gangat N; Tefferi A; Abraham RS; Nguyen P; Oliveira JL; He R; Chen D; Viswanatha D; Rodriguez V; Khan SP; Patnaik MM
Br J Haematol; 2018 Jul; 182(1):141-145. PubMed ID: 28485484
[No Abstract] [Full Text] [Related]
40. Aplastic Anemia and MDS International Foundation (AAMDSIF): Bone marrow failure disease scientific symposium 2016.
Zeidan AM; Battiwalla M; Berlyne D; Winkler T
Leuk Res; 2017 Feb; 53():8-12. PubMed ID: 27923195
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
