297 related articles for article (PubMed ID: 31306780)
1. Outcomes of Hematopoietic Cell Transplantation in Patients with Germline SAMD9/SAMD9L Mutations.
Ahmed IA; Farooqi MS; Vander Lugt MT; Boklan J; Rose M; Friehling ED; Triplett B; Lieuw K; Saldana BD; Smith CM; Schwartz JR; Goyal RK
Biol Blood Marrow Transplant; 2019 Nov; 25(11):2186-2196. PubMed ID: 31306780
[TBL] [Abstract][Full Text] [Related]
2. SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies.
Davidsson J; Puschmann A; Tedgård U; Bryder D; Nilsson L; Cammenga J
Leukemia; 2018 May; 32(5):1106-1115. PubMed ID: 29535429
[TBL] [Abstract][Full Text] [Related]
3. Germline SAMD9 and SAMD9L mutations are associated with extensive genetic evolution and diverse hematologic outcomes.
Wong JC; Bryant V; Lamprecht T; Ma J; Walsh M; Schwartz J; Del Pilar Alzamora M; Mullighan CG; Loh ML; Ribeiro R; Downing JR; Carroll WL; Davis J; Gold S; Rogers PC; Israels S; Yanofsky R; Shannon K; Klco JM
JCI Insight; 2018 Jul; 3(14):. PubMed ID: 30046003
[TBL] [Abstract][Full Text] [Related]
4. Pediatric MDS and bone marrow failure-associated germline mutations in SAMD9 and SAMD9L impair multiple pathways in primary hematopoietic cells.
Thomas ME; Abdelhamed S; Hiltenbrand R; Schwartz JR; Sakurada SM; Walsh M; Song G; Ma J; Pruett-Miller SM; Klco JM
Leukemia; 2021 Nov; 35(11):3232-3244. PubMed ID: 33731850
[TBL] [Abstract][Full Text] [Related]
5. [Association between SAMD9/SAMD9L and hematological malignancies].
Narumi S; Hasegawa T
Rinsho Ketsueki; 2018; 59(11):2475-2480. PubMed ID: 30531146
[TBL] [Abstract][Full Text] [Related]
6. Germline predisposition in myeloid neoplasms: Unique genetic and clinical features of GATA2 deficiency and SAMD9/SAMD9L syndromes.
Sahoo SS; Kozyra EJ; Wlodarski MW
Best Pract Res Clin Haematol; 2020 Sep; 33(3):101197. PubMed ID: 33038986
[TBL] [Abstract][Full Text] [Related]
7. Multiorgan failure with abnormal receptor metabolism in mice mimicking Samd9/9L syndromes.
Nagamachi A; Kanai A; Nakamura M; Okuda H; Yokoyama A; Shinriki S; Matsui H; Inaba T
J Clin Invest; 2021 Feb; 131(4):. PubMed ID: 33373325
[TBL] [Abstract][Full Text] [Related]
8. Of gains and losses: SAMD9/SAMD9L and monosomy 7 in myelodysplastic syndrome.
Cammenga J
Exp Hematol; 2024 Apr; 134():104217. PubMed ID: 38649131
[TBL] [Abstract][Full Text] [Related]
9. Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.
Sahoo SS; Pastor VB; Goodings C; Voss RK; Kozyra EJ; Szvetnik A; Noellke P; Dworzak M; Starý J; Locatelli F; Masetti R; Schmugge M; De Moerloose B; Catala A; Kállay K; Turkiewicz D; Hasle H; Buechner J; Jahnukainen K; Ussowicz M; Polychronopoulou S; Smith OP; Fabri O; Barzilai S; de Haas V; Baumann I; Schwarz-Furlan S; ; Niewisch MR; Sauer MG; Burkhardt B; Lang P; Bader P; Beier R; Müller I; Albert MH; Meisel R; Schulz A; Cario G; Panda PK; Wehrle J; Hirabayashi S; Derecka M; Durruthy-Durruthy R; Göhring G; Yoshimi-Noellke A; Ku M; Lebrecht D; Erlacher M; Flotho C; Strahm B; Niemeyer CM; Wlodarski MW
Nat Med; 2021 Oct; 27(10):1806-1817. PubMed ID: 34621053
[TBL] [Abstract][Full Text] [Related]
10. Prevalence of germline GATA2 and SAMD9/9L variants in paediatric haematological disorders with monosomy 7.
Yoshida M; Tanase-Nakao K; Shima H; Shirai R; Yoshida K; Osumi T; Deguchi T; Mori M; Arakawa Y; Takagi M; Miyamura T; Sakaguchi K; Toyoda H; Ishida H; Sakata N; Imamura T; Kawahara Y; Morimoto A; Koike T; Yagasaki H; Ito S; Tomizawa D; Kiyokawa N; Narumi S; Kato M
Br J Haematol; 2020 Dec; 191(5):835-843. PubMed ID: 32770553
[TBL] [Abstract][Full Text] [Related]
11. Emerging phenotypes linked to variants in
Suntharalingham JP; Ishida M; Del Valle I; Stalman SE; Solanky N; Wakeling E; Moore GE; Achermann JC; Buonocore F
Front Endocrinol (Lausanne); 2022; 13():953707. PubMed ID: 36060959
[TBL] [Abstract][Full Text] [Related]
12. The Neuropathology of MIRAGE Syndrome.
Viaene AN; Harding BN
J Neuropathol Exp Neurol; 2020 Apr; 79(4):458-462. PubMed ID: 32106287
[TBL] [Abstract][Full Text] [Related]
13. Discovery of MIRAGE syndrome.
Narumi S
Pediatr Int; 2022 Jan; 64(1):e15283. PubMed ID: 35972063
[TBL] [Abstract][Full Text] [Related]
14. Spontaneous remission and loss of monosomy 7: a window of opportunity for young children with SAMD9L syndrome.
Erlacher M; Andresen F; Sukova M; Stary J; De Moerloose B; Bosch JVWT; Dworzak M; Seidel MG; Polychronopoulou S; Beier R; Kratz CP; Nathrath M; Frühwald MC; Göhring G; Bergmann AK; Mayerhofer C; Lebrecht D; Ramamoorthy S; Yoshimi A; Strahm B; Wlodarski MW; Niemeyer CM
Haematologica; 2024 Feb; 109(2):422-430. PubMed ID: 37584291
[TBL] [Abstract][Full Text] [Related]
15. Cord Blood Transplantation in 2 Infants Presenting Monosomy 7 Clonal Hematopoiesis: SAMD9 / SAMD9L Germline Mutation.
Hirai M; Yagasaki H; Kanezawa K; Ueno M; Shimozawa K; Imai K; Morio T; Kato M; Gocho Y; Narumi S; Ebihara Y; Morioka I
J Pediatr Hematol Oncol; 2023 Mar; 45(2):e290-e293. PubMed ID: 36730951
[TBL] [Abstract][Full Text] [Related]
16. Two patients with MIRAGE syndrome lacking haematological features: role of somatic second-site reversion SAMD9 mutations.
Shima H; Koehler K; Nomura Y; Sugimoto K; Satoh A; Ogata T; Fukami M; Jühlen R; Schuelke M; Mohnike K; Huebner A; Narumi S
J Med Genet; 2018 Feb; 55(2):81-85. PubMed ID: 29175836
[TBL] [Abstract][Full Text] [Related]
17. [Novel germline SAMD9 mutation in an elderly patient with myelodysplastic syndrome].
Uchida T; Fujii T; Ohara S; Imai Y; Inoue M; Harada Y; Harada H; Hagihara M
Rinsho Ketsueki; 2022; 63(8):865-869. PubMed ID: 36058856
[TBL] [Abstract][Full Text] [Related]
18. Inherited thrombocytopenia and platelet disorders with germline predisposition to myeloid neoplasia.
Galera P; Dulau-Florea A; Calvo KR
Int J Lab Hematol; 2019 May; 41 Suppl 1():131-141. PubMed ID: 31069978
[TBL] [Abstract][Full Text] [Related]
19. The International Consensus Classification (ICC) of hematologic neoplasms with germline predisposition, pediatric myelodysplastic syndrome, and juvenile myelomonocytic leukemia.
Rudelius M; Weinberg OK; Niemeyer CM; Shimamura A; Calvo KR
Virchows Arch; 2023 Jan; 482(1):113-130. PubMed ID: 36445482
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
