Detalhe da pesquisa
1.
Disrupted lymphocyte homeostasis in hepatitis-associated acquired aplastic anemia is associated with short telomeres.
Am J Hematol
; 91(2): 243-7, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26615915
2.
Clonal hematopoiesis in patients with dyskeratosis congenita.
Am J Hematol
; 91(12): 1227-1233, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27622320
3.
Ribosomal and hematopoietic defects in induced pluripotent stem cells derived from Diamond Blackfan anemia patients.
Blood
; 122(6): 912-21, 2013 Aug 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-23744582
4.
Single nucleotide polymorphism array analysis of bone marrow failure patients reveals characteristic patterns of genetic changes.
Br J Haematol
; 164(1): 73-82, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24116929
5.
Baseline characteristics and disease burden in patients in the International Paroxysmal Nocturnal Hemoglobinuria Registry.
Haematologica
; 99(5): 922-9, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24488565
6.
Diagnosis and treatment of pediatric acquired aplastic anemia (AAA): an initial survey of the North American Pediatric Aplastic Anemia Consortium (NAPAAC).
Pediatr Blood Cancer
; 61(5): 869-74, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-24285674
7.
Liver failure due to hepatic angiosarcoma in an adolescent with dyskeratosis congenita.
J Pediatr Hematol Oncol
; 36(4): 312-5, 2014 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-23588325
8.
Somatic Mutations and Clonal Hematopoiesis in Aplastic Anemia.
N Engl J Med
; 373(17): 1673, 2015 10 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-26488703
9.
3'UTR-truncated Hmga2 cDNA causes MPN-like hematopoiesis by conferring a clonal growth advantage at the level of HSC in mice.
Blood
; 117(22): 5860-9, 2011 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-21460244
10.
Common polymorphic deletion of glutathione S-transferase theta predisposes to acquired aplastic anemia: Independent cohort and meta-analysis of 609 patients.
Am J Hematol
; 88(10): 862-7, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23798465
11.
A family with Hoyeraal-Hreidarsson syndrome and four variants in two genes of the telomerase core complex.
Pediatr Blood Cancer
; 60(6): E4-6, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23335200
12.
Comment on: Acquired monosomy 7 myelodysplastic syndrome in a child with clinical features of dyskeratosis congenita and IMAGe association.
Pediatr Blood Cancer
; 65(1)2018 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-28834235
13.
Clonal Replacement Underlies Spontaneous Remission in Paroxysmal Nocturnal Haemoglobinuria.
Br J Haematol
; 176(3): 487-490, 2017 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-26913981
14.
Recent insights into inherited bone marrow failure syndromes.
Curr Opin Pediatr
; 24(1): 23-32, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22227778
15.
TERC and TERT gene mutations in patients with bone marrow failure and the significance of telomere length measurements.
Blood
; 113(2): 309-16, 2009 Jan 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-18931339
16.
SnoRNA microarray analysis reveals changes in H/ACA and C/D RNA levels caused by dyskerin ablation in mouse liver.
Biochem J
; 429(1): 33-41, 2010 Jul 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20423331
17.
A pathogenic dyskerin mutation impairs proliferation and activates a DNA damage response independent of telomere length in mice.
Proc Natl Acad Sci U S A
; 105(29): 10173-8, 2008 Jul 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-18626023
18.
Effect of eculizumab on haemolysis-associated nitric oxide depletion, dyspnoea, and measures of pulmonary hypertension in patients with paroxysmal nocturnal haemoglobinuria.
Br J Haematol
; 149(3): 414-25, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20230403
19.
The role of human ribosomal proteins in the maturation of rRNA and ribosome production.
RNA
; 14(9): 1918-29, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18697920
20.
Poikiloderma with neutropenia: beginning at the end.
Blood
; 121(6): 872-4, 2013 Feb 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-23393019