Detalhe da pesquisa
1.
SAMHD1 is mutated recurrently in chronic lymphocytic leukemia and is involved in response to DNA damage.
Blood
; 123(7): 1021-31, 2014 Feb 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-24335234
2.
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Am J Med Genet A
; 167A(2): 296-312, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25604658
3.
A retrospective real-world study of the current treatment pathways for myelofibrosis in the United Kingdom: the REALISM UK study.
Ther Adv Hematol
; 13: 20406207221084487, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35371428
4.
Guideline for the diagnosis and management of the rare coagulation disorders: a United Kingdom Haemophilia Centre Doctors' Organization guideline on behalf of the British Committee for Standards in Haematology.
Br J Haematol
; 167(3): 304-26, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25100430
5.
Rarity of IgH translocations in Waldenström macroglobulinemia.
Cancer Genet Cytogenet
; 163(1): 77-80, 2005 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-16271961
6.
Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.
Lancet Neurol
; 12(12): 1159-69, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24183309
7.
IgM myeloma with t(4;14)(p16;q32).
Cancer Genet Cytogenet
; 162(2): 183-4, 2005 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-16213370
8.
Efficacy of stroke prevention in atrial fibrillation: a way of improvement.
Future Hosp J
; 2(Suppl 2): s29, 2015 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31098157