Detalhe da pesquisa
1.
Two SERPINC1 variants affecting N-glycosylation of Asn224 cause severe thrombophilia not detected by functional assays.
Blood
; 140(2): 140-151, 2022 07 14.
Artigo
Inglês
| MEDLINE | ID: mdl-35486842
2.
Usefulness and Limitations of Multiple Ligation-Dependent Probe Amplification in Antithrombin Deficiency.
Int J Mol Sci
; 24(5)2023 Mar 06.
Artigo
Inglês
| MEDLINE | ID: mdl-36902454
3.
Paroxysmal Nocturnal Hemoglobinuria: Biology and Treatment.
Medicina (Kaunas)
; 59(9)2023 Sep 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37763731
4.
Molecular and clinical characterization of transient antithrombin deficiency: A new concept in congenital thrombophilia.
Am J Hematol
; 97(2): 216-225, 2022 02 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34800304
5.
High penetrance of inferior vena cava system atresia in severe thrombophilia caused by homozygous antithrombin Budapest 3 variant: Description of a new syndrome.
Am J Hematol
; 96(11): 1363-1373, 2021 11 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34324211
6.
The whole is greater than the sum of its parts: Long-read sequencing for solving clinical problems in haematology.
J Cell Mol Med
; 28(3): e17961, 2024 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-38260950
7.
Unclassified Dots in the Blood Cell Counter Graphs from a Cancer Patient with Fever and Hypotension.
Clin Chem
; 67(8): 1162-1163, 2021 08 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36103282
8.
A pilot study on the impact of congenital thrombophilia in COVID-19.
Eur J Clin Invest
; 51(5): e13546, 2021 May.
Artigo
Inglês
| MEDLINE | ID: mdl-33738814
9.
Enhanced therapeutic effect using sequential administration of antigenically distinct oncolytic viruses expressing oncostatin M in a Syrian hamster orthotopic pancreatic cancer model.
Mol Cancer
; 14: 210, 2015 Dec 16.
Artigo
Inglês
| MEDLINE | ID: mdl-26671477
10.
Double hit B cell precursor leukemia/lymphoma in a patient with a prior diagnosis of follicular lymphoma: a diagnostic and therapeutic dilemma.
Ann Hematol
; 99(2): 391-393, 2020 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-31858188
11.
Identification of the first large intronic deletion responsible of type I antithrombin deficiency not detected by routine molecular diagnostic methods.
Br J Haematol
; 186(4): e82-e86, 2019 08.
Artigo
Inglês
| MEDLINE | ID: mdl-30941754
12.
Double hit B cell precursor leukemia/lymphoma in a patient with a prior diagnosis of follicular lymphoma: a diagnostic and therapeutic dilemma.
Ann Hematol
; 98(12): 2837-2839, 2019 Dec.
Artigo
Inglês
| MEDLINE | ID: mdl-31712881
13.
A tower of babel of acronyms? The shadowlands of MGUS/MBL/CHIP/TCUS.
Semin Hematol
; 61(1): 43-50, 2024 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-38350765
14.
Immunotherapy in Acute Myeloid Leukemia: A Literature Review of Emerging Strategies.
Bioengineering (Basel)
; 10(10)2023 Oct 20.
Artigo
Inglês
| MEDLINE | ID: mdl-37892958
15.
Antithrombin Deficiency Is Associated with Prothrombotic Plasma Fibrin Clot Phenotype.
Thromb Haemost
; 123(9): 880-891, 2023 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-37201530
16.
Impact of genetic structural variants in factor XI deficiency: identification, accurate characterization, and inferred mechanism by long-read sequencing.
J Thromb Haemost
; 21(7): 1779-1788, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-36940803
17.
Scalable production of tissue-like vascularized liver organoids from human PSCs.
Exp Mol Med
; 55(9): 2005-2024, 2023 09.
Artigo
Inglês
| MEDLINE | ID: mdl-37653039
18.
Persistent Large Granular Lymphocyte Clonal Expansions: "The Root of Many Evils"-And of Some Goodness.
Cancers (Basel)
; 14(5)2022 Mar 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35267648
19.
Full-length antithrombin frameshift variant with aberrant C-terminus causes endoplasmic reticulum retention with a dominant-negative effect.
JCI Insight
; 7(19)2022 10 10.
Artigo
Inglês
| MEDLINE | ID: mdl-36214221
20.
Molecular Dissection of Structural Variations Involved in Antithrombin Deficiency.
J Mol Diagn
; 24(5): 462-475, 2022 05.
Artigo
Inglês
| MEDLINE | ID: mdl-35218943