Detalles de la búsqueda
1.
Peculiar Congenital Factor VII Defect with the Proposita and Her Mother Showing the Same Compound Heterozygosity for Thr384Met and Arg413Gln.
Acta Haematol
; 144(1): 100-104, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-32396910
2.
Long-term safety outcomes of prekallikrein (Fletcher factor) deficiency: A systematic literature review of case reports.
Allergy Asthma Proc
; 41(1): 10-18, 2020 01 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-31888778
3.
Heterozygous FXII deficiency is not associated with an increased incidence of thrombotic events: Results of a long term study.
Blood Cells Mol Dis
; 77: 8-11, 2019 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-30884321
4.
Thrombotic events in severe FXII deficiency in comparison with unaffected family members during a long observation period.
J Thromb Thrombolysis
; 47(3): 481-485, 2019 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-30694429
5.
Long-term safety outcomes of prekillikrein (Fletcher factor) deficiency: A systematic literature review of case reports.
Allergy Asthma Proc
; 2019 Sep 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-31530337
6.
Prevalence of bleeding manifestations in 128 heterozygotes for Factor X deficiency, mainly for FX Friuli, matched versus 128 unaffected family members, during a long sequential observation period (23.5 years).
Eur J Haematol
; 97(6): 547-553, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27124643
7.
A Rare Cause of Isolated Prothrombin Time Prolongation: Congenital Factor X Deficiency.
J Pediatr Hematol Oncol
; 43(8): e1248-e1250, 2021 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-33902062
8.
A comment on congenital prothrombin abnormalities associated with thrombosis but not with bleeding.
J Thromb Thrombolysis
; 51(2): 513-515, 2021 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-32607654
9.
The slow but progressive disappearance of the patients with the Pro343Ser (FX Friuli) mutation.
Br J Haematol
; 191(2): e50-e52, 2020 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-32748957
10.
Complex history of the discovery and characterization of congenital factor X deficiency.
Semin Thromb Hemost
; 41(4): 359-65, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25875733
11.
The Story of Serum Prothrombin Conversion Accelerator, Proconvertin, Stable Factor, Cothromboplastin, Prothrombin Accelerator or Autoprothrombin I, and Their Subsequent Merging into Factor VII.
Semin Thromb Hemost
; 41(4): 366-73, 2015 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-25973586
12.
Venous thrombosis in rare or unusual sites: a diagnostic challenge.
Semin Thromb Hemost
; 40(1): 81-7, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24347377
13.
The old and the new in prekallikrein deficiency: historical context and a family from Argentina with PK deficiency due to a new mutation (Arg541Gln) in exon 14 associated with a common polymorphysm (Asn124Ser) in exon 5.
Semin Thromb Hemost
; 40(5): 592-9, 2014 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-25075649
14.
Discrepant ratios of arterial versus venous thrombosis in hemophilia A as compared with hemophilia B.
J Thromb Thrombolysis
; 37(3): 293-7, 2014 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23681676
15.
Discrepant ratios of arterial vs. venous thrombosis in hemophilias A and B as compared to FVII deficiency.
Eur J Haematol
; 91(2): 152-6, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23621110
16.
A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern Italy.
Eur J Haematol
; 88(3): 229-36, 2012 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-21999818
17.
Myocardial infarction in two cousins heterozygous for ASN41HIS autosomal dominant variant of Bernard-Soulier syndrome.
J Thromb Thrombolysis
; 34(4): 513-7, 2012 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-22569901
18.
Spectrum of 5'UTR mutations in ANKRD26 gene in patients with inherited thrombocytopenia: c.-140C>G mutation is more frequent than expected.
Platelets
; 28(6): 621-624, 2017 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-28277066
19.
Worldwide diffusion of FVII Arg304Gln coagulation defect (FVII Padua).
Eur J Haematol
; 86(2): 135-9, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-20958793
20.
Congenital FVII deficiency and thrombotic events after replacement therapy.
J Thromb Thrombolysis
; 32(3): 362-7, 2011 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-21681394