Detalles de la búsqueda
1.
Healthcare Risk Management and Monitoring of patient falls in Italian National Service. The experience of a Local Health Authority.
Ig Sanita Pubbl
; 80(2): 30-40, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38739439
2.
Thromboses and hemorrhages are common in MPN patients with high JAK2V617F allele burden.
Ann Hematol
; 96(8): 1297-1302, 2017 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-28585070
3.
Meat intake and non-Hodgkin lymphoma: a meta-analysis of observational studies.
Cancer Causes Control
; 27(5): 595-606, 2016 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-27076059
4.
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
5.
Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients.
J Thromb Thrombolysis
; 42(4): 586-92, 2016 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-27379499
6.
Defective ADAMTS13 synthesis as a possible consequence of NASH in an obese patient with recurrent thrombotic thrombocytopenic purpura.
Eur J Haematol
; 92(6): 497-501, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24460705
7.
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
8.
A novel germ-line mutation of c-mpl gene in a sporadic case of essential thrombocythemia.
Blood Cells Mol Dis
; 64: 51-52, 2017 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-28391042
9.
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
10.
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
11.
The clinical significance of the lack of arterial or venous thrombosis in patients with congenital prothrombin or FX deficiency.
J Thromb Thrombolysis
; 29(3): 299-302, 2010 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-19412729
12.
Relapsing thrombotic thrombocytopenic purpura with low ADAMTS13 antigen levels: An indication for splenectomy?
Hematol Rep
; 11(1): 7904, 2019 Feb 19.
Artículo
en Inglés
| MEDLINE | ID: mdl-30996851
13.
Multi-segment rupture of the 2016 Amatrice-Visso-Norcia seismic sequence (central Italy) constrained by the first high-quality catalog of Early Aftershocks.
Sci Rep
; 9(1): 6921, 2019 05 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-31061514
14.
Link between von Willebrand factor multimers, relapses and coronary microcirculation in patients with thrombotic thrombocytopenic purpura in remission.
Thromb Res
; 173: 42-47, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30471507
15.
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant.
Haematologica
; 93(11): 1743-7, 2008 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-18815197
16.
Genetic study in patients with factor XII deficiency: a report of three new mutations exon 13 (Q501STOP), exon 14 (P547L) and -13C>T promoter region in three compound heterozygotes.
Blood Coagul Fibrinolysis
; 19(7): 639-43, 2008 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-18832903
17.
A case of Bernard-Soulier Syndrome due to a homozygous four bases deletion (TGAG) of GPIbalpha gene: lack of GPIbalpha but absence of bleeding.
Platelets
; 19(5): 388-91, 2008 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-18791947
18.
A structure-function analysis in patients with prekallikrein deficiency.
Hematology
; 23(6): 346-350, 2018 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-29165051
19.
Factor X Friuli Coagulation Disorder: Almost 50 Years Later.
Clin Appl Thromb Hemost
; 24(1): 33-40, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-28030967
20.
Congenital prothrombin defects: they are not only associated with bleeding but also with thrombosis: a new classification is needed.
Hematology
; 23(2): 105-110, 2018 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-28762299