Bibliografia UJ CM

1/14
Magdalena Mrożek, Ewa Wypasek, Martine Alhenc-Gelas, Daniel P. Potaczek, Anetta Undas.
Novel Splice Site Mutation in the PROS1 Gene in a Polish Patient with Venous Thromboembolism : c.602-2delA, Splice Acceptor Site of Exon 7.
Medicina
2020 : Vol. 56, nr 9, il., bibliogr. 17 poz., abstr.
Autor korespondencyjny: Daniel P. Potaczek.
Open Access Creative Commons Attribution License CC-BY 4.0.
p-ISSN: 1010-660X
AZ
KAZ
AIF
IF: 2.430
Adres url:
Streszczenie w PubMed:
2/14
Ewa Wypasek, Javier Corral, Martine Alhenc-Gelas, Wojciech Sydor, Teresa Iwaniec, Magdalena Celińska-Lowenhoff, Daniel P. Potaczek, Aleksandra Blecharczyk, Krystyna Zawilska, Jacek Musiał, Anetta Undas.
Genetic characterization of antithrombin, protein C and protein S deficiencies in Polish patients.
Polskie Archiwum Medycyny Wewnętrznej
2017 : Vol. 127, nr 7-8, s. 512-523, bibliogr. 47 poz., abstr.
Open Access Creative Commons Attribution License CC-BY 4.0.
Autor korespondencyjny: Ewa Wypasek.
p-ISSN: 0032-3772
AP
ORG
AIF
IF: 2.658
Adres url:
Streszczenie w PubMed:
3/14
Ewa Wypasek, Javier Corral, Martine Alhenc-Gelas, Wojciech Sydor, Teresa Iwaniec, Magdalena Celińska-Lowenhoff, Daniel P. Potaczek, Aleksandra Blecharczyk, Krystyna Zawilska, Jacek Musiał, Anetta Undas.
Genetic characterization of antithrombin, protein C and protein S deficiencies in polish patients.
Acta Haematologica Polonica
2017 : Vol. 48, suppl. 1, s. s17-s18
XXVII Zjazd Polskiego Towarzystwa Hematologów i Transfuzjologów, Warszawa, 21-23 września 2017 r.
p-ISSN: 0001-5814
SZP
AWZ
4/14
Ewa Wypasek, Marek Karpinski, Martine Alhenc-Gelas, Anetta Undas.
Venous thromboembolism associated with protein S deficiency due to Arg451* mutation in PROS1 gene: a case report and a literature review.
Journal of Genetics
2017 : Vol. 96, nr 6, s. 1047-1056, il., bibliogr., abstr.
Autor korespondencyjny: Anetta Undas.
p-ISSN: 0022-1333
AZ
POG
AIF
IF: 0.672
Adres url:
Streszczenie w PubMed:
5/14
Marek Cieśla, Ewa Wypasek, Javier Corral, Martine Alhenc-Gelas, Anetta Undas.
Antithrombin Katowice: exon 1 deletion in the SERPINC1 gene associated with type I antithrombin deficiency.
Blood Coagulation and Fibrinolysis
2015 : Vol. 26, nr 1, s. 95-97, il., bibliogr. 12 poz.
p-ISSN: 0957-5235
AZ
KAZ
AIF
IF: 1.242
Streszczenie w PubMed:
6/14
Ewa Wypasek, Daniel P. Potaczek, Martine Alhenc-Gelas, Anetta Undas.
Heerlen polymorphism associated with type III protein S deficiency and factor V Leiden mutation in a Polish patient with deep vein thrombosis.
Blood Coagulation and Fibrinolysis
2014 : Vol. 25, nr 1, s. 84-85, bibliogr. 9 poz.
p-ISSN: 0957-5235
AZ
KAZ
AIF
IF: 1.403
7/14
Ewa Wypasek, Daniel P. Potaczek, Martine Alhenc-Gelas, Anetta Undas.
Novel missense mutation C106R in the PROC gene associated with type I protein C deficiency in a young Polish man with high-risk pulmonary embolism.
Polskie Archiwum Medycyny Wewnętrznej
2014 : Vol. 124, nr 1-2, s. 75-76, bibliogr. 7 poz.
p-ISSN: 1897-9483
LR
AIF
IF: 2.121
Adres url:
Streszczenie w PubMed:
8/14
Ewa Wypasek, Daniel P. Potaczek, Martine Alhenc-Gelas, Anetta Undas.
PROS1 mutations associated with protein S deficiency in Polish patients with residual vein obstruction on rivaroxaban therapy.
Thrombosis Research
2014 : Vol. 134, nr 1, s. 199-201, il., bibliogr. 17 poz.
p-ISSN: 0049-3848
LR
AIF
IF: 2.447
9/14
Ewa Wypasek, Oksana Pankiw-Bembenek, Daniel P. Potaczek, Martine Alhenc-Gelas, Jaroslaw Trebacz, Anetta Undas.
A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction.
International Journal of Cardiology
2013 : Vol. 167, nr 5, s. e146-e148, il., bibliogr. 9 poz.
p-ISSN: 0167-5273
LR
AIF
IF: 6.175
Adres url:
Streszczenie w PubMed:
10/14
Magdalena Szymańska, Martine Alhenc-Gelas, Anetta Undas.
Antithrombin Rybnik: a new point mutation (nt 683 G>T) associated with type I antithrombin deficiency in a patient with venous thromboembolism and recurrent superficial venous thrombosis.
Blood Coagulation and Fibrinolysis
2013 : Vol. 24, nr 5, s. 579-580, bibliogr. 13 poz.
p-ISSN: 0957-5235
LR
AIF
IF: 1.380
11/14
Ewa Wypasek, Martine Alhenc-Gelas, Anetta Undas.
First report of a large PROS1 deletion from exon 1 through 12 detected in Polish patients with deep-vein thrombosis.
Thrombosis Research
2013 : Vol. 132, nr 1, s. 143-144, il., bibliogr. 11 poz.
p-ISSN: 0049-3848
LR
AIF
IF: 2.427
Adres url:
12/14
Ewa Wypasek, Daniel P. Potaczek, Joanna Płonka, Martine Alhenc-Gelas, Anetta Undas.
Protein S deficiency and Heerlen polymorphism in a Polish patient with acute myocardial infarction and previous venous thromboembolism.
Thrombosis Research
2013 : Vol. 132, nr 6, s. 776-777, il., bibliogr. 4 poz.
p-ISSN: 0049-3848
LR
AIF
IF: 2.427
Adres url:
13/14
Magdalena Szymańska, Martine Alhenc-Gelas, Anetta Undas.
Recurrent ischemic cerebrovascular events in a patient with type I antithrombin deficiency caused by 9788 G>A splice site mutation: a case report.
Blood Coagulation and Fibrinolysis
2013 : Vol. 24, nr 2, s. 213-215, bibliogr. 16 poz.
p-ISSN: 0957-5235
AZ
KAZ
AIF
IF: 1.380
14/14
Magdalena Celinska-Lowenhoff, Teresa Iwaniec, Martine Alhenc-Gelas, Jacek Musial, Anetta Undas.
Antithrombin Krakow II (c.624+1 G > T): a novel mutation leading to type 1 antithrombin deficiency.
Blood Coagulation and Fibrinolysis
2012 : Vol. 23, nr 5, s. 454-455, bibliogr. 8 poz.
p-ISSN: 0957-5235
AZ
KAZ
AIF
IF: 1.248
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