Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ana C, Kempfer"'
Autor:
Adriana I. Woods, Ana C. Kempfer, Maria A. Lazzari, Emilse Bermejo, Analía Sánchez-Luceros, Maria Fabiana Alberto, S. H. Grosso, Juvenal Paiva
Publikováno v:
Seminars in Thrombosis and Hemostasis. 40:151-160
Platelet-type von Willebrand disease (PT-VWD) and type 2B von Willebrand disease (2B-VWD) are rare bleeding disorders characterized by increased ristocetin-induced platelet aggregation (RIPA) at low concentrations of ristocetin. Diagnosis of either c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd30eaa0975a66a7c5907391e029e92e
https://doi.org/10.1055/s-0033-1364183
https://doi.org/10.1055/s-0033-1364183
Autor:
Adriana I. Woods, Ana C. Kempfer, Susana S. Meschengieser, Maria A. Lazzari, J. C. Calderazzo Pereyra, Analía Sánchez-Luceros, Alicia N. Blanco, Yanina Powazniak
Publikováno v:
Haemophilia. 18:112-116
Most mutations identified in 2A VWD patients are localized in the A2 domain, although missense substitutions have also been recognized in the A1 domain. We describe a novel heterozygous missense mutation in the A1 domain of VWF gene responsible for t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7183c5b4e0ffbc3ff927357f641893bc
https://doi.org/10.1111/j.1365-2516.2011.02569.x
https://doi.org/10.1111/j.1365-2516.2011.02569.x
Autor:
Emilse Bermejo, Juan Pablo Frontroth, Maria A. Lazzari, Ana C. Kempfer, Cristina Elena Farias
Publikováno v:
Thrombosis Research. 68:131-136
In order to determine the binding of vWF, subendothelium from everted human umbilical arteries was perfused with dialysed serum containing different concentrations of purified vWF using an annular perfusion chamber at a wall shear rate of 1100 sec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72558a75927eb8c87d74647feab3287a
https://doi.org/10.1016/0049-3848(92)90028-9
https://doi.org/10.1016/0049-3848(92)90028-9
Autor:
Patricia, Casais, Gonzalo A, Carballo, Adriana I, Woods, Ana C, Kempfer, Cristina E, Farías, Silvia H, Grosso, María A, Lazzari
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Von Willebrand disease (VWD) type 2 comprises the qualitative defects of VWF molecule (1). Among them, VWD 2N is the result of mutations in the D’ or D3 domains in the N-terminal region that cause VWF with a defective binding capacity to FVIII, res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::3a763e3ba0b3132ef5731a6ed3b64304
https://www.ncbi.nlm.nih.gov/pubmed/?term=16894469
https://www.ncbi.nlm.nih.gov/pubmed/?term=16894469
Autor:
Susana S. Meschengieser, Ana C. Kempfer, Maria A. Lazzari, Karina Turdó, Adriana I. Woods, Patricia Casais, Adriana Arizó, Analía Sánchez-Luceros, Alicia N. Blanco
Publikováno v:
Thrombosis research. 120(3)
Fil: Sánchez Luceros, Analía Gabriela. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Academia Nacional de Medicina de Buenos Aires. Instituto de Investigaciones Hematológicas "Mariano R. Castex"; Argentina Fil: Meschengi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7e806864a6307e418b7e834f1ffd471
https://pubmed.ncbi.nlm.nih.gov/17056101
https://pubmed.ncbi.nlm.nih.gov/17056101
Autor:
Julio Cesar Calderazzo, Adriana I. Woods, Ana C. Kempfer, Analía Sánchez-Luceros, Silvia H. Grosso, Maria A. Lazzari
Publikováno v:
Haemophilia. 19:e180-e181
von Willebrand's disease (VWD)-type Vicenza is characterized by a mild-moderate bleeding tendency, presence of ultralarge multimers (ULVWF), low von Willebrand's factor (VWF) and factor VIII (FVIII:C), attributed to reduced VWF survival, and the prop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d60b7e75d149c776ebbb8d241b81cb7
https://doi.org/10.1111/hae.12126
https://doi.org/10.1111/hae.12126
Autor:
Marco Cattaneo, Adriana I. Woods, A. Chang, Ana C. Kempfer, Emmanuel J. Favaloro, David Lillicrap, A. Hubbard, Maria A. Lazzari, Alicia N. Blanco, Susana S. Meschengieser, C. Mazurier
Publikováno v:
Scopus-Elsevier
von Willebrand disease is the most common inherited bleeding disorder in humans. VWD can be classified into three major types, designated Types 1, 2 and 3; Type 2 can be further separated into subtypes 2A, 2B, 2M and 2N. The diagnosis of VWD requires
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7eb7f174d26317d5b5fd5c2bda55bf7
https://pubmed.ncbi.nlm.nih.gov/15479392
https://pubmed.ncbi.nlm.nih.gov/15479392
Autor:
María Marta, Amaral, Ana C, Kempfer, Cristina E, Farías, Gonzalo A, Carballo, María R, Silaf, María A, Lazzari
Publikováno v:
Medicina. 63(2)
The von Willebrand factor cleaving protease (VWFCP) modulates the von Willebrand factor (VWF) multimeric size in normal plasma. VWFCP activity levels are decreased in different physiological and pathologic situations. Different techniques have been d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::70f80e59f840c690c05a3c93d9f895ed
https://pubmed.ncbi.nlm.nih.gov/12793081
https://pubmed.ncbi.nlm.nih.gov/12793081
Publikováno v:
Thrombosis research. 96(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb9a7829123cd39e5691e9fd04c1e811
https://pubmed.ncbi.nlm.nih.gov/10574594
https://pubmed.ncbi.nlm.nih.gov/10574594
Autor:
Ana C. Kempfer, Elisa Singer, María T. Santarelli, Adriana I. Woods, Maria A. Lazzari, Juan C. Giménez, Cristina Elena Farias
Publikováno v:
Thrombosis research. 88(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1238997c59c06d9491a8337f9589cb3d
https://pubmed.ncbi.nlm.nih.gov/9336877
https://pubmed.ncbi.nlm.nih.gov/9336877