Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Anna Paszulewicz"'
Publikováno v:
Advances in Dermatology and Allergology/Postȩpy Dermatologii I Alergologii
Introduction: Administration of human C1 esterase inhibitor (Berinert ® P) from target import is the most widespread treatment strategy for patients with hereditary angioedema (HAE). However, a therapeutic health program includ ing Ruconest ® (cone
Publikováno v:
Archives of Medical Science. 5:767-775
INTRODUCTION: Sipuleucel-T is a novel active cellular immunotherapy for the treatment of asymptomatic or minimally symptomatic metastatic castrate-resistant prostate cancer (mCRPC). It is assumed to be associated with less adverse events than convent
Autor:
Paweł, Kawalec, Monika, Szkultecka-Debek, Justyna, Maks, Anna, Paszulewicz, Aneta, Kaweczyńska-Lasoń, Andrzej, Pilc
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 35(205)
Cytomegalovirus infection is particularly dangerous for patients undergoing solid organs transplantation. Among these patients cytomegalovirus disease (CMV) may occur. CMV disease is associated with increased mortality, organ damage and reduced graft
Autor:
Paweł, Kawalec, Przemysław, Holko, Monika, Szkultecka-Debek, Anna, Paszulewicz, Maria, Boratyńska, Maciej, Głyda, Ewa, Ignacak, Justyna, Maks, Monika, Russel-Szymczyk, Aneta, Kaweczyńska-Lasoń
Publikováno v:
Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 34(204)
Standard procedure for cytomegalovirus disease (CMV) prophylaxis in kidney transplant patients was the administration of valganciclovir for up to 110 days after organ transplant. This prophylaxis has been extended up to 200 days in Poland since 2011.
Publikováno v:
Pneumonologia i alergologia polska. 81(2)
Hereditary angioedema (HAE) is a genetic disease caused by C1-esterase inhibitor deficiency, characterized by recurrent attacks of intense, massive, localized subcutaneous oedema that can involve all parts of the body. The aim of this study is a comp
Publikováno v:
Advances in Respiratory Medicine; Volume 81; Issue 2; Pages: 95-104
Introduction: Hereditary angioedema (HAE) is a genetic disease caused by C1-esterase inhibitor deficiency, characterized by recurrent attacks of intense, massive, localized subcutaneous oedema that can involve all parts of the body. The aim of this s