Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Krzysztof, Szmyd"'
Autor:
Krzysztof Szmyd, Zbigniew Chmielewski
Publikováno v:
Social Communication. 6:42-52
The paper presents results of research related to familiarity and understanding of home hospice term and shows how the social media discourse of palliative care looks like. Answers and conclusions are crucial for palliative care organisations as thei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a78d7490abd9ed94569ca3fd49b737b
https://doi.org/10.2478/sc-2020-0005
https://doi.org/10.2478/sc-2020-0005
Autor:
Grażyna Ohia, Paweł Krajewski, Agnieszka Jalowska, Maria M. Sąsiadek, Piotr Stawiński, Robert Śmigiel, Anna Walczak, Elżbieta Szmida, Krzysztof Szmyd, Anna Biernacka, Bożena Głowska, Waldemar Golebiowski, Rafał Płoski, Mateusz Biela, Marzena Zielińska, Wojciech Walas, Michał Błoch, Joanna Kosińska, Barbara Królak-Olejnik, Paweł Skiba, Małgorzata Rydzanicz, Piotr Gasperowicz, Jolanta Sykut-Cegielska
Publikováno v:
Journal of Clinical Medicine; Volume 9; Issue 7; Pages: 2220
Journal of Clinical Medicine, Vol 9, Iss 2220, p 2220 (2020)
Journal of Clinical Medicine
Journal of Clinical Medicine, Vol 9, Iss 2220, p 2220 (2020)
Journal of Clinical Medicine
Genetic disorders are the leading cause of infant morbidity and mortality. Due to the large number of genetic diseases, molecular and phenotype heterogeneity and often severe course, these diseases remain undiagnosed. In infants with a suspected acut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c15e2f611919c7b7f9e4cac9f4e737c1
Autor:
Agnieszka, Jalowska, Joanna, Krzeszowiak, Agnieszka, Stembalska, Krzysztof, Szmyd, Mariusz, Zimmer, Gizela, Jagielska, Małgorzata, Raś, Agnieszka, Pasławska, Agnieszka, Szafrańska, Dorota, Paluszyńska, Tomasz, Fuchs, Karolina, Pesz, Maria, Sąsiadek, Barbara, Królak-Olejnik, Robert, Śmigiel
Publikováno v:
Developmental period medicine. 23(4)
Lethal defects lead to the intrauterine death of the fetus or the passing away of the child immediately after birth or in early infancy, regardless of the treatment used. In the case of lethal defects, it is not possible to effectively help the child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::813b3bf28ee638f31256b4eef7d9773d
https://pubmed.ncbi.nlm.nih.gov/31913141
https://pubmed.ncbi.nlm.nih.gov/31913141
Autor:
Krzysztof Szmyd, Robert Śmigiel, Olgierd Pankiewicz, Barbara Królak-Olejnik, Jadwiga Węcławek-Tompol
Publikováno v:
Pediatria Polska. 92:796-801
The decision to terminate causative treatment greatly affects the course of treatment and the patient's future. There is a serious conflict when there is a significant difference in opinion about further treatment between the physician and the patien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53df233ba886af776760889445ce5cd3
https://doi.org/10.1016/j.pepo.2017.06.004
https://doi.org/10.1016/j.pepo.2017.06.004
Autor:
Agnieszka, Jalowska, Joanna, Krzeszowiak, Agnieszka, Stembalska, Krzysztof, Szmyd, Mariusz, Zimmer, Gizela, Jagielska, Małgorzata, Raś, Agnieszka, Pasławska, Agnieszka, Szafrańska, Dorota, Paluszyńska, Tomasz, Fuchs, Karolina, Pesz, Maria, Sąsiadek, Barbara, Królak-Olejnik, Robert, Śmigiel
Publikováno v:
Journal of mother and childPiśmiennictwo. 23(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0914f249395ff9a7627bb75e93504d19
https://pubmed.ncbi.nlm.nih.gov/34705354
https://pubmed.ncbi.nlm.nih.gov/34705354
Publikováno v:
Pediatria Polska. 89:389-394
Congenital defects are some of the most common reasons of neonatal morbidity and in some cases those may have lethal prognosis. Progress in the diagnostics of congenital defects enables most cases to be diagnosed prenatally. Because of that reason, t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13d0160f8e70342ca08b628a1633f733
https://doi.org/10.1016/j.pepo.2014.08.004
https://doi.org/10.1016/j.pepo.2014.08.004
Autor:
Katarzyna Pawelec, Alicja Chybicka, Mariusz Wysocki, Tomasz Urasiński, Andrzej Kurylak, Michał Matysiak, Dawid Szpecht, Wojciech Młynarski, Barbara Kaczorowska-Hać, Małgorzata Salamonowicz, Krzysztof Szmyd, Ewa Zaleska-Czepko, Tomasz Szczepański, Maryna Krawczuk-Rybak, Monika Bulas, Jerzy Kowalczyk, Anna Balcerska, Jarosław Peregud-Pogorzelski, Walentyna Balwierz, Halina Bubała, Anna Panasiuk, Jacek Wachowiak, Elzbieta Leszczynska, Urszula Demkow
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9783319100173
Immunosuppressive therapy is the treatment of choice in children with acquired severe aplastic anemia (AA) and no HLA-matched family donor. The paper presents results of a multicenter study of 63 children with AA treated with rabbit antithymocyte glo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::55b13d49efaccdcccb656573dfcb2900
https://doi.org/10.1007/5584_2014_38
https://doi.org/10.1007/5584_2014_38
Autor:
Robert, Smigiel, Dariusz, Patkowski, Beata, Pyrek, Marzena, Zielińska, Waldemar, Gołebiowski, Małgorzata, Czyzewska, Krzysztof, Szmyd, Maria M, Sasiadek
Publikováno v:
Medycyna wieku rozwojowego. 15(1)
Oesophageal atresia is a congenital defect of alimentary tract concerning the interruption of oesophagus with or without connection with the trachea. Its incidence is 1:3000-3500 of live-born. Associated anomalies including genetic disorders occur in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f1caf1bec0a5dfdbe350b5baa953857
https://pubmed.ncbi.nlm.nih.gov/21786507
https://pubmed.ncbi.nlm.nih.gov/21786507
Autor:
Krzysztof, Szmyd, Olga, Haus
Publikováno v:
Medycyna pracy. 62(1)
The majority of antineoplastic agents have been found to show mutagenic, teratogenic and carcinogenic potential. Biological effects of long-term contact with low levels of cytostatic drugs are not well known. The results of many studies are ambiguous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bffd1f5620e3864a139378bdad655763
https://pubmed.ncbi.nlm.nih.gov/21748879
https://pubmed.ncbi.nlm.nih.gov/21748879
Autor:
Maria Pilarska, M Schab, Anna Junkiert-Czarnecka, Olga Haus, Hanna Janiszewska, Krzysztof Szmyd, Aneta Bąk
Publikováno v:
Hereditary Cancer in Clinical Practice, Vol 9, Iss Suppl 2, p A2 (2011)
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice
Background Many studies on the genetic background of common neoplastic diseases indicate that they may be the result of hereditary mutations in cancer susceptibility genes, such as BRCA1, CHEK2, CDKN2A, NOD2, NBS1. The cancer occurrence in geneticall
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf63ba04a699c571f87fef267dc0f848
http://www.hccpjournal.com/content/9/S2/A2
http://www.hccpjournal.com/content/9/S2/A2