Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Anna Kubiak-Dydo"'
Autor:
Marcin Bednarek, Marek Trybus, Monika Kolanowska, Mateusz Koziej, Beata Kiec‐Wilk, Artur Dobosz, Marta Kotlarek‐Łysakowska, Anna Kubiak‐Dydo, Ewelina Użarowska‐Gąska, Julia Staręga‐Rosłan, Paweł Gaj, Izabela Górzyńska, Katarzyna Serwan, Michał Świerniak, Adam Kot, Krystian Jażdżewski, Anna Wójcicka
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Abstract Background Brachydactylies are a group of inherited conditions, characterized mainly by the presence of shortened fingers and toes. Based on the patients’ phenotypes, brachydactylies have been subdivided into 10 subtypes. In this study, we
Externí odkaz:
https://doaj.org/article/affdf9a585db42bda2bb63ae2877b1ff
Autor:
Agnieszka Furmańczyk-Zawiska, Anna Kubiak-Dydo, Ewelina Użarowska-Gąska, Marta Kotlarek-Łysakowska, Katarzyna Salata, Monika Kolanowska, Michał Świerniak, Paweł Gaj, Beata Leszczyńska, Maria Daniel, Krystian Jażdżewski, Magdalena Durlik, Anna Wójcicka
Publikováno v:
Journal of Personalized Medicine, Vol 11, Iss 4, p 304 (2021)
Atypical hemolytic uremic syndrome (aHUS) is a rare disease triggered by dysregulation of the alternative complement pathway, consisting of a characteristic triad of nonimmune hemolytic anemia, thrombocytopenia, and renal failure. The risk of aHUS on
Externí odkaz:
https://doaj.org/article/12475646fa0642a3b7b6b5785d600ecb
Autor:
Monika Kolanowska, Krystian Jazdzewski, Marta Kotlarek-Łysakowska, Magdalena Durlik, Anna Kubiak-Dydo, Katarzyna Salata, Agnieszka Furmańczyk-Zawiska, Pawel Gaj, Michał Świerniak, Anna Wojcicka, Ewelina Użarowska-Gąska, Beata Leszczyńska, Maria Daniel
Publikováno v:
Journal of Personalized Medicine
Journal of Personalized Medicine, Vol 11, Iss 304, p 304 (2021)
Journal of Personalized Medicine, Vol 11, Iss 304, p 304 (2021)
Atypical hemolytic uremic syndrome (aHUS) is a rare disease triggered by dysregulation of the alternative complement pathway, consisting of a characteristic triad of nonimmune hemolytic anemia, thrombocytopenia, and renal failure. The risk of aHUS on
Autor:
Ewelina Użarowska-Gąska, Izabela Górzyńska, Mateusz Koziej, Anna Kubiak-Dydo, Katarzyna Serwan, Pawel Gaj, Marta Kotlarek-Łysakowska, Krystian Jazdzewski, Anna Wojcicka, Julia Staręga-Rosłan, Michał Świerniak, Monika Kolanowska, Adam Kot, Marcin Bednarek, Beata Kieć-Wilk, Artur Dobosz, Marek Trybus
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 3, Pp n/a-n/a (2021)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Background Brachydactylies are a group of inherited conditions, characterized mainly by the presence of shortened fingers and toes. Based on the patients’ phenotypes, brachydactylies have been subdivided into 10 subtypes. In this study, we have ide
Autor:
Furmańczyk-Zawiska, Agnieszka, Kubiak-Dydo, Anna, Użarowska-Gąska, Ewelina, Kotlarek-Łysakowska, Marta, Salata, Katarzyna, Kolanowska, Monika, Świerniak, Michał, Gaj, Paweł, Leszczyńska, Beata, Daniel, Maria, Jażdżewski, Krystian, Durlik, Magdalena, Wójcicka, Anna
Publikováno v:
Journal of Personalized Medicine; Apr2021, Vol. 11 Issue 4, p304-304, 1p