Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Jana Volejnikova"'
Autor:
D. Matthew Gianferante, Marcin W. Wlodarski, Evangelia Atsidaftos, Lydie Da Costa, Polyxeni Delaporta, Jason E. Farrar, Frederick D. Goldman, Maryam Hussain, Antonis Kattamis, Thierry Leblanc, Jeffrey M. Lipton, Charlotte M. Niemeyer, Dagmar Pospisilova, Paola Quarello, Ugo Ramenghi, Vijay G. Sankaran, Adrianna Vlachos, Jana Volejnikova, Blanche P. Alter, Sharon A. Savage, Neelam Giri
Publikováno v:
Haematologica, Vol 106, Iss 5 (2020)
Diamond Blackfan anemia (DBA) is predominantly an autosomal dominant inherited red cell aplasia primarily caused by pathogenic germline variants in ribosomal protein genes. DBA due to pathogenic RPL35A variants has been associated with large 3q29 del
Externí odkaz:
https://doaj.org/article/6dcaa279444c45d49f67d28d56e40b5d
Publikováno v:
Biomedical Papers, Vol 162, Iss 2, Pp 154-158 (2018)
Background: Henoch-Schönlein purpura (HSP) is a systemic disorder characterized by leukocytoclastic vasculitis involving the capillaries and by the deposition of IgA immune complexes. An association between HSP and atypical bacteria is uncommon in c
Externí odkaz:
https://doaj.org/article/59a7bc3437be4d7a83d993c4378a3d0b
Autor:
Jana Volejnikova, Jirina Zapletalova, Marie Jarosova, Helena Urbankova, Petr Vojta, Eva Klaskova, Marshall S. Horwitz, Marian Hajduch, Vladimir Mihal
Publikováno v:
Biomedical Papers, Vol 162, Iss 1, Pp 65-70 (2018)
Background: Leri-Weill syndrome (LWS) ranks among conditions with short stature homeobox gene (SHOX) haploinsufficiency. Data on possible association of SHOX aberrations with malignant diseases are scarce. Methods and Results: We report a unique case
Externí odkaz:
https://doaj.org/article/587fce9b91bd4cf8b81ee17a06ff42b2
Autor:
Jana Volejnikova, Viera Bajciova, Lucie Sulovska, Marie Geierova, Eva Buriankova, Marie Jarosova, Marian Hajduch, Jaroslav Sterba, Vladimir Mihal
Publikováno v:
Biomedical Papers, Vol 160, Iss 3, Pp 456-460 (2016)
Background: Malignant melanoma in childhood is infrequent and can arise within congenital melanocytic nevi. Spread of malignant melanoma to the bone marrow, especially in children, is extremely rare. Methods and Results: Reported is a case of a 5-yea
Externí odkaz:
https://doaj.org/article/6642853b11b54c34a6bc5b5a6470413c
Autor:
Jana Volejnikova, Ester Mejstrikova, Tatana Valova, Leona Reznickova, Ladislava Hodonska, Vladimir Mihal, Jaroslav Sterba, Yahia Jabali, Daniela Prochazkova, Bohumir Blazek, Jiri Hak, Zdenka Cerna, Ondrej Hrusak, Jan Stary, Jan Trka, Eva Fronkova
Publikováno v:
Haematologica, Vol 96, Iss 12 (2011)
Background Most minimal residual disease-directed treatment interventions in current treatment protocols for acute lymphoblastic leukemia are based on bone marrow testing, which is a consequence of previous studies showing the superiority of bone mar
Externí odkaz:
https://doaj.org/article/56f8f534185b4b1abc8f07c8bc916afb
Autor:
Ester Mejstrikova, Jana Volejnikova, Eva Fronkova, Katerina Zdrahalova, Tomas Kalina, Jaroslav Sterba, Yahia Jabali, Vladimir Mihal, Bohumir Blazek, Zdena Cerna, Daniela Prochazkova, Jiri Hak, Zuzana Zemanova, Marie Jarosova, Alexandra Oltova, Petr Sedlacek, Jiri Schwarz, Jan Zuna, Jan Trka, Jan Stary, Ondrej Hrusak
Publikováno v:
Haematologica, Vol 95, Iss 6 (2010)
Background Mixed phenotype acute leukemia (MPAL) represents a diagnostic and therapeutic dilemma. The European Group for the Immunological Classification of Leukemias (EGIL) scoring system unambiguously defines MPAL expressing aberrant lineage marker
Externí odkaz:
https://doaj.org/article/00e3c2b1f9cb4fb2adcf9b49b33ebc86
Autor:
Vratislav, Smolka, Marie, Rohanova, Miroslav, Seda, Eva, Karaskova, Oksana, Tkachyk, Martin, Zapalka, Jana, Volejnikova
Publikováno v:
Hepatobiliary & Pancreatic Diseases International. 22:317-322
Pediatric acute pancreatitis (AP) is rare but increasing. Severe AP is associated with higher morbidity and mortality. However, there are no universally accepted prognostic criteria for AP.This retrospective study included children with AP admitted t
Autor:
Agata Kubickova, Zuzana Maceckova, Petr Vojta, Martin Ondra, Jana Volejnikova, Pavla Koralkova, Alexandra Jungova, Ondřej Jahoda, Renata Mojzikova, Ivana Hadacova, Jaroslav Cermak, Monika Horvathova, Dagmar Pospisilova, Marian Hajduch
Publikováno v:
Blood cells, moleculesdiseases. 97
Diamond-Blackfan anemia (DBA) is predominantly underlined by mutations in genes encoding ribosomal proteins (RP); however, its etiology remains unexplained in approximately 25 % of patients. We previously reported a novel heterozygous RPS7 mutation h
Autor:
Jana Volejnikova, Dagmar Pospisilova, Blanche P. Alter, Sharon A. Savage, Marcin W. Wlodarski, Antonis Kattamis, Polyxeni Delaporta, Paola Quarello, D. Matthew Gianferante, Thierry Leblanc, Ugo Ramenghi, Adrianna Vlachos, Jeffrey M. Lipton, Frederick D. Goldman, Evangelia Atsidaftos, Maryam Hussain, Lydie Da Costa, Vijay G. Sankaran, Charlotte M. Niemeyer, Neelam Giri, Jason E. Farrar
Publikováno v:
Haematologica. 106:1303-1310
Diamond Blackfan anemia (DBA) is predominantly an autosomal dominant inherited red cell aplasia primarily caused by pathogenic germline variants in ribosomal protein genes. DBA due to pathogenic RPL35A variants has been associated with large 3q29 del
Autor:
Jiri Ehrmann, Jana Volejnikova, Eva Karásková, Vratislav Smolka, Martin Zápalka, Oksana Tkachyk
Publikováno v:
Hepatobiliary & Pancreatic Diseases International. 19:17-21
Background Autoimmune hepatitis (AIH) is a rare progressive liver disease, which manifests as acute hepatitis in 40%-50% of pediatric cases. This refers predominantly to spontaneous exacerbations of previously unrecognized subclinical AIH with labora