Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Beata Olchowik"'
Autor:
Małgorzata Łukawska, Anna Potulska-Chromik, Marta Lipowska, Dorota Hoffman-Zacharska, Beata Olchowik, Magdalena Figlerowicz, Karolina Kanabus, Edyta Rosiak, Anna Kostera-Pruszczyk
Publikováno v:
Frontiers in Neurology, Vol 12 (2022)
Externí odkaz:
https://doaj.org/article/155442a6133a4994bb511fc4f017b414
Autor:
Małgorzata Łukawska, Anna Potulska-Chromik, Marta Lipowska, Dorota Hoffman-Zacharska, Beata Olchowik, Magdalena Figlerowicz, Karolina Kanabus, Edyta Rosiak, Anna Kostera-Pruszczyk
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Background: Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare acquired polyneuropathy that especially among youngest children should be differentiated with hereditary neuropathies. Even though upon diagnosis treatment options are sim
Externí odkaz:
https://doaj.org/article/81c19a58a6cf4a00a0b008a53c63fcf0
Autor:
Anna Kostera-Pruszczyk, Karolina Kanabus, Beata Olchowik, Marta Lipowska, Dorota Hoffman-Zacharska, Małgorzata Łukawska, Edyta Rosiak, Anna Potulska-Chromik, Magdalena Figlerowicz
Publikováno v:
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology
Frontiers in Neurology
Background: Chronic inflammatory demyelinating polyneuropathy (CIDP) is a rare acquired polyneuropathy that especially among youngest children should be differentiated with hereditary neuropathies. Even though upon diagnosis treatment options are sim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6072d103d0a569b43d020ba6ac274043
https://www.frontiersin.org/articles/10.3389/fneur.2021.667378/full
https://www.frontiersin.org/articles/10.3389/fneur.2021.667378/full
Autor:
Krzysztof Sendrowski, Anna Potulska-Chromik, Anna Kostera-Pruszczyk, Beata Olchowik, Małgorzata Łukawska
Publikováno v:
Child Neurology. 26:71-74
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::32c85da1b5434e004730c091470e2d21
https://doi.org/10.20966/chn.2017.53.414
https://doi.org/10.20966/chn.2017.53.414
Autor:
Joanna Śmigielska-Kuzia, Magdalena Cholewa, Leszek Boćkowski, Krzysztof Sendrowski, Wojciech Sobaniec, Adam Lukasiewicz, Urszula Lebkowska, Beata Olchowik
Publikováno v:
ResearcherID
Background and purpose Down syndrome (DS) is the most common genetic cause of mental retardation with deficits in language and memory. Mental retardation of varying degrees is the most consistent feature of DS. The objective of this study was to use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61529e9256d97aa5231dccfff8d92528
https://doi.org/10.1016/s0028-3843(14)60107-9
https://doi.org/10.1016/s0028-3843(14)60107-9
Autor:
Elżbieta Poskrobko, Małgorzata Rusak, Beata Olchowik, Anna Galicka, Anna Jakubiuk-Tomaszuk, Wojciech Sobaniec, Agata Nędzi
Publikováno v:
Pharmacological reports : PR. 67(6)
Background Down Syndrome is by far the most common and best known chromosomal disorder in humans. It expresses multiple systemic complications with both structural and functional defects as part of the clinical manifestation. The mechanisms of immune
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4897d7443e87078ebd6d9cc53ac47c12
https://pubmed.ncbi.nlm.nih.gov/26481531
https://pubmed.ncbi.nlm.nih.gov/26481531
Publikováno v:
Psychiatria polska. 43(2)
Prader-Willi syndrome, induced by a loss of function of paternal genes in the subcentrometric region of the chromosome 15 (q11.2q13), is a complex neurodevelopmental disorder with characteristic obesity resulting from hyperphagia. In addition behavio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8cf8ea58777a671a51035b3717aa098c
https://pubmed.ncbi.nlm.nih.gov/19697785
https://pubmed.ncbi.nlm.nih.gov/19697785
Publikováno v:
Psychiatria polska. 43(2)
Prader-Willi syndrome, induced by a function changes of paternal genes in the subcentrometric region of the chromosome 15 (q11.2q13), is the most common genetic cause of obesity resulting from hyperphagia. Behavioural disturbancies with compulsions i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e4c6af12b21d3f050bfd286688d03602
https://pubmed.ncbi.nlm.nih.gov/19697784
https://pubmed.ncbi.nlm.nih.gov/19697784