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Page 1
Next-generation sequencing in children with epilepsy: The importance of precise genotype-phenotype correlation.
Epilepsy Behav. 2022 Mar;128:108564. doi: 10.1016/j.yebeh.2022.108564. Epub 2022 Jan 19.
Epilepsy Behav. 2022.
PMID: 35065395
Causes of Intensive Care Unit Admissions in Children with SARS-CoV-2: A Single-Centre Observational Study.
Homola L, Klučka J, Fabián D, Štourač P, Šikula J, Vávrová E, Jeřábková B, Sihlovec M, Musil V, Španělová K, Mužlayová P, Danhofer P.
Homola L, et al. Among authors: jerabkova b.
Children (Basel). 2022 Dec 30;10(1):75. doi: 10.3390/children10010075.
Children (Basel). 2022.
PMID: 36670627
Free PMC article.
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Improved nutritional outcomes and gastrointestinal symptoms in adult cystic fibrosis patients treated with elexacaftor/tezacaftor/ivacaftor.
Stastna N, Kunovsky L, Svoboda M, Pokojova E, Homola L, Mala M, Gracova Z, Jerabkova B, Skrickova J, Trna J.
Stastna N, et al. Among authors: jerabkova b.
Dig Dis. 2024 Apr 3. doi: 10.1159/000538606. Online ahead of print.
Dig Dis. 2024.
PMID: 38569478
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Impulsivity in patients with borderline personality disorder: a comprehensive profile compared with healthy people and patients with ADHD.
Linhartová P, Látalová A, Barteček R, Širůček J, Theiner P, Ejova A, Hlavatá P, Kóša B, Jeřábková B, Bareš M, Kašpárek T.
Linhartová P, et al. Among authors: jerabkova b.
Psychol Med. 2020 Aug;50(11):1829-1838. doi: 10.1017/S0033291719001892. Epub 2019 Aug 23.
Psychol Med. 2020.
PMID: 31439062
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Analysis of the COL7A1 gene in Czech patients with dystrophic epidermolysis bullosa reveals novel and recurrent mutations.
Jerábková B, Kopecková L, Bucková H, Veselý K, Valícková J, Fajkusová L.
Jerábková B, et al.
J Dermatol Sci. 2010 Aug;59(2):136-40. doi: 10.1016/j.jdermsci.2010.05.007. Epub 2010 Jun 8.
J Dermatol Sci. 2010.
PMID: 20598510
No abstract available.
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