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Page 1
Exome Sequencing Reveals Novel Variants and Expands the Genetic Landscape for Congenital Microcephaly.
Genes (Basel). 2021 Dec 18;12(12):2014. doi: 10.3390/genes12122014.
Genes (Basel). 2021.
PMID: 34946966
Free PMC article.
Glucose transporter type 1 deficiency due to SLC2A1 gene mutations--a rare but treatable cause of metabolic epilepsy and extrapyramidal movement disorder; own experience and literature review.
Szczepanik E, Terczyńska I, Kruk M, Lipiec A, Dudko E, Tryfon J, Jurek M, Hoffman-Zacharska D.
Szczepanik E, et al. Among authors: lipiec a.
Dev Period Med. 2015 Oct-Dec;19(4):454-63.
Dev Period Med. 2015.
PMID: 26982753
Review.
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Genetic Risk Factors for Neurological Disorders in Children with Adverse Events Following Immunization: A Descriptive Study of a Polish Case Series.
Charzewska A, Terczyńska I, Lipiec A, Mazurczak T, Górka-Skoczylas P, Szlendak R, Kanabus K, Tataj R, Dawidziuk M, Wojtaś B, Gielniewski B, Bal J, Stawicka E, Hoffman-Zacharska D.
Charzewska A, et al. Among authors: lipiec a.
Int J Mol Sci. 2023 Jan 6;24(2):1117. doi: 10.3390/ijms24021117.
Int J Mol Sci. 2023.
PMID: 36674629
Free PMC article.
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Functional Characteristics of the Nav1.1 p.Arg1596Cys Mutation Associated with Varying Severity of Epilepsy Phenotypes.
Witkowski G, Szulczyk B, Nurowska E, Jurek M, Pasierski M, Lipiec A, Charzewska A, Dawidziuk M, Milewski M, Owsiak S, Rola R, Sienkiewicz Jarosz H, Hoffman-Zacharska D.
Witkowski G, et al. Among authors: lipiec a.
Int J Mol Sci. 2024 Feb 1;25(3):1745. doi: 10.3390/ijms25031745.
Int J Mol Sci. 2024.
PMID: 38339022
Free PMC article.
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[Cat scratch disease--course, diagnosis].
Sala E, Lipiec A, Zygmunt A, Burdzel Z, Ogórek M, Chyla M.
Sala E, et al. Among authors: lipiec a.
Przegl Epidemiol. 2006;60(2):307-13.
Przegl Epidemiol. 2006.
PMID: 16964683
Polish.
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