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Year Number of Results
2006 1
2007 3
2009 2
2010 2
2011 1
2012 4
2013 2
2014 3
2015 5
2016 4
2017 2
2018 3
2019 9
2020 15
2021 20
2022 15
2023 10
2024 3

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Page 1
Editorial.
Jezela-Stanek A. Jezela-Stanek A. J Mother Child. 2022 Sep 2;25(4):243. doi: 10.34763/jmotherandchild.20212504.edit.2021_25_04. eCollection 2021 Dec 1. J Mother Child. 2022. PMID: 36047172 Free PMC article. No abstract available.
Editorial.
Jezela-Stanek A. Jezela-Stanek A. J Mother Child. 2021 Oct 11;25(1):1. doi: 10.34763/jmotherandchild.20212501.edit.2021_25_01. J Mother Child. 2021. PMID: 34643349 Free PMC article. No abstract available.
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP.
Van Dijck A, Vulto-van Silfhout AT, Cappuyns E, van der Werf IM, Mancini GM, Tzschach A, Bernier R, Gozes I, Eichler EE, Romano C, Lindstrand A, Nordgren A; ADNP Consortium; Kvarnung M, Kleefstra T, de Vries BBA, Küry S, Rosenfeld JA, Meuwissen ME, Vandeweyer G, Kooy RF. Van Dijck A, et al. Biol Psychiatry. 2019 Feb 15;85(4):287-297. doi: 10.1016/j.biopsych.2018.02.1173. Epub 2018 Mar 15. Biol Psychiatry. 2019. PMID: 29724491 Free PMC article.
Editorial: Inherited Protein Glycosylation Defects in Humans.
Jezela-Stanek A, Stepien KM, Tylki-Szymanska A. Jezela-Stanek A, et al. Front Genet. 2022 Mar 14;13:851438. doi: 10.3389/fgene.2022.851438. eCollection 2022. Front Genet. 2022. PMID: 35368693 Free PMC article. No abstract available.
Interstitial Lung Disease in Rare Congenital Syndromes.
Jezela-Stanek A. Jezela-Stanek A. J Mother Child. 2020 Jul 29;24(1):47-52. doi: 10.34763/jmotherandchild.2020241.1931.000004. J Mother Child. 2020. PMID: 33074183 Free PMC article. Review.
PIGN encephalopathy: Characterizing the epileptology.
Bayat A, de Valles-Ibáñez G, Pendziwiat M, Knaus A, Alt K, Biamino E, Bley A, Calvert S, Carney P, Caro-Llopis A, Ceulemans B, Cousin J, Davis S, des Portes V, Edery P, England E, Ferreira C, Freeman J, Gener B, Gorce M, Heron D, Hildebrand MS, Jezela-Stanek A, Jouk PS, Keren B, Kloth K, Kluger G, Kuhn M, Lemke JR, Li H, Martinez F, Maxton C, Mefford HC, Merla G, Mierzewska H, Muir A, Monfort S, Nicolai J, Norman J, O'Grady G, Oleksy B, Orellana C, Orec LE, Peinhardt C, Pronicka E, Rosello M, Santos-Simarro F, Schwaibold EMC, Stegmann APA, Stumpel CT, Szczepanik E, Terczyńska I, Thevenon J, Tzschach A, Van Bogaert P, Vittorini R, Walsh S, Weckhuysen S, Weissman B, Wolfe L, Reymond A, De Nittis P, Poduri A, Olson H, Striano P, Lesca G, Scheffer IE, Møller RS, Sadleir LG. Bayat A, et al. Among authors: jezela stanek a. Epilepsia. 2022 Apr;63(4):974-991. doi: 10.1111/epi.17173. Epub 2022 Feb 18. Epilepsia. 2022. PMID: 35179230
Expanding the Knowledge of KIF1A-Dependent Disorders to a Group of Polish Patients.
Paprocka J, Jezela-Stanek A, Śmigiel R, Walczak A, Mierzewska H, Kutkowska-Kaźmierczak A, Płoski R, Emich-Widera E, Steinborn B. Paprocka J, et al. Among authors: jezela stanek a. Genes (Basel). 2023 Apr 25;14(5):972. doi: 10.3390/genes14050972. Genes (Basel). 2023. PMID: 37239332 Free PMC article.
Genetic causes of syndromic craniosynostoses.
Jezela-Stanek A, Krajewska-Walasek M. Jezela-Stanek A, et al. Eur J Paediatr Neurol. 2013 May;17(3):221-4. doi: 10.1016/j.ejpn.2012.09.009. Epub 2012 Oct 11. Eur J Paediatr Neurol. 2013. PMID: 23062756 Review.
90 results