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Page 1
Epigenetic Findings in Twins with Esophageal Atresia.
Genes (Basel). 2023 Sep 20;14(9):1822. doi: 10.3390/genes14091822.
Genes (Basel). 2023.
PMID: 37761962
Free PMC article.
The Impact of Congenital Esophageal Atresia on the Family Functioning.
Rozensztrauch A, Śmigiel R, Błoch M, Patkowski D.
Rozensztrauch A, et al. Among authors: bloch m.
J Pediatr Nurs. 2020 Jan-Feb;50:e85-e90. doi: 10.1016/j.pedn.2019.04.009. Epub 2019 Apr 23.
J Pediatr Nurs. 2020.
PMID: 31027866
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Rapid Whole-Exome Sequencing as a Diagnostic Tool in a Neonatal/Pediatric Intensive Care Unit.
Śmigiel R, Biela M, Szmyd K, Błoch M, Szmida E, Skiba P, Walczak A, Gasperowicz P, Kosińska J, Rydzanicz M, Stawiński P, Biernacka A, Zielińska M, Gołębiowski W, Jalowska A, Ohia G, Głowska B, Walas W, Królak-Olejnik B, Krajewski P, Sykut-Cegielska J, Sąsiadek MM, Płoski R.
Śmigiel R, et al. Among authors: bloch m.
J Clin Med. 2020 Jul 13;9(7):2220. doi: 10.3390/jcm9072220.
J Clin Med. 2020.
PMID: 32668698
Free PMC article.
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Further evidence for GRIN2B mutation as the cause of severe epileptic encephalopathy.
Smigiel R, Kostrzewa G, Kosinska J, Pollak A, Stawinski P, Szmida E, Bloch M, Szymanska K, Karpinski P, Sasiadek MM, Ploski R.
Smigiel R, et al. Among authors: bloch m.
Am J Med Genet A. 2016 Dec;170(12):3265-3270. doi: 10.1002/ajmg.a.37887. Epub 2016 Sep 8.
Am J Med Genet A. 2016.
PMID: 27605359
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Occurrence of Esophageal Atresia With Tracheoesophageal Fistula in Siblings From Three-Generation Family Affected by Variable Expressivity MYCN Mutation: A Case Report.
Klaniewska M, Toczewski K, Rozensztrauch A, Bloch M, Dzielendziak A, Gasperowicz P, Slezak R, Ploski R, Rydzanicz M, Smigiel R, Patkowski D.
Klaniewska M, et al. Among authors: bloch m.
Front Pediatr. 2021 Dec 2;9:783553. doi: 10.3389/fped.2021.783553. eCollection 2021.
Front Pediatr. 2021.
PMID: 34926353
Free PMC article.
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Metatropic dysplasia in four-year-old boy--physiotherapy and orthopaedic care problems--case report.
Kleszczyński J, Błoch M, Hofbauer K, Dominiak P.
Kleszczyński J, et al. Among authors: bloch m.
Ortop Traumatol Rehabil. 2012 May-Jun;14(3):289-302. doi: 10.5604/15093492.1002258.
Ortop Traumatol Rehabil. 2012.
PMID: 22764341
English, Polish.
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Phenotype analysis of Polish patients with mandibulofacial dysostosis type Guion-Almeida associated with esophageal atresia and choanal atresia caused by EFTUD2 gene mutations.
Smigiel R, Bezniakow N, Jakubiak A, Błoch M, Patkowski D, Obersztyn E, Sasiadek MM.
Smigiel R, et al. Among authors: bloch m.
J Appl Genet. 2015 May;56(2):199-204. doi: 10.1007/s13353-014-0255-4. Epub 2014 Nov 12.
J Appl Genet. 2015.
PMID: 25387991
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