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Genetic and Environmental Risk Factors for Isolated Hemangiomas in Infants.
Materna-Kiryluk A, Wiśniewska K, Więckowska B, Wróblewska-Seniuk K, Jaroszewska-Świątek B, Helwich E, Latos-Bieleńska A. Materna-Kiryluk A, et al. Among authors: latos bielenska a. Children (Basel). 2020 Sep 25;7(10):E150. doi: 10.3390/children7100150. Children (Basel). 2020. PMID: 32992757 Free article.
Prenatal genetic diagnosis of cranioectodermal dysplasia in a Polish family with compound heterozygous variants in WDR35.
Walczak-Sztulpa J, Wawrocka A, Leszczynska B, Mikulska B, Arts HH, Bukowska-Olech E, Daniel M, Krawczynski MR, Latos-Bielenska A, Obersztyn E. Walczak-Sztulpa J, et al. Among authors: latos bielenska a. Am J Med Genet A. 2020 Oct;182(10):2417-2425. doi: 10.1002/ajmg.a.61785. Epub 2020 Aug 17. Am J Med Genet A. 2020. PMID: 32804427
Hi-C Identifies Complex Genomic Rearrangements and TAD-Shuffling in Developmental Diseases.
Melo US, Schöpflin R, Acuna-Hidalgo R, Mensah MA, Fischer-Zirnsak B, Holtgrewe M, Klever MK, Türkmen S, Heinrich V, Pluym ID, Matoso E, Bernardo de Sousa S, Louro P, Hülsemann W, Cohen M, Dufke A, Latos-Bieleńska A, Vingron M, Kalscheuer V, Quintero-Rivera F, Spielmann M, Mundlos S. Melo US, et al. Among authors: latos bielenska a. Am J Hum Genet. 2020 Jun 4;106(6):872-884. doi: 10.1016/j.ajhg.2020.04.016. Epub 2020 May 28. Am J Hum Genet. 2020. PMID: 32470376
Maternal risk factors for the VACTERL association: A EUROCAT case-control study.
van de Putte R, van Rooij IALM, Haanappel CP, Marcelis CLM, Brunner HG, Addor MC, Cavero-Carbonell C, Dias CM, Draper ES, Etxebarriarteun L, Gatt M, Khoshnood B, Kinsner-Ovaskainen A, Klungsoyr K, Kurinczuk JJ, Latos-Bielenska A, Luyt K, O'Mahony MT, Miller N, Mullaney C, Nelen V, Neville AJ, Perthus I, Pierini A, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiesel A, Zymak-Zakutnia N, Loane M, Barisic I, de Walle HEK, Bergman JEH, Roeleveld N. van de Putte R, et al. Among authors: latos bielenska a. Birth Defects Res. 2020 May 15;112(9):688-698. doi: 10.1002/bdr2.1686. Epub 2020 Apr 22. Birth Defects Res. 2020. PMID: 32319733 Free PMC article.
Compound heterozygous IFT140 variants in two Polish families with Sensenbrenner syndrome and early onset end-stage renal disease.
Walczak-Sztulpa J, Posmyk R, Bukowska-Olech EM, Wawrocka A, Jamsheer A, Oud MM, Schmidts M, Arts HH, Latos-Bielenska A, Wasilewska A. Walczak-Sztulpa J, et al. Among authors: latos bielenska a. Orphanet J Rare Dis. 2020 Feb 1;15(1):36. doi: 10.1186/s13023-020-1303-2. Orphanet J Rare Dis. 2020. PMID: 32007091 Free PMC article.
Exploring Research Priorities of Parents Who Have Children With Down Syndrome, Cleft Lip With or Without Cleft Palate, Congenital Heart Defects, or Spina Bifida Using ConnectEpeople: A Social Media Coproduction Research Study.
Sinclair M, McCullough JE, Elliott D, Latos-Bielenska A, Braz P, Cavero-Carbonell C, Jamry-Dziurla A, João Santos A, Páramo-Rodríguez L. Sinclair M, et al. Among authors: latos bielenska a. J Med Internet Res. 2019 Nov 25;21(11):e15847. doi: 10.2196/15847. J Med Internet Res. 2019. PMID: 31763986 Free PMC article.
Clinical and ultrastructural findings in an ataxic variant of Kufor-Rakeb syndrome.
Pietrzak A, Badura-Stronka M, Kangas-Kontio T, Felczak P, Kozubski W, Latos-Bielenska A, Wierzba-Bobrowicz T, Florczak-Wyspianska J. Pietrzak A, et al. Among authors: latos bielenska a. Folia Neuropathol. 2019;57(3):285-294. doi: 10.5114/fn.2019.88459. Folia Neuropathol. 2019. PMID: 31588715 Free article.
Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study.
van de Putte R, van Rooij IALM, Marcelis CLM, Guo M, Brunner HG, Addor MC, Cavero-Carbonell C, Dias CM, Draper ES, Etxebarriarteun L, Gatt M, Haeusler M, Khoshnood B, Klungsoyr K, Kurinczuk JJ, Lanzoni M, Latos-Bielenska A, Luyt K, O'Mahony MT, Miller N, Mullaney C, Nelen V, Neville AJ, Perthus I, Pierini A, Randrianaivo H, Rankin J, Rissmann A, Rouget F, Schaub B, Tucker D, Wellesley D, Wiesel A, Zymak-Zakutnia N, Loane M, Barisic I, de Walle HEK, Roeleveld N, Bergman JEH. van de Putte R, et al. Among authors: latos bielenska a. Pediatr Res. 2020 Feb;87(3):541-549. doi: 10.1038/s41390-019-0561-y. Epub 2019 Sep 9. Pediatr Res. 2020. PMID: 31499513
Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia.
Hordyjewska-Kowalczyk E, Sowińska-Seidler A, Olech EM, Socha M, Glazar R, Kruczek A, Latos-Bieleńska A, Tylzanowski P, Jamsheer A. Hordyjewska-Kowalczyk E, et al. Among authors: latos bielenska a. Clin Genet. 2019 Nov;96(5):429-438. doi: 10.1111/cge.13610. Epub 2019 Jul 31. Clin Genet. 2019. PMID: 31347140
Phenotypic description of two adult brothers presenting with mild form of Smith-Lemli-Opitz syndrome.
Olech EM, Matuszewska K, Piechota M, Latos-Bieleńska A, Jamsheer A. Olech EM, et al. Among authors: latos bielenska a. Clin Dysmorphol. 2019 Jul;28(3):154-156. doi: 10.1097/MCD.0000000000000276. Clin Dysmorphol. 2019. PMID: 30925529 No abstract available.
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