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Page 1
Clinical characteristics of Polish patients with molecularly confirmed Mowat-Wilson syndrome.
J Appl Genet. 2021 Sep;62(3):477-485. doi: 10.1007/s13353-021-00636-1. Epub 2021 May 12.
J Appl Genet. 2021.
PMID: 33982229
Free PMC article.
Prenatal Diagnosis by Array Comparative Genomic Hybridization in Fetuses with Cardiac Abnormalities.
Kowalczyk K, Bartnik-Głaska M, Smyk M, Plaskota I, Bernaciak J, Kędzior M, Wiśniowiecka-Kowalnik B, Jakubów-Durska K, Braun-Walicka N, Barczyk A, Geremek M, Castañeda J, Kutkowska-Kaźmierczak A, Własienko P, Dębska M, Kucińska-Chahwan A, Roszkowski T, Kozłowski S, Mikulska B, Issat T, Obersztyn E, Nowakowska BA.
Kowalczyk K, et al. Among authors: braun walicka n.
Genes (Basel). 2021 Dec 19;12(12):2021. doi: 10.3390/genes12122021.
Genes (Basel). 2021.
PMID: 34946970
Free PMC article.
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Comparative Genomic Hybridization to Microarrays in Fetuses with High-Risk Prenatal Indications: Polish Experience with 7400 Pregnancies.
Kowalczyk K, Bartnik-Głaska M, Smyk M, Plaskota I, Bernaciak J, Kędzior M, Wiśniowiecka-Kowalnik B, Deperas M, Domaradzka J, Łuszczek A, Dutkiewicz D, Kozar A, Grad D, Niemiec M, Ziemkiewicz K, Magdziak R, Braun-Walicka N, Barczyk A, Geremek M, Castañeda J, Kutkowska-Kaźmierczak A, Własienko P, Jakubów-Durska K, Dębska M, Kucińska-Chahwan A, Kozłowski S, Mikulska B, Issat T, Roszkowski T, Nawara-Baran A, Runge A, Jakubiuk-Tomaszuk A, Kruczek A, Kostyk E, Pietras G, Limon J, Zwoliński J, Ochman K, Szajner T, Węgrzyn P, Wielgoś M, Sąsiadek M, Obersztyn E, Nowakowska BA.
Kowalczyk K, et al. Among authors: braun walicka n.
Genes (Basel). 2022 Apr 14;13(4):690. doi: 10.3390/genes13040690.
Genes (Basel). 2022.
PMID: 35456496
Free PMC article.
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Research on the Pathogenesis of Cognitive and Neurofunctional Impairments in Patients with Noonan Syndrome: The Role of Rat Sarcoma-Mitogen Activated Protein Kinase Signaling Pathway Gene Disturbances.
Braun-Walicka N, Pluta A, Wolak T, Maj E, Maryniak A, Gos M, Abramowicz A, Landowska A, Obersztyn E, Bal J.
Braun-Walicka N, et al.
Genes (Basel). 2023 Dec 3;14(12):2173. doi: 10.3390/genes14122173.
Genes (Basel). 2023.
PMID: 38136995
Free PMC article.
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Spinal muscular atrophy with an overlapping syndrome - "double trouble" or a potentially better outcome?
Frączek A, Potulska-Chromik A, Bednarska-Makaruk M, Sułek A, Obersztyn E, Braun-Walicka N, Ryniewicz B, Kostera-Pruszczyk A.
Frączek A, et al. Among authors: braun walicka n.
Neurol Neurochir Pol. 2020;54(5):475-477. doi: 10.5603/PJNNS.a2020.0060. Epub 2020 Aug 5.
Neurol Neurochir Pol. 2020.
PMID: 32757203
Free article.
No abstract available.
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