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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2002 1
2003 2
2004 3
2006 2
2007 1
2008 1
2010 1
2011 4
2012 5
2013 3
2015 1
2016 4
2017 1
2018 1
2019 2
2021 3
2022 3
2024 1

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34 results

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Page 1
The COL7A1 mutation database.
Wertheim-Tysarowska K, Sobczyńska-Tomaszewska A, Kowalewski C, Skroński M, Swięćkowski G, Kutkowska-Kaźmierczak A, Woźniak K, Bal J. Wertheim-Tysarowska K, et al. Among authors: sobczynska tomaszewska a. Hum Mutat. 2012 Feb;33(2):327-31. doi: 10.1002/humu.21651. Epub 2011 Dec 20. Hum Mutat. 2012. PMID: 22058051
Familial pneumothoraces: Birt-Hogg-Dubé syndrome.
Radzikowska E, Barańska I, Sobczyńska-Tomaszewska A, Wiatr E, Roszkowski-Śliż K. Radzikowska E, et al. Among authors: sobczynska tomaszewska a. Pol Arch Med Wewn. 2016 Nov 10;126(11):897-898. doi: 10.20452/pamw.3646. Epub 2016 Nov 10. Pol Arch Med Wewn. 2016. PMID: 27906882 Free article. No abstract available.
Gitelman syndrome with normocalciuria - a case report.
Flisiński M, Skalska E, Mączyńska B, Butt-Hussaim N, Sobczyńska-Tomaszewska A, Haus O, Manitius J. Flisiński M, et al. Among authors: sobczynska tomaszewska a. BMC Nephrol. 2022 May 4;23(1):170. doi: 10.1186/s12882-022-02782-y. BMC Nephrol. 2022. PMID: 35509038 Free PMC article.
[Hereditary aspects of pancreatitis].
Bak D, Sobczyńska-Tomaszewska A, Bal J. Bak D, et al. Among authors: sobczynska tomaszewska a. Med Wieku Rozwoj. 2003 Jan-Mar;7(1):57-66. Med Wieku Rozwoj. 2003. PMID: 13130170 Review. Polish.
Immune system disturbances in Clouston syndrome.
Pietrzak A, Grywalska E, Gerkowicz A, Krasowska D, Chodorowska G, Michalska-Jakubus M, Roliński J, Wawrzycki B, Radej S, Dybiec E, Wroński J, Sobczyńska-Tomaszewska A, Rudzki M, Hadj-Rabia S. Pietrzak A, et al. Among authors: sobczynska tomaszewska a. Int J Dermatol. 2016 May;55(5):e241-9. doi: 10.1111/ijd.13152. Epub 2015 Nov 9. Int J Dermatol. 2016. PMID: 26551294
Molecular Background and Disease Prevalence of Biotinidase Deficiency in a Polish Population-Data Based on the National Newborn Screening Programme.
Jezela-Stanek A, Suchoń L, Sobczyńska-Tomaszewska A, Czerska K, Kuśmierska K, Taybert J, Ołtarzewski M, Sykut-Cegielska J. Jezela-Stanek A, et al. Among authors: sobczynska tomaszewska a. Genes (Basel). 2022 Apr 29;13(5):802. doi: 10.3390/genes13050802. Genes (Basel). 2022. PMID: 35627187 Free PMC article.
A new family with spastic paraplegia type 51 and novel mutations in AP4E1.
Winkler I, Miotła P, Lejman M, Pietrzyk A, Kacprzak M, Kubiak M, Sobczyńska-Tomaszewska A, Skrzypczak M, Jaszczuk I. Winkler I, et al. Among authors: sobczynska tomaszewska a. BMC Med Genomics. 2021 May 18;14(1):131. doi: 10.1186/s12920-021-00980-5. BMC Med Genomics. 2021. PMID: 34006278 Free PMC article.
34 results