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Expression of the energy substrate transporters in uterine fibroids.
Knapp P, Chabowski A, Posmyk R, Górski J. Knapp P, et al. Among authors: posmyk r. Prostaglandins Other Lipid Mediat. 2016 Mar;123:9-15. doi: 10.1016/j.prostaglandins.2016.02.002. Epub 2016 Feb 27. Prostaglandins Other Lipid Mediat. 2016. PMID: 26932421
Wolf-Hirschhorn syndrome due to pure and translocation forms of monosomy 4p16.1 → pter.
Iwanowski PS, Panasiuk B, Van Buggenhout G, Murdolo M, Myśliwiec M, Maas NM, Lattante S, Korniszewski L, Posmyk R, Pilch J, Zajączek S, Fryns JP, Zollino M, Midro AT. Iwanowski PS, et al. Among authors: posmyk r. Am J Med Genet A. 2011 Aug;155A(8):1833-47. doi: 10.1002/ajmg.a.34005. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744486
Some Common SNPs of the T-Cell Homeostasis-Related Genes Are Associated with Multiple Sclerosis, but Not with the Clinical Manifestations of the Disease, in the Polish Population.
Chorąży M, Wawrusiewicz-Kurylonek N, Adamska-Patruno E, Zajkowska O, Kapica-Topczewska K, Posmyk R, Krętowski AJ, Kochanowicz J, Kułakowska A. Chorąży M, et al. Among authors: posmyk r. J Immunol Res. 2020 Nov 11;2020:8838014. doi: 10.1155/2020/8838014. eCollection 2020. J Immunol Res. 2020. PMID: 33224992 Free PMC article.
The natural history of Möbius syndrome in a 32-year-old man.
Chorąży M, Leśniewicz R, Posmyk R, Halicka D, Zalewska A, Wincewicz-Pietrzykowska A, Chorąży K, Drozdowski W. Chorąży M, et al. Among authors: posmyk r. Neurol Neurochir Pol. 2011 Jan-Feb;45(1):74-9. doi: 10.1016/s0028-3843(14)60063-3. Neurol Neurochir Pol. 2011. PMID: 21384297
The FOXP3 rs3761547 Gene Polymorphism in Multiple Sclerosis as a Male-Specific Risk Factor.
Wawrusiewicz-Kurylonek N, Chorąży M, Posmyk R, Zajkowska O, Zajkowska A, Krętowski AJ, Tarasiuk J, Kochanowicz J, Kułakowska A. Wawrusiewicz-Kurylonek N, et al. Among authors: posmyk r. Neuromolecular Med. 2018 Dec;20(4):537-543. doi: 10.1007/s12017-018-8512-z. Epub 2018 Sep 18. Neuromolecular Med. 2018. PMID: 30229436 Free PMC article.
Phenotype and genotype in 103 patients with tricho-rhino-phalangeal syndrome.
Maas SM, Shaw AC, Bikker H, Lüdecke HJ, van der Tuin K, Badura-Stronka M, Belligni E, Biamino E, Bonati MT, Carvalho DR, Cobben J, de Man SA, Den Hollander NS, Di Donato N, Garavelli L, Grønborg S, Herkert JC, Hoogeboom AJ, Jamsheer A, Latos-Bielenska A, Maat-Kievit A, Magnani C, Marcelis C, Mathijssen IB, Nielsen M, Otten E, Ousager LB, Pilch J, Plomp A, Poke G, Poluha A, Posmyk R, Rieubland C, Silengo M, Simon M, Steichen E, Stumpel C, Szakszon K, Polonkai E, van den Ende J, van der Steen A, van Essen T, van Haeringen A, van Hagen JM, Verheij JB, Mannens MM, Hennekam RC. Maas SM, et al. Among authors: posmyk r. Eur J Med Genet. 2015 May;58(5):279-92. doi: 10.1016/j.ejmg.2015.03.002. Epub 2015 Mar 16. Eur J Med Genet. 2015. PMID: 25792522
35 results