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Page 1
A novel p.Ser282Pro CPA1 variant is associated with autosomal dominant hereditary pancreatitis.
Gut. 2017 Sep;66(9):1728-1730. doi: 10.1136/gutjnl-2017-313816. Epub 2017 Mar 3.
Gut. 2017.
PMID: 28258133
Free PMC article.
No abstract available.
Novel Pathogenic PRSS1 Variant p.Glu190Lys in a Case of Chronic Pancreatitis.
Jancsó Z, Oracz G, Kujko AA, Kolodziejczyk E, Radisky ES, Rygiel AM, Sahin-Tóth M.
Jancsó Z, et al. Among authors: kujko aa.
Front Genet. 2019 Feb 6;10:46. doi: 10.3389/fgene.2019.00046. eCollection 2019.
Front Genet. 2019.
PMID: 30792736
Free PMC article.
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The hybrid allele 1 of carboxyl-ester lipase (CEL-HYB1) in Polish pediatric patients with chronic pancreatitis.
Oracz G, Kujko AA, Fjeld K, Wertheim-Tysarowska K, Adamus-Białek W, Steine SJ, Koziel D, Gluszek S, Molven A, Rygiel AM.
Oracz G, et al. Among authors: kujko aa.
Pancreatology. 2019 Jun;19(4):531-534. doi: 10.1016/j.pan.2019.04.006. Epub 2019 Apr 26.
Pancreatology. 2019.
PMID: 31036489
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Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.
Niepokój K, Rygiel AM, Jurczak P, Kujko AA, Śniegórska D, Sawicka J, Grabarczyk A, Bal J, Wertheim-Tysarowska K.
Niepokój K, et al. Among authors: kujko aa.
J Appl Genet. 2018 Feb;59(1):67-72. doi: 10.1007/s13353-017-0416-3. Epub 2017 Nov 18.
J Appl Genet. 2018.
PMID: 29151245
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Chymotrypsinogen C Genetic Variants, Including c.180TT, Are Strongly Associated With Chronic Pancreatitis in Pediatric Patients.
Grabarczyk AM, Oracz G, Wertheim-Tysarowska K, Kujko AA, Wejnarska K, Kolodziejczyk E, Bal J, Koziel D, Kowalik A, Gluszek S, Rygiel AM.
Grabarczyk AM, et al. Among authors: kujko aa.
J Pediatr Gastroenterol Nutr. 2017 Dec;65(6):652-657. doi: 10.1097/MPG.0000000000001767.
J Pediatr Gastroenterol Nutr. 2017.
PMID: 28968289
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