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Journal of Gastrointestinal and Liver Diseases : JGLD|September 22, 2021
Differentiating Primary Sclerosing Cholangitis from Similar Diseases of Autoimmune OriginLumir Kunovsky, Petr Dite, Lubomira Hornakova, et al.Journal of Clinical Medicine|December 24, 2021
Autoimmune Diseases of Digestive Organs-A Multidisciplinary Challenge: A Focus on Hepatopancreatobiliary ManifestationLumir Kunovsky, Petr Dite, Petr Jabandziev, et al.Molecular Genetics & Genomic Medicine|January 25, 2023
Two sisters with cardiac-urogenital syndrome secondary to pathogenic splicing variant in the MYRF gene with unaffected parents: A case of gonadal mosaicism?Katerina Slaba, Marta Jezova, Petra Pokorna, et al.World Journal of Gastrointestinal Oncology|August 30, 2021
<i>Helicobacter pylori</i> infection and other bacteria in pancreatic cancer and autoimmune pancreatitisLumir Kunovsky, Petr Dite, Petr Jabandziev, et al.Diagnostic Pathology|July 15, 2019
Triple malignancy (NET, GIST and pheochromocytoma) as a first manifestation of neurofibromatosis type-1 in an adult patientKarolina Poredska, Lumir Kunovsky, Vladimir Prochazka, et al.Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|May 20, 2021
Novel mutations in TRPM6 gene associated with primary hypomagnesemia with secondary hypocalcemia. Case reportJan Papez, Jiri Starha, Katerina Slaba, et al.Clinical Case Reports|April 8, 2026
Aicardi-Goutières Syndrome Type 6: Case Report and Structural Prediction Supporting a Dominant-Negative Effect of the <i>ADAR1</i> c.<i>3019G</i>>A VariantKaterina Turan, Petra Pokorna, Kamila Rihova, et al.Frontiers in Genetics|November 2, 2020
Novel Splicing Variant in the <i>PMM2</i> Gene in a Patient With PMM2-CDG Syndrome Presenting With Pericardial Effusion: A Case ReportKaterina Slaba, Hana Noskova, Petra Vesela, et al.Inflammatory Bowel Diseases|August 27, 2025
Tissue MicroRNA Expression Signatures as Diagnostic Biomarkers and Predictors of Residual Disease Activity and Relapse in Treatment-Naïve Pediatric Inflammatory Bowel DiseaseTereza Deissova, Dagmar Al Tukmachi, Lenka Radova, et al.Frontiers in Genetics|October 28, 2020
A Newly Observed Mutation of the <i>ABCA3</i> Gene Causing Lethal Respiratory Failure of a Full-Term Newborn: A Case ReportMartin Jouza, Tomas Jimramovsky, Eva Sloukova, et al.Pageof 4