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Journal of Hepatology|July 19, 2017
A heterozygous mutation in GOT1 is associated with familial macro-aspartate aminotransferaseMaria Kulecka, Aldona Wierzbicka, Agnieszka Paziewska, et al.
Biomedicines|February 25, 2023
A Century of Progress on Wilson Disease and the Enduring Challenges of Genetics, Diagnosis, and TreatmentLouis C Penning, Marina Berenguer, Anna Czlonkowska, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|May 11, 2010
Polymorphisms in the factor VII gene and ischemic stroke in young adultsStanislaw Lopaciuk, Jerzy Windyga, Cezary W Watala, et al.
International Journal of Molecular Sciences|December 14, 2017
Population-Specific Associations of Deleterious Rare Variants in Coding Region of P2RY1-P2RY12 Purinergic Receptor Genes in Large-Vessel Ischemic Stroke PatientsPiotr K Janicki, Ceren Eyileten, Victor Ruiz-Velasco, et al.
Stroke|March 20, 2012
Factors influencing in-hospital delay in treatment with intravenous thrombolysisRobert Mikulík, Pavla Kadlecová, Anna Czlonkowska, et al.
Liver International : Official Journal of the International Association for the Study of the Liver|September 20, 2018
Whole-exome sequencing identifies novel pathogenic variants across the ATP7B gene and some modifiers of Wilson's disease phenotypeAnna Kluska, Maria Kulecka, Tomasz Litwin, et al.
Hepatology (Baltimore, Md.)|July 28, 2021
Designing Clinical Trials in Wilson's DiseasePeter Ott, Aftab Ala, Frederick K Askari, et al.
International Journal of Molecular Sciences|May 14, 2022
Diagnostic Performance of Circulating miRNAs and Extracellular Vesicles in Acute Ischemic StrokeCeren Eyileten, Daniel Jakubik, Andleeb Shahzadi, et al.
Stroke|July 10, 2020
High-Sensitivity Cardiac Troponin T for Risk Stratification in Patients With Embolic Stroke of Undetermined SourceJan F Scheitz, Guillaume Pare, Lesly A Pearce, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2007
Evaluation of the Unified Wilson's Disease Rating Scale (UWDRS) in German patients with treated Wilson's diseaseBarbara Leinweber, J Carsten Möller, Andre Scherag, et al.
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