I. Rtskhiladze

Assessment of treatment options for patients with hepatitis C virus recombinant form 2k/1b

M. Weizenegger, J. Bartel, R. Gish, 2020, Hepatology research : the official journal of the Japan Society of Hepatology.

A questionnaire survey of radiological diagnosis and management of renal dysplasia in children

V. Tasic, A. Woolf, M. Zaniew, 2017, Journal of Nephrology.

Agammaglobulinemia with normal B-cell numbers in a patient lacking Bob1.

S. Ehl, Manuela Pendziwiat, I. Helbig, 2021, The Journal of allergy and clinical immunology.

Intrahepatic Cholestasis Is a Clinically Significant Feature Associated with Natural History of X-Linked Myotubular Myopathy (XLMTM): A Case Series and Biopsy Report

B. Kamath, M. Lawlor, R. Graham, 2021, Journal of neuromuscular diseases.

Clinical, neuroradiological, and molecular characterization of patients with atypical Zellweger spectrum disorder caused by PEX16 mutations: a case series

S. Lévesque, N. Braverman, G. Bernard, 2022, neurogenetics.

Identification of hepatitis C virus 2k/1b intergenotypic recombinants in Georgia

M. Weizenegger, J. Bartel, H. Mo, 2018, Liver international : official journal of the International Association for the Study of the Liver.

The histidine-loop is essential for transport activity of human MDR3. A novel mutation of MDR3 in a patient with progressive familial intrahepatic cholestasis type 3.

D. Häussinger, G. Engelmann, C. Flechtenmacher, 2012, Gene.

The histidine-loop is essential for transport activity of human MDR3. A novel mutation of MDR3 in a patient with progressive familial intrahepatic cholestasis type 3.

D. Häussinger, G. Engelmann, C. Flechtenmacher, 2012, Gene.