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Plos One
|
July 1, 2021
High rate of HSV-1 reactivation in invasively ventilated COVID-19 patients: Immunological findings
Jessica Seeßle, Theresa Hippchen, Paul Schnitzler, et al.
BMC Infectious Diseases
|
October 21, 2016
Pseudobacteremia outbreak of biofilm-forming Achromobacter xylosoxidans - environmental transmission
Frank Günther, Uta Merle, Uwe Frank, et al.
Transplantation Proceedings
|
June 4, 2024
Exacerbation of Myopathy in Glycogen Debrancher Deficiency After Liver Transplantation: Case Report and Review of the Literature
Conrad Rauber, Jan Pfeiffenberger, Arianeb Mehrabi, et al.
Healthcare (Basel, Switzerland)
|
April 12, 2025
Patient Perspectives on the Care in a Long COVID Outpatient Clinic-A Regional Qualitative Analysis from Germany
Lea Alexandra Gölz, Regina Poß-Doering, Uta Merle, et al.
BMC Infectious Diseases
|
June 4, 2026
Clinical characteristics and outcomes of invasive fungal infections in critically ill patients with liver cirrhosis
Jessica Seeßle, Elena Pelivan, Marietta Kirchner, et al.
Nutrients
|
September 15, 2020
Vitamin D Deficiency and Outcome of COVID-19 Patients
Aleksandar Radujkovic, Theresa Hippchen, Shilpa Tiwari-Heckler, et al.
Medicine
|
February 3, 2018
Hemophagocytic lymphohistiocytosis in an adult kidney transplant recipient successfully treated by plasmapheresis: A case report and review of the literature
Christian Nusshag, Christian Morath, Martin Zeier, et al.
BMC Gastroenterology
|
January 20, 2010
Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease
Uta Merle, Karl Heinz Weiss, Christoph Eisenbach, et al.
BMC Gastroenterology
|
July 19, 2020
Plasma Lipidome, PNPLA3 polymorphism and hepatic steatosis in hereditary hemochromatosis
Jessica Seeßle, Hongying Gan-Schreier, Marietta Kirchner, et al.
World Journal of Gastroenterology
|
April 13, 2006
Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels
Karl Heinz Weiss, Uta Merle, Mark Schaefer, et al.
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Search research articles
Search
Showing results (31-40 of 188) with videos related to
Sort By:
Page
of 19
Plos One
|
July 1, 2021
High rate of HSV-1 reactivation in invasively ventilated COVID-19 patients: Immunological findings
Jessica Seeßle, Theresa Hippchen, Paul Schnitzler, et al.
BMC Infectious Diseases
|
October 21, 2016
Pseudobacteremia outbreak of biofilm-forming Achromobacter xylosoxidans - environmental transmission
Frank Günther, Uta Merle, Uwe Frank, et al.
Transplantation Proceedings
|
June 4, 2024
Exacerbation of Myopathy in Glycogen Debrancher Deficiency After Liver Transplantation: Case Report and Review of the Literature
Conrad Rauber, Jan Pfeiffenberger, Arianeb Mehrabi, et al.
Healthcare (Basel, Switzerland)
|
April 12, 2025
Patient Perspectives on the Care in a Long COVID Outpatient Clinic-A Regional Qualitative Analysis from Germany
Lea Alexandra Gölz, Regina Poß-Doering, Uta Merle, et al.
BMC Infectious Diseases
|
June 4, 2026
Clinical characteristics and outcomes of invasive fungal infections in critically ill patients with liver cirrhosis
Jessica Seeßle, Elena Pelivan, Marietta Kirchner, et al.
Nutrients
|
September 15, 2020
Vitamin D Deficiency and Outcome of COVID-19 Patients
Aleksandar Radujkovic, Theresa Hippchen, Shilpa Tiwari-Heckler, et al.
Medicine
|
February 3, 2018
Hemophagocytic lymphohistiocytosis in an adult kidney transplant recipient successfully treated by plasmapheresis: A case report and review of the literature
Christian Nusshag, Christian Morath, Martin Zeier, et al.
BMC Gastroenterology
|
January 20, 2010
Truncating mutations in the Wilson disease gene ATP7B are associated with very low serum ceruloplasmin oxidase activity and an early onset of Wilson disease
Uta Merle, Karl Heinz Weiss, Christoph Eisenbach, et al.
BMC Gastroenterology
|
July 19, 2020
Plasma Lipidome, PNPLA3 polymorphism and hepatic steatosis in hereditary hemochromatosis
Jessica Seeßle, Hongying Gan-Schreier, Marietta Kirchner, et al.
World Journal of Gastroenterology
|
April 13, 2006
Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels
Karl Heinz Weiss, Uta Merle, Mark Schaefer, et al.
Page
of 19