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Seminars in Liver Disease
|
May 4, 2011
Genetic modifiers of liver injury in hereditary liver disease
Aftab Ala, Michael Schilsky
Seminars in Liver Disease
|
September 9, 2011
Wilson disease: pathogenesis and clinical considerations in diagnosis and treatment
Richard Rosencrantz, Michael Schilsky
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
September 25, 2002
Autonomic cardiovascular reflexes in Wilson's disease
Kirsty Bhattacharya, Miodrag Velickovic, Michael Schilsky, et al.
Hepatology (Baltimore, Md.)
|
February 22, 2005
Wilson disease in septuagenarian siblings: Raising the bar for diagnosis
Aftab Ala, Jimo Borjigin, Arnold Rochwarger, et al.
Journal of Clinical Gastroenterology
|
June 11, 2010
A clinical assessment of Wilson disease in patients with concurrent liver disease
Robert J Wong, Robert Gish, Michael Schilsky, et al.
Pediatric Gastroenterology, Hepatology & Nutrition
|
July 21, 2016
The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria
Soofia Khan, Michael Schilsky, Gary Silber, et al.
Clinical Medicine (London, England)
|
June 15, 2022
Defining and characterising a toolkit for the development of a successful European registry for rare liver diseases: a model for building a rare disease registry
Marinos Pericleous, Claire Kelly, Michael Schilsky, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
March 26, 2013
Pre-liver transplant protocols in dentistry
Reza Radmand, Michael Schilsky, Simona Jakab, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 27, 2007
Wilson disease in children: serum aminotransferases and urinary copper on triethylene tetramine dihydrochloride (trientine) treatment
Ronen Arnon, Judith Flores Calderon, Michael Schilsky, et al.
Analytica Chimica Acta
|
January 18, 2020
Biomedical copper speciation in relation to Wilson's disease using strong anion exchange chromatography coupled to triple quadrupole inductively coupled plasma mass spectrometry
Nikolay Solovyev, Aftab Ala, Michael Schilsky, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Seminars in Liver Disease
|
May 4, 2011
Genetic modifiers of liver injury in hereditary liver disease
Aftab Ala, Michael Schilsky
Seminars in Liver Disease
|
September 9, 2011
Wilson disease: pathogenesis and clinical considerations in diagnosis and treatment
Richard Rosencrantz, Michael Schilsky
Clinical Autonomic Research : Official Journal of the Clinical Autonomic Research Society
|
September 25, 2002
Autonomic cardiovascular reflexes in Wilson's disease
Kirsty Bhattacharya, Miodrag Velickovic, Michael Schilsky, et al.
Hepatology (Baltimore, Md.)
|
February 22, 2005
Wilson disease in septuagenarian siblings: Raising the bar for diagnosis
Aftab Ala, Jimo Borjigin, Arnold Rochwarger, et al.
Journal of Clinical Gastroenterology
|
June 11, 2010
A clinical assessment of Wilson disease in patients with concurrent liver disease
Robert J Wong, Robert Gish, Michael Schilsky, et al.
Pediatric Gastroenterology, Hepatology & Nutrition
|
July 21, 2016
The Challenges of Diagnosing and Following Wilson Disease in the Presence of Proteinuria
Soofia Khan, Michael Schilsky, Gary Silber, et al.
Clinical Medicine (London, England)
|
June 15, 2022
Defining and characterising a toolkit for the development of a successful European registry for rare liver diseases: a model for building a rare disease registry
Marinos Pericleous, Claire Kelly, Michael Schilsky, et al.
Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology
|
March 26, 2013
Pre-liver transplant protocols in dentistry
Reza Radmand, Michael Schilsky, Simona Jakab, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 27, 2007
Wilson disease in children: serum aminotransferases and urinary copper on triethylene tetramine dihydrochloride (trientine) treatment
Ronen Arnon, Judith Flores Calderon, Michael Schilsky, et al.
Analytica Chimica Acta
|
January 18, 2020
Biomedical copper speciation in relation to Wilson's disease using strong anion exchange chromatography coupled to triple quadrupole inductively coupled plasma mass spectrometry
Nikolay Solovyev, Aftab Ala, Michael Schilsky, et al.
Page
of 3