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B F Scharschmidt

Showing results (71-80 of 77) with videos related to

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Gastroenterology|July 1, 1997
Evidence for an ATP-dependent bile acid transport protein other than the canalicular liver ecto-ATPase in ratsT T Luther, P Hammerman, C M Rahmaoui, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Urinary phenylacetylglutamine (U-PAGN) concentration as biomarker for adherence in patients with urea cycle disorders (UCD) treated with glycerol phenylbutyrateM Mokhtarani, G A Diaz, U Lichter-Konecki, et al.
Nature Genetics|March 21, 1998
A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasisL N Bull, M J van Eijk, L Pawlikowska, et al.
Digestive Diseases and Sciences|January 20, 2016
Prospective Multicenter Observational Study of Overt Hepatic EncephalopathyC S Landis, M Ghabril, V Rustgi, et al.
Molecular Genetics and Metabolism|November 21, 2015
Glutamine and hyperammonemic crises in patients with urea cycle disordersB Lee, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|October 23, 2013
Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratioM Mokhtarani, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|September 11, 2012
Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disordersM Mokhtarani, G A Diaz, W Rhead, et al.
Pageof 8

Showing results (71-80 of 77) with videos related to

Sort By:
Pageof 8
You have reached the last page of results.This site can display upto 77 results.
Gastroenterology|July 1, 1997
Evidence for an ATP-dependent bile acid transport protein other than the canalicular liver ecto-ATPase in ratsT T Luther, P Hammerman, C M Rahmaoui, et al.
Molecular Genetics and Metabolism Reports|June 27, 2017
Urinary phenylacetylglutamine (U-PAGN) concentration as biomarker for adherence in patients with urea cycle disorders (UCD) treated with glycerol phenylbutyrateM Mokhtarani, G A Diaz, U Lichter-Konecki, et al.
Nature Genetics|March 21, 1998
A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasisL N Bull, M J van Eijk, L Pawlikowska, et al.
Digestive Diseases and Sciences|January 20, 2016
Prospective Multicenter Observational Study of Overt Hepatic EncephalopathyC S Landis, M Ghabril, V Rustgi, et al.
Molecular Genetics and Metabolism|November 21, 2015
Glutamine and hyperammonemic crises in patients with urea cycle disordersB Lee, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|October 23, 2013
Elevated phenylacetic acid levels do not correlate with adverse events in patients with urea cycle disorders or hepatic encephalopathy and can be predicted based on the plasma PAA to PAGN ratioM Mokhtarani, G A Diaz, W Rhead, et al.
Molecular Genetics and Metabolism|September 11, 2012
Urinary phenylacetylglutamine as dosing biomarker for patients with urea cycle disordersM Mokhtarani, G A Diaz, W Rhead, et al.
Pageof 8