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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Susan A Berry

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Molecular Genetics and Metabolism|August 23, 2015

Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trialsSandesh C S Nagamani, George A Diaz, William Rhead, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014

Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorderBrendan Lee, George A Diaz, William Rhead, et al.

Hepatology (Baltimore, Md.)|September 11, 2012

Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrateGeorge A Diaz, Lauren S Krivitzky, Masoud Mokhtarani, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019

Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literatureErin Torti, Boris Keren, Elizabeth E Palmer, et al.

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Search research articles

Showing results (71-80 of 74) with videos related to

Sort By:

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You have reached the last page of results.This site can display upto 74 results.

Molecular Genetics and Metabolism|August 23, 2015

Self-reported treatment-associated symptoms among patients with urea cycle disorders participating in glycerol phenylbutyrate clinical trialsSandesh C S Nagamani, George A Diaz, William Rhead, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 16, 2014

Blood ammonia and glutamine as predictors of hyperammonemic crises in patients with urea cycle disorderBrendan Lee, George A Diaz, William Rhead, et al.

Hepatology (Baltimore, Md.)|September 11, 2012

Ammonia control and neurocognitive outcome among urea cycle disorder patients treated with glycerol phenylbutyrateGeorge A Diaz, Lauren S Krivitzky, Masoud Mokhtarani, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019

Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literatureErin Torti, Boris Keren, Elizabeth E Palmer, et al.

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