Search Results - Walter, Melanie
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Succinyl-CoA:3-oxoacid coenzyme a transferase (SCOT) deficiency: a rare and potentially fatal metabolic disease by Grünert, Sarah (Author) , Foster, William (Author) , Schumann, Anke (Author) , Lund, Allan (Author) , Pontes, Christina (Author) , Roloff, Sylvia (Author) , Weinhold, Natalie (Author) , Yue, Wyatt W. (Author) , AlAsmari, Ali (Author) , Obaid, Osama A. (Author) , Faqeih, Eissa Ali (Author) , Stübbe, Lisa (Author) , Yamamoto, Raina (Author) , Gemperle-Britschgi, Corinne (Author) , Walter, Melanie (Author) , Spiekerkoetter, Ute (Author) , Mackinnon, Sabrina (Author) , Sass, Jörn Oliver (Author) ,
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Two inborn errors of metabolism in a newborn: glutaric aciduria type I combined with isobutyrylglycinuria by Popek, Manuela (Author) , Walter, Melanie (Author) , Fernando, Malkanthi (Author) , Lindner, Martin (Author) , Schwab, Karl Otfried (Author) , Sass, Jörn Oliver (Author) ,
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Related Subjects
Acylcarnitines
Glutaric acid
Glutaric aciduria
Glutaryl-coenzyme A dehydrogenase
Inborn error of metabolism
Isobutyryl-coenzyme dehydrogenase
Isobutyrylglycine
Isobutyrylglycinuria
Ketoacidosis
Ketolysis
Ketone body utilization
Metabolic acidosis
Newborn screening
Organic acids
Tandem mass spectrometry
gene