Hyperglycinemia and propionyl CoA carboxylase deficiency and episodic severe illness without consistent ketosis

Author:

Wadlington William B.,Kilroy A.nthony.,Ando Toshiyuki,Sweetman Lawrence.,Nyhan William L.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference26 articles.

1. Idiopathic hyperglycinemia and hyperglycinuria, a new disorder of amino acid metabolism;Childs;Pediatrics,1961

2. A new type of idiopathic hyperglycinemia with hypooxaluria;Gerritsen;Pediatrics,1965

3. Ketotic hyperglycinaemia;Nyhan,1972

4. The clinical findings in a patient with nonketotic hyperglycinemia;Ziter;Pediatr Res,1968

5. Observations on the coexistence of methylmalonic acidemia and glycinemia;Morrow;J Pediatr,1969

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2. Organic Acids;Volpe's Neurology of the Newborn;2018

3. Amino Acids;Volpe's Neurology of the Newborn;2018

4. Methylmalonic and propionic acidemias: clinical management update;Current Opinion in Pediatrics;2016-12

5. Organic Acidemias and Disorders of Fatty Acid Oxidation;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

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