Histidinaemia: a child and his family.

Author:

Cain A. R.,Holton J. B.

Publisher

BMJ

Subject

Pediatrics, Perinatology and Child Health

Reference24 articles.

1. Histidinemia: a new metabolic disorder (abstract);Andrews, B.F.; Crosby, P.F.; Angel, C.R.;Sth. med. J. (Bgham, Ala.),1962

2. Histidinemia: a deficiency in histidase resulting in the urinary excretion of histidine and imidazolepyruvic acid;Auerbach, V.H.; DiGeorge, A.M.; Baldridge, R.C.; Tourtellotte, C.D.; Brigham, M.P.;J. Pediat,1962

3. A method for the determination of histidine in blood;Baldridge, R.C.; Greenberg, N.;J. Lab. clin. Med,1963

4. P3-Iminazolyl-4 (or 5)-pyruvic acid;Barger, G.; Stewart, C.P.;J. Pharmacol. exp. Ther,1926

5. Berlow, S., Arends, R., and Harries, C. (1965). Studies in histidinemia. J.-Lancet, 85, 241.

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1. Biochemical Profiling of Urine Metabolome in Premature Infants Based on LC−MS Considering Maternal Influence;Nutrients;2024-01-31

2. Speech and Histidinemia: Methodology and Evaluation of Four Cases;Developmental Medicine & Child Neurology;2008-11-12

3. DELAYED SPEECH AND HISTIDINAEMIA;Developmental Medicine & Child Neurology;2008-11-12

4. Histidinemia: a biochemical variant or a disease?;Journal of the American College of Nutrition;1993-04

5. Histidinaemia. Part II: Impact; a retrospective study;Journal of Inherited Metabolic Disease;1983-09

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