Literature DB >> 13534741

An inborn error of metabolism with the urinary excretion of alpha-hydroxy-butyric acid and phenylpyruvic acid.

A J SMITH, L B STRANG.   

Abstract

Entities:  

Keywords:  KETONE BODIES/in urine; PHENYLPYRUVIC OLIGOPHRENIA/urine in

Mesh：

Substances：

Year:  1958        PMID： 13534741      PMCID： PMC2012215          DOI： 10.1136/adc.33.168.109

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  8 in total

1.  Phenylpyruvic oligophrenia (phenylketonuria).

Authors:  G A JERVIS
Journal:  Res Publ Assoc Res Nerv Ment Dis       Date:  1954

2.  Identification of alpha-aminobutyric acid enzymatically formed from threonine.

Authors:  O G LIEN; D M GREENBERG
Journal:  J Biol Chem       Date:  1953-01       Impact factor: 5.157

3.  The fate of certain organic acids and amides in the rabbit. 10. The application of paper chromatography to metabolic studies of hydroxybenzoic acids and amides.

Authors:  H G Bray; W V Thorpe; K White
Journal:  Biochem J       Date:  1950-03       Impact factor: 3.857

4.  The amino-aciduria in Fanconi syndrome. A study making extensive use of techniques based on paper partition chromatography.

Authors:  C E Dent
Journal:  Biochem J       Date:  1947       Impact factor: 3.857

5.  Estimation of phenylpyruvic acid.

Authors:  J P BERRY; L I WOOLF
Journal:  Nature       Date:  1952-02-02       Impact factor: 49.962

6.  Biochemistry of fluoroacetate poisoning; isolation of an active tricarboxylic acid fraction from poisoned kidney homogenates.

Authors:  P BUFFA; R A PETERS; R W WAKELIN
Journal:  Biochem J       Date:  1951-04       Impact factor: 3.857

7.  The coupled oxidation of pyruvate with glutathione and cysteine.

Authors:  D CAVALLINI
Journal:  Biochem J       Date:  1951-06       Impact factor: 3.857

8.  Keto-acid content of human blood and urine.

Authors:  D CAVALLINI; N FRONTALI; G TOSCHI
Journal:  Nature       Date:  1949-11-05       Impact factor: 49.962
  8 in total
  15 in total

1.  [ON THE NOMENCLATURE OF CONGENITAL METABOLIC ANOMALIES].

Authors:  I SANO
Journal:  Klin Wochenschr       Date:  1964-02-01

2.  Maple syrup urine disease.

Authors:  A D PATRICK
Journal:  Arch Dis Child       Date:  1961-06       Impact factor: 3.791

3.  Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency.

Authors:  D Y MACKENZIE; L I WOOLF
Journal:  Br Med J       Date:  1959-01-10

Review 4.  Advances in electronic-nose technologies developed for biomedical applications.

Authors:  Alphus D Wilson; Manuela Baietto
Journal:  Sensors (Basel)       Date:  2011-01-19       Impact factor: 3.576

5.  ANNOTATIONS.

Authors: 
Journal:  Br Med J       Date:  1959-01-10

6.  Smell as a diagnostic marker.

Authors:  K Liddell
Journal:  Postgrad Med J       Date:  1976-03       Impact factor: 2.401

Review 7.  Food intolerance in humans.

Authors:  R H Herman; L Hagler
Journal:  West J Med       Date:  1979-02

8.  Hypophosphatasia with phenylketonuria.

Authors:  M E Blaskovics; K N Shaw
Journal:  Z Kinderheilkd       Date:  1974

Review 9.  [Absorption and malabsorption of protein digestion products].

Authors:  D M Matthews
Journal:  Klin Wochenschr       Date:  1969-04-15

Review 10.  Lessons from inborn errors of metabolism.

Authors:  M D Milne
Journal:  Proc R Soc Med       Date:  1966-11
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