Diagnosis and follow-up of inborn errors of amino acid metabolism: Use of proton magnetic resonance of biological fluids

Amino Acids

Volumn 10, Issue 4, 1996, Pages 305-315

  Pontoni, G ^a   Rotondo, F ^a   Carteni Farina M ^a   Zappia, V ^b  

^a SECOND UNIVERSITY OF NAPLES   (Italy)

^b CNR   (Italy)

Author keywords

Amino acids; Amino acidurias; Inherited metabolic diseases; Neonatal screening; Nuclear magnetic resonance spectroscopy; Organic acidurias

Indexed keywords

AMINO ACID;

ACIDURIA; ALKAPTONURIA; AMINO ACID METABOLISM; ARTICLE; CHILD; CONTROLLED STUDY; CYSTINURIA; DIAGNOSTIC TEST; HUMAN; INBORN ERROR OF METABOLISM; MAPLE SYRUP URINE DISEASE; PHENYLKETONURIA; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SCHOOL CHILD; TYROSINEMIA; URINALYSIS;

ACER;

EID: 0030056809     PISSN: 09394451     EISSN: None     Source Type: Journal    
DOI: 10.1007/BF00805859     Document Type: Article

References (9)

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