Selective screening of amino acid disorders in the south-west of Iran, Shiraz

Journal of Inherited Metabolic Disease

Volumn 25, Issue 6, 2002, Pages 519-521

  Golbahar, J ^a   Karamizadeh, Z ^a   Honardar, Z ^a  

^a SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; THIAMINE;

AMINO ACID BLOOD LEVEL; AMINO ACID DEFICIENCY; ARTICLE; BLOOD SAMPLING; CHILD; CLINICAL FEATURE; HUMAN; INCIDENCE; IRAN; MAPLE SYRUP URINE DISEASE; PHENYLKETONURIA; SCREENING TEST; TYROSINEMIA;

ADULT; AMINO ACID METABOLISM, INBORN ERRORS; CONSANGUINITY; FEMALE; HUMANS; INFANT, NEWBORN; IRAN; MAPLE SYRUP URINE DISEASE; NEONATAL SCREENING; PHENYLKETONURIAS; PREGNANCY; TYROSINEMIAS;

EID: 12244259751     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1021219805921     Document Type: Article

References (5)

1. Moammar H, Ratard R, Cheriyan G, Mathew P (1996) Incidence and features of galactosaemia in Saudi Arabs. J Inherit Metab Dis 19: 331-334.
2. Ozand PT, Devol EB, Generoso GG (1992) Neurometabolic diseases at a national referral center: five years experience at the King Faisal Specialist Hospital and Research Centre. J Child Neurol 7(Supplement): S4-S11.
3. Teebi A (1994) Autosomal recessive disorders among Arabs: an overview from Kuwait. J Med Genet 31: 224-233.
4. Temtamy SA, Kandil MR, Demerdash AM, Hassan WA, Meguid NA, Afifi HH (1994) An epidemiological/genetic study of mental subnormality in Assiut Governorate, Egypt. Clin Genet 46: 347-351.
5. Terrlink T, van Leeuwen PAM, Houdijk A (1994) Plasma amino acids determined by liquid chromatography within 17 minutes. Clin Chem 40: 245-249.