Towards enzyme-replacement treatment in triosephosphate isomerase deficiency

Lancet

Volumn 353, Issue 9159, 1999, Pages 1155-1156

  Ationu, Art ^a   Humphries, Ann ^a   Wild, Barbara ^a   Carr, Trevor ^a   Will, Andrew ^a   Arya, Roopen ^a   Layton, D Mark ^a  

^a KING'S COLLEGE LONDON   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALBUMIN; ALCOHOL; CEPHALOSPORIN; SODIUM CHLORIDE;

ADULT; ALCOHOL ABUSE; ARTICLE; CASE REPORT; CENTRAL PONTINE MYELINOLYSIS; CRYSTALLOID; FEMALE; HUMAN; HYPONATREMIA; INFUSION; NUCLEAR MAGNETIC RESONANCE IMAGING; PLASMAPHERESIS; PRIORITY JOURNAL; TREATMENT OUTCOME;

EID: 0033519047     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(99)00474-2     Document Type: Article

References (5)

1. Schneider A.S., Valentine W.N., Hattori M., Heins J.R. Hereditary haemolytic anaemia with triosephosphate isomerase deficiency. N Engl J Med. 272:1965;229-235.
2. Arya R., Layton D.M., Bellingham A.J. Hereditary red cell enzymopathies. Blood Rev. 9:1995;165-175.
3. Ationu A., Humphries A., Bellingham A.J., Layton D.M. Metabolic correction of triosephosphate isomerase deficiency in vitro by complementation. Biochem Biophys Res Commun. 232:1997;528-531.
4. Beutler E., Blume K.G., Kaplan J.C., Lohr G.W., Ramot B., Valentine W.N. International Committee for Standardisation in Haematology: recommended methods for red cell enzyme analysis. Br J Haematol. 6:1977;163-172.
5. Bellingham A.J., Lestas A.N., William L.H.P., Nicolaides K.H. Prenatal diagnosis of a red cell enzymopathy: triosephosphate isomerase deficiency. Lancet. ii:1989;419-421.