During routine screening procedures for amino-acid disorders by thin-layer chromatography, a 16-year-old boy was found to have phenylketonuria and cystinuria. A phenylalanine and a cystine loading were carried out. The patient was found to be homozygous for phenylketonuria and heterozygous for cysti
β¦ LIBER β¦
Cystathioninuria in a patient with cystinuria
β Scribed by George W. Frimpter
- Book ID
- 115675709
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- English
- Weight
- 440 KB
- Volume
- 46
- Category
- Article
- ISSN
- 1555-7162
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Phenylketonuria in a patient with cystin
β
R. Minami; K. Olek; P. Wardenbach
π
Article
π
1975
π
Springer
π
English
β 318 KB
Cystathioninuria in patients with neurob
β
Rajnherc, J. R. ;van Gennip, A. H. ;Abeling, N. G. G. M. ;van der Zee, J. M. ;Vo
π
Article
π
1984
π
John Wiley and Sons
π
English
β 343 KB
Urinary excretion of cystathionine and dopa metabolites was analyzed in 61 patients with active neuroblastoma before, and at regular intervals during treatment. Thirty-seven patients with clinical evidence of active neuroblastoma excreted elevated levels of cystathionine before treatment was initiat
Characterization of Patients With Hetero
β
Mohamed A. Elkoushy; Sero Andonian
π
Article
π
2012
π
Elsevier Science
π
English
β 216 KB
βDisappearanceβ of cystinuria in a patie
β
Felix O. Kolb; Jerry M. Earll; Harold A. Harper
π
Article
π
1967
π
Elsevier Science
π
English
β 274 KB
Urinary cystine excretion and capacity i
β
Goldfarb, D S; Coe, F L; Asplin, J R
π
Article
π
2006
π
Nature Publishing Group
π
English
β 280 KB
Cystathioninuria in Down's syndrome
β
A. HESTNES; O. BORUD; H. LUNDE; L. GJESSING
π
Article
π
2008
π
John Wiley and Sons
π
English
β 284 KB