Literature DB >> 5844007

Homocystinuria: a report in two siblings.

C Kennedy, V E Shih, L P Rowland.   

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Year:  1965        PMID： 5844007

Source DB:  PubMed          Journal:  Pediatrics        ISSN： 0031-4005            Impact factor:   7.124


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  4 in total

1.  Detection of heterozygotes for homocystinuria. Study of sulphur-containing amino acids in plasma and urine after L-methionine loading.

Authors:  I B Sardharwalla; B Fowler; A J Robins; G M Komrower
Journal:  Arch Dis Child       Date:  1974-07       Impact factor: 3.791

2.  Amino acid patterns in cystinuric families.

Authors:  S Kelly; W Copeland
Journal:  J Med Genet       Date:  1968-12       Impact factor: 6.318

3.  Treatment of homocystinuria.

Authors:  H P Chase; S I Goodman; D O'Brien
Journal:  Arch Dis Child       Date:  1967-10       Impact factor: 3.791

4.  Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.

Authors:  G H Boers; B Fowler; A G Smals; F J Trijbels; A I Leermakers; W J Kleijer; P W Kloppenborg
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132
  4 in total

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