Literature DB >> 6061292

Treatment of homocystinuria.

H P Chase, S I Goodman, D O'Brien.   

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Year:  1967        PMID: 6061292      PMCID: PMC2019813          DOI: 10.1136/adc.42.225.514

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


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  16 in total

1.  Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.

Authors:  N A CARSON; D W NEILL
Journal:  Arch Dis Child       Date:  1962-10       Impact factor: 3.791

2.  Effect of penicillamine on cystinuria.

Authors:  J C CRAWHALL; E F SCOWEN; R W WATTS
Journal:  Br Med J       Date:  1963-03-02

3.  Cystathioninura.

Authors:  G W FRIMPTER; A HAYMOVITZ; M HORWITH
Journal:  N Engl J Med       Date:  1963-02-14       Impact factor: 91.245

4.  Use of dimercaprol or pencillamine in the treatment of cystinosis.

Authors:  B E CLAYTON; A D PATRICK
Journal:  Lancet       Date:  1961-10-21       Impact factor: 79.321

5.  Phenylketonuria-treating the disease and feeding the child.

Authors:  B UMBARGER
Journal:  Am J Dis Child       Date:  1960-12

6.  Homocystinuria: a report in two siblings.

Authors:  C Kennedy; V E Shih; L P Rowland
Journal:  Pediatrics       Date:  1965-11       Impact factor: 7.124

7.  Dietary treatment of homocystinuria.

Authors:  G M Komrower; A M Lambert; D C Cusworth; R G Westall
Journal:  Arch Dis Child       Date:  1966-12       Impact factor: 3.791

8.  Early diagnosis and treatment of homocystinuria.

Authors:  T L Perry; H G Dunn; S Hansen; L MacDougall; P D Warrington
Journal:  Pediatrics       Date:  1966-03       Impact factor: 7.124

9.  Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis.

Authors:  H G Dunn; T L Perry; C L Dolman
Journal:  Neurology       Date:  1966-04       Impact factor: 9.910

10.  Homocystinuria due to cystathionine synthase deficiency.

Authors: 
Journal:  Ann Intern Med       Date:  1965-12       Impact factor: 25.391

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  6 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.  [A case of homocystinuria with predominating musculosceletal system].

Authors:  K Szepesi; J Nábrády
Journal:  Arch Orthop Unfallchir       Date:  1973-03-26

3.  The detection of heterozygotes for homocystinuria by oral loading with L-methionine.

Authors:  B Fowler; I B Sardharwalla; A J Robins
Journal:  Biochem J       Date:  1971-03       Impact factor: 3.857

4.  Psychiatric and biochemical aspects of a case of homocystinuria.

Authors:  A C Kaeser; R Rodnight; B A Ellis
Journal:  J Neurol Neurosurg Psychiatry       Date:  1969-04       Impact factor: 10.154

5.  Treatment of homocystinuria with pyridoxine. A preliminary study.

Authors:  N A Carson; I J Carré
Journal:  Arch Dis Child       Date:  1969-06       Impact factor: 3.791

6.  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

  6 in total

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