Literature DB >> 4289134

Cystathioninuria.

K N Shaw, E Lieberman, R Koch, G N Donnell.   

Abstract

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Year:  1967        PMID： 4289134     DOI： 10.1001/archpedi.1967.02090160169027

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN： 0002-922X


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  7 in total

1.  Occurrence of secondary cystathioninuria in children with inherited metabolic disorders, liver diseases, neoplasms, cystic fibrosis and celiac disease.

Authors:  W Endres; B Wuttge
Journal:  Eur J Pediatr       Date:  1978-08-17       Impact factor: 3.183

2.  Hypophosphatasia with phenylketonuria.

Authors:  M E Blaskovics; K N Shaw
Journal:  Z Kinderheilkd       Date:  1974

3.  Absent thumbs with a ring D2 chromosome: a new deletion syndrome.

Authors:  R S Sparkes; R E Carrel; S W Wright
Journal:  Am J Hum Genet       Date:  1967-09       Impact factor: 11.025

4.  Phenylketonuria in a patient with cystinuria.

Authors:  R Minami; K Olek; P Wardenbach
Journal:  Humangenetik       Date:  1975-08-25

5.  In vitro study of cysteine oxidase in rat brain.

Authors:  C H Misra
Journal:  Neurochem Res       Date:  1983-11       Impact factor: 3.996

6.  Is a certain amount of cysteine prerequisite to produce brain damage in neonatal rats?

Authors:  C H Misra
Journal:  Neurochem Res       Date:  1989-03       Impact factor: 3.996

Review 7.  Diseases of phenylalanine metabolism.

Authors:  C E Parker
Journal:  West J Med       Date:  1979-10
  7 in total

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