Literature DB >> 5560617

Pure familial hyperprolinemia: isolated inborn error of aminoacid metabolism without other anomalies in a Sicilian family.

F Mollica, L Pavone, I Antener.   

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Year:  1971        PMID： 5560617

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


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  3 in total

1.  Asymptomatic type II hyperprolinaemia associated with hyperglycinaemia in three sibs.

Authors:  L Pavone; F Mollica; H L Levy
Journal:  Arch Dis Child       Date:  1975-08       Impact factor: 3.791

2.  Hyperprolinaemia type I and white matter disease: coincidence or causal relationship?

Authors:  M Steinlin; E Boltshauser; B Steinmann; W Wichmann; G Niemeyer
Journal:  Eur J Pediatr       Date:  1989-10       Impact factor: 3.183

3.  Type II hyperprolinaemia in a pedigree of Irish travellers (nomads).

Authors:  M P Flynn; M C Martin; P T Moore; J A Stafford; G A Fleming; J M Phang
Journal:  Arch Dis Child       Date:  1989-12       Impact factor: 3.791
  3 in total

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