Literature DB >> 14060091

PRESUMPTIVE X-LINKED INTERMEDIATE TRANSMISSION OF RETINAL DEGENERATIONS. VARIATIONS AND COINCIDENTAL OCCURRENCE WITH ATAXIA IN A LARGE FAMILY.

A F HECK.   

Abstract

Entities:  

Keywords:  ADOLESCENCE; CATARACT; COLOR BLINDNESS; FRIEDREICH'S ATAXIA; GENETICS, HUMAN; NYCTALOPIA; RETINITIS PIGMENTOSA

Mesh：

Year:  1963        PMID： 14060091     DOI： 10.1001/archopht.1963.00960050145002

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  4 in total

1.  X-linked retinitis pigmentosa.

Authors:  A C Bird
Journal:  Br J Ophthalmol       Date:  1975-04       Impact factor: 4.638

Review 2.  Refsum's disease (heredopathia atactica polyneuritiformis). An inborn error of lipid metabolism with storage of 3,7,11,15 tetramethyl hexadecanoic acid. A review of the clinical findings.

Authors:  R Richterich; H Moser; E Rossi
Journal:  Humangenetik       Date:  1965

3.  A-beta-lipoproteinaemia and colour-blindness.

Authors:  A K Khachadurian; R Freyha; M M Shamma'a; S A Baghdassarian
Journal:  Arch Dis Child       Date:  1971-12       Impact factor: 3.791

4.  Hereditary spastic ataxia with congenital miosis: four cases in one family.

Authors:  D J Dick; P K Newman; P G Cleland
Journal:  Br J Ophthalmol       Date:  1983-02       Impact factor: 4.638
  4 in total

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