Literature DB >> 2743859

Studies on Leber's optic neuropathy III.

A Palan1, A Stehouwer, L N Went.   

Abstract

Neurological investigations, HLA-typing and viral antibody studies were performed in patients with Leber's optic neuropathy (LON), in individuals at risk to develop the disease, in obligatory (female) carriers of the disease, and compared with controls. The only relevant findings were an excess of minor neurological abnormalities in patients with LON and in some individuals from the at risk group. Occasionally, an association of LON and a multiple sclerosis-like picture was observed.

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Year:  1989        PMID: 2743859     DOI: 10.1007/bf00155135

Source DB:  PubMed          Journal:  Doc Ophthalmol        ISSN: 0012-4486            Impact factor:   2.379


  25 in total

1.  A SEX-LINKED HEREDO-DEGENERATIVE NEUROLOGICAL DISORDER, ASSOCIATED WITH LEBER'S OPTIC ATROPHY. I. CLINICAL STUDIES.

Authors:  G W BRUYN; L N WENT
Journal:  J Neurol Sci       Date:  1964 Jan-Feb       Impact factor: 3.181

2.  Degenerative disease of the central nervous system in New Guinea; the endemic occurrence of kuru in the native population.

Authors:  D C GAJDUSEK; V ZIGAS
Journal:  N Engl J Med       Date:  1957-11-14       Impact factor: 91.245

Review 3.  Mendelian inheritance or transmissible agent? The lesson Kuru and the Australia antigen.

Authors:  P S Harper
Journal:  J Med Genet       Date:  1977-12       Impact factor: 6.318

4.  A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance.

Authors:  D C Wallace
Journal:  Brain       Date:  1970       Impact factor: 13.501

5.  Leber's disease. II.

Authors:  T Seedorff
Journal:  Acta Ophthalmol (Copenh)       Date:  1968

6.  Leber's disease. 3.

Authors:  T Seedorff
Journal:  Acta Ophthalmol (Copenh)       Date:  1969

7.  Leber's hereditary optic atrophy: a possible defect of cyanide metabolism.

Authors:  J Wilson
Journal:  Clin Sci       Date:  1965-12       Impact factor: 6.124

8.  The inheritance of Leber's disease. A genealogical follow-up study.

Authors:  T Seedorff
Journal:  Acta Ophthalmol (Copenh)       Date:  1985-04

9.  Leber's optic neuropathy II. Fluorescein angiographic studies.

Authors:  A Stehouwer; J A Oosterhuis; A H Renger-van Dijk; L N Went
Journal:  Doc Ophthalmol       Date:  1982-09-30       Impact factor: 2.379

10.  Ophthalmoscopic findings in Leber's hereditary optic neuropathy. I. Fundus findings in asymptomatic family members.

Authors:  E Nikoskelainen; W F Hoyt; K Nummelin
Journal:  Arch Ophthalmol       Date:  1982-10
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  4 in total

1.  Bilateral striatal necrosis, dystonia and optic atrophy in two siblings.

Authors:  V Leuzzi; E Bertini; A M De Negri; M Gallucci; B Garavaglia
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-01       Impact factor: 10.154

2.  Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.

Authors:  N Howell; I Kubacka; M Xu; D A McCullough
Journal:  Am J Hum Genet       Date:  1991-05       Impact factor: 11.025

3.  Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

Authors:  R J Oostra; P A Bolhuis; F A Wijburg; G Zorn-Ende; E M Bleeker-Wagemakers
Journal:  J Med Genet       Date:  1994-04       Impact factor: 6.318

4.  Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy.

Authors:  E K Nikoskelainen; R J Marttila; K Huoponen; V Juvonen; T Lamminen; P Sonninen; M L Savontaus
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-08       Impact factor: 10.154

  4 in total

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