Literature DB >> 14187151

LEBER'S DISEASE IN THE NETHERLANDS.

A H VANSENUS.   

Abstract

Entities:  

Keywords:  ADAPTATION, OCULAR; ADOLESCENCE; BLINDNESS; CHILD; CHROMOSOMES; COLOR PERCEPTION TESTS; ELECTRORETINOGRAPHY; GENETICS, HUMAN; GERIATRICS; INFANT; MEDICAL RECORDS; NETHERLANDS; NEUROSURGERY; OPTIC NEURITIS; PATHOLOGY; PROGNOSIS; REVIEW; STATISTICS; VISION TESTS; VISUAL FIELDS

Mesh：

Year:  1963        PMID： 14187151     DOI： 10.1007/BF00573524

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


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  34 in total

1.  [Heredity in ophthalmology].

Authors:  J FRANCOIS
Journal:  Bull Soc Belge Ophtalmol       Date:  1958

2.  Hereditary afections.

Authors:  F D CARROLL
Journal:  Trans Am Acad Ophthalmol Otolaryngol       Date:  1956 Jan-Feb

3.  [Infantile familial atrophy of the optic nerve].

Authors:  R KAYSER
Journal:  Confin Neurol       Date:  1955

4.  [Structure of the papilla of the human eye].

Authors:  J R WOLTER
Journal:  Albrecht Von Graefes Arch Ophthalmol       Date:  1956

5.  Relation of hereditary optic atrophy (leber) to the other familial degenerative diseases of central nervous system.

Authors:  M BEREDAY; S COBB
Journal:  AMA Arch Ophthalmol       Date:  1952-12

6.  Leber's hereditary optic atrophy in a Canadian family.

Authors:  A BIRD; D McEACHERN
Journal:  Can Med Assoc J       Date:  1949-10       Impact factor: 8.262

7.  Hereditary optic atrophy in family with keratodermia palmaris et plantaris (tylosis).

Authors:  H DIMSDALE
Journal:  Proc R Soc Med       Date:  1949-10

8.  Leber's Disease in Twins.

Authors:  E F King
Journal:  Proc R Soc Med       Date:  1939-05

9.  Statistical Details of three years' experience in respect to the form of Amaurosis supposed to be due to Tobacco.

Authors:  J Hutchinson
Journal:  Med Chir Trans       Date:  1867

10.  A Pedigree of Congenital Optic Atrophy Embracing Sixteen Affected Cases In Six Generations: (Section of Ophthalmology).

Authors:  A H Thompson; G T Cashell
Journal:  Proc R Soc Med       Date:  1935-08
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  26 in total

1.  Molecular genetic analysis of a sporadic case of Leber hereditary optic neuropathy.

Authors:  N Howell; D McCullough; I Bodis-Wollner
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

2.  Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.

Authors:  N Howell; L A Bindoff; D A McCullough; I Kubacka; J Poulton; D Mackey; L Taylor; D M Turnbull
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

3.  A family with sex linked optic atrophy : Ophthalmological and neurological aspects.

Authors:  H J Völker-Dieben; G H Van Lith; L N Went; J W Klawer; A Staal; E C De Vries-De Mol
Journal:  Doc Ophthalmol       Date:  1974-11       Impact factor: 2.379

4.  No evidence for 'skewed' inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers.

Authors:  R J Oostra; S Kemp; P A Bolhuis; E M Bleeker-Wagemakers
Journal:  Hum Genet       Date:  1996-04       Impact factor: 4.132

5.  A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

Authors:  J J Assink; N T Tijmes; J B ten Brink; R J Oostra; F C Riemslag; P T de Jong; A A Bergen
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

6.  A Meta-analysis of the association between different genotypes (G11778A, T14484C and G3460A) of Leber hereditary optic neuropathy and visual prognosis.

Authors:  Dong-Yu Guo; Xia-Wei Wang; Nan Hong; Yang-Shun Gu
Journal:  Int J Ophthalmol       Date:  2016-10-18       Impact factor: 1.779

7.  Analysis of mitochondrial DNA sequences in patients with isolated or combined oxidative phosphorylation system deficiency.

Authors:  R Hinttala; R Smeets; J S Moilanen; C Ugalde; J Uusimaa; J A M Smeitink; K Majamaa
Journal:  J Med Genet       Date:  2006-05-31       Impact factor: 6.318

8.  Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutation.

Authors:  A E Harding; M G Sweeney; G G Govan; P Riordan-Eva
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

9.  X-recessive angiopathic opticopathy.

Authors:  L A Bastiaensen; J J Vandoninck
Journal:  Doc Ophthalmol       Date:  1982-01-29       Impact factor: 2.379

10.  Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy.

Authors:  B A Kormann; H Schuster; T A Berninger; B Leo-Kottler
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132
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