L N Went
Overview
Explore the profile of L N Went including associated specialties, affiliations and a list of published articles.
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Articles
105
Citations
620
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Recent Articles
1.
Volker-Dieben H, Van Lith G, Went L, Klawer J, Staal A, De Vries-De Mol E
Doc Ophthalmol
. 2016 May;
37(2):307-26.
PMID: 27169914
A large family in which 8 males are affected with apparently sex linked optic atrophy is described. The disease has been present since early childhood, and the visual acuity ranges...
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de Vries D, Went L, BRUYN G, Scholte H, Hofstra R, Bolhuis P, et al.
Am J Hum Genet
. 1996 Apr;
58(4):703-11.
PMID: 8644732
A rare form of Leber hereditary optic neuropathy (LHON) that is associated with hereditary spastic dystonia has been studied in a large Dutch family. Neuropathy and ophthalmological lesions were present...
5.
BRUYN G, BOTS G, Went L, Klinkhamer P
J Neurol Sci
. 1992 Nov;
113(1):55-61.
PMID: 1469456
Neuropathological findings in a 59-year-old male case of hereditary spastic dystonia with Leber's hereditary optic atrophy included: marked depletion of myelinated nerve fibres in the posterior funiculi, corticopontine tracts and...
6.
Weitz C, Went L, Nathans J
Am J Hum Genet
. 1992 Aug;
51(2):444-6.
PMID: 1386496
No abstract available.
7.
Went L, van Schooneveld M, Oosterhuis J
J Med Genet
. 1992 May;
29(5):295-8.
PMID: 1583655
A dominant cone dystrophy spanning seven generations was found in a pedigree from the Netherlands. The onset of the decline of visual acuity started after the age of 20, while...
8.
van Everdingen J, Went L, Keunen J, Oosterhuis J
J Med Genet
. 1992 May;
29(5):291-4.
PMID: 1583654
We investigated 111 members of a five generation family with X linked cone dystrophy. The patients showed the characteristic picture of cone dystrophy. Routine ophthalmological examination of the carrier women...
9.
Weitz C, Miyake Y, Shinzato K, Montag E, Zrenner E, Went L, et al.
Am J Hum Genet
. 1992 Mar;
50(3):498-507.
PMID: 1531728
Tritanopia is an autosomal dominant genetic disorder of human vision characterize by a selective deficiency of blue spectral sensitivity. The defect is manifested within the retina and could be caused...
10.
van Schooneveld M, Went L, Oosterhuis J
Br J Ophthalmol
. 1991 Jun;
75(6):332-6.
PMID: 2043573
The results of ophthalmological and colour vision studies are reported on 13 patients from a family with a dominant cone dystrophy spanning seven generations. The onset of visual deterioration occurred...