Literature DB >> 4457103

Genetic aspects in gyrate atrophy of the choroid and retina with hyperornithinaemia.

K Takki, O Simell.   

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Year:  1974        PMID: 4457103      PMCID: PMC1215056          DOI: 10.1136/bjo.58.11.907

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


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  13 in total

1.  Atrophia choroideae et retinae.

Authors:  H C WU; C W YANG
Journal:  Chin Med J       Date:  1960-06

2.  A familial disturbance of histidine metabolism.

Authors:  H GHADIMI; M W PARTINGTON; A HUNTER
Journal:  N Engl J Med       Date:  1961-08-03       Impact factor: 91.245

3.  [Carrier of the gene of atrophia gyrata choroidae et retinae of Fuchs (Alder's anomaly)].

Authors:  J FRANCOIS; F BARBIER; A DE ROUCK
Journal:  Bull Soc Belge Ophtalmol       Date:  1959

4.  ATROPHIA GYRATA CHOROIDEAE ET RETINAE.

Authors:  J Saebø
Journal:  Br J Ophthalmol       Date:  1948-11       Impact factor: 4.638

5.  Gyrate atrophy of the choroid and retina associated with hyperornithinaemia.

Authors:  K Takki
Journal:  Br J Ophthalmol       Date:  1974-01       Impact factor: 4.638

6.  [Ornithinemia, additional disorder of amino acid metabolism with brain damage].

Authors:  H Bickel; D Feist; H Müller; G Quadbeck
Journal:  Dtsch Med Wochenschr       Date:  1968-11-22       Impact factor: 0.628

7.  [Gyrate atrophy with nystagmus and strabismus].

Authors:  W D Schäfer; A Tenner
Journal:  Klin Monbl Augenheilkd       Date:  1970-03       Impact factor: 0.700

8.  [On the presence of druse in distorted coroid and retinal atrophy].

Authors:  C Hilsdorf
Journal:  Ophthalmologica       Date:  1967       Impact factor: 3.250

9.  Further studies of hyperlysinemia.

Authors:  N C Woody; J Hutzler; J Dancis
Journal:  Am J Dis Child       Date:  1966-12

10.  Hyperornithinemia, hyperammonemia, and homocitrullinuria. A new disorder of amino acid metabolism associated with myoclonic seizures and mental retardation.

Authors:  V E Shih; M L Efron; H W Moser
Journal:  Am J Dis Child       Date:  1969-01
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  26 in total

1.  Oral lysine feeding in gyrate atrophy with hyperornithinaemia--a pilot study.

Authors:  K Peltola; O J Heinonen; K Näntö-Salonen; K Pulkki; O Simell
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

Review 2.  The Finnish Disease Heritage III: the individual diseases.

Authors:  Reijo Norio
Journal:  Hum Genet       Date:  2003-03-08       Impact factor: 4.132

3.  Gyrate atrophy of the choroid and retina: clinical, ophthalmologic, and biochemical considerations.

Authors:  C McCulloch; E B Marliss
Journal:  Trans Am Ophthalmol Soc       Date:  1975

4.  Hyperprolinaemia and gyrate atrophy of the choroid and retina in members of the same family.

Authors:  E P Douglas
Journal:  Br J Ophthalmol       Date:  1985-08       Impact factor: 4.638

5.  Presence of ornithine ketoacid aminotransferase in human ocular tissues.

Authors:  T Shiono; S Hayasaka; K Mizuno
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1982       Impact factor: 3.117

6.  Free amino acid concentrations in blood cells of two brothers with gyrate atrophy of the choroid and retina with hyperornithinaemia.

Authors:  K Fukuda; Y Nishi; T Usui; H Mishima; H Hirata; S Baba; K Choshi; Y Tanaka; S Akiya
Journal:  J Inherit Metab Dis       Date:  1983       Impact factor: 4.982

7.  Treatment of gyrate atrophy of the choroid and retina with low arginine diet.

Authors:  R R McInnes; S A Arshinoff; L Bell; C McCulloch
Journal:  Trans Am Ophthalmol Soc       Date:  1980

8.  Gyrate atrophy of choroid and retina with myopia, cataract and systemic proximal myopathy: A rare case report from rural India.

Authors:  Surekha Bangal; Akshay Bhandari; Priyanka Dhaytadak; Pratik Gogri
Journal:  Australas Med J       Date:  2012-12-31

9.  Ornithine ketoacid transaminase deficiency in gyrate atrophy of the choroid and retina.

Authors:  V E Shih; E L Berson; R Mandell; S Y Schmidt
Journal:  Am J Hum Genet       Date:  1978-03       Impact factor: 11.025

10.  Decreased transport of ornithine across the inner mitochondrial membrane as a cause of hyperornithinaemia.

Authors:  F A Hommes; C K Ho; R A Roesel; M E Coryell; B A Gordon
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

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