Literature DB >> 5516287

Dystrophia retinae pigmentosa--dysacusis syndrome (DRD): a study of the Usher- or Hallgren syndrome.

A Nuutila.   

Abstract

Entities:  

Mesh：

Year:  1970        PMID： 5516287

Source DB:  PubMed          Journal:  J Genet Hum        ISSN： 0021-7743


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  18 in total

Review 1.  The Finnish Disease Heritage III: the individual diseases.

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

2.  Usher syndrome in the city of Birmingham--prevalence and clinical classification.

Authors:  C I Hope; S Bundey; D Proops; A R Fielder
Journal:  Br J Ophthalmol       Date:  1997-01       Impact factor: 4.638

3.  Children with Usher syndrome: mental and behavioral disorders.

Authors:  Jesper Dammeyer
Journal:  Behav Brain Funct       Date:  2012-03-27       Impact factor: 3.759

4.  Usher's syndrome.

Authors:  R A Pagon
Journal:  Br J Ophthalmol       Date:  1980-02       Impact factor: 4.638

5.  CNS changes in Usher's syndrome with mental disorder: CT, MRI and PET findings.

Authors:  J Koizumi; K Ofuku; K Sakuma; H Shiraishi; M Iio; S Nawano
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-07       Impact factor: 10.154

Review 6.  Usher syndrome: Hearing loss, retinal degeneration and associated abnormalities.

Authors:  Pranav Mathur; Jun Yang
Journal:  Biochim Biophys Acta       Date:  2014-12-04

7.  Usher's syndrome: electrophysiological tests of the visual and auditory systems.

Authors:  F A Abraham; D Cohen; H Sohmer
Journal:  Doc Ophthalmol       Date:  1977-12-30       Impact factor: 2.379

8.  Biochemical characterization of native Usher protein complexes from a vesicular subfraction of tracheal epithelial cells.

Authors:  Marisa Zallocchi; Joseph H Sisson; Dominic Cosgrove
Journal:  Biochemistry       Date:  2010-02-16       Impact factor: 3.162

9.  Survey in to the prevalence of hearing loss in patients diagnosed with retinitis pigmentosa.

Authors:  Satoshi Iwasaki; Yuuka Maruyama; Yoshihiro Hotta; Yasuyuki Hashimoto; Mitsuyoshi Nagura
Journal:  Int Ophthalmol       Date:  2006-03-07       Impact factor: 2.031

10.  CDH23 mutation and phenotype heterogeneity: a profile of 107 diverse families with Usher syndrome and nonsyndromic deafness.

Authors:  L M Astuto; J M Bork; M D Weston; J W Askew; R R Fields; D J Orten; S J Ohliger; S Riazuddin; R J Morell; S Khan; S Riazuddin; H Kremer; P van Hauwe; C G Moller; C W R J Cremers; C Ayuso; J R Heckenlively; K Rohrschneider; U Spandau; J Greenberg; R Ramesar; W Reardon; P Bitoun; J Millan; R Legge; T B Friedman; W J Kimberling
Journal:  Am J Hum Genet       Date:  2002-06-19       Impact factor: 11.025
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