Literature DB >> 5312273

Usher's syndrome, with special reference to heterozygous manifestations.

E B de Haas, G H van Lith, J Rijnders, A M Rümke, C Volmer.   

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Year:  1970        PMID: 5312273     DOI: 10.1007/BF00153876

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


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  21 in total

1.  [TAPETO-RETINAL DEGENERATION OF THE X CHROMOSOME TYPE IN THE NETHERLANDS].

Authors:  J SCHAPPERT-KIMMIJSER
Journal:  Bull Mem Soc Fr Ophtalmol       Date:  1963

2.  ON VARIOUS RECESSIVE BIOTYPES OF LEBER'S CONGENITAL AMAUROSIS.

Authors:  P J WAARDENBURG; J SCHAPPERT-KIMMIJSER
Journal:  Acta Ophthalmol (Copenh)       Date:  1963

3.  [Audiometric & electroencephalographic correlations in the course of tapetoretinal degeneration; concerning 22 cases: otoneuroretinal abiotrophy].

Authors:  C PERRIN
Journal:  Rev Laryngol Otol Rhinol (Bord)       Date:  1958 Sep-Oct

4.  The association of nerve deafness and retinitis pigmentosa. Interval report.

Authors:  F H MCGOVERN
Journal:  Ann Otol Rhinol Laryngol       Date:  1960-12       Impact factor: 1.547

5.  Vestibular function in deafness and severe hardness of hearing.

Authors:  J ARNVIG
Journal:  Acta Otolaryngol       Date:  1955 Jul-Aug       Impact factor: 1.494

6.  [Differential diagnostic significance of electroretinogram in tapeto-retinal degeneration].

Authors:  A FRANCESCHETTI; P DIETERLE
Journal:  Bibl Ophthalmol       Date:  1957

7.  Consanguinity and congenital deaf mutism in the Netherlands; are the parents of deaf children detectable as heterozygotes.

Authors:  L S WILDERVANCK
Journal:  Acta Genet Stat Med       Date:  1957

8.  Familial electroretinographic and adaptometric studies in retinitis pigmentosa.

Authors:  G GOODMAN; R D GUNKEL
Journal:  Am J Ophthalmol       Date:  1958-09       Impact factor: 5.258

9.  [Retinitis pigmentosa, symmetrical inner ear deafness, typical inverse vascular fistula symptom without fistula and vestibular sensitivity disease; combined hereditary ear and eye diseases].

Authors:  H H STENGER
Journal:  Arch Ohren Nasen Kehlkopfheilkd       Date:  1956

10.  Hereditary deaf mutism, with particular reference to Northern Ireland.

Authors:  A C STEVENSON; E A CHEESEMAN
Journal:  Ann Hum Genet       Date:  1956-02       Impact factor: 1.670

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  4 in total

1.  Dark adaptation testing in heterozygotes of Usher's syndrome.

Authors:  S Sondheimer; G A Fishman; R S Young; V A Vasquez
Journal:  Br J Ophthalmol       Date:  1979-08       Impact factor: 4.638

2.  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

3.  Peripheral Anomalies in USH2A Cause Central Auditory Anomalies in a Mouse Model of Usher Syndrome and CAPD.

Authors:  Peter A Perrino; Dianne F Newbury; R Holly Fitch
Journal:  Genes (Basel)       Date:  2021-01-24       Impact factor: 4.096

4.  A Novel Mouse Model of MYO7A USH1B Reveals Auditory and Visual System Haploinsufficiencies.

Authors:  Kaitlyn R Calabro; Sanford L Boye; Shreyasi Choudhury; Diego Fajardo; James J Peterson; Wei Li; Sean M Crosson; Mi-Jung Kim; Dalian Ding; Richard Salvi; Shinichi Someya; Shannon E Boye
Journal:  Front Neurosci       Date:  2019-11-22       Impact factor: 5.152

  4 in total

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