(Q41561622)

3 October 2017

title

Inner ear anomalies in Waardenburg's syndrome associated with Hirschsprung's disease (English)

1 reference

3 October 2017

main subject

Waardenburg's syndrome

1 reference

K. E. Rarey

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6335502

1 October 2023

L. E. Davis

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6335502

1 October 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=6335502

1 October 2023

publication date

1 December 1984

1 reference

full work available at URL

3 October 2017

https://api.elsevier.com/content/article/PII:S0165587684800671?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

https://api.elsevier.com/content/article/PII:S0165587684800671?httpAccept=text/plain

1 October 2023

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

International Journal of Pediatric Otorhinolaryngology

1 October 2023

published in

1 reference

3 October 2017

volume

8

1 reference

3 October 2017

issue

2

1 reference

3 October 2017

page(s)

181-189

1 reference

Observations on the Histogenesis of the Inner Ear Degeneration of the Deaf White Cat and Its Possible Relationship to the Ætiology of Certain Unexplained Varieties of Human Congenital Deafness

3 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

Waardenburg's syndrome. A syndrome of heterochromia of the irides, lateral displacement of the medial canthi and lacrimal puncta, congenital deafness, and other characteristic associated defects

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

Deafness as part of an hereditary syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

The association of Waardenburg syndrome and Hirschsprung megacolon

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

Waardenburg's syndrome: a case report with CT scanning and cochleovestibular evaluation

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

White forelock, pigmentary disorder of irides, and long segment Hirschsprung disease: Possible variant of Waardenburg syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

Stria vascularis of deaf Hedlung mink. Light and electron microscopic studies of vascular insufficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0165-5876%2884%2980067-1

7 January 2021

Waardenburg's syndrome and Hirschsprung's disease in the same patient

6

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

Audiometric findings in 34 patients with Waardenburg's syndrome

1 October 2023

7

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

Vestibular Findings in 25 Patients With Waardenburg's Syndrome

1 October 2023

8

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

Congenital Deafness and Hirschsprung’s Disease

1 October 2023

13

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

The Migration and Differentiation of Neural Crest Cells

1 October 2023

19

1 reference

https://api.crossref.org/works/10.1016/S0165-5876(84)80067-1

1 October 2023

Identifiers

1 reference

3 October 2017

1 reference