An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.

The authors report an autosomal dominant episodic ataxia that is clinically distinct from the other episodic ataxias. Vestibular ataxia, vertigo, tinnitus, and interictal myokymia are prominent; attacks are diminished by acetazolamide. Linkage analyses of markers flanking the EA1 and EA2 loci demons...

Descrizione completa

Dettagli Bibliografici
Autori principali:	Steckley, J, Ebers, G, Cader, M, McLachlan, R
Natura:	Journal article
Lingua:	English
Pubblicazione:	2001

Documenti analoghi

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
di: Cader, M, et al.
Pubblicazione: (2005)

Editorial: Vertigo, tinnitus, and cognition
di: Xingxing Lu, et al.
Pubblicazione: (2024-05-01)

Vestibular vertigo and ataxia in emergency neurology
di: Natalia Vladimirovna Aptikeeva, et al.
Pubblicazione: (2013-12-01)

Nilotinib treatment outcomes in autosomal dominant spinocerebellar ataxia over one year
di: Woo-Jin Lee, et al.
Pubblicazione: (2024-07-01)

Clinical Phenotypes of Autosomal Recessive Ataxias
di: J Gordon Millichap
Pubblicazione: (2007-05-01)

Primary Episodic Ataxias
di: J Gordon Millichap
Pubblicazione: (2007-10-01)

Epigenetic editing for autosomal dominant neurological disorders
di: Jennifer J. Waldo, et al.
Pubblicazione: (2024-03-01)

Incidence of Hearing Loss, Tinnitus and Vertigo among Diabetes Patients
di: Rabindra N. Padhy
Pubblicazione: (2014-11-01)

Editorial: Advances in hearing loss, tinnitus, and vertigo: mechanisms and treatment
di: Lidong Zhao, et al.
Pubblicazione: (2024-01-01)

Ondansetron for intractable vertigo complicating acute brainstem disorders.
di: Rice, G, et al.
Pubblicazione: (1995)

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
di: George, A, et al.
Pubblicazione: (1993)

Febrile Episodic Ataxia with Novel Mutation
di: J Gordon Millichap
Pubblicazione: (2004-01-01)

Unilateral Pulsatile Tinnitus and Intractable Vertigo as a Manifestation of Natural Gas Toxicity
di: Kyle W. Leonard, et al.
Pubblicazione: (2023-07-01)

LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder
di: James Chettle, et al.
Pubblicazione: (2024-10-01)

Linkage analysis of candidate loci in autosomal dominant myotonia congenita.
di: Abdalla, J, et al.
Pubblicazione: (1992)

Autosomal Dominant Alternating Hemiplegia
di: J Gordon Millichap
Pubblicazione: (1993-01-01)

Autosomal Dominant Partial Epilepsies
di: J Gordon Millichap
Pubblicazione: (2000-07-01)

Genes for autosomal recessive cerebellar ataxia: order from chaos?
di: Nemeth, A, et al.
Pubblicazione: (2001)

Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene.
di: Worth, P, et al.
Pubblicazione: (1999)

Prevalence of hearing loss, tinnitus, vertigo and sudden deafness among patients with polymyositis and dermatomyositis
di: Shih-Han Hung, et al.
Pubblicazione: (2024-03-01)

Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34.
di: Németh, A, et al.
Pubblicazione: (2000)

Autosomal Dominant Juvenile Amyotrophic LS
di: J Gordon Millichap
Pubblicazione: (1999-09-01)

Autosomal recessive spinocerebellar ataxia and peripheral neuropathy with raised alpha-fetoprotein.
di: Izatt, L, et al.
Pubblicazione: (2004)

Autosomal Dominant Partial Epilepsy with Auditory Features
di: J Gordon Millichap
Pubblicazione: (2009-01-01)

Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34
di: Moreira, M, et al.
Pubblicazione: (2002)

R-Loops in proliferating cells but not in the brain : implications for AOA2 and other autosomal recessive ataxias
di: Yeo, Abrey J., et al.
Pubblicazione: (2014)

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy
di: Cansu de Muijnck, et al.
Pubblicazione: (2024-10-01)

Emergence of Venous Stenosis as the Dominant Cause of Pulsatile Tinnitus
di: Eytan Raz, et al.
Pubblicazione: (2022-07-01)

Autosomal recessive cerebellar ataxias: a diagnostic classification approach according to ocular features
di: Diego Lopergolo, et al.
Pubblicazione: (2024-02-01)

Estudo da possível associação entre zumbido e vertigem Study of possible relationship between tinnitus and vertigo
di: Poliana Palussio Vieira, et al.
Pubblicazione: (2010-08-01)

Autosomal dominant susceptibility to tuberculosis in a multi-case pedigree.
di: Campbell, S, et al.
Pubblicazione: (2001)

Intracranial aneurysms in autosomal dominant polycystic kidney disease
di: Jung Hyun Park
Pubblicazione: (2024-12-01)

Echocardiographic characteristics of autosomal dominant polycystic kidney disease
di: Agata Koska-Ścigała, et al.
Pubblicazione: (2024-12-01)

Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta
di: I. Mouna Ben Amor, et al.
Pubblicazione: (2011-01-01)

PTH infusion for seizures in autosomal dominant hypocalcemia type 1
di: Sastre, A, et al.
Pubblicazione: (2021)

Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay Secondary to a Novel Mutation in the SACS Gene
di: Akhil Sahib, et al.
Pubblicazione: (2024-10-01)

Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix–Saguenay
di: Teodora Chamova, et al.
Pubblicazione: (2024-07-01)

Compound heterozygous mutation of the SNX14 gene causes autosomal recessive spinocerebellar ataxia 20
di: Yuqi Shao, et al.
Pubblicazione: (2024-04-01)

Teaching NeuroImages: Headache with pulsatile tinnitus.
di: Armstrong, R, et al.
Pubblicazione: (2011)

Genetics of Autosomal Dominant Partial Epilepsy with Auditory Features (ADPEAF)
di: J Gordon Millichap
Pubblicazione: (2008-09-01)