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...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखकों:	Steckley, J, Ebers, G, Cader, M, McLachlan, R
स्वरूप:	Journal article
भाषा:	English
प्रकाशित:	2001

समान संसाधन

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.
द्वारा: Cader, M, और अन्य
प्रकाशित: (2005)

Editorial: Vertigo, tinnitus, and cognition
द्वारा: Xingxing Lu, और अन्य
प्रकाशित: (2024-05-01)

Vestibular vertigo and ataxia in emergency neurology
द्वारा: Natalia Vladimirovna Aptikeeva, और अन्य
प्रकाशित: (2013-12-01)

Nilotinib treatment outcomes in autosomal dominant spinocerebellar ataxia over one year
द्वारा: Woo-Jin Lee, और अन्य
प्रकाशित: (2024-07-01)

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

Primary Episodic Ataxias
द्वारा: J Gordon Millichap
प्रकाशित: (2007-10-01)

Epigenetic editing for autosomal dominant neurological disorders
द्वारा: Jennifer J. Waldo, और अन्य
प्रकाशित: (2024-03-01)

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

Editorial: Advances in hearing loss, tinnitus, and vertigo: mechanisms and treatment
द्वारा: Lidong Zhao, और अन्य
प्रकाशित: (2024-01-01)

Ondansetron for intractable vertigo complicating acute brainstem disorders.
द्वारा: Rice, G, और अन्य
प्रकाशित: (1995)

Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita).
द्वारा: George, A, और अन्य
प्रकाशित: (1993)

Febrile Episodic Ataxia with Novel Mutation
द्वारा: J Gordon Millichap
प्रकाशित: (2004-01-01)

Unilateral Pulsatile Tinnitus and Intractable Vertigo as a Manifestation of Natural Gas Toxicity
द्वारा: Kyle W. Leonard, और अन्य
प्रकाशित: (2023-07-01)

LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder
द्वारा: James Chettle, और अन्य
प्रकाशित: (2024-10-01)

Linkage analysis of candidate loci in autosomal dominant myotonia congenita.
द्वारा: Abdalla, J, और अन्य
प्रकाशित: (1992)

Autosomal Dominant Alternating Hemiplegia
द्वारा: J Gordon Millichap
प्रकाशित: (1993-01-01)

Autosomal Dominant Partial Epilepsies
द्वारा: J Gordon Millichap
प्रकाशित: (2000-07-01)

Genes for autosomal recessive cerebellar ataxia: order from chaos?
द्वारा: Nemeth, A, और अन्य
प्रकाशित: (2001)

Autosomal dominant cerebellar ataxia type III: No evidence for a large pathological CAG repeat expansion in the SCA 11 gene.
द्वारा: Worth, P, और अन्य
प्रकाशित: (1999)

Prevalence of hearing loss, tinnitus, vertigo and sudden deafness among patients with polymyositis and dermatomyositis
द्वारा: Shih-Han Hung, और अन्य
प्रकाशित: (2024-03-01)

Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34.
द्वारा: Németh, A, और अन्य
प्रकाशित: (2000)

Autosomal Dominant Juvenile Amyotrophic LS
द्वारा: J Gordon Millichap
प्रकाशित: (1999-09-01)

Autosomal recessive spinocerebellar ataxia and peripheral neuropathy with raised alpha-fetoprotein.
द्वारा: Izatt, L, और अन्य
प्रकाशित: (2004)

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

Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34
द्वारा: Moreira, M, और अन्य
प्रकाशित: (2002)

R-Loops in proliferating cells but not in the brain : implications for AOA2 and other autosomal recessive ataxias
द्वारा: Yeo, Abrey J., और अन्य
प्रकाशित: (2014)

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy
द्वारा: Cansu de Muijnck, और अन्य
प्रकाशित: (2024-10-01)

Emergence of Venous Stenosis as the Dominant Cause of Pulsatile Tinnitus
द्वारा: Eytan Raz, और अन्य
प्रकाशित: (2022-07-01)

Autosomal recessive cerebellar ataxias: a diagnostic classification approach according to ocular features
द्वारा: Diego Lopergolo, और अन्य
प्रकाशित: (2024-02-01)

Estudo da possível associação entre zumbido e vertigem Study of possible relationship between tinnitus and vertigo
द्वारा: Poliana Palussio Vieira, और अन्य
प्रकाशित: (2010-08-01)

Autosomal dominant susceptibility to tuberculosis in a multi-case pedigree.
द्वारा: Campbell, S, और अन्य
प्रकाशित: (2001)

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

Echocardiographic characteristics of autosomal dominant polycystic kidney disease
द्वारा: Agata Koska-Ścigała, और अन्य
प्रकाशित: (2024-12-01)

Genotype-Phenotype Correlations in Autosomal Dominant Osteogenesis Imperfecta
द्वारा: I. Mouna Ben Amor, और अन्य
प्रकाशित: (2011-01-01)

PTH infusion for seizures in autosomal dominant hypocalcemia type 1
द्वारा: Sastre, A, और अन्य
प्रकाशित: (2021)

Autosomal Recessive Spastic Ataxia of Charlevoix–Saguenay Secondary to a Novel Mutation in the SACS Gene
द्वारा: Akhil Sahib, और अन्य
प्रकाशित: (2024-10-01)

Clinical and genetic variability among Bulgarian patients with autosomal recessive spastic ataxia of Charlevoix–Saguenay
द्वारा: Teodora Chamova, और अन्य
प्रकाशित: (2024-07-01)

Compound heterozygous mutation of the SNX14 gene causes autosomal recessive spinocerebellar ataxia 20
द्वारा: Yuqi Shao, और अन्य
प्रकाशित: (2024-04-01)

Teaching NeuroImages: Headache with pulsatile tinnitus.
द्वारा: Armstrong, R, और अन्य
प्रकाशित: (2011)

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