A H Nemeth
Overview
Explore the profile of A H Nemeth including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
16
Citations
323
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Steventon J, Collett J, Furby H, Hamana K, Foster C, OCallaghan P, et al.
Parkinsonism Relat Disord
. 2018 Apr;
54:56-61.
PMID: 29705557
Background: Limited data suggests that an altered metabolic and cardiorespiratory exercise response may affect exercise performance in individuals with Huntington's disease (HD). There is no clear exploration of the response...
2.
Dawes H, Collett J, Debono K, Quinn L, Jones K, Kelson M, et al.
Clin Rehabil
. 2014 Aug;
29(2):196-206.
PMID: 25142278
Objective: To explore exercise response in people with Huntington's disease (HD). Design: Experimental observational study with a randomly allocated subgroup before/after interventional study. Setting: Community. Subjects: People with HD (n=30)...
3.
Webb T, Poulter M, Beck J, Uphill J, Adamson G, Campbell T, et al.
Brain
. 2008 Sep;
131(Pt 10):2632-46.
PMID: 18757886
The largest kindred with inherited prion disease P102L, historically Gerstmann-Sträussler-Scheinker syndrome, originates from central England, with émigrés now resident in various parts of the English-speaking world. We have collected data...
4.
Nemeth A, Gallen I, Crocker M, Levy E, Maher E
J Med Genet
. 2002 Jun;
39(6):E28.
PMID: 12070260
No abstract available.
5.
Rampoldi L, Dobson-Stone C, Rubio J, Danek A, Chalmers R, Wood N, et al.
Nat Genet
. 2001 May;
28(2):119-20.
PMID: 11381253
Chorea-acanthocytosis (CHAC, MIM 200150) is an autosomal recessive neurodegenerative disorder characterized by the gradual onset of hyperkinetic movements and abnormal erythrocyte morphology (acanthocytosis). Neurological findings closely resemble those observed in...
6.
Nemeth A, Bochukova E, Dunne E, Huson S, Elston J, Hannan M, et al.
Am J Hum Genet
. 2000 Oct;
67(5):1320-6.
PMID: 11022012
Ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome [AOA]; MIM 208920) is an autosomal recessive disorder characterized by ataxia, oculomotor apraxia, and choreoathetosis. These neurological features resemble those of ataxia-telangiectasia (AT), but...
7.
Muller U, Steinberger D, Nemeth A
Neurogenetics
. 2000 Mar;
1(3):165-77.
PMID: 10737119
Primary dystonias are movement disorders with dystonia as a major symptom. They are frequently inherited as Mendelian traits. There are at least eight clinically distinct autosomal dominant and two X-linked...
8.
Nemeth A, Mills K, Elston J, Williams A, Dunne E, Hyman N
Mov Disord
. 1999 Sep;
14(5):826-31.
PMID: 10495045
Gilles de la Tourette syndrome (TS) and idiopathic focal torsion dystonia are both movement disorders in which the pathologic process is thought to arise within the basal ganglia. However, despite...
9.
Nemeth A, Nolte D, Dunne E, Niemann S, Kostrzewa M, Peters U, et al.
Genomics
. 1999 Sep;
60(3):320-9.
PMID: 10493831
X-linked dystonia-parkinsonism (XDP) is a recessive disorder characterized by generalized dystonia with some patients exhibiting parkinsonism. The disease gene, DYT3, is located between DXS453 (DXS993) and DXS559, and strongest linkage...
10.
A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degeneration
Dunne E, Hyman N, Huson S, Nemeth A
Ann Neurol
. 1999 May;
45(5):652-5.
PMID: 10319888
X-linked adrenoleukodystrophy (ALD) usually presents in childhood as severe cerebral demyelination accompanied by axonal loss or in adults as a progressive spinal cord syndrome (adrenomyeloneuropathy). Rarely, patients present with adult...