Search Results - "Harding AE"

The relationship between striatal dopamine receptor binding and cognitive performance in Huntington's disease.

Authors: Lawrence AD Weeks RA Brooks DJ et al.

Source: Brain : a journal of neurology [Brain] 1998 Jul; Vol. 121 ( Pt 7), pp. 1343-55.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Print ISSN: 0006-8950 (Print) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Influence of vision on upper limb reaching movements in patients with cerebellar ataxia.

Authors: Day BL Thompson PD Harding AE et al.

Source: Brain : a journal of neurology [Brain] 1998 Feb; Vol. 121 ( Pt 2), pp. 357-72.

Publication Type: Comparative Study; Journal Article

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Print ISSN: 0006-8950 (Print) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Cortical control of movement in Huntington's disease. A PET activation study.

Authors: Weeks RA Ceballos-Baumann A Piccini P et al.

Source: Brain : a journal of neurology [Brain] 1997 Sep; Vol. 120 ( Pt 9), pp. 1569-78.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Print ISSN: 0006-8950 (Print) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

The phenotypic manifestations of chromosome 17p11.2 duplication.

Authors: Thomas PK Marques W Jr Davis MB et al.

Source: Brain : a journal of neurology [Brain] 1997 Mar; Vol. 120 ( Pt 3), pp. 465-78.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Print ISSN: 0006-8950 (Print) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Hereditary demyelinating neuropathy of infancy. A genetically complex syndrome.

Authors: Tyson J Ellis D Fairbrother U et al.

Source: Brain : a journal of neurology [Brain] 1997 Jan; Vol. 120 ( Pt 1), pp. 47-63.

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Print ISSN: 0006-8950 (Print) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

A case-control study of Leber's hereditary optic neuropathy.

Authors: Charlmers RM Harding AE

Source: Brain : a journal of neurology [Brain] 1996 Oct; Vol. 119 ( Pt 5), pp. 1481-6.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Print ISSN: 0006-8950 (Print) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

Dopa-responsive dystonia in British patients: new mutations of the GTP-cyclohydrolase I gene and evidence for genetic heterogeneity.

Authors: Bandmann O Nygaard TG Surtees R et al.

Source: Human molecular genetics [Hum Mol Genet] 1996 Mar; Vol. 5 (3), pp. 403-6.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Print ISSN: 0964-6906 (Print) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

Mutation analysis in patients with possible but apparently sporadic Huntington's disease.

Authors: Davis MB Bateman D Quinn NP et al.

Source: Lancet (London, England) [Lancet] 1994 Sep 10; Vol. 344 (8924), pp. 714-7.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 2985213R Publication Model: Print Cited Medium: Print ISSN: 0140-6736 (Print) Linking ISSN: 01406736 NLM ISO Abbreviation: Lancet Subsets: MEDLINE

Evidence for glutamate excitotoxicity in Huntington's disease with proton magnetic resonance spectroscopy.

Authors: Taylor-Robinson SD Weeks RA Sargentoni J et al.

Source: Lancet (London, England) [Lancet] 1994 May 07; Vol. 343 (8906), pp. 1170.

Publication Type: Letter

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 2985213R Publication Model: Print Cited Medium: Print ISSN: 0140-6736 (Print) Linking ISSN: 01406736 NLM ISO Abbreviation: Lancet Subsets: MEDLINE

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA.

Authors: Reardon W Ross RJ Sweeney MG et al.

Source: Lancet (London, England) [Lancet] 1992 Dec 05; Vol. 340 (8832), pp. 1376-9.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 2985213R Publication Model: Print Cited Medium: Print ISSN: 0140-6736 (Print) Linking ISSN: 01406736 NLM ISO Abbreviation: Lancet Subsets: MEDLINE

Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease.

Authors: Smith CA Gough AC Leigh PN et al.

Source: Lancet (London, England) [Lancet] 1992 Jun 06; Vol. 339 (8806), pp. 1375-7.

Publication Type: Journal Article

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 2985213R Publication Model: Print Cited Medium: Print ISSN: 0140-6736 (Print) Linking ISSN: 01406736 NLM ISO Abbreviation: Lancet Subsets: MEDLINE

Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples.

Authors: Hammans SR Sweeney MG Brockington M et al.

Source: Lancet (London, England) [Lancet] 1991 Jun 01; Vol. 337 (8753), pp. 1311-3.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Elsevier Country of Publication: England NLM ID: 2985213R Publication Model: Print Cited Medium: Print ISSN: 0140-6736 (Print) Linking ISSN: 01406736 NLM ISO Abbreviation: Lancet Subsets: MEDLINE

Clinical and laboratory findings in referrals for mitochondrial DNA analysis.

Authors: Lamont PJ Surtees R Woodward CE et al.

Source: Archives of disease in childhood [Arch Dis Child] 1998 Jul; Vol. 79 (1), pp. 22-7.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: BMJ Pub. Group [etc.] Country of Publication: England NLM ID: 0372434 Publication Model: Print Cited Medium: Internet ISSN: 1468-2044 (Electronic) Linking ISSN: 00039888 NLM ISO Abbreviation: Arch Dis Child Subsets: MEDLINE

11C-diprenorphine binding in Huntington's disease: a comparison of region of interest analysis with statistical parametric mapping.

Authors: Weeks RA Cunningham VJ Piccini P et al.

Source: Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism [J Cereb Blood Flow Metab] 1997 Sep; Vol. 17 (9), pp. 943-9.

Publication Type: Journal Article

Journal Info: Publisher: SAGE Publications Country of Publication: United States NLM ID: 8112566 Publication Model: Print Cited Medium: Print ISSN: 0271-678X (Print) Linking ISSN: 0271678X NLM ISO Abbreviation: J Cereb Blood Flow Metab Subsets: MEDLINE

A mitochondrial DNA tRNA(Val) point mutation associated with adult-onset Leigh syndrome.

Authors: Chalmers RM Lamont PJ Nelson I et al.

Source: Neurology [Neurology] 1997 Aug; Vol. 49 (2), pp. 589-92.

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Print ISSN: 0028-3878 (Print) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE

Depletion of mitochondrial DNA by ddC in untransformed human cell lines.

Authors: Nelson I Hanna MG Wood NW et al.

Source: Somatic cell and molecular genetics [Somat Cell Mol Genet] 1997 Jul; Vol. 23 (4), pp. 287-90.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Kluwer Academic/Plenum Publishers Country of Publication: United States NLM ID: 8403568 Publication Model: Print Cited Medium: Print ISSN: 0740-7750 (Print) Linking ISSN: 07407750 NLM ISO Abbreviation: Somat Cell Mol Genet Subsets: MEDLINE

Evaluation of four candidate genes encoding proteins of the dopamine pathway in familial and sporadic Parkinson's disease: evidence for association of a DRD2 allele.

Authors: Planté-Bordeneuve V Taussig D Thomas F et al.

Source: Neurology [Neurology] 1997 Jun; Vol. 48 (6), pp. 1589-93.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Print ISSN: 0028-3878 (Print) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE

Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular study.

Authors: Evans DG Mason S Huson SM et al.

Source: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 1997 Apr; Vol. 62 (4), pp. 361-6.

Publication Type: Case Reports; Journal Article

Journal Info: Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 2985191R Publication Model: Print Cited Medium: Print ISSN: 0022-3050 (Print) Linking ISSN: 00223050 NLM ISO Abbreviation: J Neurol Neurosurg Psychiatry Subsets: MEDLINE

Cerebellar presentation of multiple system atrophy.

Authors: Wenning GK Kraft E Beck R et al.

Source: Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 1997 Jan; Vol. 12 (1), pp. 115-7.

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

Journal Info: Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8610688 Publication Model: Print Cited Medium: Print ISSN: 0885-3185 (Print) Linking ISSN: 08853185 NLM ISO Abbreviation: Mov Disord Subsets: MEDLINE

Anticipation in familial Parkinson's disease: a reanalysis of 13 United Kingdom kindreds.

Authors: Maraganore DM Schaid DJ Rocca WA et al.

Source: Neurology [Neurology] 1996 Dec; Vol. 47 (6), pp. 1512-7.

Publication Type: Journal Article

Journal Info: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Print ISSN: 0028-3878 (Print) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE