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THE RELATIONSHIP BETWEEN STRIATAL DOPAMINE-RECEPTOR BINDING AND COGNITIVE PERFORMANCE IN HUNTINGTONS-DISEASE
Authors: LAWRENCE AD WEEKS RA BROOKS DJ ANDREWS TC WATKINS LHA HARDING AE ROBBINS TW SAHAKIAN BJ
Citation: Ad. Lawrence et al., THE RELATIONSHIP BETWEEN STRIATAL DOPAMINE-RECEPTOR BINDING AND COGNITIVE PERFORMANCE IN HUNTINGTONS-DISEASE, Brain (Print), 121, 1998, pp. 1343-1355
INFLUENCE OF VISION ON UPPER-LIMB REACHING MOVEMENTS IN PATIENTS WITHCEREBELLAR-ATAXIA
Authors: DAY BL THOMPSON PD HARDING AE MARSDEN CD
Citation: Bl. Day et al., INFLUENCE OF VISION ON UPPER-LIMB REACHING MOVEMENTS IN PATIENTS WITHCEREBELLAR-ATAXIA, Brain, 121, 1998, pp. 357-372
CLINICAL AND LABORATORY FINDINGS IN REFERRALS FOR MITOCHONDRIAL-DNA ANALYSIS
Authors: LAMONT PJ SURTEES R WOODWARD CE LEONARD JV WOOD NW HARDING AE
Citation: Pj. Lamont et al., CLINICAL AND LABORATORY FINDINGS IN REFERRALS FOR MITOCHONDRIAL-DNA ANALYSIS, Archives of Disease in Childhood, 79(1), 1998, pp. 22-27
CEREBELLAR PRESENTATION OF MULTIPLE SYSTEM ATROPHY
Authors: WENNING GK KRAFT E BECK R FOWLER CJ MATHIAS CJ QUINN NP HARDING AE
Citation: Gk. Wenning et al., CEREBELLAR PRESENTATION OF MULTIPLE SYSTEM ATROPHY, Movement disorders, 12(1), 1997, pp. 115-117
DEPLETION OF MITOCHONDRIAL-DNA BY DDC IN UNTRANSFORMED HUMAN CELL-LINES
Authors: NELSON I HANNA MG WOOD NW HARDING AE
Citation: I. Nelson et al., DEPLETION OF MITOCHONDRIAL-DNA BY DDC IN UNTRANSFORMED HUMAN CELL-LINES, Somatic cell and molecular genetics, 23(4), 1997, pp. 287-290
C-11 DIPRENORPHINE BINDING IN HUNTINGTONS-DISEASE - A COMPARISON OF REGION OF INTEREST ANALYSIS WITH STATISTICAL PARAMETRIC MAPPING
Authors: WEEKS RA CUNNINGHAM VJ PICCINI P WATERS S HARDING AE BROOKS DJ
Citation: Ra. Weeks et al., C-11 DIPRENORPHINE BINDING IN HUNTINGTONS-DISEASE - A COMPARISON OF REGION OF INTEREST ANALYSIS WITH STATISTICAL PARAMETRIC MAPPING, Journal of cerebral blood flow and metabolism, 17(9), 1997, pp. 943-949
A MITOCHONDRIAL-DNA TRNA(VAL) POINT MUTATION ASSOCIATED WITH ADULT-ONSET LEIGH-SYNDROME
Authors: CHALMERS RM LAMONT PJ NELSON I ELLISON DW THOMAS NH HARDING AE HAMMANS SR
Citation: Rm. Chalmers et al., A MITOCHONDRIAL-DNA TRNA(VAL) POINT MUTATION ASSOCIATED WITH ADULT-ONSET LEIGH-SYNDROME, Neurology, 49(2), 1997, pp. 589-592
EVALUATION OF 4 CANDIDATE GENES ENCODING PROTEINS OF THE DOPAMINE PATHWAY IN FAMILIAL AND SPORADIC PARKINSONS-DISEASE - EVIDENCE FOR ASSOCIATION OF A DRD2-ALLELE
Authors: PLANTEBORDENEUVE V TAUSSIG D THOMAS F SAID G WOOD NW MARSDEN CD HARDING AE
Citation: V. Plantebordeneuve et al., EVALUATION OF 4 CANDIDATE GENES ENCODING PROTEINS OF THE DOPAMINE PATHWAY IN FAMILIAL AND SPORADIC PARKINSONS-DISEASE - EVIDENCE FOR ASSOCIATION OF A DRD2-ALLELE, Neurology, 48(6), 1997, pp. 1589-1593
SPINAL AND CUTANEOUS SCHWANNOMATOSIS IS A VARIANT FORM OF TYPE-2 NEUROFIBROMATOSIS - A CLINICAL AND MOLECULAR STUDY
Authors: EVANS DGR MASON S HUSON SM PONDER M HARDING AE STRACHAN T
Citation: Dgr. Evans et al., SPINAL AND CUTANEOUS SCHWANNOMATOSIS IS A VARIANT FORM OF TYPE-2 NEUROFIBROMATOSIS - A CLINICAL AND MOLECULAR STUDY, Journal of Neurology, Neurosurgery and Psychiatry, 62(4), 1997, pp. 361-366
CORTICAL CONTROL OF MOVEMENT IN HUNTINGTONS-DISEASE - A PET ACTIVATION STUDY
Authors: WEEKS RA CEBALLOSBAUMANN A PICCINI P BOECKER H HARDING AE BROOKS DJ
Citation: Ra. Weeks et al., CORTICAL CONTROL OF MOVEMENT IN HUNTINGTONS-DISEASE - A PET ACTIVATION STUDY, Brain, 120, 1997, pp. 1569-1578
THE PHENOTYPIC MANIFESTATIONS OF CHROMOSOME 17P11.2 DUPLICATION
Authors: THOMAS PK MARQUES W DAVIS MB SWEENEY MG KING RHM BRADLEY JL MUDDLE JR TYSON J MALCOLM S HARDING AE
Citation: Pk. Thomas et al., THE PHENOTYPIC MANIFESTATIONS OF CHROMOSOME 17P11.2 DUPLICATION, Brain, 120, 1997, pp. 465-478
HEREDITARY DEMYELINATING NEUROPATHY OF INFANCY - A GENETICALLY COMPLEX SYNDROME
Authors: TYSON J ELLIS D FAIRBROTHER U KING RHM MUNTONI F JACOBS J MALCOLM S HARDING AE THOMAS PK
Citation: J. Tyson et al., HEREDITARY DEMYELINATING NEUROPATHY OF INFANCY - A GENETICALLY COMPLEX SYNDROME, Brain, 120, 1997, pp. 47-63
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 MARSDEN CD WOOD NW HARDING AE
Citation: O. Bandmann et al., DOPA-RESPONSIVE DYSTONIA IN BRITISH PATIENTS - NEW MUTATIONS OF THE GTP-CYCLOHYDROLASE-I GENE AND EVIDENCE FOR GENETIC-HETEROGENEITY, Human molecular genetics, 5(3), 1996, pp. 403-406
PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN HUNTINGTONS-DISEASE - EVIDENCE IN FAVOR OF THE GLUTAMATE EXCITOTOXIC THEORY
Authors: TAYLORROBINSON SD WEEKS RA BRYANT DJ SARGENTONI J MARCUS CD HARDING AE BROOKS DJ
Citation: Sd. Taylorrobinson et al., PROTON MAGNETIC-RESONANCE SPECTROSCOPY IN HUNTINGTONS-DISEASE - EVIDENCE IN FAVOR OF THE GLUTAMATE EXCITOTOXIC THEORY, Movement disorders, 11(2), 1996, pp. 167-173
ASSOCIATIVE LEARNING IN PATIENTS WITH CEREBELLAR-ATAXIA
Authors: TUCKER J HARDING AE JAHANSHAHI M NIXON PD RUSHWORTH M QUINN NP THOMPSON PD PASSINGHAM RE
Citation: J. Tucker et al., ASSOCIATIVE LEARNING IN PATIENTS WITH CEREBELLAR-ATAXIA, Behavioral neuroscience, 110(6), 1996, pp. 1229-1234
EXCLUSION OF THE DYT1 LOCUS IN FAMILIAL TORTICOLLIS
Authors: BRESSMAN SB WARNER TT ALMASY L UITTI RJ GREEN PE HEIMAN GA RAYMOND D FORD B DELEON D FAHN S KRAMER PL RISCH NJ MARAGANORE DM NYGAARD TG HARDING AE
Citation: Sb. Bressman et al., EXCLUSION OF THE DYT1 LOCUS IN FAMILIAL TORTICOLLIS, Annals of neurology, 40(4), 1996, pp. 681-684
SEQUENCE OF MITOCHONDRIAL-DNA IN PATIENTS WITH MULTIPLE-SCLEROSIS
Authors: CHALMERS RM ROBERTSON N COMPSTON DAS HARDING AE
Citation: Rm. Chalmers et al., SEQUENCE OF MITOCHONDRIAL-DNA IN PATIENTS WITH MULTIPLE-SCLEROSIS, Annals of neurology, 40(2), 1996, pp. 239-243
DEFICIENCY OF RESPIRATORY-CHAIN COMPLEX-I IS A COMMON-CAUSE OF LEIGH-DISEASE
Authors: MORRIS AAM LEONARD IV BROWN GK BIDOUKI SK BINDOFF LA WOODWARD CE HARDING AE LAKE BD HARDING BN FARRELL MA BELL JE MIRAKHUR M TURNBULL DM
Citation: Aam. Morris et al., DEFICIENCY OF RESPIRATORY-CHAIN COMPLEX-I IS A COMMON-CAUSE OF LEIGH-DISEASE, Annals of neurology, 40(1), 1996, pp. 25-30
STRIATAL D1 AND D2 DOPAMINE-RECEPTOR LOSS IN ASYMPTOMATIC MUTATION CARRIERS OF HUNTINGTONS-DISEASE
Authors: WEEKS RA PICCINI P HARDING AE BROOKS DJ
Citation: Ra. Weeks et al., STRIATAL D1 AND D2 DOPAMINE-RECEPTOR LOSS IN ASYMPTOMATIC MUTATION CARRIERS OF HUNTINGTONS-DISEASE, Annals of neurology, 40(1), 1996, pp. 49-54
A NOVEL POINT MUTATION IN THE MCLEOD SYNDROME GENE IN NEUROACANTHOCYTOSIS
Authors: HO MF CHALMER RM DAVIS MB HARDING AE MONACO AP
Citation: Mf. Ho et al., A NOVEL POINT MUTATION IN THE MCLEOD SYNDROME GENE IN NEUROACANTHOCYTOSIS, Annals of neurology, 39(5), 1996, pp. 672-675
DELETIONS OF CHROMOSOME 17P11.2 IN MULTIFOCAL NEUROPATHIES
Authors: TYSON J MALCOLM S THOMAS PK HARDING AE
Citation: J. Tyson et al., DELETIONS OF CHROMOSOME 17P11.2 IN MULTIFOCAL NEUROPATHIES, Annals of neurology, 39(2), 1996, pp. 180-186
ANTICIPATION IN FAMILIAL PARKINSONS-DISEASE - A REANALYSIS OF 13 UNITED-KINGDOM KINDREDS
Authors: MARAGANORE DM SCHAID DJ ROCCA WA HARDING AE
Citation: Dm. Maraganore et al., ANTICIPATION IN FAMILIAL PARKINSONS-DISEASE - A REANALYSIS OF 13 UNITED-KINGDOM KINDREDS, Neurology, 47(6), 1996, pp. 1512-1517
THE RELATIONSHIP BETWEEN STRIATAL DOPAMINE STATUS AND COGNITIVE PERFORMANCE IN ASYMPTOMATIC MUTATION CARRIERS OF HUNTINGTONS-DISEASE
Authors: WEEKS RA LAWRENCE AD SAHAKIAN BJ HARDING AE ROBBINS TW BROOKS DJ
Citation: Ra. Weeks et al., THE RELATIONSHIP BETWEEN STRIATAL DOPAMINE STATUS AND COGNITIVE PERFORMANCE IN ASYMPTOMATIC MUTATION CARRIERS OF HUNTINGTONS-DISEASE, Neurology, 46(2), 1996, pp. 40003-40003
MITOCHONDRIAL ENCEPHALOPATHY WITH MULTIPLE MITOCHONDRIAL-DNA DELETIONS - A REPORT OF 2 FAMILIES AND 2 SPORADIC CASES WITH UNUSUAL CLINICAL AND NEUROPATHOLOGICAL FEATURES
Authors: CHALMERS RM BROCKINGTON M HOWARD RS LECKY BRF MORGANHUGHES JA HARDING AE
Citation: Rm. Chalmers et al., MITOCHONDRIAL ENCEPHALOPATHY WITH MULTIPLE MITOCHONDRIAL-DNA DELETIONS - A REPORT OF 2 FAMILIES AND 2 SPORADIC CASES WITH UNUSUAL CLINICAL AND NEUROPATHOLOGICAL FEATURES, Journal of the neurological sciences, 143(1-2), 1996, pp. 41-45
THE CTP-CYCLOHYDROLASE-I GENE IN ATYPICAL PARKINSONIAN-PATIENTS - A CLINICOGENETIC STUDY
Authors: BANDMANN O DANIEL S MARSDEN CD WOOD NW HARDING AE
Citation: O. Bandmann et al., THE CTP-CYCLOHYDROLASE-I GENE IN ATYPICAL PARKINSONIAN-PATIENTS - A CLINICOGENETIC STUDY, Journal of the neurological sciences, 141(1-2), 1996, pp. 27-32
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