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    1. Valente, EM; Bentivoglio, AR; Cassetta, E; Dixon, PH; Davis, MB; Ferraris, A; Ialongo, T; Frontali, M; Wood, NW; Albanese, A
      Identification of a novel primary torsion dystonia loons (DYT13) on chromosome 1p36 in an Italian family with cranial-cervical or upper limb onset

      NEUROLOGICAL SCIENCES
    2. Rampoldi, L; Dobson-Stone, C; Rubio, JP; Danek, A; Chalmers, RM; Wood, NW; Verellen, C; Ferrer, X; Malandrini, A; Fabrizi, GM; Brown, R; Vance, J; Pericak-Vance, M; Rudolf, G; Carre, S; Alonso, E; Manfredi, M; Nemeth, AH; Monaco, AP
      A conserved sorting-associated protein is mutant in chorea-acanthocytosis

      NATURE GENETICS
    3. Sheen, VL; Dixon, PH; Fox, JW; Hong, SE; Kinton, L; Sisodiya, SM; Duncan, JS; Dubeau, F; Scheffer, IE; Schachter, SC; Wilner, A; Henchy, R; Crino, P; Kamuro, K; DiMario, F; Berg, M; Kuzniecky, R; Cole, AJ; Bromfield, E; Biber, M; Schomer, D; Wheless, J; Silver, K; Mochida, GH; Berkovic, SF; Andermann, F; Andermann, E; Dobyns, WB; Wood, NW; Walsh, CA
      Mutations in the X-linked filamin 1 gene cause periventricular nodular heterotopia in males as well as in females

      HUMAN MOLECULAR GENETICS
    4. Houlden, H; King, RHM; Hashemi-Nejad, A; Wood, NW; Mathias, CJ; Reilly, M; Thomas, PK
      A novel TRK A (NTRK1) mutation associated with hereditary sensory and autonomic neuropathy type V

      ANNALS OF NEUROLOGY
    5. Valente, EM; Bentivoglio, AR; Cassetta, E; Dixon, PH; Davis, MB; Ferraris, A; Ialongo, T; Frontali, M; Wood, NW; Albanese, A
      DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13-36.32 in an Italian family with cranial cervical or upper limb onset

      ANNALS OF NEUROLOGY
    6. Morris, HR; Schrag, A; Nath, U; Burn, D; Quinn, NP; Daniel, S; Wood, NW; Lees, AJ
      Effect of ApoE and tau on age of onset of progressive supranuclear palsy and multiple system atrophy

      NEUROSCIENCE LETTERS
    7. de Silva, R; Weiler, M; Morris, HR; Martin, ER; Wood, NW; Lees, AJ
      Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

      NEUROSCIENCE LETTERS
    8. Bandopadhyay, R; de Silva, R; Khan, N; Graham, E; Vaughan, J; Engelender, S; Ross, C; Morris, H; Morris, C; Wood, NW; Daniel, S; Lees, A
      No pathogenic mutations in the synphilin-1 gene in Parkinson's disease

      NEUROSCIENCE LETTERS
    9. Patel, H; Hart, PE; Warner, T; Allen, I; Phillimore, HE; Silver, JR; Wood, NW; Jeffery, S; Patton, MA; Crosby, AH
      Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci

      AMERICAN JOURNAL OF MEDICAL GENETICS
    10. Bird, TD; Jarvik, GP; Wood, NW
      Genetic association studies - Genes in search of diseases

      NEUROLOGY
    11. Davenport, WJ; Siegel, AM; Dichgans, J; Drigo, P; Mammi, I; Pereda, P; Wood, NW; Rouleau, GA
      CCM1 gene mutations in families segregating cerebral cavernous malformations

      NEUROLOGY
    12. Worth, PF; Wood, NW
      Spinocerebellar ataxia type 12 is rare in the United Kingdom

      NEUROLOGY
    13. Houlden, H; Baker, M; Morris, HR; MacDonald, N; Pickering-Brown, S; Adamson, J; Lees, AJ; Rossor, MN; Quinn, NP; Kertesz, A; Khan, MN; Hardy, J; Lantos, PL; George-Hyslop, PS; Munoz, DG; Mann, D; Lang, AE; Bergeron, C; Bigio, EH; Litvan, I; Bhatia, KP; Dickson, D; Wood, NW; Hutton, M
      Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

      NEUROLOGY
    14. Placzek, MR; Misbahuddin, A; Chaudhuri, KR; Wood, NW; Bhatia, KP; Warner, TT
      Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    15. Nath, U; Ben-Shlomo, Y; Thomson, RG; Morris, HR; Wood, NW; Lees, AJ; Burn, DJ
      The prevalence of progressive supranuclear palsy (Steele-Richardson-Olszewski syndrome) in the UK

      BRAIN
    16. Houlden, H; King, RHM; Wood, NW; Thomas, PK; Reilly, MM
      Mutations in the 5 ' region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin

      BRAIN
    17. Morris, HR; Al-Sarraj, S; Schwab, C; Gwinn-Hardy, K; Perez-Tur, J; Wood, NW; Hardy, J; Lees, AJ; McGeer, PL; Daniel, SE; Steele, JC
      A clinical and pathological study of motor neurone disease on Guam

      BRAIN
    18. Morris, HR; Khan, MN; Janssen, JC; Brown, JM; Perez-Tur, J; Baker, M; Ozansoy, M; Hardy, J; Hutton, M; Wood, NW; Lees, AJ; Revesz, T; Lantos, P; Rossor, MN
      The genetic and pathological classification of familial frontotemporal dementia

      ARCHIVES OF NEUROLOGY
    19. Vaughan, JR; Davis, MB; Wood, NW
      Genetics of Parkinsonism: a review

      ANNALS OF HUMAN GENETICS
    20. Holton, JL; Ghiso, J; Lashley, T; Rostagno, A; Guerin, CJ; Gibb, G; Houlden, H; Ayling, H; Martinian, L; Anderton, BH; Wood, NW; Vidal, R; Plant, G; Frangione, B; Revesz, T
      Regional distribution of amyloid-Bri deposition and its association with neurofibrillary degeneration in familial British dementia

      AMERICAN JOURNAL OF PATHOLOGY
    21. Valente, EM; Bentivoglio, AR; Dixon, PH; Ferraris, A; Ialongo, T; Frontali, M; Albanese, A; Wood, NW
      Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

      AMERICAN JOURNAL OF HUMAN GENETICS
    22. Periquet, M; Lucking, CB; Vaughan, JR; Bonifati, V; Durr, A; De Michele, G; Horstink, MW; Farrer, M; Illarioshkin, SN; Pollak, P; Borg, M; Brefel-Courbon, C; Denefle, P; Meco, G; Gasser, T; Breteler, MMB; Wood, NW; Agid, Y; Brice, A
      Origin of the mutations in the parkin gene in europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects

      AMERICAN JOURNAL OF HUMAN GENETICS
    23. Zhang, J; Hattori, N; Leroy, E; Morris, HR; Kubo, SI; Kobayashi, T; Wood, NW; Polymeropoulos, MH; Mizuno, Y
      Association between a polymorphism of ubiquitin carboxy-terminal hydrolaseL1 (UCH-L1) gene and sporadic Parkinson's disease

      PARKINSONISM & RELATED DISORDERS
    24. Worth, PF; Houlden, H; Giunti, P; Davis, MB; Wood, NW
      Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia

      NATURE GENETICS
    25. de Silva, HA; Khan, NL; Wood, NW
      The genetics of Parkinson's disease

      CURRENT OPINION IN GENETICS & DEVELOPMENT
    26. Munchau, A; Valente, EM; Davis, MB; Stinton, V; Wood, NW; Quinn, NP; Bhatia, KP
      A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia

      MOVEMENT DISORDERS
    27. Jarman, PR; Bhatia, KP; Davie, C; Heales, SJR; Turjanski, N; Taylor-Robinson, SD; Marsden, CD; Wood, NW
      Paroxysmal dystonic choreoathetosis: Clinical features and investigation of pathophysiology in a large family

      MOVEMENT DISORDERS
    28. Bandmann, O; Vaughan, JR; Holmans, P; Marsden, CD; Wood, NW
      Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease

      MOVEMENT DISORDERS
    29. Wilson, CJ; Wood, NW; Leonard, JV; Surtees, R; Rahman, S
      Mitochondrial DNA point mutation T9176C in Leigh syndrome

      JOURNAL OF CHILD NEUROLOGY
    30. Houlden, H; Baker, M; McGowan, E; Lewis, P; Hutton, M; Crook, R; Wood, NW; Kumar-Singh, S; Geddes, J; Swash, M; Scaravilli, F; Holton, JL; Lashley, T; Tomita, T; Hashimoto, T; Verkkoniemi, A; Kalimo, H; Somer, M; Paetau, A; Martin, JJ; Van Broeckhoven, C; Golde, T; Hardy, J; Haltia, M; Revesz, T
      Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-betaconcentrations

      ANNALS OF NEUROLOGY
    31. Lodi, R; Schapira, AHV; Manners, D; Styles, P; Wood, NW; Taylor, DJ; Warner, TT
      Abnormal in vivo skeletal muscle energy metabolism in Huntington's diseaseand dentatorubropallidoluysian atrophy

      ANNALS OF NEUROLOGY
    32. Lucking, CB; Durr, A; Bonifati, V; Vaughan, J; De Michele, G; Gasser, T; Harhangi, BS; Meco, G; Denefle, P; Wood, NW; Agid, Y; Brice, A
      Association between early-onset Parkinson's disease and mutations in the parkin gene

      NEW ENGLAND JOURNAL OF MEDICINE
    33. Morris, HR; Vaughan, JR; Datta, SR; Bandopadhyay, R; de Silva, HAR; Schrag, A; Cairns, NJ; Burn, D; Nath, U; Lantos, PL; Daniel, S; Lees, AJ; Quinn, NP; Wood, NW
      Multiple system atrophy/progressive supranuclear palsy: alpha-Synuclein, synphilin, tau, and APOE

      NEUROLOGY
    34. Munchau, A; Valente, EM; Shahidi, GA; Eunson, LH; Hanna, RG; Quinn, NP; Schapira, AHV; Wood, NW; Bhatia, KP
      A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    35. Valente, EM; Spacey, SD; Wali, GM; Bhatia, KP; Dixon, PH; Wood, NW; Davis, MB
      A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16

      BRAIN
    36. Elliott, PM; Hanna, MG; Ward, SA; Chinnery, PF; Turnbull, DM; Wood, NW; McKenna, WJ
      Diagnostic utility of metabolic exercise testing in a patient with cardiovascular disease

      HEART
    37. Spacey, SD; Wood, NW
      The genetics of Parkinson's disease

      CURRENT OPINION IN NEUROLOGY
    38. Abbas, N; Lucking, CB; Ricard, S; Durr, A; Bonifati, V; De Michele, G; Bouley, S; Vaughan, JR; Gasser, T; Marconi, R; Broussolle, E; Brefel-Courbon, C; Harhangi, BS; Oostra, AB; Fabrizio, E; Bohme, GA; Pradier, L; Wood, NW; Filla, A; Meco, G; Denefle, P; Agid, Y; Brice, A
      A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe

      HUMAN MOLECULAR GENETICS
    39. Morris, HR; Lees, AJ; Wood, NW
      Neurofibrillary tangle parkinsonian disorders - Tau pathology and tau genetics

      MOVEMENT DISORDERS
    40. Pulkes, T; Eunson, L; Patterson, V; Siddiqui, A; Wood, NW; Nelson, IP; Morgan-Hughes, JA; Hanna, MG
      The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS

      ANNALS OF NEUROLOGY
    41. Morris, HR; Perez-Tur, J; Janssen, JC; Brown, J; Lees, AJ; Wood, NW; Hardy, J; Hutton, M; Rossor, MN
      Mutation in the tau exon 10 splice site region in familiar frontotemporal dementia

      ANNALS OF NEUROLOGY
    42. Marques, W; Hanna, MG; Marques, SR; Sweeney, MG; Thomas, PK; Wood, NW
      Phenotypic variation of a new P0 mutation in genetically identical twins

      JOURNAL OF NEUROLOGY
    43. Flowers, JM; Leigh, PN; Davies, AM; Ninkina, NN; Buchman, VL; Vaughan, J; Wood, NW; Powell, JF
      Mutations in the gene encoding human persyn are not associated with amyotrophic lateral sclerosis or familial Parkinson's disease

      NEUROSCIENCE LETTERS
    44. Harhangi, BS; Farrer, MJ; Lincoln, S; Bonifati, V; Meco, G; De Michele, G; Brice, A; Durr, A; Martinez, M; Gasser, T; Bereznai, B; Vaughan, JR; Wood, NW; Hardy, J; Oostra, BA; Breteler, MMB
      The lle93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease

      NEUROSCIENCE LETTERS
    45. Morris, HR; Wood, NW; Lees, AJ
      Progressive supranuclear palsy (Steele-Richardson-Olszewski disease)

      POSTGRADUATE MEDICAL JOURNAL
    46. Jarman, PR; del Grosso, N; Valente, EM; Leube, B; Cassetta, E; Bentivoglio, AR; Waddy, HM; Uitti, RJ; Maraganore, DM; Albanese, A; Frontali, M; Auburger, G; Bressman, SB; Wood, NW; Nygaard, TG
      Primary torsion dystonia: the search for genes is not over

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    47. Chalmers, RM; Andreae, L; Wood, NW; Raj, RVKD; Casey, ATH
      Familial hydrocephalus

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    48. Marques, W; Sweeney, MG; Wood, NW; Wroe, SJ; Marques, W
      Central nervous system involvement in a novel connexin 32 mutation affecting identical twins

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    49. Morris, HR; Janssen, JC; Bandmann, O; Daniel, SE; Rossor, MN; Lees, AJ; Wood, NW
      The tau gene A0 polymorphism in progressive supranuclear palsy and relatedneurodegenerative diseases

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    50. Robinson, R; McCarthy, GT; Bandmann, O; Dobbie, M; Surtees, R; Wood, NW
      GTP cyclohydrolase deficiency; intrafamilial variation in clinical phenotype, including levodopa responsiveness

      JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
    51. Zuberi, SM; Eunson, LH; Spauschus, A; De Silva, R; Tolmie, J; Wood, NW; McWilliam, RC; Stephenson, JPB; Kullmann, DM; Hanna, MG
      A novel mutation in the human voltage-gated potassium channel gene (Kv1.1)associates with episodic ataxia type 1 and sometimes with partial epilepsy

      BRAIN
    52. Andrews, TC; Weeks, RA; Turjanski, N; Gunn, RN; Watkins, LHA; Sahakian, B; Hodges, JR; Rosser, AE; Wood, NW; Brooks, DJ
      Huntington's disease progression PET and clinical observations

      BRAIN
    53. Valente, EM; Povey, S; Warner, TT; Wood, NW; Davis, MB
      Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations

      ANNALS OF HUMAN GENETICS
    54. Worth, PF; Giunti, P; Gardner-Thorpe, C; Dixon, PH; Davis, MB; Wood, NW
      Autosomal dominant cerebellar ataxia type III: Linkage in a large British family to a 7.6-cM region on chromosome 15q14-21.3

      AMERICAN JOURNAL OF HUMAN GENETICS
    55. Giunti, P; Stevanin, G; Worth, PF; David, G; Brice, A; Wood, NW
      Molecular and clinical study of 18 families with ADCA type II: Evidence for genetic heterogeneity and De Novo mutation

      AMERICAN JOURNAL OF HUMAN GENETICS
    56. Clark, KM; Taylor, RW; Johnson, MA; Chinnery, PF; Chrzanowska-Lightowlers, ZMA; Andrews, RM; Nelson, IP; Wood, NW; Lamont, PJ; Hanna, MG; Lightowlers, RN; Turnbull, DM
      An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy

      AMERICAN JOURNAL OF HUMAN GENETICS
    57. VAUGHAN JR; FARRER MJ; WSZOLEK ZK; GASSER T; DURR A; AGID Y; BONIFATI V; DEMICHELE G; VOLPE G; LINCOLN S; BRETELER M; MECO G; BRICE A; MARSDEN CD; HARDY J; WOOD NW
      SEQUENCING OF THE ALPHA-SYNUCLEIN GENE IN A LARGE SERIES OF CASES OF FAMILIAL PARKINSONS-DISEASE FAILS TO REVEAL ANY FURTHER MUTATIONS

      Human molecular genetics
    58. BANDMANN O; MARSDEN CD; WOOD NW
      GENETIC-ASPECTS OF PARKINSONS-DISEASE

      Movement disorders
    59. HANNA MG; DAVIS MB; SWEENEY MG; NOURSADEGHI M; ELLIS CJ; ELLIOT P; WOOD NW; MARSDEN CD
      GENERALIZED CHOREA IN 2 PATIENTS HARBORING THE FRIEDREICHS ATAXIA GENE TRINUCLEOTIDE REPEAT EXPANSION

      Movement disorders
    60. BANDMANN O; VALENTE EM; HOLMANS P; SURTEES RAH; WALTERS JH; WEVERS RA; MARSDEN CD; WOOD NW
      DOPA-RESPONSIVE DYSTONIA - A CLINICAL AND MOLECULAR-GENETIC STUDY

      Annals of neurology
    61. WOOD NW
      GENETIC RISK-FACTORS IN PARKINSONS-DISEASE

      Annals of neurology
    62. VAUGHAN J; DURR A; TASSIN J; BEREZNAI B; GASSER T; BONIFATI V; DEMICHELE G; FABRIZIO E; VOLPE G; BANDMANN O; JOHNSON WG; GOLBE LI; BRETELER M; MECO G; AGID Y; BRICE A; MARSDEN CD; WOOD NW
      THE ALPHA-SYNUCLEIN ALA53THR MUTATION IS NOT A COMMON-CAUSE OF FAMILIAL PARKINSONS-DISEASE - A STUDY OF 230 EUROPEAN CASES

      Annals of neurology
    63. MARQUES W; THOMAS PK; SWEENEY MG; CARR L; WOOD NW
      DEJERINE-SOTTAS NEUROPATHY AND PMP22 POINT MUTATIONS - A NEW BASE-PAIR SUBSTITUTION AND A POSSIBLE HOT-SPOT ON SER72

      Annals of neurology
    64. LUCKING CB; ABBAS N; DURR A; BONIFATI V; BONNET AM; DEBROUCKER T; DEMICHELE G; WOOD NW; AGID Y; BRICE A
      HOMOZYGOUS DELETIONS IN PARKIN GENE IN EUROPEAN AND NORTH-AFRICAN FAMILIES WITH AUTOSOMAL RECESSIVE JUVENILE PARKINSONISM

      Lancet
    65. BANDMANN O; WOOD NW
      ACETYLATOR GENOTYPE AND PARKINSONS-DISEASE - REPLY

      Lancet
    66. NICHOLL DJ; VAUGHAN JR; ALDOUS DEW; PICCINI P; DANIEL SE; BROOKS DJ; WOOD NW; WILLIAMS AC
      A LARGE BRITISH KINDRED WITH AUTOSOMAL-DOMINANT PARKINSONS-DISEASE

      Neurology
    67. KAPOOR R; MILLER DH; JONES SJ; PLANT GT; BRUSA A; GASS A; HAWKINS CP; PAGE R; WOOD NW; COMPSTON DAS; MOSELEY IF; MCDONALD WI
      EFFECTS OF INTRAVENOUS METHYLPREDNISOLONE ON OUTCOME IN MRI-BASED PROGNOSTIC SUBGROUPS IN ACUTE OPTIC NEURITIS

      Neurology
    68. HANNA MG; NELSON IP; MORGANHUGHES JA; WOOD NW
      MELAS - A NEW DISEASE-ASSOCIATED MITOCHONDRIAL-DNA MUTATION AND EVIDENCE FOR FURTHER GENETIC-HETEROGENEITY

      Journal of Neurology, Neurosurgery and Psychiatry
    69. HANNA MG; STEWART J; SCHAPIRA AHV; WOOD NW; MORGANHUGHES JA; MURRAY NMF
      SALBUTAMOL TREATMENT IN A PATIENT WITH HYPERKALEMIC PERIODIC PARALYSIS DUE TO A MUTATION IN THE SKELETAL-MUSCLE SODIUM-CHANNEL GENE (SCN4A)

      Journal of Neurology, Neurosurgery and Psychiatry
    70. GIUNTI P; SABBADINI G; SWEENEY MG; DAVIS MB; VENEZIANO L; MANTUANO E; FEDERICO A; PLASMATI R; FRONTALI M; WOOD NW
      THE ROLE OF THE SCA2 TRINUCLEOTIDE REPEAT EXPANSION IN 89 AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA FAMILIES - FREQUENCY, CLINICAL AND GENETIC CORRELATES

      Brain
    71. Valente, EM; Warner, TT; Jarman, PR; Mathen, D; Fletcher, NA; Marsden, CD; Bhatia, KP; Wood, NW
      The role of DYT1 in primary torsion dystonia in Europe

      BRAIN
    72. LAMONT PJ; SURTEES R; WOODWARD CE; LEONARD JV; WOOD NW; HARDING AE
      CLINICAL AND LABORATORY FINDINGS IN REFERRALS FOR MITOCHONDRIAL-DNA ANALYSIS

      Archives of Disease in Childhood
    73. WOOD NW
      DIAGNOSING FRIEDREICH-ATAXIA

      Archives of Disease in Childhood
    74. HANNA MG; NELSON IP; RAHMAN S; LANE RJM; LAND J; HEALES S; COOPER MJ; SCHAPIRA AHV; MORGANHUGHES JA; WOOD NW
      CYTOCHROME-C-OXIDASE DEFICIENCY ASSOCIATED WITH THE FIRST STOP-CODON POINT MUTATION IN HUMAN MTDNA

      American journal of human genetics
    75. KOMPOLITI K; PAPPERT EJ; GOETZ CG; FORD B; WOOD NW
      PROGRESSIVE COGNITIVE DECLINE WITH TRUNCAL LIMB ATAXIA AND BALLISTIC MOVEMENTS/

      Movement disorders
    76. NELSON I; HANNA MG; WOOD NW; HARDING AE
      DEPLETION OF MITOCHONDRIAL-DNA BY DDC IN UNTRANSFORMED HUMAN CELL-LINES

      Somatic cell and molecular genetics
    77. LODI R; TAYLOR DJ; TABRIZI SJ; KUMAR S; SWEENEY M; WOOD NW; STYLES P; RADDA GK; SCHAPIRA AHV
      IN-VIVO SKELETAL-MUSCLE MITOCHONDRIAL-FUNCTION IN LEBERS HEREDITARY OPTIC NEUROPATHY ASSESSED BY P-31 MAGNETIC-RESONANCE SPECTROSCOPY

      Annals of neurology
    78. HANNA MG; NELSON IP; RAHMAN S; SCHAPIRA AHV; MORGANHUGHES JA; WOOD NW
      CYTOCHROME-C-OXIDASE DEFICIENCY ASSOCIATED WITH A NEW STOP CODON MUTATION IN MITOCHONDRIAL-DNA

      Annals of neurology
    79. BANDMANN O; SWEENEY MG; DANIEL SE; MARSDEN CD; WOOD NW
      MITOCHONDRIAL-DNA POLYMORPHISMS IN PATHOLOGICALLY PROVEN PARKINSONS-DISEASE

      Journal of neurology
    80. BANDMANN O; VAUGHAN J; HOLMANS P; MARSDEN CD; WOOD NW
      ASSOCIATION OF SLOW ACETYLATOR GENOTYPE FOR N-ACETYLTRANSFERASE-2 WITH FAMILIAL PARKINSONS-DISEASE

      Lancet
    81. BANDMANN O; SWEENEY MG; DANIEL SE; WENNING GK; QUINN N; MARSDEN CD; WOOD NW
      MULTIPLE-SYSTEM ATROPHY IS GENETICALLY DISTINCT FROM IDENTIFIED INHERITED CAUSES OF SPINOCEREBELLAR DEGENERATION

      Neurology
    82. PLANTEBORDENEUVE V; TAUSSIG D; THOMAS F; SAID G; WOOD NW; MARSDEN CD; HARDING AE
      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
    83. BANDMANN O; MARSDEN CD; WOOD NW
      GENETIC POLYMORPHISMS OF 3 DETOXIFICATION ENZYMES IN FAMILIAL AND SPORADIC PARKINSONS-DISEASE

      Neurology
    84. JARMAN PR; DAVIS MB; MARSDEN CD; WOOD NW
      GENETIC-LINKAGE AND CANDIDATE GENE STUDIES IN A BRITISH FAMILY WITH PAROXYSMAL DYSTONIC CHOREOATHETOSIS

      Neurology
    85. JARMAN PR; BANDMANN O; MARSEN CD; WOOD NW
      GTP CYCLOHYDROLASE-I MUTATIONS IN PATIENTS WITH DYSTONIA RESPONSIVE TO ANTICHOLINERGIC DRUGS

      Journal of Neurology, Neurosurgery and Psychiatry
    86. CHALMERS RM; RIORDANEVA P; WOOD NW
      AUTOSOMAL RECESSIVE INHERITANCE OF HEREDITARY MOTOR AND SENSORY NEUROPATHY WITH OPTIC ATROPHY

      Journal of Neurology, Neurosurgery and Psychiatry
    87. GIUNTI P; SWEENEY MG; DAVIS MB; WOOD NW
      CHARACTERIZATION OF THE SCA2 CAG REPEAT EXPANSION IN ADCA TYPE-I FAMILIES

      Journal of Medical Genetics
    88. SWEENEY M; GIUNTI P; WOOD NW; DAVIS MB
      GENETIC-ANALYSIS OF LATE-ONSET PURE CEREBELLAR-ATAXIA (SCA6)

      Journal of Medical Genetics
    89. LAMONT PJ; DAVIS MB; WOOD NW
      IDENTIFICATION AND SIZING OF THE GAA TRINUCLEOTIDE REPEAT EXPANSION OF FRIEDREICHS ATAXIA IN 56 PATIENTS - CLINICAL AND GENETIC CORRELATES

      Brain
    90. JARMAN PR; DAVIS MB; HODGSON SV; MARSDEN CD; WOOD NW
      PAROXYSMAL DYSTONIC CHOREOATHETOSIS - GENETIC-LINKAGE STUDIES IN A BRITISH FAMILY

      Brain
    91. JARMAN PR; WOOD NW; DAVIS MT; DAVIS PV; BHATIA KP; MARSDEN CD; DAVIS MB
      HEREDITARY GENIOSPASM - LINKAGE TO CHROMOSOME 9Q13-Q21 AND EVIDENCE FOR GENETIC-HETEROGENEITY

      American journal of human genetics
    92. RIORDANEVA P; WOOD NW
      MITOCHONDRIAL DISORDERS IN NEUROOPHTHALMOLOGY

      Current opinion in neurology
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ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/10/20 alle ore 23:32:00