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    1. Street, VA; Goldy, JD; Golden, AS; Tempel, BL; Bird, TD; Chance, PF
      Mapping of Charcot-Marie-Tooth disease type 1C to chromosome 16p identifies a novel locus for demyelinating neuropathies

      AMERICAN JOURNAL OF HUMAN GENETICS
    2. Bird, TD
      The hound that did not bark in the night and Silver blaze - Reply

      ANNALS OF NEUROLOGY
    3. Bird, TD; Schellenberg, GD
      The case of the missing tau, or, why didn't the mRNA bark?

      ANNALS OF NEUROLOGY
    4. Bird, TD
      Frontotemporal dementia: genotypes, phenotypes and more problems to be solved

      NEUROBIOLOGY OF AGING
    5. Pinsky, LE; Burke, W; Bird, TD
      Why should primary care physicians know about the genetics of dementia?

      WESTERN JOURNAL OF MEDICINE
    6. Bird, TD; Jarvik, GP; Wood, NW
      Genetic association studies - Genes in search of diseases

      NEUROLOGY
    7. La Spada, AR; Bird, TD
      Late-onset SCA2: 33 CAG repeats are sufficient to cause disease - Reply

      NEUROLOGY
    8. Jeannet, PY; Watts, GDJ; Bird, TD; Chance, PF
      Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy

      NEUROLOGY
    9. Payami, H; Lee, N; Zareparsi, S; McNeal, MG; Camicioli, R; Bird, TD; Sexton, G; Gancher, S; Kaye, J; Calhoun, D; Swanson, PD; Nutt, J
      Parkinson's disease, CYP2D6 polymorphism, and age

      NEUROLOGY
    10. Poorkaj, P; Grossman, M; Steinbart, E; Payami, H; Sadovnick, A; Nochlin, D; Tabira, T; Trojanowski, JQ; Borson, S; Galasko, D; Reich, S; Quinn, B; Schellenberg, G; Bird, TD
      Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia

      ARCHIVES OF NEUROLOGY
    11. Bird, TD
      Thoughts on the relationship of the human genome project to neurology

      ARCHIVES OF NEUROLOGY
    12. Steinbart, EJ; Smith, CO; Poorkaj, P; Bird, TD
      Impact of DNA testing for early-onset familial Alzheimer disease and frontotemporal dementia

      ARCHIVES OF NEUROLOGY
    13. Poorkaj, P; Tsuang, D; Wijsman, E; Steinbart, E; Garruto, RM; Craig, UK; Chapman, NH; Anderson, L; Bird, TD; Plato, CC; Perl, DP; Weiderholt, W; Galasko, D; Schellenberg, GD
      TAU as a susceptibility gene for amyotropic lateral sclerosis-parkinsonismdementia complex of Guam

      ARCHIVES OF NEUROLOGY
    14. Piccardo, P; Liepnieks, JJ; William, A; Dlouhy, SR; Farlow, MR; Young, K; Nochlin, D; Bird, TD; Nixon, RR; Ball, MJ; DeCarli, C; Bugiani, O; Tagliavini, F; Benson, MD; Ghetti, B
      Prion proteins with different conformations accumulate in Geustmann-Straussler-Scheinker disease caused by A117V and F198S mutations

      AMERICAN JOURNAL OF PATHOLOGY
    15. Mathews, PM; Cataldo, AM; Kao, BH; Rudnicki, AG; Qin, X; Yang, JL; Jiang, Y; Picciano, M; Hulette, C; Lippa, CF; Bird, TD; Nochlin, D; Walter, J; Haass, C; Levesque, L; Fraser, PE; Andreadis, A; Nixon, RA
      Brain expression of presenilins in sporadic and early-onset, familial Alzheimer's disease

      MOLECULAR MEDICINE
    16. Moseley, ML; Schut, LJ; Bird, TD; Day, JW; Ranum, LPW
      Large, expanded repeats in SCA8 are not confined to patients with cerebellar ataxia - Reply

      NATURE GENETICS
    17. Moseley, ML; Schut, MJ; Bird, TD; Koob, MD; Day, JW; Ranum, LPW
      SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance

      HUMAN MOLECULAR GENETICS
    18. Furukawa, K; D'Souza, I; Crudder, CH; Onodera, H; Itoyama, Y; Poorkaj, P; Bird, TD; Schellenberg, GD
      Pro-apoptotic effects of tau mutations in chromosome 17 frontotemporal dementia and parkinsonism

      NEUROREPORT
    19. Lippa, CF; Swearer, JM; Kane, KJ; Nochlin, D; Bird, TD; Ghetti, B; Nee, LE; St George-Hyslop, P; Pollen, DA; Drachman, DA
      Familial Alzheimer's disease: Site of mutation influences clinical phenotype

      ANNALS OF NEUROLOGY
    20. Fernandez, M; McCain, ME; Martinez, RA; Snow, K; Lipe, H; Ravits, J; Bird, TD; La Spada, AR
      Late-onset SCA2: 33 CAG repeats are sufficient to cause disease

      NEUROLOGY
    21. Kertesz, A; Kawarai, T; Rogaeva, E; St George-Hyslop, P; Poorkaj, P; Bird, TD; Munoz, DG
      Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions

      NEUROLOGY
    22. Bird, TD
      Sporadic cases of possible genetic diseases - To test or not to test?

      ARCHIVES OF NEUROLOGY
    23. Tsuang, D; Almqvist, EW; Lipe, H; Strgar, F; DiGiacomo, L; Hoff, D; Eugenio, C; Hayden, MR; Bird, TD
      Familial aggregation of psychotic symptoms in Huntington's disease

      AMERICAN JOURNAL OF PSYCHIATRY
    24. Daw, EW; Payami, H; Nemens, EJ; Nochlin, D; Bird, TD; Schellenberg, GD; Wijsman, EM
      The number of trait loci in late-onset Alzheimer disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    25. Koob, MD; Moseley, ML; Schut, LJ; Benzow, KA; Bird, TD; Day, JW; Ranum, LPW
      An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

      NATURE GENETICS
    26. Lieberman, AP; Trojanowski, JQ; Leonard, DGB; Chen, KL; Barnett, JL; Leverenz, JB; Bird, TD; Robitaille, Y; Malandrini, A; Fischbeck, KH
      Ataxin 1 and ataxin 3 in neuronal intranuclear inclusion disease

      ANNALS OF NEUROLOGY
    27. Houlden, H; Rizzu, P; Stevens, M; de Knijff, P; van Duijn, CM; van Swieten, JC; Heutink, P; Perez-Tur, J; Thomas, V; Baker, M; Morris, H; Rossor, M; Jannsen, JC; Petersen, RC; Dodd, P; Dark, F; Boeve, B; Dickson, D; Davies, P; Pickering-Brown, S; Mann, D; Adamson, J; Lynch, T; Payami, H; Poorkaj, P; Bird, TD; Schellenberg, GD; Chakraverty, S; Norton, J; Morris, JC; Goate, A; Hutton, M; Hardy, J
      Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutations

      NEUROSCIENCE LETTERS
    28. Bird, TD
      Risks and benefits of DNA testing for neurogenetic disorders

      SEMINARS IN NEUROLOGY
    29. Figlewicz, DA; Bird, TD
      "Pure" hereditary spastic paraplegias - The story becomes complicated

      NEUROLOGY
    30. D'Souza, I; Poorkaj, P; Hong, M; Nochlin, D; Lee, VMY; Bird, TD; Schellenberg, GD
      Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    31. Gomez-Isla, T; Growdon, WB; McNamara, MJ; Nochlin, D; Bird, TD; Arango, JC; Lopera, F; Kosik, KS; Lantos, PL; Cairns, NJ; Hyman, BT
      The impact of different presenilin 1 and presenilin 2 mutations on amyloiddeposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain - Evidence for other phenotype-modifying factors

      BRAIN
    32. Bird, TD; Nochlin, D; Poorkaj, P; Cherrier, M; Payami, H; Peskind, E; Lampe, TH; Nemens, E; Boyer, PJ; Schellenberg, GD
      A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tan gene (P301L) (vol 122, pg 741, 1999)

      BRAIN
    33. Bird, TD; Nochlin, D; Poorkaj, P; Cherrier, M; Kaye, J; Payami, H; Peskind, E; Lampe, TH; Nemens, E; Boyer, PJ; Schellenberg, GD
      A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

      BRAIN
    34. Yasuda, M; Maeda, K; Hashimoto, M; Yamashita, H; Ikejiri, Y; Bird, TD; Tanaka, C; Schellenberg, GD
      A pedigree with a novel presenilin 1 mutation at a residue that is not conserved in presenilin 2

      ARCHIVES OF NEUROLOGY
    35. Bird, TD
      Outrageous fortune: The risk of suicide in genetic testing for Huntington disease

      AMERICAN JOURNAL OF HUMAN GENETICS
    36. Kamino, K; Wijsman, E; Anderson, L; Nemens, E; Yamagata, H; Ohta, S; Bird, TD; Schellenberg, GD
      A family with late-onset Alzheimer's disease carrying a Val91Met mutation of the apolipoprotein A-II gene suggests altered plasma lipid metabolism inAlzheimer's disease

      ALZHEIMER'S DISEASE AND RELATED DISORDERS
    37. Armstrong, RA; Wade, KM; Nochlin, D; Bird, TD
      Is neuropathological heterogeneity in Alzheimer's disease related to apolipoprotein genotype?

      ALZHEIMERS REPORTS
    38. KOOB MD; BENZOW KA; BIRD TD; DAY JW; MOSELEY ML; RANUM LPW
      RAPID CLONING OF EXPANDED TRINUCLEOTIDE REPEAT SEQUENCES FROM GENOMICDNA

      Nature genetics
    39. POORKAJ P; SHARMA V; ANDERSON L; NEMENS E; ALONSO ME; ORR H; WHITE J; HESTON L; BIRD TD; SCHELLENBERG GD
      MISSENSE MUTATIONS IN THE CHROMOSOME-14 FAMILIAL ALZHEIMERS-DISEASE PRESENILIN-1 GENE

      Human mutation
    40. SPILLANTINI MG; BIRD TD; GHETTI B
      FRONTOTEMPORAL DEMENTIA AND PARKINSONISM LINKED TO CHROMOSOME-17 - A NEW GROUP OF TAUOPATHIES

      Brain pathology
    41. BENSON KF; HORWITZ M; WOLFF J; FRIEND K; THOMPSON E; WHITE S; RICHARDS RI; RASKIND WH; BIRD TD
      CAG REPEAT EXPANSION IN AUTOSOMAL-DOMINANT FAMILIAL SPASTIC PARAPARESIS - NOVEL EXPANSION IN A SUBSET OF PATIENTS

      Human molecular genetics (Print)
    42. Tsuang, D; Bird, TD
      Genetics of dementia

      JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
    43. Levy-Lahad, E; Tsuang, D; Bird, TD
      Recent advances in the genetics of Alzheimer's disease

      JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
    44. IKEUCHI T; SANPEI K; TAKANO H; SASAKI H; TASHIRO K; CANCEL G; BRICE A; BIRD TD; SCHELLENBERG GD; PERICAKVANCE MA; WELSHBOHMER KA; CLARK LN; WILHELMSEN K; TSUJI S
      A NOVEL LONG AND UNSTABLE CAG CTG TRINUCLEOTIDE REPEAT ON CHROMOSOME 17Q/

      Genomics
    45. BIRD TD
      PENETRATING OBSERVATIONS OF DYSTONIA

      Annals of neurology
    46. POORKAJ P; BIRD TD; WIJSMAN E; NEMENS E; GARRUTO RM; ANDERSON L; ANDREADIS A; WIEDERHOLT WC; RASKIND M; SCHELLENBERG GD
      TAU IS A CANDIDATE GENE FOR CHROMOSOME-17 FRONTOTEMPORAL DEMENTIA

      Annals of neurology
    47. NOCHLIN D; BIRD TD; NEMENS EJ; BALL MJ; SUMI SM
      AMYLOID ANGIOPATHY IN A VOLGA GERMAN FAMILY WITH ALZHEIMERS-DISEASE AND A PRESENILIN-2 MUTATION ((NI)-I-141)

      Annals of neurology
    48. RASKIND WH; BOLIN T; WOLFF J; FINK J; MATSUSHITA M; LITT M; LIPE H; BIRD TD
      FURTHER LOCALIZATION OF A GENE FOR PAROXYSMAL DYSTONIC CHOREOATHETOSIS TO A 5-CM REGION ON CHROMOSOME 2Q34

      Human genetics
    49. TSUANG D; DIGIACOMO L; LIPE H; BIRD TD
      FAMILIAL AGGREGATION OF SCHIZOPHRENIA-LIKE SYMPTOMS IN HUNTINGTONS-DISEASE

      American journal of medical genetics
    50. BIRD TD
      GENETIC TESTING

      Western journal of medicine
    51. Hong, M; Zhukareva, V; Vogelsberg-Ragaglia, V; Wszolek, Z; Reed, L; Miller, BI; Geschwind, DH; Bird, TD; McKeel, D; Goate, A; Morris, JC; Wilhelmsen, KC; Schellenberg, GD; Trojanowski, JQ; Lee, VMY
      Mutation-specific functional impairments in distinct Tau isoforms of hereditary FTDP-17

      SCIENCE
    52. BIRD TD
      GENOTYPES, PHENOTYPES, AND FRONTOTEMPORAL DEMENTIA - TAKE YOUR PICK

      Neurology
    53. FURUKAWA Y; LANG AE; TRUGMAN JM; BIRD TD; HUNTER A; SADEH M; TAGAWA T; STGEORGEHYSLOP PH; GUTTMAN M; MORRIS LW; HORNYKIEWICZ O; SHIMADZU M; KISH SJ
      GENDER-RELATED PENETRANCE AND DE-NOVO GTP-CYCLOHYDROLASE-I GENE-MUTATIONS IN DOPA-RESPONSIVE DYSTONIA

      Neurology
    54. Moseley, ML; Benzow, KA; Schut, LJ; Bird, TD; Gomez, CM; Barkhaus, PE; Blindauer, KA; Labuda, M; Pandolfo, M; Koob, MD; Ranum, LPW
      Incidence of dominant spinocerebellar and Friedreich triplet repeats among361 ataxia families

      NEUROLOGY
    55. Carter, GT; Jensen, MP; Galer, BS; Kraft, GH; Crabtree, LD; Beardsley, RM; Abresch, RT; Bird, TD
      Neuropathic pain in Charcot-Marie-Tooth disease

      ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
    56. LIPPA CF; FUJIWARA H; MANN DMA; GIASSON B; BABA M; SCHMIDT ML; NEE LE; OCONNELL B; POLLEN DA; GEORGEHYSLOP PS; GHETTI B; NOCHLIN D; BIRD TD; CAIRNS NJ; LEE VMY; IWATSUBO T; TROJANOWSKI JQ
      LEWY BODIES CONTAIN ALTERED ALPHA-SYNUCLEIN IN BRAINS OF MANY FAMILIAR ALZHEIMERS-DISEASE PATIENTS WITH MUTATIONS IN PRESENILIN AND AMYLOIDPRECURSOR PROTEIN GENES

      The American journal of pathology
    57. Bird, TD
      The chromosome 1 type of familiar Alzheimer disease

      GENETIC TESTING FOR ALZHEIMER DISEASE
    58. KLESERT TR; OTTEN AD; BIRD TD; TAPSCOTT SJ
      TRINUCLEOTIDE REPEAT EXPANSION AT THE MYOTONIC-DYSTROPHY LOCUS REDUCES EXPRESSION OF DMAHP

      Nature genetics
    59. FOSTER NL; WILHELMSEN K; SIMA AAF; JONES MZ; DAMATO CJ; GILMAN S; SPILLANTINI MG; LYNCH T; MAYEUX RP; GASKELL PC; HULETTE CM; PERICAKVANCE MA; WELSHBOHMER KA; DICKSON DW; HEUTINK P; KROS J; VANSWIETEN JC; ARWERT F; GHETTI MB; MURRELL J; LANNFELT L; HUTTON M; JONES M; PHELPS CH; SNYDER DS; OLIVER E; BALL MJ; CUMMINGS JL; MILLER BL; KATZMAN R; REED L; SCHELPER RL; LANDSKA DJ; BRUN A; FINK JK; KUHL DE; KNOPMAN DS; WSZOLEK Z; MILLER CA; BIRD TD; LENDON C; ELECHI C
      FRONTOTEMPORAL DEMENTIA AND PARKINSONISM LINKED TO CHROMOSOME-17 - A CONSENSUS CONFERENCE

      Annals of neurology
    60. LEVEY AI; HEILMAN CJ; LAH JJ; NASH NR; REES HD; WAKAI M; MIRRA SS; RYE DB; NOCHLIN D; BIRD TD; MUFSON EJ
      PRESENILIN-1 PROTEIN EXPRESSION IN FAMILIAL AND SPORADIC ALZHEIMERS-DISEASE

      Annals of neurology
    61. BIRD TD; KRAFT GH; LIPE HP; KENNEY KL; SUMI SM
      CLINICAL AND PATHOLOGICAL PHENOTYPE OF THE ORIGINAL FAMILY WITH CHARCOT-MARIE-TOOTH TYPE 1B - A 20-YEAR STUDY

      Annals of neurology
    62. MANN DMA; IWATSUBO T; NOCHLIN D; SUMI SM; LEVYLAHAD E; BIRD TD
      AMYLOID (A-BETA) DEPOSITION IN CHROMOSOME 1-LINKED ALZHEIMERS-DISEASE- THE VOLGA GERMAN FAMILIES

      Annals of neurology
    63. PELLEGRINO JE; GEORGE RAV; BIEGEL J; FARLOW MR; GARDNER K; CARESS J; BROWN MJ; REBBECK TR; BIRD TD; CHANCE PF
      HEREDITARY NEURALGIC AMYOTROPHY - EVIDENCE FOR GENETIC HOMOGENEITY AND MAPPING TO CHROMOSOME 17Q25

      Human genetics
    64. RASKIND WH; PERICAKVANCE MA; LENNON F; WOLFF J; LIPE HP; BIRD TD
      FAMILIAL SPASTIC PARAPARESIS - EVALUATION OF LOCUS HETEROGENEITY, ANTICIPATION, AND HAPLOTYPE MAPPING OF THE SPG4 LOCUS ON THE SHORT ARM OFCHROMOSOME-2

      American journal of medical genetics
    65. POST SG; WHITEHOUSE PJ; BINSTOCK RH; BIRD TD; ECKERT SK; FARRER LA; FLECK LM; GAINES AD; JEUNGST ET; KARLINSKY H; MILES S; MURRAY TD; QUAID KA; RELKIN NR; ROSES AD; STGEORGEHYSLOP PH; SACHS GA; STEINBOCK B; TRUSCHKE EF; ZINN AB
      THE CLINICAL INTRODUCTION OF GENETIC TESTING FOR ALZHEIMER-DISEASE - AN ETHICAL PERSPECTIVE

      JAMA, the journal of the American Medical Association
    66. COPLIN WM; KIM DK; KLIOT M; BIRD TD
      MUTISM IN AN ADULT FOLLOWING HYPERTENSIVE CEREBELLAR HEMORRHAGE - NOSOLOGICAL DISCUSSION AND ILLUSTRATIVE CASE

      Brain and language
    67. PAYAMI H; SCHELLENBERG GD; ZAREPARSI S; KAYE J; SEXTON GJ; HEAD MA; MATSUYAMA SS; JARVIK LF; MILLER B; MCMANUS DQ; BIRD TD; KATZMAN R; HESTON L; NORMAN D; SMALL GW
      EVIDENCE FOR ASSOCIATION OF HLA-A2 ALLELE WITH ONSET AGE OF ALZHEIMERS-DISEASE

      Neurology
    68. BIRD TD; WIJSMAN EM; NOCHLIN D; LEEHEY M; SUMI SM; PAYAMI H; POORKAJ P; NEMENS E; RAFKIND M; SCHELLENBERG GD
      CHROMOSOME-17 AND HEREDITARY DEMENTIA - LINKAGE STUDIES IN 3 NON-ALZHEIMER FAMILIES AND KINDREDS WITH LATE-ONSET FAD

      Neurology
    69. LEWIS RA; GARBERN JY; SHY ME; BIRD TD; KRAFT GH; SIMA A; HODES ME; KAMHOLZ JA
      ABSENCE OF PROTEOLIPID PROTEIN EXPRESSION CAUSES AN INHERITED DEMYELINATING PERIPHERAL NEUROPATHY

      Neurology
    70. BIRD TD; WIJSMAN E; NOCHLIN D; LEEHEY M; SUMI M; PAYAMI H; NEMENS E; SCHELLENBERG G
      GENETIC-STUDIES OF THE CHROMOSOME-17 FORM OF HEREDITARY DEMENTIA

      Neurology
    71. GOMEZISLA T; NOCHLIN D; BIRD TD; SUMI SM; HYMAN BT
      PHENOTYPIC CHARACTERIZATION OF PS1 AND PS2 RELATED ALZHEIMERS-DISEASE

      Journal of neuropathology and experimental neurology
    72. TSUANG D; RASKIND MA; LEVERENZ J; PESKIND ER; SCHELLENBERG G; BIRD TD
      THE EFFECT OF APOLIPOPROTEIN-E GENOTYPE ON EXPRESSION OF AN AUTOSOMAL-DOMINANT SCHIZOPHRENIFORM DISORDER WITH PROGRESSIVE DEMENTIA AND NEUROFIBRILLARY TANGLES

      Biological psychiatry
    73. PELLEGRINO JE; GEORGE RAV; BIEGEL J; FARLOW MR; GARDNER K; CARESS J; BROWN MJ; REBBECK TR; BIRD TD; CHANCE PF
      HEREDITARY NEURALGIC AMYOTROPHY - REFINED MAPPING TO CHROMOSOME 17Q25

      American journal of human genetics
    74. MOSELEY ML; GOMEZ C; BENZOW KA; SCHUT LJ; STEPHENS K; BIRD TD; KOOB MD; RANUM LPW
      SPINOCEREBELLAR ATAXIA TYPE-1, TYPE-2, TYPE-3, TYPE-6 AND FRIEDREICHSATAXIA - FREQUENCY OF TRINUCLEOTIDE EXPANSIONS AMONG 354 FAMILIES WITH DOMINANT, RECESSIVE, OR SPORADIC ATAXIA

      American journal of human genetics
    75. SCHEUNER D; ECKMAN C; JENSEN M; SONG X; CITRON M; SUZUKI N; BIRD TD; HARDY J; HUTTON M; KUKULL W; LARSON E; LEVYLAHAD E; VIITANEN M; PESKIND E; POORKAJ P; SCHELLENBERG G; TANZI R; WASCO W; LANNFELT L; SELKOE D; YOUNKIN S
      SECRETED AMYLOID BETA-PROTEIN SIMILAR TO THAT IN THE SENILE PLAQUES OF ALZHEIMERS-DISEASE IS INCREASED IN-VIVO BY THE PRESENILIN-1 AND PRESENILIN-2 AND APP MUTATIONS LINKED TO FAMILIAL ALZHEIMERS-DISEASE

      Nature medicine
    76. LEVYLAHAD E; BIRD TD
      GENETIC-FACTORS IN ALZHEIMERS-DISEASE - A REVIEW OF RECENT ADVANCES

      Annals of neurology
    77. IKEDA M; SHARMA V; SUMI M; ROGAEVA EA; POORKAJ P; SHERRINGTON R; NEE L; TSUDA T; ODA N; WATANABE M; AOKI M; SHOJI M; ABE K; ITOYAMA Y; HIRAI S; SCHELLENBERG GD; BIRD TD; STGEORGEHYSLOP PH
      THE CLINICAL PHENOTYPE OF 2 MISSENSE MUTATIONS IN THE PRESENILIN-I GENE IN JAPANESE PATIENTS

      Annals of neurology
    78. BIRD TD; LEVYLAHAD E; POORKAJ P; SHARMA V; NEMENS E; LAHAD A; LAMPE TH; SCHELLENBERG GD
      WIDE-RANGE IN AGE-OF-ONSET FOR CHROMOSOME 1-RELATED FAMILIAL ALZHEIMERS-DISEASE

      Annals of neurology
    79. MANN DMA; IWATSUBO T; CAIRNS NJ; LANTOS PL; NOCHLIN D; SUMI SM; BIRD TD; POORKAJ P; HARDY J; HUTTON M; PRIHAR G; CROOK R; ROSSOR MN; HALTIA M
      AMYLOID-BETA PROTEIN (A-BETA) DEPOSITION IN CHROMOSOME 14-LINKED ALZHEIMERS-DISEASE - PREDOMINANCE OF A-BETA(42(43))

      Annals of neurology
    80. GREENSTEIN PE; MOORE D; LEVYLAHAD E; STEPHENS K; BIRD TD
      9 FAMILIES WITH THE SCA3 MACHADO-JOSEPH DISEASE TYPE OF INHERITED ATAXIA/

      Neurology
    81. PELLEGRINO JE; REBBECK TR; BROWN MJ; BIRD TD; CHANCE PF
      MAPPING OF HEREDITARY NEURALGIC AMYOTROPHY (FAMILIAL BRACHIAL-PLEXUS NEUROPATHY) TO DISTAL CHROMOSOME 17Q

      Neurology
    82. PELLEGRINO JE; REBBECK TR; BROWN MJ; FARLOW MR; BROWN RH; BUSIS NA; CARESS J; LIPE H; BIRD TD; CHANCE PF
      GENETIC-ANALYSIS IN HEREDITARY NEURALGIC AMYOTROPHY

      Neurology
    83. MURPHY GM; FORNO LS; ELLIS WG; NOCHLIN D; LEVYLAHAD E; POORKAJ P; BIRD TD; JIANG ZL; CORDELL B
      ANTIBODIES TO PRESENILIN PROTEINS DETECT NEUROFIBRILLARY TANGLES IN ALZHEIMERS-DISEASE

      The American journal of pathology
    84. PAYAMI H; ZAREPARSI S; MONTEE KR; SEXTON GJ; KAYE JA; BIRD TD; YU CE; WIJSMAN EM; HESTON LL; LITT M; SCHELLENBERG GD
      GENDER DIFFERENCE IN APOLIPOPROTEIN E-ASSOCIATED RISK FOR FAMILIAL ALZHEIMER-DISEASE - A POSSIBLE CLUE TO THE HIGHER INCIDENCE OF ALZHEIMER-DISEASE IN WOMEN

      American journal of human genetics
    85. KAMINO K; NAGANO K; KATSUYA T; NISHIWAKI Y; TAKEDA M; TANABE H; NISHIMURA T; II K; FUJIMOTO K; TSUJIMURA R; NONOMURA Y; YONEDA H; SAKAI T; NAKAJIMA T; IMAGAWA M; MARTIN GM; BIRD TD; SCHELLENBERG GS; MIKI T; OGIHARA T
      LINKAGE AND HAPLOTYPE ANALYSIS OF FAMILIAL EARLY-ONSET ALZHEIMER-DISEASE IN JAPANESE POPULATION

      Japanese journal of human genetics
    86. SCHELLENBERG GD; SHARMA V; POORKAJ P; HISAMA F; WIJSMAN EM; WEISSMAN SM; BIRD TD
      THE CHROMOSOME-14 ALZHEIMERS-DISEASE LOCUS

      Journal of cellular biochemistry
    87. COPLIN WM; BIRD TD
      OLIVOPONTOCEREBELLAR ATROPHY

      Annals of neurology
    88. BIRD TD
      APOLIPOPROTEIN-E GENOTYPING IN THE DIAGNOSIS OF ALZHEIMERS-DISEASE - A CAUTIONARY VIEW - REPLY

      Annals of neurology
    89. BIRD TD
      APOLIPOPROTEIN-E GENOTYPING IN THE DIAGNOSIS OF ALZHEIMERS-DISEASE - REPLY

      Annals of neurology
    90. LEVYLAHAD E; LAHAD A; WIJSMAN EM; BIRD TD; SCHELLENBERG GD
      APOLIPOPROTEIN-E GENOTYPES AND AGE-OF-ONSET IN EARLY-ONSET FAMILIAL ALZHEIMERS-DISEASE

      Annals of neurology
    91. BIRD TD; BENNETT RL
      WHY DO DNA TESTING - PRACTICAL AND ETHICAL IMPLICATIONS OF NEW NEUROGENETIC TESTS

      Annals of neurology
    92. BIRD TD
      APOLIPOPROTEIN-E GENOTYPING IN THE DIAGNOSIS OF ALZHEIMERS-DISEASE - A CAUTIONARY VIEW

      Annals of neurology
    93. BIRD TD
      IDIOPATHIC PROGRESSIVE SPASTIC PARAPARESIS

      JAMA, the journal of the American Medical Association
    94. LEVYLAHAD E; WIJSMAN EM; NEMENS E; ANDERSON L; GODDARD KAB; WEBER JL; BIRD TD; SCHELLENBERG GD
      A FAMILIAL ALZHEIMERS-DISEASE LOCUS ON CHROMOSOME-1

      Science
    95. LEVYLAHAD E; WASCO W; POORKAJ P; ROMANO DM; OSHIMA J; PETTINGELL WH; YU CE; JONDRO PD; SCHMIDT SD; WANG K; CROWLEY AC; FU YH; GUENETTE SY; GALAS D; NEMENS E; WIJSMAN EM; BIRD TD; SCHELLENBERG GD; TANZI RE
      CANDIDATE GENE FOR THE CHROMOSOME-1 FAMILIAL ALZHEIMERS-DISEASE LOCUS

      Science
    96. TAGLIAVINI F; PRELLI F; PORRO M; ROSSI G; GIACCONE G; BIRD TD; DLOUHY SR; YOUNG K; PICCARDO P; GHETTI B; BUGIANI O; FRANGIONE B
      ONLY MUTANT PRP PARTICIPATES IN AMYLOID FORMATION IN GERSTMANN-STRAUSSLER-SCHEINKER-DISEASE WITH ALA-GREATER-THAN-VAL SUBSTITUTION AT CODON-117

      Journal of neuropathology and experimental neurology
    97. LEVYLAHAD E; WIJSMAN EM; BIRD TD; SCHELLENBERG GD
      ALZHEIMERS-DISEASE IN THE VOLGA GERMANS - PHENOCOPY ANALYSIS IN A COMMON, COMPLEX DISEASE

      American journal of human genetics
    98. TSUANG DW; LEVERENZ JB; PESKIND ER; BIRD TD; SCHELLENBERG G; RASKIND MA
      THE EFFECT OF APOLIPOPROTEIN-E GENOTYPE ON EXPRESSION OF AN AUTOSOMAL-DOMINANT SCHIZOPHRENIFORM DISORDER WITH PROGRESSIVE DEMENTIA AND NEUROFIBRILLARY TANGLES

      American journal of human genetics
    99. RANUM LPW; LUNDGREN JK; SCHUT LJ; AHRENS MJ; PERLMAN S; AITA J; BIRD TD; GOMEZ C; ORR HT
      SPINOCEREBELLAR ATAXIA TYPE-I AND MACHADO-JOSEPH DISEASE - INCIDENCE OF CAG EXPANSIONS AMONG ADULT-ONSET ATAXIA PATIENTS FROM 311 FAMILIES WITH DOMINANT, RECESSIVE, OR SPORADIC ATAXIA

      American journal of human genetics
    100. HEARN MG; EDLAND SD; OGBURN CE; SMITH AC; BIRD TD; MARTIN GM; FUKUCHI KI
      TRYPSIN-INHIBITOR ACTIVITIES OF FIBROBLASTS INCREASE WITH AGE OF DONOR AND ARE UNALTERED IN FAMILIAL ALZHEIMERS-DISEASE

      Experimental gerontology


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 25/01/21 alle ore 12:28:43