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La ricerca find articoli where authors phrase all words ' WILHELMSEN KC' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 47 riferimenti
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    1. Takacs, Z; Wilhelmsen, KC; Sorota, S
      Snake alpha-neurotoxin binding site on the Egyptian cobra (Naja haje) nicotinic acetylcholine receptor is conserved

      MOLECULAR BIOLOGY AND EVOLUTION
    2. Geschwind, DH; Robidoux, J; Alarcon, M; Miller, BL; Wilhelmsen, KC; Cummings, JL; Nasreddine, ZS
      Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia

      ANNALS OF NEUROLOGY
    3. Wilhelmsen, KC; Miller, B; Geschwind, D
      Neuronal subpopulations and genetic background in tauopathies: a catch 22 story?

      NEUROBIOLOGY OF AGING
    4. Lynch, T; Sano, M; Marder, KS; Bell, KL; Foster, NL; Defendini, RF; Sima, AAF; Keohane, C; Nygaard, TG; Fahn, S; Mayeux, R; Rowland, LP; Wilhelmsen, KC
      Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex

      NEUROLOGY
    5. Wilhelmsen, KC; Clark, LN; Miller, BL; Geschwind, DH
      Tau mutations in frontotemporal dementia

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    6. Goedert, M; Spillantini, MG; Crowther, RA; Chen, SG; Parchi, P; Tabaton, M; Lanska, DJ; Markesbery, WR; Wilhelmsen, KC; Dickson, DW; Petersen, RB; Gambetti, P
      Tau gene mutation in familial progressive subcortical gliosis

      NATURE MEDICINE
    7. Nasreddine, ZS; Loginov, M; Clark, LN; Lamarche, J; Miller, BL; Lamontagne, A; Zhukareva, V; Lee, VMY; Wilhelmsen, KC; Geschwind, DH
      From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

      ANNALS OF NEUROLOGY
    8. Wilhelmsen, KC
      The tangled biology of tau

      PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
    9. WILHELMSEN KC
      CHROMOSOME 17-LINKED DEMENTIAS

      Cellular and molecular life sciences
    10. Wilhelmsen, KC
      Frontotemporal dementia genetics

      JOURNAL OF GERIATRIC PSYCHIATRY AND NEUROLOGY
    11. MIREL DB; MARDER K; GRAZIANO J; FREYER G; ZHAO QQ; MAYEUX R; WILHELMSEN KC
      CHARACTERIZATION OF THE HUMAN MITOCHONDRIAL ACONITASE GENE (ACO2)

      Gene
    12. 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
    13. LENDON CL; LYNCH T; NORTON J; MCKEEL DW; BUSFIELD F; CRADDOCK N; CHAKRAVERTY S; GOPALAKRISHNAN G; SHEARS SD; GRIMMETT W; WILHELMSEN KC; HANSEN L; MORRIS JC; GOATE AM
      HEREDITARY DYSPHASIC DISINHIBITION DEMENTIA - A FRONTOTEMPORAL DEMENTIA LINKED TO 17Q21-22

      Neurology
    14. CLARK LN; POORKAJ P; WSZOLEK Z; GESCHWIND DH; NASREDDINE ZS; MILLER B; LI D; PAYAMI H; AWERT F; MARKOPOULOU K; ANDREADIS A; DSOUZA I; LEE VMY; REED L; TROJANOWSKI JQ; ZHUKAREVA V; BIRD T; SCHELLENBERG G; WILHELMSEN KC
      PATHOGENIC IMPLICATIONS OF MUTATIONS IN THE TAU GENE IN PALLIDO-PONTO-NIGRAL DEGENERATION AND RELATED NEURODEGENERATIVE DISORDERS LINKED TOCHROMOSOME-17

      Proceedings of the National Academy of Sciences of the United Statesof America
    15. MORSE JH; JONES AC; BARST RJ; HODGE SE; WILHELMSEN KC; NYGAARD TG
      FAMILIAL PRIMARY PULMONARY-HYPERTENSION LOCUS MAPPED TO CHROMOSOME 2Q31-Q32

      Chest
    16. WILHELMSEN KC
      FRONTOTEMPORAL DEMENTIA IS ON THE MAP-TAU

      Annals of neurology
    17. WILHELMSEN KC
      DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEX (DDPAC) IS A NON-ALZHEIMERS FRONTOTEMPORAL DEMENTIA

      Journal of neural transmission. Supplementum
    18. WILHELMSEN KC
      DOES TUMOR-NECROSIS-FACTOR PLAY A ROLE IN ALCOHOLIC STEATOHEPATITIS -THE POTENTIAL PITFALLS OF A CASE-CONTROLLED ALLELIC ASSOCIATION ANALYSIS

      Hepatology
    19. MORSE JH; JONES AC; BARST RJ; HODGE SE; WILHELMSEN KC; NYGAARD TG
      MAPPING OF FAMILIAL PRIMARY PULMONARY-HYPERTENSION LOCUS (PPH1) TO CHROMOSOME 2Q31-Q32

      Circulation
    20. MIREL DB; FREYER G; GRAZIANO J; MARDER K; MAYEUX R; WILHELMSEN KC
      CHARACTERIZATION OF THE HUMAN MITOCHONDRIAL ACONITASE GENE (ACO2)

      American journal of human genetics
    21. CLARK LN; MILLER BL; WSZOLEK ZK; WILHELMSEN KC
      REFINED MAPPING AND CANDIDATE GENE ANALYSIS OF CHROMOSOME 17Q21-22 LINKED FRONTOTEMPORAL DEMENTIA

      American journal of human genetics
    22. TSUJIMOTO S; CLARK L; WILHELMSEN KC
      FINE MAPPING STRATEGY FOR IDENTIFYING THE GENETIC CAUSE OF LUBAG, X-LINKED DYSTONIA-PARKINSONISM (XDPD)

      American journal of human genetics
    23. ISOZUMI K; DELONG R; KAPLAN J; DENG HX; IQBAL Z; HUNG WY; WILHELMSEN KC; HENTATI A; PERICAKVANCE MA; SIDDIQUE T
      LINKAGE OF SCAPULOPERONEAL SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 12Q24.1-Q24.31

      Human molecular genetics
    24. WIJKER M; WSZOLEK ZK; WOLTERS ECH; ROOIMANS MA; PALS G; PFEIFFER RF; LYNCH T; RODNITZKY RL; WILHELMSEN KC; ARWERT F
      LOCALIZATION OF THE GENE FOR RAPIDLY PROGRESSIVE AUTOSOMAL-DOMINANT PARKINSONISM AND DEMENTIA WITH PALLIDO-PONTO-NIGRAL DEGENERATION TO CHROMOSOME 17Q21

      Human molecular genetics
    25. ISOZUMI K; DELONG R; DENG HX; KAPLAN J; IQBAL Z; HUNG WY; WILHELMSEN KC; HENTATI A; PERICAKVANCE MA; SIDDIQUE T
      LINKAGE OF SCAPULOPERONEAL SPINAL MUSCULAR-ATROPHY TO CHROMOSOME 12Q24.1-Q24.31

      Annals of neurology
    26. SIMA AAF; DEFENDINI R; KEOHANE C; DAMATO C; FOSTER NL; PARCHI P; GAMBETTI P; LYNCH T; WILHELMSEN KC
      THE NEUROPATHOLOGY OF CHROMOSOME 17-LINKED DEMENTIA

      Annals of neurology
    27. WILHELMSEN KC; BLAKE DM; LYNCH T; MABUTAS J; DEVERA M; NEYSTAT M; BERNSTEIN M; HIRANO M; GILLIAM TC; MURPHY PL; SOLA MD; BONILLA E; SCHOTLAND DL; HAYS AP; ROWLAND LP
      CHROMOSOME 12-LINKED AUTOSOMAL-DOMINANT SCAPULOPERONEAL MUSCULAR-DYSTROPHY

      Annals of neurology
    28. WILHELMSEN KC; WSZOLEK ZK; CURRIER RC; LANSKA DJ
      THE CLINICAL SPECTRUM OF CHROMOSOME 17Q21-22-LINKED DEGENERATIVE SYNDROMES

      Neurology
    29. OTTMAN R; RISCH N; HAUSER WA; PEDLEY TA; LEE JH; BARKERCUMMINGS C; LUSTENBERGER A; NAGLE KJ; LEE KS; SCHEUER ML; NEYSTAT M; SUSSER M; WILHELMSEN KC
      LOCALIZATION OF A GENE FOR PARTIAL EPILEPSY TO CHROMOSOME 10Q

      Nature genetics
    30. WEEKS DE; NYGAARD TG; NEYSTAT M; HARBY LD; WILHELMSEN KC
      A HIGH-RESOLUTION GENETIC-LINKAGE MAP OF THE PERICENTROMERIC REGION OF THE HUMAN X-CHROMOSOME

      Genomics
    31. WILHELMSEN KC; LYNCH T; ARWERT F; WSZOLEK Z
      2 LARGE PARKINSONIAN KINDREDS LINKED TO WLD LOCUS ON CHROMOSOME-17Q-21-22

      Annals of neurology
    32. PETERSEN RB; TABATON M; CHEN SG; MONARI L; RICHARDSON SL; LYNCHES T; MANETTO V; LANSKA DJ; MARKESBERY WR; CURRIER RD; AUTILIOGAMBETTI L; WILHELMSEN KC; GAMBETTI P
      FAMILIAL PROGRESSIVE SUBCORTICAL GLIOSIS - PRESENCE OF PRIONS AND LINKAGE TO CHROMOSOME-17

      Neurology
    33. SIMA AAF; DAMATO C; FOSTER NL; LYNCH T; DEFENDINI RF; WILHELMSEN KC
      NEURONAL AND GLIAL INCLUSIONS IN FAMILIAL PROGRESSIVE LIMBIC LOBE SCLEROSIS

      Journal of neuropathology and experimental neurology
    34. BRESSMAN SB; HUNT AL; HEIMAN GA; BRIN MF; BURKE RE; FAHN S; TRUGMAN JM; DELEON D; KRAMER PL; WILHELMSEN KC; NYGAARD TG
      EXCLUSION OF THE DYT1 LOCUS IN A NON-JEWISH FAMILY WITH EARLY-ONSET DYSTONIA

      Movement disorders
    35. BRESSMAN SB; HUNT AL; HEIMAN GA; BRIN MF; BURKE RE; FAHN S; TRUGMAN JM; DELEON D; KRAMER PL; WILHELMSEN KC; NYGAARD TG
      EXCLUSION OF THE DYT1 LOCUS IN A NON-JEWISH FAMILY WITH EARLY-ONSET DYSTONIA

      Movement disorders
    36. LEW MF; SHINDO M; MOSKOWITZ CB; WILHELMSEN KC; FAHN S; WATERS CH
      ADDUCTOR LARYNGEAL BREATHING DYSTONIA IN A PATIENT WITH LUBAG (X-LINKED DYSTONIA-PARKINSONISM SYNDROME)

      Movement disorders
    37. LASSER DM; DEVIVO DC; GARVIN J; WILHELMSEN KC
      TURCOTS-SYNDROME - EVIDENCE FOR LINKAGE TO THE ADENOMATOUS POLYPOSIS-COLI (APC) LOCUS

      Neurology
    38. NYGAARD TG; BARCLAY CL; SEGAWA M; FLETCHER NA; DUFF J; NOMURA Y; HARDING AE; LANG AE; WILHELMSEN KC; GEORGEHYSLOP PHS; TSUJI S; FAHN S; RISCH NJ; WEEKS DE
      GENETIC-LINKAGE MAPPING OF DOPA-RESPONSIVE DYSTONIA (DRD)

      Neurology
    39. LYNCH T; SANO M; MARDER KS; BELL KL; FOSTER NL; DEFENDINI RF; SIMA AAF; KEOHANE C; NYGAARD TG; FAHN S; MAYEUX R; ROWLAND LP; WILHELMSEN KC
      CLINICAL CHARACTERISTICS OF A FAMILY WITH CHROMOSOME 17-LINKED DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEX

      Neurology
    40. WILHELMSEN KC; LYNCH T; PAVLOU E; HIGGINS M; NYGAARD TG
      LOCALIZATION OF DISINHIBITION-DEMENTIA-PARKINSONISM-AMYATROPHY COMPLEX TO 17Q21-22

      American journal of human genetics
    41. KRAMER PL; HEIMAN GA; GASSER T; OZELIUS LJ; DELEON D; BRIN MF; BURKE RE; HEWETT J; HUNT AL; MOSKOWITZ C; NYGAARD TG; WILHELMSEN KC; FAHN S; BREAKEFIELD XO; RISCH NJ; BRESSMAN SB
      THE DYTI GENE ON 9Q34 IS RESPONSIBLE FAR MOST CASES OF EARLY LIMB-ONSET IDIOPATHIC TORSION DYSTONIA IN NON-JEWS

      American journal of human genetics
    42. NYGAARD TG; WILHELMSEN KC; RISCH NJ; BROWN DL; TRUGMAN JM; GILLIAM TC; FAHN S; WEEKS DE
      LINKAGE MAPPING OF DOPA-RESPONSIVE DYSTONIA (DRD) TO CHROMOSOME 14Q

      Nature genetics
    43. LASSER DM; WILHELMSEN KC; NYGAARD TG; TANTRAVAHI U
      CHARACTERIZATION OF MICROSATELLITE POLYMORPHISMS DXS691 AND DXS692 - GENETIC-MAPPING TO XQ26.2-XQ27 AND XQ25-XQ26.2

      Genomics
    44. WATERS CH; TAKAHASHI H; WILHELMSEN KC; SHUBIN R; SNOW BJ; NYGAARD TG; MOSKOWITZ CB; FAHN S; CALNE DB
      PHENOTYPIC-EXPRESSION OF X-LINKED DYSTONIA-PARKINSONISM (LUBAG) IN 2 WOMEN

      Neurology
    45. LASSER DM; DEVIVO DC; GARVIN J; WILHELMSEN KC
      GENETICS OF TURCOTS-SYNDROME

      Neurology
    46. PICA A; BLAKE D; STEINGLASS J; NYGAARD TG; ROWLAND LP; WILHELMSEN KC
      SCAPULOPERONEAL MUSCULAR-DYSTROPHY IS GENETICALLY DISTINCT FROM FASCIOSCAPULOHUMERAL MUSCULAR-DYSTROPHY

      Neurology
    47. WILHELMSEN KC; PEREZ M; GAMEZ G; PASCILES O; SOBREVEGA EE; ROSALES R; MOSKOWITZ C; NEYSTAT M; NYGAARD T; FAHN S
      IDENTIFICATION OF PRESYMPTOMATIC CARRIERS OF LUBAG (X-LINKED DYSTONIA-PARKINSONISM)

      Neurology


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Documento generato il 04/08/20 alle ore 02:16:34