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    1. Davidsson, P; Bogdanovic, N; Lannfelt, L; Blennow, K
      Reduced expression of amyloid precursor protein, presenilin-1 and rab3a incortical brain regions in Alzheimer's disease

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    2. Blomberg, M; Jensen, M; Basun, H; Lannfelt, L; Wahlund, LO
      Cerebrospinal fluid tau levels increase with age in healthy individuals

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    3. Nilsberth, C; Westlind-Danielsson, A; Eckman, CB; Condron, MM; Axelman, K; Forsell, C; Stenh, C; Luthman, J; Teplow, DB; Younkin, SG; Naslund, J; Lannfelt, L
      The 'Arctic' APP mutation (E693G) causes Alzheimer's disease by enhanced Abeta protofibril formation

      NATURE NEUROSCIENCE
    4. Forsell, C; Enmark, E; Axelman, K; Blomberg, M; Wahlund, LO; Gustafsson, JA; Lannfelt, L
      Investigations of a CA repeat in the oestrogen receptor beta gene in patients with Alzheimer's disease

      EUROPEAN JOURNAL OF HUMAN GENETICS
    5. Ingelson, M; Fabre, SF; Lilius, L; Andersen, C; Viitanen, M; Almkvist, O; Wahland, LO; Lannfelt, L
      Increased risk for frontotemporal dementia through interaction between taupolymorpisms and apolipoprotein E & EPSILON;4 (vol 12, pg 905, 2001)

      NEUROREPORT
    6. Ingelson, M; Fabre, SF; Lilius, L; Andersen, C; Viitanen, M; Almkvist, O; Wahlund, LO; Lannfelt, L
      Increased risk for frontotemporal dementia through interaction between taupolymorphisms and apolipoprotein E epsilon 4

      NEUROREPORT
    7. Bogdanovica, N; Bretillon, L; Lund, EG; Diczfalusy, U; Lannfelt, L; Winblad, B; Russell, DW; Bjorkhem, I
      On the turnover of brain cholesterol in patients with Alzheimer's disease.Abnormal induction of the cholesterol-catabolic enzyme CYP46 in glial cells

      NEUROSCIENCE LETTERS
    8. Russo, C; Schettini, G; Saido, TC; Hulette, C; Lippa, C; Lannfelt, L; Ghetti, B; Gambetti, P; Tabaton, M; Teller, JK
      Alzheimer's disease - Molecular consequences of presenilin-1 mutation - Reply

      NATURE
    9. Fabre, SF; Forsell, C; Viitanen, M; Sjogren, M; Wallin, A; Blennow, K; Blomberg, M; Andersen, C; Wahlund, LO; Lannfelt, L
      Clinic-based cases with frontotemporal dementia show increased cerebrospinal fluid tau and high apolipoprotein E epsilon 4 frequency, but no tau genemutations

      EXPERIMENTAL NEUROLOGY
    10. Guo, ZC; Fratiglioni, L; Viitanen, M; Lannfelt, L; Basun, H; Fastbom, J; Winblad, B
      Apolipoprotein E genotypes and the incidence of Alzheimer's disease among persons aged 75 years and older: Variation by use of antihypertensive medication?

      AMERICAN JOURNAL OF EPIDEMIOLOGY
    11. Ito, C; Morisset, S; Krebs, MO; Olie, JP; Loo, H; Poirier, MF; Lannfelt, L; Schwartz, JC; Arrang, JM
      Histamine H-2 receptor gene variants: lack of association with schizophrenia

      MOLECULAR PSYCHIATRY
    12. Jensen, M; Hartmann, T; Engvall, B; Wang, R; Uljon, SN; Sennvik, K; Naslund, J; Muehlhauser, F; Nordstedt, C; Beyreuther, K; Lannfelt, L
      Quantification of Alzheimer amyloid beta peptides ending at residues 40 and 42 by novel ELISA systems

      MOLECULAR MEDICINE
    13. Andersen, C; Jensen, M; Lannfelt, L; Lindau, M; Wahlund, LO
      Amyloid A beta(40) CSF concentrations correlate to frontal lobe atrophy infrontotemporal dementia

      NEUROREPORT
    14. Andersen, C; Fabre, SF; Ostberg, P; Lannfelt, L; Wahlund, LO
      Tau protein in cerebrospinal fluid from semantic dementia patients

      NEUROSCIENCE LETTERS
    15. Mattila, KM; Axelman, K; Rinne, JO; Blomberg, M; Lehtimaki, T; Laippala, P; Roytta, M; Viitanen, M; Wahlund, LO; Winblad, B; Lannfelt, L
      Interaction between estrogen receptor 1 and the epsilon 4 allele of apolipoprotein E increases the risk of familial Alzheimer's disease in women

      NEUROSCIENCE LETTERS
    16. Lannfelt, L; Nordstedt, C
      Genetics of Alzheimer's disease - routes to the pathophysiology

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    17. Russo, C; Schettini, G; Saido, TC; Hulette, C; Lippall, C; Lannfelt, L; Ghetti, B; Gambetti, P; Tabaton, M; Teller, JK
      Neurobiology - Presenilin-1 mutations in Alzheimer's disease

      NATURE
    18. Savioz, A; Leuba, G; Forsell, C; Lilius, L; Rossier, C; Saini, K; Bouras, C; Lannfelt, L
      No detected mutations in the genes for the amyloid precursor protein and presenilins 1 and 2 in a Swiss early-onset Alzheimer's disease family with adominant mode of inheritance

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    19. Ingelson, M; Blomberg, M; Benedikz, E; Wahlund, LO; Karlsson, E; Vanmechelen, E; Lannfelt, L
      Tau immunoreactivity detected in human plasma, but no obvious increase in dementia

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    20. Mustafa, A; Lannfelt, L; Lilius, L; Islam, A; Winblad, B; Adem, A
      Decreased plasma insulin-like growth factor-I level in familial Alzheimer's disease patients carrying the Swedish APP 670/671 mutation

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    21. Wahlund, LO; Basun, H; Almkvist, O; Julin, P; Axelman, K; Shigeta, M; Jelic, V; Nordberg, A; Lannfelt, L
      A follow-up study of the family with the Swedish APP 670/671 Alzheimer's disease mutation

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    22. Wahlund, LO; Julin, P; Lannfelt, L; Lindqvist, J; Svensson, L
      Inheritance of the ApoE epsilon 4 allele increases the rate of brain atrophy in dementia patients

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    23. Bronge, L; Fernaeus, SE; Blomberg, M; Ingelson, M; Lannfelt, L; Isberg, B; Wahlund, LO
      White matter lesions in Alzheimer patients are influenced by apolipoprotein E genotype

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    24. Axelman, K; Basun, H; Lannfelt, L
      Apolipoprotein E and alpha(1)-antichymotrypsin genotypes and age of onset of familial Alzheimer's disease

      DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
    25. Nishimura, M; Yu, G; Levesque, G; Zhang, DM; Ruel, L; Chen, F; Milman, P; Holmes, E; Liang, Y; Kawarai, T; Jo, E; Supala, A; Rogaeva, E; Xu, DM; Janus, C; Levesque, L; Bi, Q; Duthie, M; Rozmahel, R; Mattila, K; Lannfelt, L; Westaway, D; Mount, HTJ; Woodgett, J; Fraser, PE; St George-Hyslop, P
      Presenilin mutations associated with Alzheimer disease cause defective intracellular trafficking of beta-catenin, a component of the presenilin protein complex

      NATURE MEDICINE
    26. Vestling, M; Cedazo-Minguez, A; Adem, A; Wiehager, B; Racchi, M; Lannfelt, L; Cowburn, RF
      Protein kinase C and amyloid precursor protein processing in skin fibroblasts from sporadic and familial Alzheimer's disease cases

      BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
    27. Froelich, S; Houlden, H; Rizzu, P; Chakraverty, S; Baker, M; Kwon, J; Nowotny, P; Isaacs, A; Nowotny, V; Wauters, E; van Baren, MJ; Oostra, BA; Hardy, J; Lannfelt, L; Goate, A; Hutton, M; Lendon, CL; Heutink, P
      Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21

      GENOMICS
    28. Jensen, M; Schroder, J; Blomberg, M; Engvall, B; Pantel, J; Ida, N; Basun, H; Wahlund, LO; Werle, E; Jauss, M; Beyreuther, K; Lannfelt, L; Hartmann, T
      Cerebrospinal fluid A beta 42 is increased early in sporadic Alzheimer's disease and declines with disease progression

      ANNALS OF NEUROLOGY
    29. Sheu, KFR; Brown, AM; Haroutunian, V; Kristal, BS; Thaler, H; Lesser, M; Kalaria, RN; Relkin, NR; Mohs, RC; Lilius, L; Lannfelt, L; Blass, JP
      Modulation by DLST of the genetic risk of Alzheimer's disease in a very elderly population

      ANNALS OF NEUROLOGY
    30. Lilius, L; Fabre, SF; Basun, H; Forsell, C; Axelman, K; Mattila, K; Andreadis, A; Viitanen, M; Winblad, B; Fratiglioni, L; Lannfelt, L
      Tau gene polymorphisms and apolipoprotein E epsilon 4 may interact to increase risk for Alzheimer's disease

      NEUROSCIENCE LETTERS
    31. Johnston, JA; Jensen, M; Lannfelt, L; Walker, B; Williams, CH
      Inhibition of prolylendopeptidase does not affect gamma-secretase processing of amyloid precursor protein in a human neuroblastoma cell line

      NEUROSCIENCE LETTERS
    32. Sheu, KFR; Brown, AM; Kristal, BS; Kalaria, RN; Lilius, L; Lannfelt, L; Blass, JP
      A DLST genotype associated with reduced risk for Alzheimer's disease

      NEUROLOGY
    33. Marutle, A; Warpman, U; Bogdanovic, N; Lannfelt, L; Nordberg, A
      Neuronal nicotinic receptor deficits in Alzheimer patients with the Swedish amyloid precursor protein 670/671 mutation

      JOURNAL OF NEUROCHEMISTRY
    34. Nilsberth, C; Luthman, J; Lannfelt, L; Schultzberg, M
      Expression of presenilin 1 mRNA in rat peripheral organs and brain

      HISTOCHEMICAL JOURNAL
    35. Kostulas, K; Huang, WX; Crisby, M; Jin, YP; He, B; Lannfelt, L; Eggertsen, G; Kostulas, V; Hillert, J
      An angiotensin-converting enzyme gene polymorphism suggests a genetic distinction between ischaemic stroke and carotid stenosis

      EUROPEAN JOURNAL OF CLINICAL INVESTIGATION
    36. CORDER EH; LANNFELT L; BOGDANOVIC N; FRATIGLIONI L; MORI H
      THE ROLE OF APOE POLYMORPHISMS IN LATE-ONSET DEMENTIAS

      Cellular and molecular life sciences
    37. CORDER EH; ROBERTSON K; LANNFELT L; BOGDANOVIC N; EGGERTSEN G; WILKINS J; HALL C
      HIV-INFECTED SUBJECTS WITH THE E4 ALLELE FOR APOE HAVE EXCESS DEMENTIA AND PERIPHERAL NEUROPATHY

      Nature medicine
    38. JELIC V; BLOMBERG M; DIERKS T; BASUN H; SHIGETA M; JULIN P; JENSEN M; LANNFELT L; WINBLAD B; WAHLUND LO
      EEG SLOWING AND CEREBROSPINAL-FLUID TAU-LEVEL IN PATIENTS WITH COGNITIVE DECLINE

      NeuroReport
    39. LEUBA G; SAVIOZ A; LANNFELT L; FORSELL C; LILIUS L; SAINI K
      EXCLUSION STUDY OF FAD GENE-MUTATIONS IN A LARGE SWISS PEDIGREE WITH EARLY-ONSET ALZHEIMERS-DISEASE

      European journal of neuroscience
    40. JULIN P; ALMKVIST O; BASUN H; LANNFELT L; SVENSSON L; WINBLAD B; WAHLUND LO
      BRAIN VOLUMES AND REGIONAL CEREBRAL BLOOD-FLOW IN CARRIERS OF THE SWEDISH ALZHEIMER AMYLOID PROTEIN MUTATION

      Alzheimer disease and associated disorders
    41. Yamada, H; Dahl, ML; Viitanen, M; Winblad, B; Sjoqvist, F; Lannfelt, L
      No association between familial Alzheimer disease and cytochrome P450 polymorphisms

      ALZHEIMER DISEASE & ASSOCIATED DISORDERS
    42. GIBSON GE; ZHANG H; SHEU KFR; BOGDANOVICH N; LINDSAY JG; LANNFELT L; VESTLING M; COWBURN RF
      ALPHA-KETOGLUTARATE DEHYDROGENASE IN ALZHEIMER BRAINS BEARING THE APP670 671 MUTATION/

      Annals of neurology
    43. Mattila, KM; Forsell, C; Pirttila, T; Rinne, JO; Lehtimaki, T; Roytta, M; Lilius, L; Eerola, A; St George-Hyslop, PH; Frey, H; Lannfelt, L
      The Glu318Gly mutation of the presenilin-1 gene does not necessarily causeAlzheimer's disease

      ANNALS OF NEUROLOGY
    44. Almkvist, O; Basun, H; Backman, L; Herlitz, A; Lannfelt, L; Small, B; Viitanen, M; Wahlund, LO; Winblad, B
      Mild cognitive impairment - an early stage of Alzheimer's disease?

      JOURNAL OF NEURAL TRANSMISSION
    45. LANNFELT L
      BIOCHEMICAL DIAGNOSTIC MARKERS TO DETECT EARLY ALZHEIMERS-DISEASE

      Neurobiology of aging
    46. REZNIKWOLF H; MACHADO J; HAROUTUNIAN V; DEMARCO L; WALTER GF; GOLDMAN B; DAVIDSON M; JOHNSTON JA; LANNFELT L; DANI SU; FRIEDMAN E
      SOMATIC MUTATION ANALYSIS OF THE APP AND PRESENILIN-1 AND 2 GENES IN ALZHEIMERS-DISEASE BRAINS

      Journal of neurogenetics
    47. CORDER E; LANNFELT L; MULDER M
      APOLIPOPROTEIN-E AND HERPES-SIMPLEX VIRUS-1 IN ALZHEIMERS-DISEASE

      Lancet
    48. YAMADA H; DAHL ML; LANNFELT L; VIITANEN M; WINBLAD B; SJOQVIST F
      CYP2D6 AND CYP2C19 GENOTYPES IN AN ELDERLY SWEDISH POPULATION

      European Journal of Clinical Pharmacology
    49. GARBARG M; LANNFELT L; BLOMBERG M; WAHLUND LO; FREEDMAN SB; SCHWARTZ C
      BIOCHEMICAL MARKERS OF HISTAMINERGIC NEURONS IN CEREBROSPINAL-FLUID OF ALZHEIMER PATIENTS AND IN AN ANIMAL-MODEL OF ALZHEIMERS-DISEASE

      Naunyn-Schmiedeberg's archives of pharmacology
    50. HUTTON M; LENDON CL; RIZZU P; BAKER M; FROELICH S; HOULDEN H; PICKERINGBROWN S; CHAKRAVERTY S; ISAACS A; GROVER A; HACKETT J; ADAMSON J; LINCOLN S; DICKSON D; DAVIES P; PETERSEN RC; STEVENS M; DEGRAAFF E; WAUTERS E; VANBAREN J; HILLEBRAND M; JOOSSE M; KWON JM; NOWOTNY P; CHE LK; NORTON J; MORRIS JC; REED LA; TROJANOWSKI J; BASUN H; LANNFELT L; NEYSTAT M; FAHN S; DARK F; TANNENBERG T; DODD PR; HAYWARD N; KWOK JBJ; SCHOFIELD PR; ANDREADIS A; SNOWDEN J; CRAUFURD D; NEARY D; OWEN F; OOSTRA BA; HARDY J; GOATE A; VANSWIETEN J; MANN D; LYNCH T; HEUTINK P
      ASSOCIATION OF MISSENSE AND 5'-SPLICE-SITE MUTATIONS IN TAU WITH THE INHERITED DEMENTIA FTDP-17

      Nature
    51. KOSTULAS K; CRISBY M; HUANG WX; LANNFELT L; HAGENFELDT L; EGGERTSEN G; KOSTULAS V; HILLERT J
      A METHYLENETETRAHYDROFOLATE REDUCTASE GENE POLYMORPHISM IN ISCHEMIC STROKE AND IN CAROTID-ARTERY STENOSIS

      European journal of clinical investigation
    52. FORSELL Y; BASUN H; CORDER EH; LANNFELT L; WINBLAD B
      PSYCHOTIC SYMPTOMS AND APOLIPOPROTEIN-E GENOTYPES IN AN ELDERLY POPULATION

      Biological psychiatry
    53. AXELMAN K; BASUN H; LANNFELT L
      WIDE-RANGE OF DISEASE ONSET IN A FAMILY WITH ALZHEIMER-DISEASE AND A HIS163TYR MUTATION IN THE PRESENILIN-1 GENE

      Archives of neurology
    54. KOWALSKA A; WENDER M; LANNFELT L
      LACK OF ASSOCIATION BETWEEN AN INTRONIC POLYMORPHISM IN THE PRESENILIN-1 GENE AND SPORADIC - LATE-ONSET ALZHEIMER-DISEASE IN POLISH PATIENTS

      Dementia and geriatric cognitive disorders
    55. BOGDANOVIC N; CORDER EH; LANNFELT L; BASUN H; WINBLAD B
      APOE POLYMORPHISM AND DISEASE DURATION DETERMINE ALZHEIMERS-DISEASE NEUROPATHOLOGY IN SWEDISH APP DOUBLE MUTATION CARRIERS

      Brain pathology
    56. KOSTULAS K; CRISBY M; HUANG WX; LANNFELT L; KOSTULAS V; HILLERT J
      A METHYLENETETRAHYDROFOLATE REDUCTASE GENE POLYMORPHISM IN ISCHEMIC STROKE AND IN CAROTID-ARTERY STENOSIS

      Brain pathology
    57. VESTLING M; ADEM A; RACCHI M; GIBSON GE; LANNFELT L; COWBURN RF
      DIFFERENTIAL REGULATION OF ADENYLYL-CYCLASE IN FIBROBLASTS FROM SPORADIC AND FAMILIAL ALZHEIMERS-DISEASE CASES WITH PS1 AND APP MUTATIONS

      NeuroReport
    58. LANNFELT L
      THE GENETICS AND PATHOPHYSIOLOGY OF ALZHEIMERS-DISEASE

      Journal of internal medicine
    59. JOHNSTON JA; LANNFELT L; WIEHAGER B; ONEILL C; COWBURN RF
      AMYLOID PRECURSOR PROTEIN HEAT-SHOCK RESPONSE IN LYMPHOBLASTOID CELL-LINES BEARING PRESENILIN-1 MUTATIONS

      Biochimica et biophysica acta. Molecular basis of disease
    60. 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
    61. FORSELL C; FROELICH S; AXELMAN K; VESTLING M; COWBURN RF; LILIUS L; JOHNSTON JA; ENGVALL B; JOHANSSON K; DAHLKILD A; INGELSON M; STGEORGEHYSLOP PH; LANNFELT L
      A NOVEL PATHOGENIC MUTATION (LEU262PHE) FOUND IN THE PRESENILIN-1 GENE IN EARLY-ONSET ALZHEIMERS-DISEASE

      Neuroscience letters
    62. SHANAHAN C; GIBSON GE; COWBURN RF; JOHNSTON JA; WIEHAGER B; LANNFELT L; ONEILL C
      G-PROTEIN SUBUNIT LEVELS IN FIBROBLASTS FROM FAMILIAL ALZHEIMERS-DISEASE PATIENTS - LOWER LEVELS OF THE HIGH-MOLECULAR-WEIGHT GS-ALPHA ISOFORM IN PATIENTS WITH DECREASED BETA-ADRENERGIC-RECEPTOR STIMULATED CAMP FORMATION

      Neuroscience letters
    63. SVENSSON AL; WARPMAN U; HELLSTROMLINDAHL E; BOGDANOVIC N; LANNFELT L; NORDBERG A
      NICOTINIC RECEPTORS, MUSCARINIC RECEPTORS AND CHOLINE-ACETYLTRANSFERASE ACTIVITY IN THE TEMPORAL CORTEX OF ALZHEIMER PATIENTS WITH DIFFERING APOLIPOPROTEIN-E GENOTYPES

      Neuroscience letters
    64. LINDH M; BLOMBERG M; JENSEN M; BASUN H; LANNFELT L; ENGVALL B; SCHARNAGEL H; MARZ W; WAHLUND LO; COWBURN RF
      CEREBROSPINAL-FLUID APOLIPOPROTEIN-E (APOE) LEVELS IN ALZHEIMERS-DISEASE PATIENTS ARE INCREASED AT FOLLOW-UP AND SHOW A CORRELATION WITH LEVELS OF TAU-PROTEIN

      Neuroscience letters
    65. GIBSON GE; VESTLING M; ZHANG H; SZOLOSI S; ALKON D; LANNFELT L; GANDY S; COWBURN RF
      ABNORMALITIES IN ALZHEIMERS-DISEASE FIBROBLASTS BEARING THE APP670 671 MUTATION/

      Neurobiology of aging
    66. FROELICH S; BASUN H; FORSELL C; LILIUS L; AXELMAN K; ANDREADIS A; LANNFELT L
      MAPPING OF A DISEASE LOCUS FOR FAMILIAL RAPIDLY PROGRESSIVE FRONTOTEMPORAL DEMENTIA TO CHROMOSOME 17Q12-21

      American journal of medical genetics
    67. JELIC V; JULIN P; SHIGETA M; NORDBERG A; LANNFELT L; WINBLAD B; WAHLUND LO
      APOLIPOPROTEIN-E EPSILON-4 ALLELE DECREASES FUNCTIONAL CONNECTIVITY IN ALZHEIMERS-DISEASE AS MEASURED BY EEG COHERENCE

      Journal of Neurology, Neurosurgery and Psychiatry
    68. LARGE V; HELLSTROM L; REYNISDOTTIR S; LONNQVIST F; ERIKSSON P; LANNFELT L; ARNER P
      HUMAN BETA-2 ADRENOCEPTOR GENE POLYMORPHISMS ARE HIGHLY FREQUENT IN OBESITY AND ASSOCIATE WITH ALTERED ADIPOCYTE BETA-2 ADRENOCEPTOR FUNCTION

      The Journal of clinical investigation
    69. BERGEM ALM; LANNFELT L
      APOLIPOPROTEIN-E TYPE EPSILON-4 ALLELE, HERITABILITY AND AGE AT ONSETIN TWINS WITH ALZHEIMER-DISEASE AND VASCULAR DEMENTIA

      Clinical genetics
    70. FORSELL Y; CORDER EH; BASUN H; LANNFELT L; VIITANEN M; WINBLAD B
      DEPRESSION AND DEMENTIA IN RELATION TO APOLIPOPROTEIN-E POLYMORPHISM IN A POPULATION-SAMPLE AGE 75+

      Biological psychiatry
    71. BASUN H; ALMKVIST O; AXELMAN K; BRUN A; CAMPBELL TA; COLLINGE J; FORSELL C; FROELICH S; WAHLUND LO; WETTERBERG L; LANNFELT L
      CLINICAL CHARACTERISTICS OF A CHROMOSOME 17-LINKED RAPIDLY PROGRESSIVE FAMILIAL FRONTOTEMPORAL DEMENTIA

      Archives of neurology
    72. ALMKVIST O; BASUN H; WAGNER SL; ROWE BA; WAHLUND LO; LANNFELT L
      CEREBROSPINAL-FLUID LEVELS OF ALPHA-SECRETASE-CLEAVED SOLUBLE AMYLOIDPRECURSOR PROTEIN MIRROR COGNITION IN A SWEDISH FAMILY WITH ALZHEIMER-DISEASE AND A GENE MUTATION

      Archives of neurology
    73. CORDER EH; JELIC V; BASUN H; LANNFELT L; VALIND S; WINBLAD B; NORDBERG A
      NO DIFFERENCE IN CEREBRAL GLUCOSE-METABOLISM IN PATIENTS WITH ALZHEIMER-DISEASE AND DIFFERING APOLIPOPROTEIN-E GENOTYPES

      Archives of neurology
    74. 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
    75. SHERRINGTON R; FROELICH S; SORBI S; CAMPION D; CHI H; ROGAEVA EA; LEVESQUE G; ROGAEV EI; LIN C; LIANG Y; IKEDA M; MAR L; BRICE A; AGID Y; PERCY ME; CLERGETDARPOUX F; PIACENTINI S; MARCON G; NACMIAS B; AMADUCCI L; FREBOURG T; LANNFELT L; ROMMENS JM; STGEORGEHYSLOP PH
      ALZHEIMERS-DISEASE ASSOCIATED WITH MUTATIONS IN PRESENILIN-2 IS RARE AND VARIABLY PENETRANT

      Human molecular genetics
    76. KALARIA RN; COHEN DL; GREENBERG BD; SAVAGE MJ; BOGDANOVIC NE; WINBLAD B; LANNFELT L; ADEM A
      ABUNDANCE OF THE LONGER A-BETA(42) IN NEOCORTICAL AND CEREBROVASCULARAMYLOID-BETA DEPOSITS IN SWEDISH FAMILIAL ALZHEIMERS-DISEASE AND DOWNS-SYNDROME

      NeuroReport
    77. JONSSON E; LANNFELT L; ENGVALL B; SEDVALL G
      LACK OF ASSOCIATION BETWEEN SCHIZOPHRENIA AND THE APOLIPOPROTEIN E-EPSILON-4 ALLELE

      European archives of psychiatry and clinical neuroscience
    78. INGELSON M; VANMECHELEN E; LANNFELT L
      MICROTUBULE-ASSOCIATED PROTEIN-TAU IN HUMAN FIBROBLASTS WITH THE SWEDISH ALZHEIMER MUTATION

      Neuroscience letters
    79. BLOMBERG M; JENSEN M; BASUN H; LANNFELT L; WAHLUND LO
      INCREASING CEREBROSPINAL-FLUID TAU-LEVELS IN A SUBGROUP OF ALZHEIMER PATIENTS WITH APOLIPOPROTEIN-E ALLELE EPSILON-4 DURING 14 MONTHS FOLLOW-UP

      Neuroscience letters
    80. JOHNSTON JA; NORGREN S; ANNEREN G; COWBURN RF; LANNFELT L
      A NEW QUANTITATIVE SOLUTION HYBRIDIZATION-RNASE PROTECTION ASSAY FOR APP AND APLP2 MESSENGER-RNA

      Molecular brain research
    81. JOHNSTON JA; NORGREN S; RAVID R; WASCO W; WINBLAD B; LANNFELT L; COWBURN RF
      QUANTIFICATION OF APP AND APLP2 MESSENGER-RNA IN APOE GENOTYPED ALZHEIMERS-DISEASE BRAINS

      Molecular brain research
    82. LIU L; FORSELL C; LILIUS L; AXELMAN K; CORDER EH; LANNFELT L
      ALLELIC ASSOCIATION BUT ONLY WEAK EVIDENCE FOR LINKAGE TO THE APOLIPOPROTEIN-E LOCUS IN LATE-ONSET SWEDISH ALZHEIMER FAMILIES

      American journal of medical genetics
    83. CORDER EH; BASUN H; LANNFELT L; VIITANEN M; WINBLAD B
      ATTENUATION OF APOLIPOPROTEIN-E EPSILON-4 ALLELE GENE DOSE IN LATE AGE

      Lancet
    84. BASUN H; CORDER EH; GUO Z; LANNFELT L; CORDER LS; MANTON KG; WINBLAD B; VIITANEN M
      APOLIPOPROTEIN-E POLYMORPHISM AND STROKE IN A POPULATION-SAMPLE AGED 75 YEARS OR MORE

      Stroke
    85. STGEORGEHYSLOP PH; SHERRINGTON R; ROGAEV E; TSUDA T; IKEDA M; POLLEN D; ROSES A; PERICAKVANCE M; NEE L; POLINSKY R; RAINERO I; PINESSI L; VAULA G; SORBI S; AMADUCCI L; BRUNI A; MONTESI M; FONCIN JF; ABE K; AOKI M; SHOJI M; HIRAI S; WATANABE M; LANNFELT L
      ANALYSIS OF MUTATIONS IN 2 HOMOLOGOUS GENES CAUSING FAMILIAL ALZHEIMERS-DISEASE

      Neurology
    86. JOHNSTON JA; FROELICH S; LANNFELT L; COWBURN RF
      QUANTIFICATION OF PRESENILIN-1 MESSENGER-RNA IN ALZHEIMERS-DISEASE BRAINS

      FEBS letters
    87. JONSSON E; SEDVALL G; BRENE S; GUSTAVSSON JP; GEIJER T; TERENIUS L; CROCQ MA; LANNFELT L; TYLEC A; SOKOLOFF P; SCHWARTZ JC; WIESEL FA
      DOPAMINE-RELATED GENES AND THEIR RELATIONSHIPS TO MONOAMINE METABOLITES IN CSF

      Biological psychiatry
    88. YOUNKIN SG; SONG XH; SCHEUNER D; ECKMAN C; PRADA CM; JENSEN J; LANNFELT L; HARDY J; TANZI R; SCHELLENBERG G; SELKOE D; SUZUKI N
      THE EFFECT OF AMYLOID PRECURSOR PROTEIN AND PRESENILIN MUTATIONS ON AMYLOID-BETA PROTEIN

      Biological psychiatry
    89. CORDER EH; LANNFELT L; VIITANEN M; CORDER LS; MANTON KG; WINBLAD B; BASUN H
      APOLIPOPROTEIN-E GENOTYPE DETERMINES SURVIVAL IN THE OLDEST-OLD (85 YEARS OR OLDER) WHO HAVE GOOD COGNITION

      Archives of neurology
    90. MANN DMA; IWATSUBO T; IHARA Y; CAIRNS NJ; LANTOS PL; BOGDANOVIC N; LANNFELT L; WINBLAD B; MAATSCHIEMAN MLC; ROSSOR MN
      PREDOMINANT DEPOSITION OF AMYLOID-BETA(42(43)) IN PLAQUES IN CASES OFALZHEIMERS-DISEASE AND HEREDITARY CEREBRAL-HEMORRHAGE ASSOCIATED WITHMUTATIONS IN THE AMYLOID PRECURSOR PROTEIN GENE

      The American journal of pathology
    91. LANNFELT L
      GENETICS OF ALZHEIMERS-DISEASE

      Acta neurologica Scandinavica
    92. LANNFELT L; BASUN H; WAHLUND LO; ROWE BA; WAGNER SL
      DECREASED ALPHA-SECRETASE-CLEAVED AMYLOID PRECURSOR PROTEIN AS A DIAGNOSTIC MARKER FOR ALZHEIMERS-DISEASE

      Nature medicine
    93. HAASS C; LEMERE CA; CAPELL A; CITRON M; SEUBERT P; SCHENK D; LANNFELT L; SELKOE DJ
      THE SWEDISH MUTATION CAUSES EARLY-ONSET ALZHEIMERS-DISEASE BY BETA-SECRETASE CLEAVAGE WITHIN THE SECRETORY PATHWAY

      Nature medicine
    94. CLARK RF; HUTTON M; FULDNER RA; FROELICH S; KARRAN E; TALBOT C; CROOK R; LENDON C; PRIHAR G; HE C; KORENBLAT K; MARTINEZ A; WRAGG M; BUSFIELD F; BEHRENS MI; MYERS A; NORTON J; MORRIS J; MEHTA N; PEARSON C; LINCOLN S; BAKER M; DUFF K; ZEHR C; PEREZTUR J; HOULDEN H; RUIZ A; OSSA J; LOPERA F; ARCOS M; MADRIGAL L; COLLINGE J; HUMPHREYS C; ASHWORTH A; SARNER S; FOX N; HARVEY R; KENNEDY A; ROQUES P; CLINE RT; PHILLIPS CA; VENTER JC; FORSELL L; AXELMAN K; LILIUS L; JOHNSTON J; COWBURN R; VIITANEN M; WINBLAD B; KOSIK K; HALTIA M; POYHONEN M; DICKSON D; MANN D; NEARY D; SNOWDEN J; LANTOS P; LANNFELT L; ROSSOR M; ROBERTS GW; ADAMS MD; HARDY J; GOATE A
      THE STRUCTURE OF THE PRESENILIN-1 (S182) GENE AND IDENTIFICATION OF 6NOVEL MUTATIONS IN EARLY-ONSET AD FAMILIES

      Nature genetics
    95. PEREZTUR J; FROELICH S; PRIHAR G; CROOK R; BAKER M; DUFF K; WRAGG M; BUSFIELD F; LENDON C; CLARK RF; ROQUES P; FULDNER RA; JOHNSTON J; COWBURN R; FORSELL C; AXELMAN K; LILIUS L; HOULDEN H; KARRAN E; ROBERTS GW; ROSSOR M; ADAMS MD; HARDY J; GOATE A; LANNFELT L; HUTTON M
      A MUTATION IN ALZHEIMERS-DISEASE DESTROYING A SPLICE ACCEPTOR SITE INTHE PRESENILIN-1 GENE

      NeuroReport
    96. ANDERSSON C; THUNELL S; FLODERUS Y; FORSELL C; LUNDIN G; ANVRET M; LANNFELT L; WETTERBERG L; LITHNER F
      DIAGNOSIS OF ACUTE INTERMITTENT PORPHYRIA IN NORTHERN SWEDEN - AN EVALUATION OF MUTATION ANALYSIS AND BIOCHEMICAL METHODS

      Journal of internal medicine
    97. VESTLING M; COWBURN RF; VENIZELOS N; LANNFELT L; WINBLAD B; ADEM A
      CHARACTERIZATION OF MUSCARINIC ACETYLCHOLINE-RECEPTORS IN CULTURED ADULT SKIN FIBROBLASTS - EFFECTS OF THE SWEDISH ALZHEIMERS-DISEASE APP-670 671 MUTATION ON BINDING LEVELS/

      Journal of neural transmission. Parkinson's disease and dementia section
    98. NASLUND J; THYBERG J; TJERNBERG LO; WERNSTEDT C; KARLSTROM AR; BOGDANOVIC N; GANDY SE; LANNFELT L; TERENIUS L; NORDSTEDT C
      CHARACTERIZATION OF STABLE COMPLEXES INVOLVING APOLIPOPROTEIN-E AND THE AMYLOID-BETA PEPTIDE IN ALZHEIMERS-DISEASE BRAIN

      Neuron
    99. LANNFELT L; PEDERSEN NL; LILIUS L; AXELMAN K; JOHANSSON K; VIITANEN M; GATZ M
      APOLIPOPROTEIN EPSILON-4 ALLELE IN SWEDISH TWINS AND SIBLINGS WITH ALZHEIMER-DISEASE

      Alzheimer disease and associated disorders
    100. LANNFELT L; BASUN H; VIGOPELFREY C; WAHLUND LO; WINBLAD B; LIEBERBURG I; SCHENK D
      AMYLOID BETA-PEPTIDE IN CEREBROSPINAL-FLUID IN INDIVIDUALS WITH THE SWEDISH ALZHEIMER AMYLOID PRECURSOR PROTEIN MUTATION

      Neuroscience letters


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 09/08/20 alle ore 01:56:14