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    1. Bonifati, V; De Michele, G; Lucking, CB; Durr, A; Fabrizio, E; Ambrosio, G; Vanacore, N; De Mari, M; Marconi, R; Capus, L; Breteler, MMB; Gasser, T; Oostra, B; Wood, N; Agid, Y; Filla, A; Meco, G; Brice, A
      The parkin gene and its phenotype

      NEUROLOGICAL SCIENCES
    2. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; Leguern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    3. Gasser, T; Dichgans, M; Finsterer, J; Hausmanowa-Petrusewicz, I; Jurkat-Rott, K; Klopstock, T; LeGuern, E; Lehesjoki, AE; Lehmann-Horn, F; Lynch, T; Morris, H; Rossor, M; Steinlein, OK; Wood, N; Zaremba, J; Zeviani, M; Zoharn, A
      EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts

      EUROPEAN JOURNAL OF NEUROLOGY
    4. Zimprich, A; Grabowski, M; Asmus, F; Naumann, M; Berg, D; Bertram, M; Scheidtmann, K; Kern, P; Winkelmann, F; Muller-Myhsok, B; Riedel, L; Bauer, M; Muller, T; Castro, M; Meitinger, T; Strom, TM; Gasser, T
      Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome

      NATURE GENETICS
    5. West, AB; Zimprich, A; Lockhart, PJ; Farrer, M; Singleton, A; Holtom, B; Lincoln, S; Hofer, A; Hill, L; Muller-Myhsok, B; Wszolek, ZK; Hardy, J; Gasser, T
      Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes

      EUROPEAN JOURNAL OF HUMAN GENETICS
    6. Grohme, K; von Maravic, M; Gasser, T; Borasio, GD
      A case of amyotrophic lateral sclerosis with a very slow progression over 44 years

      NEUROMUSCULAR DISORDERS
    7. Wunderlich, S; Reiners, K; Gasser, T; Naumann, M
      Cervical dystonia in monozygotic twins: Case report and review of the literature

      MOVEMENT DISORDERS
    8. Asmus, F; Zimprich, A; Naumann, M; Berg, D; Bertram, M; Ceballos-Baumann, A; Pruszak-Seel, R; Kabus, C; Dichgans, M; Fuchs, S; Muller-Myhsok, B; Gasser, T
      Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families

      ANNALS OF NEUROLOGY
    9. Goebels, N; Helmchen, C; Abele-Horn, M; Gasser, T; Pfister, HW
      Extensive myelitis associated with Mycoplasma pneumoniae infection: Magnetic resonance imaging and clinical long-term follow-up

      JOURNAL OF NEUROLOGY
    10. Gasser, T
      Genetics of Parkinson's disease

      JOURNAL OF NEUROLOGY
    11. Bauer, M; Meyer, M; Sautter, J; Gasser, T; Ueffing, M; Widmer, HR
      Liposome-mediated gene transfer to fetal human ventral mesencephalic explant cultures

      NEUROSCIENCE LETTERS
    12. Vela-Navarrete, R; Benoit, G; Gasser, T
      Renal transplantation

      EUROPEAN UROLOGY
    13. Gasser, T; Sheehy, A; Largo, RH
      Statistical characterization of the pubertal growth spurt

      ANNALS OF HUMAN BIOLOGY
    14. Gasser, T; Sheehy, A; Molinari, L; Largo, RH
      Growth processes leading to a large or small adult size

      ANNALS OF HUMAN BIOLOGY
    15. Gasser, T; Sheehy, A; Molinari, L; Largo, RH
      Growth of early and late maturers

      ANNALS OF HUMAN BIOLOGY
    16. Zink, M; Grimm, L; Wszolek, ZK; Gasser, T
      Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha)

      JOURNAL OF NEURAL TRANSMISSION
    17. Thiel, G; Vogelbach, P; Gurke, L; Gasser, T; Lehmann, K; Voegele, T; Kiss, A; Kirste, G
      Crossover renal transplantation: Hurdles to be cleared!

      TRANSPLANTATION PROCEEDINGS
    18. Iannucci, G; Dichgans, M; Rovaris, M; Bruning, R; Gasser, T; Giacomotti, L; Yousry, TA; Filippi, M
      Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy

      STROKE
    19. Pfefferkorn, T; von Stuckrad-Barre, S; Herzog, J; Gasser, T; Hamann, GF; Dichgans, M
      Reduced cerebrovascular CO2 reactivity in CADASIL - A transcranial Dopplersonography study

      STROKE
    20. Auer, DP; Putz, B; Gossl, C; Elbel, GK; Gasser, T; Dichgans, M
      Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison

      RADIOLOGY
    21. Dichgans, M; Herzog, J; Gasser, T
      NOTCH3 mutation involving three cysteine residues in a family with typicalCADASIL

      NEUROLOGY
    22. Dodel, RC; Lohmuller, F; Du, Y; Eastwood, B; Gocke, P; Oertel, WH; Gasser, T
      A polymorphism in the intronic region of the IL-1 alpha gene and the risk for Parkinson's disease

      NEUROLOGY
    23. Nocito, A; Bubendorf, L; Tinner, EM; Suess, K; Wagner, U; Forster, T; Kononen, J; Fijan, A; Bruderer, J; Schmid, U; Ackermann, D; Maurer, R; Alund, G; Knonagel, H; Rist, M; Anabitarte, M; Hering, F; Hardmeier, T; Schoenenberger, AJ; Flury, R; Jager, P; Fehr, JL; Schraml, P; Moch, H; Mihatsch, MJ; Gasser, T; Sauter, G
      Microarrays of bladder cancer tissue are highly representative of proliferation index and histological grade

      JOURNAL OF PATHOLOGY
    24. Largo, RH; Caflisch, JA; Hug, F; Muggli, K; Molnar, AA; Molinari, L; Sheehy, A; Gasser, T
      Neuromotor development from 5 to 18 years. Part 1: timed performance

      DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
    25. Simon, R; Richter, J; Wagner, U; Fijan, A; Bruderer, J; Schmid, U; Ackermann, D; Maurer, R; Alund, G; Knonagel, H; Rist, M; Wilber, K; Anabitarte, M; Hering, F; Hardmeier, T; Schonenberger, A; Flury, R; Jager, P; Fehr, JL; Schraml, P; Moch, H; Mihatsch, MJ; Gasser, T; Sauter, G
      High-throughout tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1)copy number alterations in urinary bladder cancer

      CANCER RESEARCH
    26. Schraml, P; Struckmann, K; Bednar, R; Fu, WT; Gasser, T; Wilber, K; Kononen, J; Sauter, G; Mihatsch, MJ; Moch, H
      CDKN2A mutation analysis, protein expression, and deletion mapping of chromosome 9p in conventional clear-cell renal carcinomas - Evidence for a second tumor suppressor gene proximal to CDKN2A

      AMERICAN JOURNAL OF PATHOLOGY
    27. 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
    28. Seifert, B; Gasser, T
      Data adaptive ridging in local polynomial regression

      JOURNAL OF COMPUTATIONAL AND GRAPHICAL STATISTICS
    29. Bauer, M; Meyer, M; Grimm, L; Meitinger, T; Zimmer, J; Gasser, T; Ueffing, M; Widmer, HR
      Nonviral glial cell-derived neurotrophic factor gene transfer enhances survival of cultured dopaminergic neurons and improves their function after transplantation in a rat model of Parkinson's disease

      HUMAN GENE THERAPY
    30. Dichgans, M; Ludwig, H; Muller-Hocker, J; Messerschmidt, A; Gasser, T
      Small in-frame deletions and missense mutations in CADASIL: 3D models predict misfolding of Notch3 EGF-like repeat domains

      EUROPEAN JOURNAL OF HUMAN GENETICS
    31. Kamm, C; Naumann, M; Mueller, J; Mai, N; Riedel, L; Wissel, J; Gasser, T
      The DYT1 GAG deletion is infrequent in sporadic and familial writer's cramp

      MOVEMENT DISORDERS
    32. Hauffa, BP; Schlippe, G; Roos, M; Gillessen-Kaesbach, G; Gasser, T
      Spontaneous growth in German children and adolescents with genetically confirmed Prader-Willi syndrome

      ACTA PAEDIATRICA
    33. Warner, T; Camfield, L; Marsden, CD; Nemeth, AH; Hyman, N; Harley, D; Wissel, J; Poewe, W; Marttila, RJ; Erjanti, H; Burbaud, P; Lagueny, A; Kamm, C; Gasser, T; Franz, D; Castelon-Konkiewitz, E; Trender, I; Ceballos-Baumann, A; Nebe, A; Freudenberg, B; Bentivoglio, A; Cassetta, E; Albanese, A; Curra, A; Vacca, L; Berardelli, A; Ferreira, J; Sampaio, C; Passao, V; Marti, F; Tolosa, E; Claveria, L; Duarte, J; Ben-Shlomo, Y; Newton, A
      A prevalence study of primary dystonia in eight European countries

      JOURNAL OF NEUROLOGY
    34. Fattinger, K; Roos, M; Vergeres, P; Holenstein, C; Kind, B; Masche, U; Stocker, DN; Braunschweig, S; Kullak-Ublick, GA; Galeazzi, RL; Follath, F; Gasser, T; Meier, PJ
      Epidemiology of drug exposure and adverse drug reactions in two Swiss departments of internal medicine

      BRITISH JOURNAL OF CLINICAL PHARMACOLOGY
    35. Gasser, T
      Autosomal-dominantly inherited forms of Parkinson's disease

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    36. Sheehy, A; Gasser, T; Molinari, L; Largo, RH
      Contribution of growth phases to adult size

      ANNALS OF HUMAN BIOLOGY
    37. Gasser, T; Sheehy, A; Molinari, L; Largo, RH
      Sex dimorphism in growth

      ANNALS OF HUMAN BIOLOGY
    38. Eiholzer, U; l'Alleman, D; van der Sluis, I; Steinert, H; Gasser, T; Ellis, K
      Body composition abnormalities in children with Prader-Willi syndrome and long-term effects of growth hormone therapy

      HORMONE RESEARCH
    39. Winkelmann, J; Wetter, TC; Collado-Seidel, V; Gasser, T; Dichgans, M; Yassouridis, A; Trenkwalder, C
      Clinical characteristics and frequency of the hereditary restless legs syndrome in a population of 300 patients

      SLEEP
    40. 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
    41. Du, Y; Dodel, RC; Eastwood, BJ; Bales, KR; Gao, F; Lohmuller, F; Muller, U; Kurz, A; Zimmer, R; Evans, RM; Hake, A; Gasser, T; Oertel, WH; Griffin, WST; Paul, SM; Farlow, MR
      Association of an interleukin 1 alpha polymorphism with Alzheimer's disease

      NEUROLOGY
    42. Klopstock, T; Querner, V; Schmidt, F; Gekeler, F; Walter, M; Hartard, M; Hennig, M; Gasser, T; Pongratz, D; Straube, A; Dieterich, M; Muller-Felber, W
      A placebo-controlled crossover trial of creatine in mitochondrial diseases

      NEUROLOGY
    43. Dodel, RC; Du, Y; Bales, KR; Gao, F; Eastwood, B; Glazier, B; Zimmer, R; Cordell, B; Hake, A; Evans, R; Gallagher-Thompson, D; Thompson, LW; Tinklenberg, JR; Pfefferbaum, A; Sullivan, EV; Yesavage, J; Altstiel, L; Gasser, T; Farlow, MR; Murphy, GM; Paul, SM
      alpha 2 macroglobulin and the risk of Alzheimer's disease

      NEUROLOGY
    44. Gasser, T; Dichgans, M; Jurkat-Rott, K; Klockgether, T; Klopstock, T; Kretzschmar, H; Lehmann-Horn, F; Reichmann, H; Rolfs, A; Sander, T; Stogbauer, F
      Molecular diagnosis of hereditary neurological diseases. A position paper

      NERVENARZT
    45. Jager, M; von Rosen, F; Fesl, G; Gasser, T
      Typical anticipation in spinocerebellar ataxia type 7

      NERVENARZT
    46. Schraml, P; Muller, D; Bednar, R; Gasser, T; Sauter, G; Mihatsch, MJ; Moch, H
      Allelic loss at the D9S171 focus on chromosome 9p13 is associated with progression of papillary renal cell carcinoma

      JOURNAL OF PATHOLOGY
    47. Moch, H; Gasser, T; Amin, MB; Torhorst, J; Sauter, G; Mihatsch, MJ
      Prognostic utility of the recently recommended histologic classification and revised TNM staging system of renal cell carcinoma - A Swiss experience with 588 tumors

      CANCER
    48. Schwarz, J; Linke, R; Kerner, M; Mozley, PD; Trenkwalder, C; Gasser, T; Tatsch, K
      Striatal dopamine transporter binding assessed by [I-123]IPT and single photon emission computed tomography in patients with early Parkinson's disease - Implications for a preclinical diagnosis

      ARCHIVES OF NEUROLOGY
    49. Gasser, T
      Modern medical therapy for idiopathic Parkinson syndrome

      ANAESTHESIST
    50. Richter, J; Wagner, U; Kononen, J; Fijan, A; Bruderer, J; Schmid, U; Ackermann, D; Maurer, R; Alund, G; Knonagel, H; Rist, M; Wilber, K; Anabitarte, R; Hering, F; Hardmeier, T; Schonenberger, A; Flury, R; Jager, P; Fehr, JL; Schraml, P; Moch, H; Mihatsch, MJ; Gasser, T; Kallioniemi, OP; Sauter, G
      High-throughput tissue microarray analysis of cyclin E gene amplification and overexpression in urinary bladder cancer

      AMERICAN JOURNAL OF PATHOLOGY
    51. Cheng, MY; Gasser, T; Hall, P
      Nonparametric density estimation under unimodality and monotonicity constraints

      JOURNAL OF COMPUTATIONAL AND GRAPHICAL STATISTICS
    52. 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
    53. Kamm, C; Castelon-Konkiewitz, E; Naumann, M; Heinen, F; Brack, M; Nebe, A; Ceballos-Baumann, A; Gasser, T
      GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany

      MOVEMENT DISORDERS
    54. Mayer, M; Straube, A; Bruening, R; Uttner, I; Pongratz, D; Gasser, T; Dichgans, M; Muller-Hocker, J
      Muscle and skin biopsies are a sensitive diagnostic tool in the diagnosis of CADASIL

      JOURNAL OF NEUROLOGY
    55. 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
    56. Bauer, M; Ueffing, M; Meitinger, T; Gasser, T
      Somatic gene therapy in animal models of Parkinson's disease

      JOURNAL OF NEURAL TRANSMISSION-SUPPLEMENT
    57. Dichgans, M; Gasser, T
      Clinical findings and diagnostic approach in CADASIL

      AKTUELLE NEUROLOGIE
    58. Sheehy, A; Gasser, T; Molinari, L; Largo, RH
      An analysis of variance of the pubertal and midgrowth spurts for length and width

      ANNALS OF HUMAN BIOLOGY
    59. Wang, KM; Gasser, T
      Synchronizing sample curves nonparametrically

      ANNALS OF STATISTICS
    60. Warner, T; Camfield, L; Marsden, CD; Wissel, J; Poewe, W; Marttila, RJ; Erjanti, H; Burbaud, P; Lagueny, A; Kamm, C; Gasser, T; Franz, P; Castelon-Konkiewitz, E; Trender, I; Ceballos-Baumann, A; Nebe, A; Freudenberg, B; Bentivoglio, A; Cassetta, E; Albanese, A; Curra, A; Vacca, L; Berardelli, A; Ferreira, J; Sampaio, C; Passao, V; Marti, F; Tolosa, E; Claveria, L; Duarte, J; Nemeth, AH; Hyman, N; Harley, D; Warner, T; Ben-Shlomo, Y; Newton, A
      Sex-related influences on the frequency and age of onset of primary dystonia

      NEUROLOGY
    61. Klopstock, T; Jaksch, M; Gasser, T
      Age and cause of death in mitochondrial diseases

      NEUROLOGY
    62. Dichgans, M; Wick, M; Gasser, T
      Cerebrospinal fluid findings in CADASIL

      NEUROLOGY
    63. Dichgans, M; Filippi, M; Bruning, R; Iannucci, G; Berchtenbreiter, C; Minicucci, L; Uttner, I; Crispin, A; Ludwig, H; Gasser, T; Yousry, TA
      Quantitative MRI in CADASIL - Correlation with disability and cognitive performance

      NEUROLOGY
    64. Dichgans, M; Schols, L; Herzog, J; Stevanin, G; Weirich-Schwaiger, H; Rouleau, G; Burk, K; Klockgether, T; Zuhlke, C; Laccone, F; Riess, O; Gasser, T
      Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families

      NEUROLOGY
    65. Klopstock, T; Gasser, T
      Genetic counseling and prenatal diagnosis in mitochondrial diseases

      NERVENARZT
    66. Gasser, T
      Modern pharamacotherapy of idiopathic Parkinson's syndrome

      INTERNIST
    67. Dodel, RC; Bales, KR; Farlow, MR; Gasser, T; Paul, SM; Du, YS
      Rapid detection of a pentanucleotide deletion polymorphism in the human alpha(2)-macroglobulin gene

      CLINICAL CHEMISTRY
    68. Klein, C; Vieregge, P; Hagenah, J; Sieberer, M; Doyle, E; Jacobs, H; Gasser, T; Breakefield, XO; Risch, NJ; Ozelius, LJ
      Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from Northern Germany

      ANNALS OF HUMAN GENETICS
    69. Moch, H; Schraml, P; Bubendorf, L; Mirlacher, M; Kononen, J; Gasser, T; Mihatsch, MJ; Kallioniemi, OP; Sauter, G
      High-throughput tissue microarray analysis to evaluate genes uncovered by cDNA microarray screening in renal cell carcinoma

      AMERICAN JOURNAL OF PATHOLOGY
    70. Klopstock, T; Chahrokh-Zadeh, S; Holinski-Feder, E; Meindl, A; Gasser, T; Pongratz, D; Muller-Felber, W
      Markedly different course of Friedreich's ataxia in sib pairs with similarGAA repeat expansions in the frataxin gene

      ACTA NEUROPATHOLOGICA
    71. GASSER T; HALL P; PRESNELL B
      NONPARAMETRIC-ESTIMATION OF THE MODE OF A DISTRIBUTION OF RANDOM CURVES

      Journal of the Royal Statistical Society. Series B: Methodological
    72. GASSER T; MULLERMYHSOK B; WSZOLEK ZK; OEHLMANN R; CALNE DB; BONIFATI V; BEREZNAI B; FABRIZIO E; VIEREGGE P; HORSTMANN RD
      A SUSCEPTIBILITY LOCUS FOR PARKINSONS-DISEASE MAPS TO CHROMOSOME 2P13

      Nature genetics
    73. 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
    74. SCHWARZ J; TATSCH K; GASSER T; ARNOLD G; POGARELL O; KUNIG G; OERTEL WH
      I-123 IBZM BINDING COMPARED WITH LONG-TERM CLINICAL FOLLOW-UP IN PATIENTS WITH DE-NOVO PARKINSONISM

      Movement disorders
    75. DICHGANS M; MAYER M; UTTNER I; BRUNING R; MULLERHOCKER J; RUNGGER G; EBKE M; KLOCKGETHER T; GASSER T
      THE PHENOTYPIC SPECTRUM OF CADASIL - CLINICAL FINDINGS IN 102 CASES

      Annals of neurology
    76. GASSER T
      GENETICS OF PARKINSONS-DISEASE

      Annals of neurology
    77. 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
    78. GASSER T; WINDGASSEN K; BEREZNAI B; KABUS C; LUDOLPH AC
      PHENOTYPIC-EXPRESSION OF THE DYT1 MUTATION - A FAMILY WITH WRITERS CRAMP OF JUVENILE-ONSET

      Annals of neurology
    79. Wang, KM; Gasser, T
      Asymptotic and bootstrap confidence bounds for the structural average of curves

      ANNALS OF STATISTICS
    80. DICHGANS M; FORDERREUTHER S; DEITERICH M; PFAFFENRATH V; GASSER T
      THE D2 RECEPTOR NCOI ALLELE - ABSENCE OF ALLELIC ASSOCIATION WITH MIGRAINE WITH AURA

      Neurology
    81. FARRER M; GASSER T; GWINN K; LYNCH T; NEWMAN S; VAUGHAN J; WOOD N; HARDY J; WSZOLEK Z
      SEQUENCING THE ALPHA-SYNUCLEIN GENE IN A LARGE NUMBER OF FAMILIES WITH PARKINSONS-DISEASE

      Neurology
    82. SCHWARZ J; TATSCH K; KERNER M; LINKE R; STORCH A; TRENKWALDER C; GASSER T; MOZELEY D
      COMBINATION OF DOPAMINE TRANSPORTER AND DOPAMINE D2 RECEPTOR-BINDING IN THE DIFFERENTIAL-DIAGNOSIS OF PATIENTS WITH PARKINSONS-DISEASE

      Neurology
    83. LEROY E; BOYER R; AUBURGER G; LEUBE B; ULM G; MEZEY E; HARTA G; BROWNSTEIN MJ; JONNALAGADA S; CHERNOVA T; DEHEJIA A; LAVEDAN C; GASSER T; STEINBACH PJ; WILKINSON KD; POLYMEROPOULOS MH
      THE UBIQUITIN PATHWAY IN PARKINSONS-DISEASE

      Nature
    84. JIANG F; MOCH H; RICHTER J; EGENTER C; GASSER T; BUBENDORF L; GSCHWIND R; SAUTER G; MIHATSCH MJ
      COMPARATIVE GENOMIC HYBRIDIZATION REVEALS FREQUENT CHROMOSOME 13Q AND4Q LOSSES IN RENAL CARCINOMAS WITH SARCOMATOID TRANSFORMATION

      Journal of pathology
    85. GASSER T
      GENETICS OF PARKINSONS-DISEASE

      Clinical genetics
    86. JIANG F; RICHTER J; SCHRAML P; BUBENDORF L; GASSER T; SAUTER G; MIHATSCH MJ; MOCH H
      CHROMOSOMAL IMBALANCES IN PAPILLARY RENAL-CELL CARCINOMA - GENETIC-DIFFERENCES BETWEEN HISTOLOGICAL SUBTYPES

      The American journal of pathology
    87. DICHGANS M; GASSER T
      CADASIL - CLINICAL AND DIAGNOSTIC FEATURES

      Deutsche Medizinische Wochenschrift
    88. GASSER T
      IDIOPATHIC, MYOCLONIC AND DOPA-RESPONSIVE DYSTONIA

      Current opinion in neurology
    89. BEREZNAI B; WINKLER A; BORASIO GD; GASSER T
      A NOVEL SOD1 MUTATION IN AN AUSTRIAN FAMILY WITH AMYOTROPHIC-LATERAL-SCLEROSIS

      Neuromuscular disorders
    90. BINET I; BOCK AH; VOGELBACH P; GASSER T; KISS A; BRUNNER F; THIEL G
      OUTCOME IN EMOTIONALLY RELATED LIVING KIDNEY DONOR TRANSPLANTATION

      Nephrology, dialysis, transplantation
    91. SCHWARZ J; TATSCH K; GASSER T; ARNOLD G; OERTEL WH
      [(123)]IBZM BINDING PREDICTS DOPAMINERGIC RESPONSIVENESS IN PATIENTS WITH PARKINSONISM AND PREVIOUS DOPAMINOMIMETIC THERAPY

      Movement disorders
    92. GASSER T
      ADVANCES IN THE GENETICS OF MOVEMENT-DISORDERS - IMPLICATIONS FOR MOLECULAR DIAGNOSIS

      Journal of neurology
    93. SCHEIDTMANN K; SCHWARZ J; HOLINSKI E; GASSER T; TRENKWALDER C
      PAROXYSMAL CHOREOATHETOSIS A DISORDER RELATED TO HUNTINGTONS-DISEASE

      Journal of neurology
    94. BIANCHETTI M; FRISCHMUTH N; GASSER T; VOGELBACH P; THIEL G
      UROLOGIC COMPLICATIONS AFTER 2 DIFFERENT TECHNIQUES OF URETERAL ANASTOMOSIS FOR RENAL-TRANSPLANTATION WITH THE USE OF PROPHYLACTIC URETERALSTENTS

      Kidney international
    95. BOCK HA; BINET I; FRISCHMUTH N; VOGELBACH P; GASSER T; THIEL G
      NO EVIDENCE FOR HYPERFILTRATION INJURY IN SIZE MISMATCHED ADULT LIVING DONOR KIDNEYS

      Kidney international
    96. GASSER T; MULLERMYHSOK B; WSZOLEK ZK; DURR A; VAUGHAN JR; BONIFATI V; MECO G; BEREZNAI B; OEHLMANN R; AGID Y; BRICE A; WOOD N
      GENETIC COMPLEXITY AND PARKINSONS-DISEASE

      Science
    97. MOCH H; SAUTER G; GASSER T; RICHTER J; FENG J; MIHATSCH MJ
      P53-PROTEIN AND MDM2-PROTEIN EXPRESSION IN RENAL-CANCER

      Laboratory investigation
    98. EBKE M; DICHGANS M; BERGMANN M; VOELTER HU; RIEGER P; GASSER T; SCHWENDEMANN G
      CADASIL - SKIN BIOPSY ALLOWS DIAGNOSIS IN EARLY STAGES

      Acta neurologica Scandinavica
    99. BOCK HA; BINET I; FRISCHMUTH N; VOGELBACH P; GASSER T; THIEL G
      NO EVIDENCE FOR HYPERFILTRATION INJURY IN SIZE MISMATCHED ADULT LIVING DONOR KIDNEYS

      Journal of the American Society of Nephrology
    100. DICHGANS M; MAYER M; MULLERMYHSOK B; STRAUBE A; GASSER T
      IDENTIFICATION OF A KEY RECOMBINANT NARROWS THE CADASIL GENE REGION TO 8 CM AND ARGUES AGAINST ALLELISM OF CADASIL AND FAMILIAL HEMIPLEGIC MIGRAINE

      Genomics


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 26/05/20 alle ore 15:58:42