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Results: 1-25 | 26-50 | 51-71
Results: 1-25/71
The parkin gene and its phenotype
Authors: 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
Citation: V. Bonifati et al., The parkin gene and its phenotype, NEUROL SCI, 22(1), 2001, pp. 51-52
EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts
Authors: 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
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - Second of two parts, EUR J NEUR, 8(5), 2001, pp. 407-424
EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts
Authors: 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
Citation: T. Gasser et al., EFNS task force on molecular diagnosis of neurologic disorders - Guidelines for the molecular diagnosis of inherited neurologic diseases - First of two parts, EUR J NEUR, 8(4), 2001, pp. 299-314
Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome
Authors: 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
Citation: A. Zimprich et al., Mutations in the gene encoding epsilon-sarcoglycan cause myoclonus-dystonia syndrome, NAT GENET, 29(1), 2001, pp. 66-69
Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes
Authors: 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
Citation: Ab. West et al., Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes, EUR J HUM G, 9(9), 2001, pp. 659-666
A case of amyotrophic lateral sclerosis with a very slow progression over 44 years
Authors: Grohme, K von Maravic, M Gasser, T Borasio, GD
Citation: K. Grohme et al., A case of amyotrophic lateral sclerosis with a very slow progression over 44 years, NEUROMUSC D, 11(4), 2001, pp. 414-416
Cervical dystonia in monozygotic twins: Case report and review of the literature
Authors: Wunderlich, S Reiners, K Gasser, T Naumann, M
Citation: S. Wunderlich et al., Cervical dystonia in monozygotic twins: Case report and review of the literature, MOVEMENT D, 16(4), 2001, pp. 714-718
Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families
Authors: 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
Citation: F. Asmus et al., Inherited myoclonus-dystonia syndrome: Narrowing the 7q21-q31 locus in German families, ANN NEUROL, 49(1), 2001, pp. 121-124
Extensive myelitis associated with Mycoplasma pneumoniae infection: Magnetic resonance imaging and clinical long-term follow-up
Authors: Goebels, N Helmchen, C Abele-Horn, M Gasser, T Pfister, HW
Citation: N. Goebels et al., Extensive myelitis associated with Mycoplasma pneumoniae infection: Magnetic resonance imaging and clinical long-term follow-up, J NEUROL, 248(3), 2001, pp. 204-208
Genetics of Parkinson's disease
Authors: Gasser, T
Citation: T. Gasser, Genetics of Parkinson's disease, J NEUROL, 248(10), 2001, pp. 833-840
Liposome-mediated gene transfer to fetal human ventral mesencephalic explant cultures
Authors: Bauer, M Meyer, M Sautter, J Gasser, T Ueffing, M Widmer, HR
Citation: M. Bauer et al., Liposome-mediated gene transfer to fetal human ventral mesencephalic explant cultures, NEUROSCI L, 308(3), 2001, pp. 169-172
Renal transplantation
Authors: Vela-Navarrete, R Benoit, G Gasser, T
Citation: R. Vela-navarrete et al., Renal transplantation, EUR UROL, 40(2), 2001, pp. 1-8
Statistical characterization of the pubertal growth spurt
Authors: Gasser, T Sheehy, A Largo, RH
Citation: T. Gasser et al., Statistical characterization of the pubertal growth spurt, ANN HUM BIO, 28(4), 2001, pp. 395-402
Growth processes leading to a large or small adult size
Authors: Gasser, T Sheehy, A Molinari, L Largo, RH
Citation: T. Gasser et al., Growth processes leading to a large or small adult size, ANN HUM BIO, 28(3), 2001, pp. 319-327
Growth of early and late maturers
Authors: Gasser, T Sheehy, A Molinari, L Largo, RH
Citation: T. Gasser et al., Growth of early and late maturers, ANN HUM BIO, 28(3), 2001, pp. 328-336
Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha)
Authors: Zink, M Grimm, L Wszolek, ZK Gasser, T
Citation: M. Zink et al., Autosomal-dominant Parkinson's disease linked to 2p13 is not caused by mutations in transforming growth factor alpha (TGF alpha), J NEURAL TR, 108(8-9), 2001, pp. 1029-1034
Crossover renal transplantation: Hurdles to be cleared!
Authors: Thiel, G Vogelbach, P Gurke, L Gasser, T Lehmann, K Voegele, T Kiss, A Kirste, G
Citation: G. Thiel et al., Crossover renal transplantation: Hurdles to be cleared!, TRANSPLAN P, 33(1-2), 2001, pp. 811-816
Correlations between clinical findings and magnetization transfer imaging metrics of tissue damage in individuals with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
Authors: Iannucci, G Dichgans, M Rovaris, M Bruning, R Gasser, T Giacomotti, L Yousry, TA Filippi, M
Citation: G. Iannucci et al., 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, 32(3), 2001, pp. 643-648
Reduced cerebrovascular CO2 reactivity in CADASIL - A transcranial Dopplersonography study
Authors: Pfefferkorn, T von Stuckrad-Barre, S Herzog, J Gasser, T Hamann, GF Dichgans, M
Citation: T. Pfefferkorn et al., Reduced cerebrovascular CO2 reactivity in CADASIL - A transcranial Dopplersonography study, STROKE, 32(1), 2001, pp. 17-21
Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison
Authors: Auer, DP Putz, B Gossl, C Elbel, GK Gasser, T Dichgans, M
Citation: Dp. Auer et al., Differential lesion patterns in CADASIL and sporadic subcortical arteriosclerotic encephalopathy: MR imaging study with statistical parametric group comparison, RADIOLOGY, 218(2), 2001, pp. 443-451
NOTCH3 mutation involving three cysteine residues in a family with typicalCADASIL
Authors: Dichgans, M Herzog, J Gasser, T
Citation: M. Dichgans et al., NOTCH3 mutation involving three cysteine residues in a family with typicalCADASIL, NEUROLOGY, 57(9), 2001, pp. 1714-1717
A polymorphism in the intronic region of the IL-1 alpha gene and the risk for Parkinson's disease
Authors: Dodel, RC Lohmuller, F Du, Y Eastwood, B Gocke, P Oertel, WH Gasser, T
Citation: Rc. Dodel et al., A polymorphism in the intronic region of the IL-1 alpha gene and the risk for Parkinson's disease, NEUROLOGY, 56(7), 2001, pp. 982-983
Microarrays of bladder cancer tissue are highly representative of proliferation index and histological grade
Authors: 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
Citation: A. Nocito et al., Microarrays of bladder cancer tissue are highly representative of proliferation index and histological grade, J PATHOLOGY, 194(3), 2001, pp. 349-357
Neuromotor development from 5 to 18 years. Part 1: timed performance
Authors: Largo, RH Caflisch, JA Hug, F Muggli, K Molnar, AA Molinari, L Sheehy, A Gasser, T
Citation: Rh. Largo et al., Neuromotor development from 5 to 18 years. Part 1: timed performance, DEVELOP MED, 43(7), 2001, pp. 436-443
High-throughout tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1)copy number alterations in urinary bladder cancer
Authors: 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
Citation: R. Simon et al., High-throughout tissue microarray analysis of 3p25 (RAF1) and 8p12 (FGFR1)copy number alterations in urinary bladder cancer, CANCER RES, 61(11), 2001, pp. 4514-4519
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