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Results:
1-17
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Results: 17
Authors:
Pal, PK
Wszolek, ZK
Uitti, R
Markopoulou, K
Calne, SM
Stoessl, AJ
Calne, DB
Citation: Pk. Pal et al., Positron emission tomography of dopamine pathways in familial Parkinsoniansyndromes, PARKINS R D, 8(1), 2001, pp. 51-56
Authors:
Pal, PK
Wszolek, ZK
Kishore, A
de la Fuente-Fernandez, R
Sossi, V
Uitti, RJ
Dobko, T
Stoessl, AJ
Citation: Pk. Pal et al., Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene), PARKINS R D, 7(2), 2001, pp. 81-88
Authors:
McRae, CA
Diem, G
Yamazaki, TG
Mitek, A
Wszolek, ZK
Citation: Ca. Mcrae et al., Interest in genetic testing in pallido-ponto-nigral degeneration (PPND): afamily with frontotemporal dementia with Parkinsonism linked to chromosome17, EUR J NEUR, 8(2), 2001, pp. 179-183
Authors:
Arvanitakis, Z
Wszolek, ZK
Citation: Z. Arvanitakis et Zk. Wszolek, Recent advances in the understanding of tau protein and movement disorders, CURR OP NEU, 14(4), 2001, pp. 491-497
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
Authors:
Wszolek, ZK
Kardon, RH
Wolters, EC
Pfeiffer, RF
Citation: Zk. Wszolek et al., Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17): PPND family. A longitudinal videotape demonstration, MOVEMENT D, 16(4), 2001, pp. 756-760
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
Authors:
Reed, LA
Wszolek, ZK
Hutton, M
Citation: La. Reed et al., Phenotypic correlations in FTDP-17, NEUROBIOL A, 22(1), 2001, pp. 89-107
Authors:
Wszolek, ZK
Tsuboi, Y
Uitti, RJ
Reed, L
Hutton, ML
Dickson, DW
Citation: Zk. Wszolek et al., Progressive supranuclear palsy as a disease phenotype caused by the S305S tau gene mutation, BRAIN, 124, 2001, pp. 1666-1668
Authors:
Uitti, RJ
Wharen, RE
Duffy, JR
Lucas, JA
Schneider, SL
Rippeth, JD
Wszolek, ZK
Obwegeser, AA
Turk, MF
Atkinson, EJ
Citation: Rj. Uitti et al., Unilateral pallidotomy for Parkinson's disease: speech, motor, and neuropsychological outcome measurements, PARKINS R D, 6(3), 2000, pp. 133-143
Authors:
Wszolek, ZK
Tsuboi, Y
Uitti, RJ
Reed, L
Citation: Zk. Wszolek et al., Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene, NEUROLOGY, 55(12), 2000, pp. 1939-1939
Authors:
Wszolek, ZK
Uitti, RJ
Hutton, M
Citation: Zk. Wszolek et al., A mutation in the microtubule-associated protein tan in pallido-nigro-luysian degeneration, NEUROLOGY, 54(10), 2000, pp. 2028-2029
Authors:
Lynch, HT
McComb, RD
Osborn, NK
Wolpert, PA
Lynch, JF
Wszolek, ZK
Sidransky, D
Steg, RE
Citation: Ht. Lynch et al., Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome, CANCER, 88(2), 2000, pp. 433-439
Authors:
Wszolek, ZK
Markopoulou, K
Citation: Zk. Wszolek et K. Markopoulou, Molecular genetics of familial parkinsonism, PARKINS R D, 5(4), 1999, pp. 145-155
Authors:
Markopoulou, K
Wszolek, ZK
Pfeiffer, RF
Chase, BA
Citation: K. Markopoulou et al., Reduced expression of the G209A alpha-synuclein allele in familial parkinsonism, ANN NEUROL, 46(3), 1999, pp. 374-381
Authors:
Steg, RE
Kessinger, A
Wszolek, ZK
Citation: Re. Steg et al., Cortical blindness and seizures in a patient receiving FK506 after bone marrow transplantation, BONE MAR TR, 23(9), 1999, pp. 959-962
Authors:
Samii, A
Markopoulou, K
Wszolek, ZK
Sossi, V
Dobko, T
Mak, E
Calne, DB
Stoessl, AJ
Citation: A. Samii et al., PET studies of parkinsonism associated with mutation in the alpha-synuclein gene, NEUROLOGY, 53(9), 1999, pp. 2097-2102
Risultati:
1-17
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