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Results:
1-24
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Results: 24
Authors:
Alarcon, M
Cantor, RM
Liu, JJ
Gilliam, TC
Geschwind, DH
Citation: M. Alarcon et al., Evidence for a language quantitative trait locus on chromosome 7q in multiplex autism families, AM J HU GEN, 70(1), 2002, pp. 60-71
Authors:
Geschwind, DH
Citation: Dh. Geschwind, Sharing gene expression data: an array of options, NAT REV NEU, 2(6), 2001, pp. 435-438
Authors:
Kornblum, HI
Geschwind, DH
Citation: Hi. Kornblum et Dh. Geschwind, Molecular markers in CNS stem cell research: hitting a moving target, NAT REV NEU, 2(11), 2001, pp. 843-846
Authors:
Boone, KB
Swerdloff, RS
Miller, BL
Geschwind, DH
Razani, J
Lee, A
Gonzalo, IG
Haddal, A
Rankin, K
Lu, P
Paul, L
Citation: Kb. Boone et al., Neuropsychological profiles of adults with Klinefelter syndrome, J INT NEURO, 7(4), 2001, pp. 446-456
Authors:
Luo, Z
Geschwind, DH
Citation: Z. Luo et Dh. Geschwind, Microarray applications in neuroscience, NEUROBIOL D, 8(2), 2001, pp. 183-193
Authors:
Kornblum, HL
Geschwind, DH
Citation: Hl. Kornblum et Dh. Geschwind, The use of representational difference analysis and cDNA microarrays in neural repair research, REST NEUROL, 18(2-3), 2001, pp. 89-94
Authors:
Geschwind, DH
Ou, J
Easterday, MC
Dougherty, JD
Jackson, RL
Chen, ZG
Antoine, H
Terskikh, A
Weissman, IL
Nelson, SF
Kornblum, HI
Citation: Dh. Geschwind et al., A genetic analysis of neural progenitor differentiation, NEURON, 29(2), 2001, pp. 325-339
Authors:
Geschwind, DH
Robidoux, J
Alarcon, M
Miller, BL
Wilhelmsen, KC
Cummings, JL
Nasreddine, ZS
Citation: Dh. Geschwind et al., Dementia and neurodevelopmental predisposition: Cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia, ANN NEUROL, 50(6), 2001, pp. 741-746
Authors:
Geschwind, DH
Miller, BL
Citation: Dh. Geschwind et Bl. Miller, Molecular approaches to cerebral laterality: Development and neurodegeneration, AM J MED G, 101(4), 2001, pp. 370-381
Authors:
Sobrido, MJ
Cholfin, JA
Perlman, S
Pulst, SM
Geschwind, DH
Citation: Mj. Sobrido et al., SCA8 repeat expansions in ataxia: A controversial association, NEUROLOGY, 57(7), 2001, pp. 1310-1312
Authors:
Terskikh, AV
Easterday, MC
Li, LH
Hood, L
Kornblum, HI
Geschwind, DH
Weissman, IL
Citation: Av. Terskikh et al., From hematopoiesis to neuropoiesis: Evidence of overlapping genetic programs, P NAS US, 98(14), 2001, pp. 7934-7939
Authors:
Jen, J
Geschwind, DH
Citation: J. Jen et Dh. Geschwind, Ataxia and calcium channels - What a headache!, ARCH NEUROL, 58(2), 2001, pp. 179-180
Authors:
Cholfin, JA
Sobrido, MJ
Perlman, S
Pulst, SM
Geschwind, DH
Citation: Ja. Cholfin et al., The SCA12 mutation as a rare cause of spinocerebellar ataxia, ARCH NEUROL, 58(11), 2001, pp. 1833-1835
Authors:
Figueroa, KP
Chan, P
Schols, L
Tanner, C
Riess, O
Perlman, SL
Geschwind, DH
Pulst, SM
Citation: Kp. Figueroa et al., Association of moderate polyglutamine tract expansions in the slow calcium-activated potassium channel type 3 with ataxia, ARCH NEUROL, 58(10), 2001, pp. 1649-1653
Authors:
Geschwind, DH
Sowinski, J
Lord, C
Iversen, P
Shestack, J
Jones, P
Ducat, L
Spence, SJ
Citation: Dh. Geschwind et al., The Autism Genetic Resource Exchange: A resource for the study of autism and related neuropsychiatric conditions, AM J HU GEN, 69(2), 2001, pp. 463-466
Authors:
Geschwind, DH
Boone, KB
Miller, BL
Swerdloff, RS
Citation: Dh. Geschwind et al., Neurobehavioral phenotype of Klinefelter syndrome, MENT RET D, 6(2), 2000, pp. 107-116
Authors:
Geschwind, DH
Citation: Dh. Geschwind, Mice, microarrays, and the genetic diversity of the brain, P NAS US, 97(20), 2000, pp. 10676-10678
Authors:
Wilhelmsen, KC
Clark, LN
Miller, BL
Geschwind, DH
Citation: Kc. Wilhelmsen et al., Tau mutations in frontotemporal dementia, DEMENT G C, 10, 1999, pp. 88-92
Authors:
Nasreddine, ZS
Loginov, M
Clark, LN
Lamarche, J
Miller, BL
Lamontagne, A
Zhukareva, V
Lee, VMY
Wilhelmsen, KC
Geschwind, DH
Citation: Zs. Nasreddine et al., From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation, ANN NEUROL, 45(6), 1999, pp. 704-715
Authors:
Geschwind, DH
Citation: Dh. Geschwind, Founders and CAG repeats - Cause or effect?, NEUROLOGY, 52(4), 1999, pp. 685-686
Authors:
Chow, TW
Miller, BL
Hayashi, VN
Geschwind, DH
Citation: Tw. Chow et al., Inheritance of frontotemporal dementia, ARCH NEUROL, 56(7), 1999, pp. 817-822
Authors:
Geschwind, DH
Citation: Dh. Geschwind, Focusing attention on cognitive impairment in spinocerebellar ataxia, ARCH NEUROL, 56(1), 1999, pp. 20-22
Authors:
Geschwind, DH
Loginov, M
Stern, JM
Citation: Dh. Geschwind et al., Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease), AM J HU GEN, 65(3), 1999, pp. 764-772
Authors:
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
Citation: M. Hong et al., Mutation-specific functional impairments in distinct Tau isoforms of hereditary FTDP-17, SCIENCE, 282(5395), 1998, pp. 1914-1917
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