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Mon Jun 6 15:35:15 2005

Papers found in a Web of Science
topic search of "Fragile-X" AND "Parkinson*"

Nodes: 37, Authors: 175, Journals: 26, Outer References: 1801, Words: 183
Collection span: 1994 - 2005
View: Overview. Sorted by LCS.
#LCRNCRNode / Date / Journal / AuthorLCSGCS
10109 2001 NEUROLOGY 57 (1): 127-130
Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; et al.
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
1980
213614 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72 (4): 869-878
Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; et al.
Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates
1347
335523 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291 (4): 460-469
Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; et al.
Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population
817
413115 2003 ANNALS OF NEUROLOGY 53 (5): 616-623
Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al.
Tremor and ataxia in fragile X premutation carriers: Blinded videotape study
716
568020 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74 (5): 805-816
Hagerman PJ; Hagerman RJ
The fragile-X premutation: A maturing perspective
417
621028 2004 NEUROLOGY 63 (2): 362-363
Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al.
Fragile X premutation alleles in SCA, ET, and parkinsonism in an Asian cohort
44
71616 2003 CLINICAL GENETICS 64 (1): 54-56
Rogers C; Partington MW; Turner GM
Tremor, ataxia and dementia in older men may indicate a carrier of the fragile X syndrome
34
842327 2004 MOVEMENT DISORDERS 19 (8): 930-933
Arocena DG; Louis ED; Tassone F; Gilliam TC; Ottman R; et al.
Screen for expanded FMR1 alleles in patients with essential tremor
22
90823 1996 HUMAN MOLECULAR GENETICS 5 (5): 607-616
Margolis RL; Stine OC; McInnis MG; Ranen NG; Rubinsztein DC; et al.
cDNA cloning of a human homologue of the Caenorhabditis elegans cell fate-determining gene mab-21: Expression, chromosomal localization and analysis of a highly polymorphic (CAG)(n) trinucleotide repeat
132
1001384 1996 MEDICAL HYPOTHESES 47 (4): 289-298
Fischer KM
Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression
14
#LCRNCRNode / Date / Journal / AuthorLCSGCS
1102519 2003 PARKINSON'S DISEASE: THE LIFE CYCLE OF THE DOPAMINE NEURON 991: 333-338
Wissler JH
Redox-and metalloregulated RNA bioaptamer targets of proteins associated with Parkinson's and other neurodegenerative diseases - Factors of relevance in the life cycle of cells
11
1234121 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109 (2): 154-164
Jacquemont S; Farzin F; Hall D; Leehey M; Tassone F; et al.
Aging in individuals with the FMR1 mutation
17
1301751 1994 JOURNAL OF THE NEUROLOGICAL SCIENCES 124 (2): 119-140
MULLER U; GRAEBER MB; HABERHAUSEN G; KOHLER A
MOLECULAR-BASIS AND DIAGNOSIS OF NEUROGENETIC DISORDERS
014
140312 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58 (6): 1120-1126
Lindsay S; Splitt M; Edney S; Berney TP; Knight SJL; et al.
PPM-X: A new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28
014
151805 1997 HUMAN GENETICS 100 (1): 114-122
Margolis RL; Abraham MR; Gatchell SB; Li SH; Kidwai AS; et al.
cDNAs with long CAG trinucleotide repeats from human brain
056
1611276 1997 MEDICAL HYPOTHESES 49 (4): 337-345
Fischer KM
Parkinson's disease, amyotrophic lateral sclerosis and spinal muscular atrophy are caused by an unstable (CAG)(n) trinucleotide repeat microsatellite
01
170267 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 88 (1): 25-28
Schuback DE; Mulligan EL; Sims KB; Tivol EA; Greenberg BD; et al.
Screen for MAOA mutations in target human groups
010
1801448 2000 ANNUAL REVIEW OF NEUROSCIENCE 23: 343-391
Cowan WM; Harter DH; Kandel ER
The emergence of modern neuroscience: Some implications for neurology and psychiatry
014
19012910 2002 DEVELOPMENT AND PSYCHOPATHOLOGY 14 (3): 437-461
Kopnisky KL; Cowan WM; Hyman SE
Levels of analysis in psychiatric research
00
200011 2002 MOVEMENT DISORDERS 17: S351-S351
Leehey MA; Grigsby J; Rubinstein D; Jacquemont S; Greco C; et al.
Parkinsonism, tremor and ataxia in a female fragile X carrier
01
#LCRNCRNode / Date / Journal / AuthorLCSGCS
210012 2002 NEUROLOGY 58 (6): 987-987
Munoz DG
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
00
220013 2002 NEUROLOGY 58 (6): 987-988
Hagerman RJ; Greco C; Jacquemont S; Leehy M; Hagerman P
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X - Reply
00
2302817 2003 CURRENT OPINION IN NEUROLOGY 16 (4): 481-485
Sethi KD
Tremor
02
2406018 2003 NEUROBIOLOGY OF AGING 24 (8): 1105-1111
Glanzer JG; Eberwine JH
Mechanisms of translational control in dendrites
01
2515122 2004 CIRCULATING NUCLEIC ACIDS IN PLASMA/SERUM III AND SERUM PROTEOMICS 1022: 163-184
Wissler JH
Extracellular and circulating redox-and metalloregulated eRNA and eRNP - Copper ion-structured RNA cytokines (angiotropin ribokines) and bioaptamer targets imparting RNA chaperone and novel biofunctions to S100-EF-hand and disease-associated proteins
00
263924 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 292 (14): 1685-1686
Deng H; Le WD; Jankovic J
Premutation Alleles associated with Parkinson disease and essential tremor
01
27312825 2004 LANCET NEUROLOGY 3 (11): 652-662
Healy DG; Abou-Sleiman PM; Wood NW
PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism
02
2845526 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10 (1): 25-30
Hagerman PJ; Hagerman RJ
Fragile X-associated tremor/ataxia syndrome (FXTAS)
02
2911929 2004 NEUROSCIENCE LETTERS 368 (1): 21-24
Annesi G; Nicoletti G; Tarantino P; Cutuli N; Annesi F; et al.
FRAXE intermediate alleles are associated with Parkinson's disease
00
3042030 2005 ANNALS OF NEUROLOGY 57 (1): 144-147
Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG
Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation
01
#LCRNCRNode / Date / Journal / AuthorLCSGCS
3143131 2005 CLINICAL GENETICS 67 (5): 412-417
Loesch DZ; Churchyard A; Brotchie P; Marot M; Tassone F
Evidence for, and a spectrum of, neurological involvement in carriers of the fragile X pre-mutation: FXTAS and beyond
00
3261532 2005 EUROPEAN JOURNAL OF HUMAN GENETICS 13 (1): 2-3
Jacquemont S
Screening for FXTAS
00
332833 2005 JOURNAL OF CLINICAL NEUROSCIENCE 12 (1): 42-43
Storey E; Billimoria P
Increased T-2 signal in the middle cerebellar peduncles on MRI is not specific for fragile X premutation syndrome
00
34044934 2005 MOLECULAR PSYCHIATRY 10 (2): 160-184
Geuze E; Vermetten E; Bremner JD
MR-based in vivo hippocampal volumetrics: 2. Findings in neuropsychiatric disorders
01
3552035 2005 MOVEMENT DISORDERS 20 (2): 230-233
Toft M; Aasly J; Bisceglio G; Adler CH; Uitti RJ; et al.
Parkinsonism, FXTAS, and FMR1 premutations
00
363636 2005 NEUROGENETICS 6 (1): 51-52
Tan EK; Zhao Y; Puong KY; Law HY; Chan LL; et al.
Expanded FMR1 alleles are rare in idiopathic Parkinson's disease
00
3754637 2005 REVISTA DE NEUROLOGIA 40 (7): 431-437
Castro-Volio I; Cuenca-Berger P
Neurodevelopmental (fragile X syndrome) and neurodegenerative (tremoriataxia syndrome) disorders associated to the 'growth' of a gene
00

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