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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 date.
#LCRNCRNode / Date / Journal / AuthorLCSGCS
101751 1994 JUL [15] 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
20823 1996 MAY [15] 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
30312 1996 JUN [15] 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
401384 1996 OCT [15] 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
51805 1997 JUL [15] 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
611276 1997 OCT [15] 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
70267 1999 FEB 5 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
801448 2000 [JUN 30] 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
90109 2001 JUL 10 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
100012 2002 MAR 26 NEUROLOGY 58 (6): 987-987
Munoz DG
Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X
00
#LCRNCRNode / Date / Journal / AuthorLCSGCS
110013 2002 MAR 26 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
120011 2002 [JUN 30] 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
13012910 2002 SUM [JUL 15] DEVELOPMENT AND PSYCHOPATHOLOGY 14 (3): 437-461
Kopnisky KL; Cowan WM; Hyman SE
Levels of analysis in psychiatric research
00
1413614 2003 APR [15] 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
1513115 2003 MAY [15] 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
1602519 2003 [JUN 30] 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
171616 2003 JUL [15] 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
1802817 2003 AUG [15] CURRENT OPINION IN NEUROLOGY 16 (4): 481-485
Sethi KD
Tremor
02
1906018 2003 DEC [15] NEUROBIOLOGY OF AGING 24 (8): 1105-1111
Glanzer JG; Eberwine JH
Mechanisms of translational control in dendrites
01
2035523 2004 JAN 28 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
#LCRNCRNode / Date / Journal / AuthorLCSGCS
2134121 2004 MAR [15] 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
2268020 2004 MAY [15] AMERICAN JOURNAL OF HUMAN GENETICS 74 (5): 805-816
Hagerman PJ; Hagerman RJ
The fragile-X premutation: A maturing perspective
417
2315122 2004 [JUN 30] 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
2445526 2004 [JUN 30] MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10 (1): 25-30
Hagerman PJ; Hagerman RJ
Fragile X-associated tremor/ataxia syndrome (FXTAS)
02
2521028 2004 JUL 27 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
2642327 2004 AUG [15] 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
2711929 2004 SEP 16 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
283924 2004 OCT 13 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
29312825 2004 NOV [15] LANCET NEUROLOGY 3 (11): 652-662
Healy DG; Abou-Sleiman PM; Wood NW
PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism
02
3042030 2005 JAN [15] 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
3161532 2005 JAN [15] EUROPEAN JOURNAL OF HUMAN GENETICS 13 (1): 2-3
Jacquemont S
Screening for FXTAS
00
322833 2005 JAN [15] 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
33044934 2005 FEB [15] MOLECULAR PSYCHIATRY 10 (2): 160-184
Geuze E; Vermetten E; Bremner JD
MR-based in vivo hippocampal volumetrics: 2. Findings in neuropsychiatric disorders
01
3452035 2005 FEB [15] MOVEMENT DISORDERS 20 (2): 230-233
Toft M; Aasly J; Bisceglio G; Adler CH; Uitti RJ; et al.
Parkinsonism, FXTAS, and FMR1 premutations
00
353636 2005 FEB [15] 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
3654637 2005 APR 1 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
3743131 2005 MAY [15] 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

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