Symptomatic treatment in the fragile X-associated tremor/ataxia syndrome
There is no established treatment for the neurological features of the recently discovered fragile X–associated tremor/ataxia syndrome (FXTAS). Fifty‐six patients with FXTAS completed a questionnaire to determine whether any medications had been effective for neurological symptoms. Of 11 subjects wi...
Saved in:
Published in | Movement disorders Vol. 21; no. 10; pp. 1741 - 1744 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.10.2006
Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 0885-3185 1531-8257 |
DOI | 10.1002/mds.21001 |
Cover
Abstract | There is no established treatment for the neurological features of the recently discovered fragile X–associated tremor/ataxia syndrome (FXTAS). Fifty‐six patients with FXTAS completed a questionnaire to determine whether any medications had been effective for neurological symptoms. Of 11 subjects with definite FXTAS, 8 (70%) were on medications for their neurological symptoms, whereas most subjects with possible or probable FXTAS, 31 (70%) of 45 subjects, were not on medications. Although no therapy was uniformly effective for intention tremor, ataxia, Parkinsonism, memory loss, or anxiety, some subjects with intention tremor or Parkinsonism reported improvement with medications frequently used in other movement disorders. Overall, all 22 subjects on medications reported improvement in one or more symptoms. Lack of insight, recall bias, and cognitive impairment may have resulted in an underestimation of the beneficial effect of medical therapy. This study suggests that patients with FXTAS can derive improvement from medication treatment for some of their symptoms. © 2006 Movement Disorder Society |
---|---|
AbstractList | There is no established treatment for the neurological features of the recently discovered fragile X-associated tremor/ataxia syndrome (FXTAS). Fifty-six patients with FXTAS completed a questionnaire to determine whether any medications had been effective for neurological symptoms. Of 11 subjects with definite FXTAS, 8 (70%) were on medications for their neurological symptoms, whereas most subjects with possible or probable FXTAS, 31 (70%) of 45 subjects, were not on medications. Although no therapy was uniformly effective for intention tremor, ataxia, Parkinsonism, memory loss, or anxiety, some subjects with intention tremor or Parkinsonism reported improvement with medications frequently used in other movement disorders. Overall, all 22 subjects on medications reported improvement in one or more symptoms. Lack of insight, recall bias, and cognitive impairment may have resulted in an underestimation of the beneficial effect of medical therapy. This study suggests that patients with FXTAS can derive improvement from medication treatment for some of their symptoms.There is no established treatment for the neurological features of the recently discovered fragile X-associated tremor/ataxia syndrome (FXTAS). Fifty-six patients with FXTAS completed a questionnaire to determine whether any medications had been effective for neurological symptoms. Of 11 subjects with definite FXTAS, 8 (70%) were on medications for their neurological symptoms, whereas most subjects with possible or probable FXTAS, 31 (70%) of 45 subjects, were not on medications. Although no therapy was uniformly effective for intention tremor, ataxia, Parkinsonism, memory loss, or anxiety, some subjects with intention tremor or Parkinsonism reported improvement with medications frequently used in other movement disorders. Overall, all 22 subjects on medications reported improvement in one or more symptoms. Lack of insight, recall bias, and cognitive impairment may have resulted in an underestimation of the beneficial effect of medical therapy. This study suggests that patients with FXTAS can derive improvement from medication treatment for some of their symptoms. There is no established treatment for the neurological features of the recently discovered fragile X-associated tremor/ataxia syndrome (FXTAS). Fifty-six patients with FXTAS completed a questionnaire to determine whether any medications had been effective for neurological symptoms. Of 11 subjects with definite FXTAS, 8 (70%) were on medications for their neurological symptoms, whereas most subjects with possible or probable FXTAS, 31 (70%) of 45 subjects, were not on medications. Although no therapy was uniformly effective for intention tremor, ataxia, Parkinsonism, memory loss, or anxiety, some subjects with intention tremor or Parkinsonism reported improvement with medications frequently used in other movement disorders. Overall, all 22 subjects on medications reported improvement in one or more symptoms. Lack of insight, recall bias, and cognitive impairment may have resulted in an underestimation of the beneficial effect of medical therapy. This study suggests that patients with FXTAS can derive improvement from medication treatment for some of their symptoms. There is no established treatment for the neurological features of the recently discovered fragile X–associated tremor/ataxia syndrome (FXTAS). Fifty‐six patients with FXTAS completed a questionnaire to determine whether any medications had been effective for neurological symptoms. Of 11 subjects with definite FXTAS, 8 (70%) were on medications for their neurological symptoms, whereas most subjects with possible or probable FXTAS, 31 (70%) of 45 subjects, were not on medications. Although no therapy was uniformly effective for intention tremor, ataxia, Parkinsonism, memory loss, or anxiety, some subjects with intention tremor or Parkinsonism reported improvement with medications frequently used in other movement disorders. Overall, all 22 subjects on medications reported improvement in one or more symptoms. Lack of insight, recall bias, and cognitive impairment may have resulted in an underestimation of the beneficial effect of medical therapy. This study suggests that patients with FXTAS can derive improvement from medication treatment for some of their symptoms. © 2006 Movement Disorder Society |
Author | Rice, Cathlin D. Hagerman, Paul J. Hagerman, Randi J. Berry-Kravis, Elizabeth Leehey, Maureen A. Hall, Deborah A. |
Author_xml | – sequence: 1 givenname: Deborah A. surname: Hall fullname: Hall, Deborah A. email: deborah.hall@uchsc.edu organization: Department of Neurology, University of Colorado Health Sciences Center at Denver, Denver, Colorado, USA – sequence: 2 givenname: Elizabeth surname: Berry-Kravis fullname: Berry-Kravis, Elizabeth organization: Departments of Neurological Sciences, Pediatrics Biochemistry, RUSH University Medical Center, Chicago, Illinois, USA – sequence: 3 givenname: Randi J. surname: Hagerman fullname: Hagerman, Randi J. organization: M.I.N.D. Institute, University of California at Davis Medical Center, Sacramento, California, USA – sequence: 4 givenname: Paul J. surname: Hagerman fullname: Hagerman, Paul J. organization: Department of Biochemistry and Molecular Medicine, University of California at Davis School of Medicine, Davis, California, USA – sequence: 5 givenname: Cathlin D. surname: Rice fullname: Rice, Cathlin D. organization: Department of Clinical Genetics and Metabolism, The Children's Hospital, Denver, Colorado, USA – sequence: 6 givenname: Maureen A. surname: Leehey fullname: Leehey, Maureen A. organization: Department of Neurology, University of Colorado Health Sciences Center at Denver, Denver, Colorado, USA |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18263883$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/16773616$$D View this record in MEDLINE/PubMed |
BookMark | eNqF0c1uEzEUBWALFdG0sOAF0GxA6mIa3_H4Z5Yo0BYpFERAZWfd8ThgmBkH21Gbt69D0lZCIFb24jtX9j1H5GD0oyXkOdBToLSaDl08rfINHpEJcAalqrg8IBOqFC8ZKH5IjmL8kQFwEE_IIQgpmQAxIReLzbBKfsDkTJGCxTTYMRVuLNJ3WywDfnO9Lb6WGKM3DpPttmrwYYoJbxwWcTN2wQ_2KXm8xD7aZ_vzmHw5e_t5dlHOP5y_m72el6ZWavuyBmpoLHSiBqzy28AYUG1bt0pypIxDjUJWTBmFS0qlqdqKSWMaxRXQmh2TV7u5q-B_rW1MenDR2L7H0fp11KLJ35QA_4VVNlTxJsMXe7huB9vpVXADho2-W1IGL_cAo8E-L2U0Lj44VQmmFMtuunMm-BiDXWrjUl6sH1NA12ugeluXznXp33XlxMkfifuhf7H76de5kc2_oX7_ZnGXKHcJF5O9uU9g-KmFZJLrq8tz_XHOF-LTbKGv2C0jzrCd |
CitedBy_id | crossref_primary_10_1016_j_nrleng_2014_10_018 crossref_primary_10_1016_S1474_4422_13_70125_X crossref_primary_10_1038_ejhg_2011_55 crossref_primary_10_1038_ncpneuro0373 crossref_primary_10_1016_j_jns_2015_03_031 crossref_primary_10_5582_irdr_2014_01029 crossref_primary_10_1016_j_genhosppsych_2007_03_003 crossref_primary_10_1007_s12041_018_0948_2 crossref_primary_10_1002_mds_24958 crossref_primary_10_1242_dmm_049485 crossref_primary_10_1055_a_1165_7378 crossref_primary_10_3389_fneur_2022_977380 crossref_primary_10_1016_j_lpm_2008_12_035 crossref_primary_10_1016_j_parkreldis_2014_12_015 crossref_primary_10_1016_j_nlm_2011_12_006 crossref_primary_10_1002_mds_22354 crossref_primary_10_1016_S0035_3787_07_74182_6 crossref_primary_10_1097_WNF_0b013e31816a48e2 crossref_primary_10_2310_JIM_0b013e3181af59c4 crossref_primary_10_1111_ner_12150 crossref_primary_10_2217_fnl_14_11 crossref_primary_10_1016_j_nrl_2014_10_009 crossref_primary_10_25100_cm_v48i3_3019 crossref_primary_10_1007_s00415_011_6161_3 crossref_primary_10_1038_nrneurol_2016_82 crossref_primary_10_1177_0891988716666379 crossref_primary_10_1097_JCP_0b013e3181f1d10a crossref_primary_10_3389_fnmol_2016_00071 crossref_primary_10_3390_cells12182330 crossref_primary_10_1097_RMR_0b013e31804c99d4 crossref_primary_10_1002_ajmg_b_30732 crossref_primary_10_1002_mdc3_12637 crossref_primary_10_1016_j_parkreldis_2019_05_010 crossref_primary_10_1002_mds_21493 crossref_primary_10_1016_j_neurol_2008_03_022 crossref_primary_10_1007_s00115_009_2846_6 crossref_primary_10_1016_S1474_4422_06_70676_7 crossref_primary_10_1002_ajmg_a_34113 crossref_primary_10_1016_j_ncl_2013_04_008 |
Cites_doi | 10.1086/374321 10.1002/mds.10208 10.1352/0895-8017(2004)109<154:AIIWTF>2.0.CO;2 10.1212/WNL.57.1.127 10.1212/01.wnl.0000188821.51055.52 10.1212/01.wnl.0000192393.05850.ec |
ContentType | Journal Article |
Copyright | Copyright © 2006 Movement Disorder Society 2006 INIST-CNRS |
Copyright_xml | – notice: Copyright © 2006 Movement Disorder Society – notice: 2006 INIST-CNRS |
DBID | BSCLL AAYXX CITATION IQODW CGR CUY CVF ECM EIF NPM 7TK 7X8 8BM |
DOI | 10.1002/mds.21001 |
DatabaseName | Istex CrossRef Pascal-Francis Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed Neurosciences Abstracts MEDLINE - Academic ComDisDome |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) Neurosciences Abstracts ComDisDome MEDLINE - Academic |
DatabaseTitleList | ComDisDome Neurosciences Abstracts CrossRef MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Medicine |
EISSN | 1531-8257 |
EndPage | 1744 |
ExternalDocumentID | 16773616 18263883 10_1002_mds_21001 MDS21001 ark_67375_WNG_PL5S6RCS_W |
Genre | article Research Support, Non-U.S. Gov't Journal Article Research Support, N.I.H., Extramural |
GrantInformation_xml | – fundername: National Institute of Neurological Disorders and Stroke funderid: NS43532; NS044299 – fundername: National Institute of Child Development funderid: HD36071; HD02274 – fundername: American Academy of Neurology Clinical Research Fellowship – fundername: NINDS NIH HHS grantid: NS43532 – fundername: NICHD NIH HHS grantid: HD36071 – fundername: NICHD NIH HHS grantid: HD02274 – fundername: NINDS NIH HHS grantid: NS044299 |
GroupedDBID | --- .3N .GA .GJ .Y3 05W 0R~ 10A 123 1CY 1L6 1OB 1OC 1ZS 31~ 33P 3PY 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5VS 66C 6PF 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHQN AAIPD AAMMB AAMNL AANHP AANLZ AAONW AASGY AAWTL AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABIJN ABJNI ABLJU ABPVW ABQWH ABXGK ACAHQ ACBWZ ACCZN ACGFS ACGOF ACMXC ACPOU ACPRK ACRPL ACSCC ACXBN ACXQS ACYXJ ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADNMO ADOZA ADXAS ADZMN AEFGJ AEIGN AEIMD AENEX AEUYR AEYWJ AFBPY AFFPM AFGKR AFWVQ AFZJQ AGHNM AGQPQ AGXDD AGYGG AHBTC AHMBA AIACR AIDQK AIDYY AIQQE AITYG AIURR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB ASPBG ATUGU AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMXJE BROTX BRXPI BSCLL BY8 C45 CS3 D-6 D-7 D-E D-F DCZOG DPXWK DR1 DR2 DRFUL DRMAN DRSTM DU5 EBD EBS EJD EMOBN F00 F01 F04 F5P FEDTE FUBAC FYBCS G-S G.N GNP GODZA H.X HBH HF~ HGLYW HHY HHZ HVGLF HZ~ IX1 J0M JPC KBYEO KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M6M MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG OVD P2P P2W P2X P2Z P4B P4D PALCI PQQKQ Q.N Q11 QB0 QRW R.K RIWAO RJQFR ROL RX1 RYL SAMSI SUPJJ SV3 TEORI TWZ UB1 V2E V9Y W8V W99 WBKPD WHWMO WIB WIH WIJ WIK WJL WOHZO WQJ WVDHM WXI WXSBR XG1 XV2 ZGI ZZTAW ~IA ~WT AAHHS AAYXX ACCFJ AEEZP AEQDE AIWBW AJBDE CITATION IQODW AEUQT AFPWT CGR CUY CVF ECM EIF NPM RWD RWI WRC WUP YCJ 7TK 7X8 8BM |
ID | FETCH-LOGICAL-c4881-8291419e1d641a21851cc18bb4b875a03514a67238c8af007c2b237cc98581043 |
IEDL.DBID | DR2 |
ISSN | 0885-3185 |
IngestDate | Thu Jul 10 18:05:55 EDT 2025 Fri Jul 11 12:29:49 EDT 2025 Wed Feb 19 01:45:26 EST 2025 Mon Jul 21 09:14:01 EDT 2025 Tue Jul 01 02:32:47 EDT 2025 Thu Apr 24 22:56:12 EDT 2025 Sun Sep 21 06:17:23 EDT 2025 Sun Sep 21 06:18:32 EDT 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Keywords | Chromosome fragility Nervous system diseases Tremor fragile X Cerebral disorder Involuntary movement Chemotherapy Treatment Central nervous system disease FXTAS medications Ataxia Fragile X syndrome Neurological disorder |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor CC BY 4.0 |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c4881-8291419e1d641a21851cc18bb4b875a03514a67238c8af007c2b237cc98581043 |
Notes | ArticleID:MDS21001 American Academy of Neurology Clinical Research Fellowship ark:/67375/WNG-PL5S6RCS-W National Institute of Neurological Disorders and Stroke - No. NS43532; No. NS044299 istex:E0ACDE2CD8CA96094819E80DA32DAE52F9BD6DEE National Institute of Child Development - No. HD36071; No. HD02274 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
PMID | 16773616 |
PQID | 21130859 |
PQPubID | 23462 |
PageCount | 4 |
ParticipantIDs | proquest_miscellaneous_69001711 proquest_miscellaneous_21130859 pubmed_primary_16773616 pascalfrancis_primary_18263883 crossref_citationtrail_10_1002_mds_21001 crossref_primary_10_1002_mds_21001 wiley_primary_10_1002_mds_21001_MDS21001 istex_primary_ark_67375_WNG_PL5S6RCS_W |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | October 2006 |
PublicationDateYYYYMMDD | 2006-10-01 |
PublicationDate_xml | – month: 10 year: 2006 text: October 2006 |
PublicationDecade | 2000 |
PublicationPlace | Hoboken |
PublicationPlace_xml | – name: Hoboken – name: Hoboken, NJ – name: United States |
PublicationTitle | Movement disorders |
PublicationTitleAlternate | Mov. Disord |
PublicationYear | 2006 |
Publisher | Wiley Subscription Services, Inc., A Wiley Company Wiley |
Publisher_xml | – name: Wiley Subscription Services, Inc., A Wiley Company – name: Wiley |
References | Benito-Leon J, Louis E, Bermigo-Pareja F. Population-based case-control study of cognitive function in essential tremor. Neurology 2006; 66: 69-74. Ceravolo R, Antonini A, Volterrani D, et al. Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers. Neurology 2005; 65: 1971-1973. Hagerman RJ, Leehey MA, Heinreichs W, et al. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 2001; 57: 127-130. Leehey MA, Hagerman RJ, Landau WM, et al. Tremor/ataxia syndrome in Fragile X carrier males. Mov Disord 2002; 17: 744-745. Jacquemont S, Hagerman RJ, Leehey MA, et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet 2003; 72: 869-878. Jacquemont S, Farzin F, Hall DA, et al. Aging in individuals with the FMR1 mutation. Am J Mental Retard 2004; 109: 154-164. 2004; 109 2002; 17 2003; 72 2001; 57 2005; 65 2006; 66 e_1_2_6_7_2 e_1_2_6_2_2 e_1_2_6_4_2 e_1_2_6_3_2 e_1_2_6_6_2 e_1_2_6_5_2 |
References_xml | – reference: Jacquemont S, Farzin F, Hall DA, et al. Aging in individuals with the FMR1 mutation. Am J Mental Retard 2004; 109: 154-164. – reference: Ceravolo R, Antonini A, Volterrani D, et al. Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers. Neurology 2005; 65: 1971-1973. – reference: Benito-Leon J, Louis E, Bermigo-Pareja F. Population-based case-control study of cognitive function in essential tremor. Neurology 2006; 66: 69-74. – reference: Hagerman RJ, Leehey MA, Heinreichs W, et al. Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X. Neurology 2001; 57: 127-130. – reference: Jacquemont S, Hagerman RJ, Leehey MA, et al. Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates. Am J Hum Genet 2003; 72: 869-878. – reference: Leehey MA, Hagerman RJ, Landau WM, et al. Tremor/ataxia syndrome in Fragile X carrier males. Mov Disord 2002; 17: 744-745. – volume: 109 start-page: 154 year: 2004 end-page: 164 article-title: Aging in individuals with the mutation publication-title: Am J Mental Retard – volume: 17 start-page: 744 year: 2002 end-page: 745 article-title: Tremor/ataxia syndrome in Fragile X carrier males publication-title: Mov Disord – volume: 66 start-page: 69 year: 2006 end-page: 74 article-title: Population‐based case‐control study of cognitive function in essential tremor publication-title: Neurology – volume: 57 start-page: 127 year: 2001 end-page: 130 article-title: Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X publication-title: Neurology – volume: 72 start-page: 869 year: 2003 end-page: 878 article-title: Fragile X premutation tremor/ataxia syndrome: molecular, clinical, and neuroimaging correlates publication-title: Am J Hum Genet – volume: 65 start-page: 1971 year: 2005 end-page: 1973 article-title: Dopamine transporter imaging study in parkinsonism occurring in fragile X premutation carriers publication-title: Neurology – ident: e_1_2_6_3_2 doi: 10.1086/374321 – ident: e_1_2_6_4_2 doi: 10.1002/mds.10208 – ident: e_1_2_6_5_2 doi: 10.1352/0895-8017(2004)109<154:AIIWTF>2.0.CO;2 – ident: e_1_2_6_2_2 doi: 10.1212/WNL.57.1.127 – ident: e_1_2_6_6_2 doi: 10.1212/01.wnl.0000188821.51055.52 – ident: e_1_2_6_7_2 doi: 10.1212/01.wnl.0000192393.05850.ec |
SSID | ssj0011516 |
Score | 2.07686 |
Snippet | There is no established treatment for the neurological features of the recently discovered fragile X–associated tremor/ataxia syndrome (FXTAS). Fifty‐six... There is no established treatment for the neurological features of the recently discovered fragile X-associated tremor/ataxia syndrome (FXTAS). Fifty-six... |
SourceID | proquest pubmed pascalfrancis crossref wiley istex |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 1741 |
SubjectTerms | Adrenergic beta-Antagonists - therapeutic use Aged Anxiety Disorders - drug therapy ataxia Benzodiazepines - therapeutic use Biological and medical sciences Carbidopa - therapeutic use Central Nervous System Agents - therapeutic use Cerebellar Ataxia - drug therapy Cholinesterase Inhibitors - therapeutic use Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Dopamine Agonists - therapeutic use Female fragile X Fragile X Syndrome - drug therapy FXTAS Humans Levodopa - therapeutic use Male Medical sciences medications Memory Disorders - drug therapy Middle Aged Nervous system (semeiology, syndromes) Nervous system as a whole Neurologic Examination - drug effects Neurology Parkinsonian Disorders - drug therapy Serotonin Uptake Inhibitors - therapeutic use Treatment Outcome tremor Tremor - drug therapy |
Title | Symptomatic treatment in the fragile X-associated tremor/ataxia syndrome |
URI | https://api.istex.fr/ark:/67375/WNG-PL5S6RCS-W/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fmds.21001 https://www.ncbi.nlm.nih.gov/pubmed/16773616 https://www.proquest.com/docview/21130859 https://www.proquest.com/docview/69001711 |
Volume | 21 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
journalDatabaseRights | – providerCode: PRVWIB databaseName: Wiley Online Library - Core collection (SURFmarket) issn: 0885-3185 databaseCode: DR2 dateStart: 19990101 customDbUrl: isFulltext: true eissn: 1531-8257 dateEnd: 99991231 omitProxy: false ssIdentifier: ssj0011516 providerName: Wiley-Blackwell |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1fSxwxEB9EofSl1art9Y9dpIgve7fZzWYT-lS0VsST4lW8h0JIsrki9vbkbg9sn_od-g37STrJ_jmuKBTf8jCb7CQzyS_J5DcA7yjLLROjOIxihRuUXPNQRZaGkckYExZnB-POIftn7PiCngzT4Qq8b97CVPwQ7YGb8ww_XzsHV3rWW5CGjvNZN3YMQjj_kiT1V7TnLXUUAh2f9hSdKPUvhBtWoSjutV8urUVrrltvXWykmmH3jKq8FncBz2Uc6xeio6fwtVGhij-57s5L3TU__2F3fKCO6_CkBqjBh8qiNmDFFs_gUb--gt-Ek8GP8U058UyvQRumHlwVAULJAPX5hi0Fwz-_fqt65G3u5MaTaU-V6vZKBQ1LwhZcHH38cnAc1gkZQoN-TkIeC0KJsCRnlCgEBykxhnCtqcZtj3KXklQxl8bMcDVC9GFiHSeZMYKnHPd9yTasFpPCvoDAMK6STJGEUY3rY6QjwanGgjVC5Mx0YL8ZGmlqtnKXNOO7rHiWY4l9I33fdGC3Fb2pKDruEtrz49tKqOm1i2nLUnl59kl-Pk0H7PxgIC87sLNkAIsqcSOWcJ504G1jERJd0d2vqMJO5q4hBAQ8FfdLMOH5ifBvnlemtKidZVnCCEO9vUHcr4nsHw584eX_i76Cx_7oyAchvobVcjq3bxBMlXrHe81f9aEYug |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LTxsxEB5RkFoufbekD1hVVdXLJut9eG2plwpKU5pEFQGRC7Jsr4MQZIPCRgJO_Q_9h_0lHXsfUSqQqt58mLV37Bn7sz3-BuB9TDND-Tj0g1DiBiVTzJeBif1Ap5Ryg7ODtueQ_QHtHsZ7o2S0Ap_qtzAlP0Rz4GY9w83X1sHtgXRnwRo6yS7boaUQugdr9n7OuuXOfkMehVDHJT5FN0rcG-GaVygIO82nS6vRmu3YKxsdKS-xg8ZlZovboOcyknVL0e4jOK6VKCNQztrzQrX1zV_8jv-r5WN4WGFU73NpVE9gxeRP4X6_uoV_BnvD68lFMXVkr14Tqe6d5h6iSQ8VOsGmvNHvn79kNfgms3KT6awjC3l1Kr2aKOE5HO5-Odju-lVOBl-jqxOfhZzEhBuS0ZhIxAcJ0ZowpWKFOx9p7yVjSW0mM83kGAGIDlUYpVpzljDc-kUvYDWf5mYDPE2ZjFJJIhorXCIDFXAWKywYzXlGdQs-1mMjdEVYbvNmnIuSajkU2DfC9U0L3jWiFyVLx21CH9wANxJydmbD2tJEHA2-ih-9ZEj3t4fiqAWbSxawqBL3YhFjUQu2apMQ6I32ikXmZjq3DSEmYAm_W4JyR1GEf_OytKVF7TRNI0oo6u0s4m5NRH9n6Aqv_l10Cx50D_o90fs2-P4a1t1JkotJfAOrxWxu3iK2KtSmc6E_cZ8c1g |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LTxsxEB5RkFAvLX2HUlhVVdXLJvvwem31VEFTSkmESBE5IFm216kQZBOFjUR76n_gH_JLOvY-olQgVb3tYdbesWfW39jjbwDeEZoZykeRH0QSA5RMMV8GhviBTinlBv8O2u5D9vp0_4QcDJPhCnys78KU_BDNhpv1DPe_tg4-zUadBWnoOLtqR5ZB6AGsEYrRlUVExw13FCIdV_cUvShxV4RrWqEg6jSvLi1Ga3Zcr21ypLzC8RmVhS3uQp7LQNatRN3HcFbrUCagXLTnhWrrX3_RO_6nkhvwqEKo3qfSpJ7AismfwnqvOoN_BgeDn-NpMXFUr16Tp-6d5x5iSQ_1-YE9ecPb3zeymnqTWbnxZNaRhbw-l15Nk_AcTrqfv-_u-1VFBl-jo4c-i3hIQm7CjJJQIjpIQq1DphRRGPdIeypJJLV1zDSTI4QfOlJRnGrNWcIw8ItfwGo-yc0r8DRlMk5lGFOicIEMVMAZUfhgNOcZ1S34UE-N0BVdua2acSlKouVI4NgINzYteNuITkuOjruE3rv5bSTk7MImtaWJOO1_EUeHyYAe7w7EaQu2lwxg0SRGYjFjcQt2aosQ6Iv2gEXmZjK3HSEiYAm_X4JyR1CEX_OyNKVF6zRNYxpS1NsZxP2aiN7ewD1s_rvoDqwf7XXF4df-t9fw0G0juYTELVgtZnPzBoFVobadA_0BBiobhQ |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Symptomatic+treatment+in+the+fragile+X-associated+tremor%2Fataxia+syndrome&rft.jtitle=Movement+disorders&rft.au=Hall%2C+Deborah+A&rft.au=Berry-Kravis%2C+Elizabeth&rft.au=Hagerman%2C+Randi+J&rft.au=Hagerman%2C+Paul+J&rft.date=2006-10-01&rft.issn=0885-3185&rft.volume=21&rft.issue=10&rft.spage=1741&rft.epage=1744&rft_id=info:doi/10.1002%2Fmds.21001&rft.externalDBID=NO_FULL_TEXT |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0885-3185&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0885-3185&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0885-3185&client=summon |