Inicia sesión Registrate Mi Biblioteca idioma

Idioma

biblioteca idioma abrir menu

Bibliografía Científica

Artículos por temáticas

En este apartado encontrará la selección de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por International Parkinson & Movement Disorder Society.

Ataxia

408 ARTíCULOS , VIENDO DEL 361 AL 375

PUBMED

The cardiomyopathy in Friedreich's ataxia - New biomarker for staging cardiac involvement.

Weidemann F, Liu D, Hu K, Florescu C, Niemann M, Herrmann S, Kramer B, Klebe S, Doppler K, Üçeyler N, Ritter CO, Ertl G, Störk S.

Int J Cardiol. 2015 Sep 1;194:50-7. doi: 10.1016/j.ijcard.2015.05.074.

0

0

0

PUBMED

Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28.

Gorman GS, Pfeffer G, Griffin H, Blakely EL, Kurzawa-Akanbi M, Gabriel J, Sitarz K, Roberts M, Schoser B, Pyle A, Schaefer AM, McFarland R, Turnbull DM, Horvath R, Chinnery PF, Taylor RW.

JAMA Neurol. 2015 Jan;72(1):106-11. doi: 10.1001/jamaneurol.2014.1753.

0

0

0

PUBMED

SPG7 mutations are a common cause of undiagnosed ataxia.

[No authors listed]

Neurology. 2015 May 5;84(18):1911. doi: 10.1212/WNL.0000000000001628. No abstract available.

0

0

0

PUBMED

Small fiber neuropathy in a woman with fragile X-associated tremor/ataxia syndrome (FXTAS).

Chanson JB, Boehm N, Samama B, Echaniz-Laguna A, Anheim M.

J Neurol. 2015 Jan;262(1):226-7. doi: 10.1007/s00415-014-7597-z. No abstract available.

0

0

0

PUBMED

Low-dose Methylphenidate Monotherapy for Features of Attention-Deficit/Hyperactivity Disorder Secondary to Hereditary Cerebellar Ataxia.

Hu LY, Lin YL, Chang HS, Lu T, Lin WS.

CNS Neurosci Ther. 2015 Aug;21(8):672-3. doi: 10.1111/cns.12403. No abstract available.

0

0

0

PUBMED

Visual scanning area is abnormally enlarged in hereditary pure cerebellar ataxia.

Matsuda S, Matsumoto H, Furubayashi T, Fukuda H, Hanajima R, Tsuji S, Ugawa Y, Terao Y.

Cerebellum. 2015 Apr;14(2):63-71. doi: 10.1007/s12311-014-0600-5.

0

0

0

PUBMED

A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndrome.

Johnson JO, Stevanin G, van de Leemput J, Hernandez DG, Arepalli S, Forlani S, Zonozi R, Gibbs JR, Brice A, Durr A, Singleton AB.

Mov Disord. 2015 Feb;30(2):262-6. doi: 10.1002/mds.26059.

0

0

0

PUBMED

Characteristics of Handwriting of People With Cerebellar Ataxia: Three-Dimensional Movement Analysis of the Pen Tip, Finger, and Wrist.

Fujisawa Y, Okajima Y.

Phys Ther. 2015 Nov;95(11):1547-58. doi: 10.2522/ptj.20140118.

0

0

0

PUBMED

Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptoms.

Wang TY, Jao CW, Soong BW, Wu HM, Shyu KK, Wang PS, Wu YT.

PLoS One. 2015 Apr 21;10(4):e0118828. doi: 10.1371/journal.pone.0118828.

0

0

0

PUBMED

Diffusion tensor imaging and tract-based spatial statistics analysis in Friedreich's ataxia patients.

Vieira Karuta SC, Raskin S, de Carvalho Neto A, Gasparetto EL, Doring T, Teive HA.

Parkinsonism Relat Disord. 2015 May;21(5):504-8. doi: 10.1016/j.parkreldis.2015.02.021.

0

0

0

PUBMED

Exome sequencing & homozygosity mapping for identification of genetic aetiology for spastic ataxia in a consanguineous family.

Dalal A, Bhowmik AD, Agarwal D, Phadke SR.

Indian J Med Res. 2015 Aug;142(2):220-4. doi: 10.4103/0971-5916.164262. No abstract available.

0

0

0

PUBMED

Comparison of major lymphocyte subpopulations and recent thymic emigrants in patients with ataxia telangiectasia and age-matched healthy groups.

Celiksoy MH, Topal E, Yıldıran A.

Allergol Immunopathol (Madr). 2015 Sep-Oct;43(5):477-81. doi: 10.1016/j.aller.2014.06.007.

0

0

0

PUBMED

Sensorimotor processing for balance in spinocerebellar ataxia type 6.

Bunn LM, Marsden JF, Voyce DC, Giunti P, Day BL.

Mov Disord. 2015 Aug;30(9):1259-66. doi: 10.1002/mds.26227.

0

0

0

PUBMED

From Mice to Men: TRPC3 in Cerebellar Ataxia.

Becker EB.

Cerebellum. 2015 Mar 14. [Epub ahead of print]

0

0

0

Comentarios

En ningún caso la información facilitada constituye asesoramiento por parte de Zambon

Con el aval de:

Logo SEN Logo HONcode Logo WIS

En colaboración con:

Zambon Neuroacademy