| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Lijuan Zhang, Fei Wang, Yan Shi, Jianhua Wang, Qingfan Xi. [Plum-blossom needle tapping at Jiaji(EX-B 2) combined with rehabilitation for ataxia of cerebellar apoplexy: a randomized controlled trial]. Zhongguo zhen jiu = Chinese acupuncture & moxibustion. vol 36. issue 2. 2016-07-26. PMID:27348907. |
[plum-blossom needle tapping at jiaji(ex-b 2) combined with rehabilitation for ataxia of cerebellar apoplexy: a randomized controlled trial]. |
2016-07-26 |
2023-08-13 |
Not clear |
| Lijuan Zhang, Fei Wang, Yan Shi, Jianhua Wang, Qingfan Xi. [Plum-blossom needle tapping at Jiaji(EX-B 2) combined with rehabilitation for ataxia of cerebellar apoplexy: a randomized controlled trial]. Zhongguo zhen jiu = Chinese acupuncture & moxibustion. vol 36. issue 2. 2016-07-26. PMID:27348907. |
to compare the effects between plum-blossom needle tapping at jiaji (ex-b 2) combined with rehabilitation and simple rehabilitation for ataxia of cerebellar apoplexy. |
2016-07-26 |
2023-08-13 |
Not clear |
| Alberto Benussi, Giacomo Koch, Maria Cotelli, Alessandro Padovani, Barbara Borron. Cerebellar transcranial direct current stimulation in patients with ataxia: A double-blind, randomized, sham-controlled study. Movement disorders : official journal of the Movement Disorder Society. vol 30. issue 12. 2016-07-25. PMID:26274840. |
cerebellar transcranial direct current stimulation in patients with ataxia: a double-blind, randomized, sham-controlled study. |
2016-07-25 |
2023-08-13 |
Not clear |
| Alberto Benussi, Giacomo Koch, Maria Cotelli, Alessandro Padovani, Barbara Borron. Cerebellar transcranial direct current stimulation in patients with ataxia: A double-blind, randomized, sham-controlled study. Movement disorders : official journal of the Movement Disorder Society. vol 30. issue 12. 2016-07-25. PMID:26274840. |
the present study investigated whether a single session of cerebellar anodal transcranial direct current stimulation could improve symptoms in patients with ataxia. |
2016-07-25 |
2023-08-13 |
Not clear |
| Jana Hartmann, Arthur Konnert. TRPC3-dependent synaptic transmission in central mammalian neurons. Journal of molecular medicine (Berlin, Germany). vol 93. issue 9. 2016-07-22. PMID:26041382. |
finally, we address the deleterious consequences of distorted trpc3 synaptic signaling for cerebellar function in different mouse models and present trpc3 as an emerging candidate protein implicated in various forms of ataxia in humans. |
2016-07-22 |
2023-08-13 |
mouse |
| K Feil, N Böttcher, O Kremmyda, C Muth, J Teufel, A Zwergal, T Brandt, M Strup. [Pharmacotherapy of Vestibular Disorders, Nystagmus and Cerebellar Disorders]. Fortschritte der Neurologie-Psychiatrie. vol 83. issue 9. 2016-07-12. PMID:26421856. |
there are ongoing rcts on treatment of vestibular paroxysmia with carbamazepine (vespa), acute unilateral vestibulopathy with betahistine (betavest), vestibular migraine with metoprolol (provemig), benign paroxysmal positional vertigo with vitamin d (vitd@bppv), ea2 with 4-aminopyridine versus acetazolamide (eat-2-treat), and cerebellar ataxias with acetyl-dl-leucine (alcat). |
2016-07-12 |
2023-08-13 |
Not clear |
| Maria Isabel Bahamonde, Selma Angèlica Serra, Oliver Drechsel, Rubayte Rahman, Anna Marcé-Grau, Marta Prieto, Stephan Ossowski, Alfons Macaya, José M Fernández-Fernánde. A Single Amino Acid Deletion (ΔF1502) in the S6 Segment of CaV2.1 Domain III Associated with Congenital Ataxia Increases Channel Activity and Promotes Ca2+ Influx. PloS one. vol 10. issue 12. 2016-07-12. PMID:26716990. |
however, some hm-linked gain-of-function mutations are also associated to congenital ataxia and/or cerebellar atrophy, including the deletion of a highly conserved phenylalanine located at the s6 pore region of α1a domain iii (Δf1502). |
2016-07-12 |
2023-08-13 |
human |
| Mercedes Serrano, Víctor de Diego, Jordi Muchart, Daniel Cuadras, Ana Felipe, Alfons Macaya, Ramón Velázquez, M Pilar Poo, Carmen Fons, M Mar O'Callaghan, Angels García-Cazorla, Cristina Boix, Bernabé Robles, Francisco Carratalá, Marisa Girós, Paz Briones, Laura Gort, Rafael Artuch, Celia Pérez-Cerdá, Jaak Jaeken, Belén Pérez, Belén Pérez-Dueña. Phosphomannomutase deficiency (PMM2-CDG): ataxia and cerebellar assessment. Orphanet journal of rare diseases. vol 10. 2016-07-06. PMID:26502900. |
phosphomannomutase deficiency (pmm2-cdg): ataxia and cerebellar assessment. |
2016-07-06 |
2023-08-13 |
Not clear |
| Václav Marcián, Pavel Filip, Martin Bareš, Milan Brázdi. Cerebellar Dysfunction and Ataxia in Patients with Epilepsy: Coincidence, Consequence, or Cause? Tremor and other hyperkinetic movements (New York, N.Y.). vol 6. 2016-07-04. PMID:27375960. |
cerebellar dysfunction and ataxia in patients with epilepsy: coincidence, consequence, or cause? |
2016-07-04 |
2023-08-13 |
Not clear |
| Václav Marcián, Pavel Filip, Martin Bareš, Milan Brázdi. Cerebellar Dysfunction and Ataxia in Patients with Epilepsy: Coincidence, Consequence, or Cause? Tremor and other hyperkinetic movements (New York, N.Y.). vol 6. 2016-07-04. PMID:27375960. |
tracing the evolution of this line of inquiry from the observed coincidence of cerebellar atrophy and cerebellar dysfunction (most apparently manifested as ataxia) in epilepsy to their close association, this review considers converging clinical, physiological, histological, and neuroimaging evidence that support incorporating the cerebellum into epilepsy pathology. |
2016-07-04 |
2023-08-13 |
Not clear |
| Václav Marcián, Pavel Filip, Martin Bareš, Milan Brázdi. Cerebellar Dysfunction and Ataxia in Patients with Epilepsy: Coincidence, Consequence, or Cause? Tremor and other hyperkinetic movements (New York, N.Y.). vol 6. 2016-07-04. PMID:27375960. |
we examine reports of still controversial cerebellar epilepsy, studies of cerebellar stimulation alleviating paroxysmal epileptic activity, studies and case reports of cerebellar lesions directly associated with seizures, and conditions in which ataxia is accompanied by epileptic seizures. |
2016-07-04 |
2023-08-13 |
Not clear |
| Vasfiye Burcu Doga. An anti-GAD autoantibody-associated cerebellar syndrome case: a curable cause of ataxia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 36. issue 10. 2016-06-29. PMID:26058956. |
an anti-gad autoantibody-associated cerebellar syndrome case: a curable cause of ataxia. |
2016-06-29 |
2023-08-13 |
Not clear |
| Marie Mongin, Cécile Delorme, Timothée Lenglet, Claude Jardel, Catherine Vignal, Emmanuel Roz. Progressive Ataxia and Palatal Tremor: Think about POLG Mutations. Tremor and other hyperkinetic movements (New York, N.Y.). vol 6. 2016-06-29. PMID:27351300. |
progressive ataxia and palatal tremor (papt) can be observed in both acquired brainstem or cerebellar lesions and genetic disorders. |
2016-06-29 |
2023-08-13 |
Not clear |
| Elizabeth A Bowman, Mark Walterfang, Larry Abel, Patricia Desmond, Michael Fahey, Dennis Velakouli. Longitudinal changes in cerebellar and subcortical volumes in adult-onset Niemann-Pick disease type C patients treated with miglustat. Journal of neurology. vol 262. issue 9. 2016-06-27. PMID:26092521. |
this study explored how changes in cerebellar grey and white matter volumes, and in subcortical volumes, related to patient treatment status and disability and ataxia ratings. |
2016-06-27 |
2023-08-13 |
Not clear |
| Elizabeth A Bowman, Mark Walterfang, Larry Abel, Patricia Desmond, Michael Fahey, Dennis Velakouli. Longitudinal changes in cerebellar and subcortical volumes in adult-onset Niemann-Pick disease type C patients treated with miglustat. Journal of neurology. vol 262. issue 9. 2016-06-27. PMID:26092521. |
semi-automated cerebellar and subcortical segmentation was undertaken, and the rates of change in putamen, hippocampal, thalamic and caudal volumes, and grey and white matter cerebellar volumes, were compared to rates of change in iturriaga disability score, brief ataxia rating scale (bars), and horizontal saccadic gain. |
2016-06-27 |
2023-08-13 |
Not clear |
| Sarah Doss, Jan Leo Rinnenthal, Tanja Schmitz-Hübsch, Alexander U Brandt, Sebastian Papazoglou, Silke Lux, Stephan Maul, Jens Würfel, Matthias Endres, Thomas Klockgether, Martina Minnerop, Friedemann Pau. Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency. Journal of neurology. vol 262. issue 8. 2016-06-22. PMID:26041613. |
autosomal dominant ataxia type 14 (sca14) is a rare usually adult-onset progressive disorder with cerebellar neurodegeneration caused by mutations in protein kinase c gamma. |
2016-06-22 |
2023-08-13 |
Not clear |
| Sarah Doss, Jan Leo Rinnenthal, Tanja Schmitz-Hübsch, Alexander U Brandt, Sebastian Papazoglou, Silke Lux, Stephan Maul, Jens Würfel, Matthias Endres, Thomas Klockgether, Martina Minnerop, Friedemann Pau. Cerebellar neurochemical alterations in spinocerebellar ataxia type 14 appear to include glutathione deficiency. Journal of neurology. vol 262. issue 8. 2016-06-22. PMID:26041613. |
in the cerebellum, we found in addition to signs of neurodegeneration a glutathione reduction, which has been associated with cellular damage by oxidative stress in other neurodegenerative diseases such as parkinson's disease and friedreich's ataxia. |
2016-06-22 |
2023-08-13 |
Not clear |
| Wouter Hoogkamer, Sjoerd M Bruijn, Stefan Sunaert, Stephan P Swinnen, Frank Van Calenbergh, Jacques Duysen. Adaptation and aftereffects of split-belt walking in cerebellar lesion patients. Journal of neurophysiology. vol 114. issue 3. 2016-06-17. PMID:26203113. |
these results confirm that deficits in gait adaptation vary with ataxia severity and between patients with different types of cerebellar damage. |
2016-06-17 |
2023-08-13 |
Not clear |
| Xinlu Li, Marie Ménade, Guennadi Kozlov, Zheping Hu, Zheng Dai, Peter S McPherson, Bernard Brais, Kalle Gehrin. High-Throughput Screening for Ligands of the HEPN Domain of Sacsin. PloS one. vol 10. issue 9. 2016-06-17. PMID:26366743. |
sacsin is a large protein implicated in the neurodevelopmental and neurodegenerative disease autosomal recessive spastic ataxia of charlevoix-saguenay (arsacs), which features the loss of purkinje neurons in the cerebellum. |
2016-06-17 |
2023-08-13 |
Not clear |
| Andy W Yang, Andrew J Sachs, Arne M Nystue. Deletion of Inpp5a causes ataxia and cerebellar degeneration in mice. Neurogenetics. vol 16. issue 4. 2016-06-13. PMID:26051944. |
deletion of inpp5a causes ataxia and cerebellar degeneration in mice. |
2016-06-13 |
2023-08-13 |
mouse |