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by Koutsis, G. et al.From mild ataxia to huntington disease phenocopy: the multiple faces of spinocerebellar ataxia 17.Case. Rep. Neurol. Med. 2014; 643289[See paper]

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by Alvarez-Mora, M.I. et al.MicroRNA expression profiling in blood from fragile X-associated tremor/ataxia syndrome patients.Genes Brain Behav. 2013; 6:595-603[See paper]

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by Wang, X. et al.The du(2J) mouse model of ataxia and absence epilepsy has deficient cannabinoid CB₁ receptor-mediated signalling.J. Physiol. (Lond.). 2013; Pt 16:3919-33[See paper]

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by Jiménez-Jiménez, F.J. et al.Section of Neurology, Hospital Universitario del Sureste, Arganda del Rey, Madrid, SpainHereditary Coproporphyria Associated with the Q306X Mutation in the...

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by Hall, D.A. et al.Department of Neurological Sciences, Rush University, Chicago, Illinois, United States of America Premutation carriers may present with a Parkinson disease phenotype or...

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by Maejima, T. et al.Department of Zoology and Neurobiology, Ruhr University Bochum, D-44780 Bochum, Germany Phenotypic analysis revealed that quirky mice display ataxia, dyskinesia, and absence...

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by Hussain, R.S. et al.Warren Alpert Medical School of Brown University, Providence, RI 02912, USA Though corticosteroids and acyclovir are not recommended therapy in patients presenting with...

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by Margolin, D.H. et al.Department of Neurology, Massachusetts General Hospital, Boston 02115, USAAtaxia, dementia, and hypogonadotropism caused by disordered ubiquitination.N. Engl. J. Med. 2013;...

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by Brashear, A. et al.Department of Neurology, Wake Forest School of Medicine, Winston-Salem, NC 27157, USA At age 4 years, he had episodic slurred speech, followed by ataxia, drooling, and...

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by Zannolli, R. et al.Child Neurology and Psychiatry Unit, Azienda Ospedaliera Universitaria Senese/University of Siena, Policlinico Le Scotte, Siena, Italy In conclusion, Oral betamethasone could be...

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by Karmon, Y. et al.Baird MS Center, Jacobs Neurological Institute, SUNY Buffalo School of Medicine and Biomedical Sciences, United StatesLimb ataxia originating from peri-central sulcus demyelinating...

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by Brown, S.A. et al.Richard D, Berlin Center for Cell Analysis & Modeling, University of Connecticut Health Center, 400 Farmington Ave, USAComputational analysis of calcium signaling and membrane...

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by Juncos, J.L. et al.Department of Neurology, Emory University School of Medicine, Atlanta, USAOlfactory dysfunction in fragile X tremor ataxia syndrome.Mov. Disord. 2012; 12:1556-9[See paper]

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by Labate, A. et al.Institute of Neurology, University Magna Graecia, Catanzaro, ItalyInstitute of Neurological Sciences, Italy This family provides strong evidence that homozygous PRRT2 mutations...

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by Jordan, J.T. et al.Slowly progressive ataxia, neuropathy, and oculomotor dysfunction.Arch. Neurol. 2012; 10:1366-71[See paper]

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by Thevenon, J. et al.Hôpital d'Enfants, Centre de Génétique, 10 Bd Maréchal de Lattre de Tassigny, Dijon 21079, France;Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or...

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by Müller, K.I. et al.Department of Neurology, University Hospital of North Norway, Tromsø, NorwayEpilepsy in a patient with ataxia caused by vitamin E deficiency.BMJ. Case. Rep. 2011; [See paper]

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by Mahfouz, W. et al.Jewish General Hospital, McGill University, Montreal, Quebec, CanadaManagement of detrusor external sphincter dyssynergia in neurogenic bladder.Eur. J. Phys. Rehabil. Med. 2011;...

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by Jacobi, H. et al.Department of Neurology, University Hospital of Bonn, Sigmund-Freud-Straße 25, 53105, GermanySpinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and...

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by Fogel, B.L. et al.Program in Neurogenetics, Department of Neurology, David Geffen School of Medicine, University of California at Los Angeles, USAThe rare genetic ataxias examined here do not...

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