Monday, January 4, 2016

Using stem cells to battle brain diseases

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Esther B. E. Becker, Atlas of Science Although scientific progress is being made, neurodegenerative diseases remain incurable. Research i...
Sunday, January 3, 2016

2,2′-dipyridyl induces pexophagy

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Ai Lin Jin, Joon No Lee, Min Soo Kim, SeongAe Kwak, Se-Jin Kim, Kyung Song, Seong-Kyu Choe, Raekil Park, Biochemical and Biophysical Researc...
Friday, January 1, 2016

Pseudocyst of the auricle in patients with movement disorders: report of two patients with ataxia-associated auricular pseudocysts

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Beutler BD, Cohen PR; Dermatol Pract Concept. 2015 Oct 31;5(4):59-64. doi: 10.5826/dpc.0504a15. eCollection 2015. Pseudocyst of the auricl...
Thursday, December 31, 2015

Rare diseases: matching wheelchair users with rare metabolic, neuromuscular or neurological disorders to electric powered indoor/outdoor wheelchairs (EPIOCs)

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Lorraine H. De Souza & Andrew O. Frank. Disabil Rehabil. 2015 Dec 30:1-10. [Epub ahead of print] DOI:10.3109/09638288.2015.1106599 The...
Wednesday, December 30, 2015

Identification of potential mitochondrial CLPXP protease interactors and substrates suggests its central role in energy metabolism

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Fabian Fischer, Julian D. Langer & Heinz D. Osiewacz; (NATURE) Scientific Reports 5, Article number: 18375 (2015) doi:10.1038/srep18375 ...
Tuesday, December 29, 2015

The first therapeutics based on genome-editing tools will treat diseases caused by single genes, but many other factors dictate what is currently possible.

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Virginia Gewin, Medicine: Expanding possibilities, Nature 528, S10–S11 (03 December 2015) doi:10.1038/528S10a Published online 02 December 2...
Monday, December 28, 2015

Treatments for Syndromes of Progressive Ataxia and Weakness Disorders - PMR Market Insight Report to 2020

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Persistence Market Research (PMR) Stringent regulations and standard requires for approval process of new drugs impede growth of the treat...
Sunday, December 27, 2015

Burden of mitochondrial DNA variations in Friedreich's Ataxia (FRDA) patients and sharing of mitochondrial lineage with Caucasians

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Inder singh, Sunil Sakhya, Madhuri Behari, M.V. Padma Srivastava, Garima Shukla, Vinay Goyal, Achal Kumar Srivastava, Mohd. Faruq, Parkinson...
Saturday, December 26, 2015

Compound heterozygous FXN mutations and clinical outcome in Friedreich ataxia

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Charles A. Galea, Aamira Huq, Paul J. Lockhart, Geneieve Tai, Louise A. Corben, Eppie M. Yiu, Lyle C. Gurrin, David R. Lynch, Sarah Gelbard,...
Thursday, December 24, 2015

Diagnosis and management of hypertrophic cardiomyopathy

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Antonis Pantazis MD, Annina S Vischer MD, Maria Carrillo Perez-Tome MD and Silvia Castelletti MD;  Echo Res Pract. 2015 Mar 1;2(1):R45-53. ...