Schneider SA - Search Results

1

Stem cell reprogramming: basic implications and future perspective for movement disorders.

Brändl B, Schneider SA, Loring JF, Hardy J, Gribbon P, Müller FJ. Brändl B, et al. Among authors: schneider sa. Mov Disord. 2015 Mar;30(3):301-12. doi: 10.1002/mds.26113. Epub 2014 Dec 27. Mov Disord. 2015. PMID: 25546831 Review.

2

Iron accumulation in syndromes of neurodegeneration with brain iron accumulation 1 and 2: causative or consequential?

Schneider SA, Hardy J, Bhatia KP. Schneider SA, et al. J Neurol Neurosurg Psychiatry. 2009 Jun;80(6):589-90. doi: 10.1136/jnnp.2008.169953. Epub 2009 Jan 15. J Neurol Neurosurg Psychiatry. 2009. PMID: 19147629 No abstract available.

3

Complicated recessive dystonia parkinsonism syndromes.

Schneider SA, Bhatia KP, Hardy J. Schneider SA, et al. Mov Disord. 2009 Mar 15;24(4):490-9. doi: 10.1002/mds.22314. Mov Disord. 2009. PMID: 19185014 Review.

4

GLUT1 gene mutations cause sporadic paroxysmal exercise-induced dyskinesias.

Schneider SA, Paisan-Ruiz C, Garcia-Gorostiaga I, Quinn NP, Weber YG, Lerche H, Hardy J, Bhatia KP. Schneider SA, et al. Mov Disord. 2009 Aug 15;24(11):1684-8. doi: 10.1002/mds.22507. Mov Disord. 2009. PMID: 19630075

5

ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation.

Schneider SA, Paisan-Ruiz C, Quinn NP, Lees AJ, Houlden H, Hardy J, Bhatia KP. Schneider SA, et al. Mov Disord. 2010 Jun 15;25(8):979-84. doi: 10.1002/mds.22947. Mov Disord. 2010. PMID: 20310007

6

Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms.

Aggarwal A, Schneider SA, Houlden H, Silverdale M, Paudel R, Paisan-Ruiz C, Desai S, Munshi M, Sanghvi D, Hardy J, Bhatia KP, Bhatt M. Aggarwal A, et al. Among authors: schneider sa. Mov Disord. 2010 Jul 30;25(10):1424-31. doi: 10.1002/mds.23095. Mov Disord. 2010. PMID: 20629144

7

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.

Paisán-Ruiz C, Guevara R, Federoff M, Hanagasi H, Sina F, Elahi E, Schneider SA, Schwingenschuh P, Bajaj N, Emre M, Singleton AB, Hardy J, Bhatia KP, Brandner S, Lees AJ, Houlden H. Paisán-Ruiz C, et al. Among authors: schneider sa. Mov Disord. 2010 Sep 15;25(12):1791-800. doi: 10.1002/mds.23221. Mov Disord. 2010. PMID: 20669327 Free PMC article.

8

Syndromes of neurodegeneration with brain iron accumulation (NBIA): an update on clinical presentations, histological and genetic underpinnings, and treatment considerations.

Schneider SA, Hardy J, Bhatia KP. Schneider SA, et al. Mov Disord. 2012 Jan;27(1):42-53. doi: 10.1002/mds.23971. Epub 2011 Oct 26. Mov Disord. 2012. PMID: 22031173 Review.

9

Alternating hemiplegia of childhood and rapid-onset dystonia parkinsonism are allelic disorders due to ATP1A3 gene mutations.

Alexoudi A, Schneider SA. Alexoudi A, et al. Among authors: schneider sa. Mov Disord. 2012 Oct;27(12):1494. doi: 10.1002/mds.25222. Mov Disord. 2012. PMID: 23460948 No abstract available.

10

Submandibular gland biopsy for the diagnosis of Parkinson's disease.

Alexoudi A, Schneider SA, Deuschl G. Alexoudi A, et al. Among authors: schneider sa. Mov Disord. 2013 Jun;28(6):734. doi: 10.1002/mds.25467. Epub 2013 May 29. Mov Disord. 2013. PMID: 23720221 No abstract available.

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