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118 results

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Page 1
A practical approach to diagnosing adult onset leukodystrophies.
Ahmed RM, Murphy E, Davagnanam I, Parton M, Schott JM, Mummery CJ, Rohrer JD, Lachmann RH, Houlden H, Fox NC, Chataway J. Ahmed RM, et al. Among authors: davagnanam i. J Neurol Neurosurg Psychiatry. 2014 Jul;85(7):770-81. doi: 10.1136/jnnp-2013-305888. Epub 2013 Dec 19. J Neurol Neurosurg Psychiatry. 2014. PMID: 24357685 No abstract available.
Pisa syndrome in Parkinson's disease: a mobile or fixed deformity?
Doherty KM, Davagnanam I, Molloy S, Silveira-Moriyama L, Lees AJ. Doherty KM, et al. Among authors: davagnanam i. J Neurol Neurosurg Psychiatry. 2013 Dec;84(12):1400-3. doi: 10.1136/jnnp-2012-304700. Epub 2013 Mar 26. J Neurol Neurosurg Psychiatry. 2013. PMID: 23532719 Free PMC article.
Lymphomatosis cerebri: a treatable cause of rapidly progressive dementia.
Samani A, Davagnanam I, Cockerell OC, Ramsay A, Patani R, Chataway J. Samani A, et al. Among authors: davagnanam i. J Neurol Neurosurg Psychiatry. 2015 Feb;86(2):238-40. doi: 10.1136/jnnp-2013-307327. Epub 2014 May 20. J Neurol Neurosurg Psychiatry. 2015. PMID: 24847165 Free PMC article. No abstract available.
Analysis of Mutations in AARS2 in a Series of CSF1R-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia.
Lynch DS, Zhang WJ, Lakshmanan R, Kinsella JA, Uzun GA, Karbay M, Tüfekçioglu Z, Hanagasi H, Burke G, Foulds N, Hammans SR, Bhattacharjee A, Wilson H, Adams M, Walker M, Nicoll JA, Chataway J, Fox N, Davagnanam I, Phadke R, Houlden H. Lynch DS, et al. Among authors: davagnanam i. JAMA Neurol. 2016 Dec 1;73(12):1433-1439. doi: 10.1001/jamaneurol.2016.2229. JAMA Neurol. 2016. PMID: 27749956
Redefining the phenotype of ALSP and AARS2 mutation-related leukodystrophy.
Lakshmanan R, Adams ME, Lynch DS, Kinsella JA, Phadke R, Schott JM, Murphy E, Rohrer JD, Chataway J, Houlden H, Fox NC, Davagnanam I. Lakshmanan R, et al. Among authors: davagnanam i. Neurol Genet. 2017 Feb 15;3(2):e135. doi: 10.1212/NXG.0000000000000135. eCollection 2017 Apr. Neurol Genet. 2017. PMID: 28243630 Free PMC article. Review.
Clinical and genetic characterization of leukoencephalopathies in adults.
Lynch DS, Rodrigues Brandão de Paiva A, Zhang WJ, Bugiardini E, Freua F, Tavares Lucato L, Macedo-Souza LI, Lakshmanan R, Kinsella JA, Merwick A, Rossor AM, Bajaj N, Herron B, McMonagle P, Morrison PJ, Hughes D, Pittman A, Laurà M, Reilly MM, Warren JD, Mummery CJ, Schott JM, Adams M, Fox NC, Murphy E, Davagnanam I, Kok F, Chataway J, Houlden H. Lynch DS, et al. Among authors: davagnanam i. Brain. 2017 May 1;140(5):1204-1211. doi: 10.1093/brain/awx045. Brain. 2017. PMID: 28334938 Free PMC article.
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination.
Chelban V, Patel N, Vandrovcova J, Zanetti MN, Lynch DS, Ryten M, Botía JA, Bello O, Tribollet E, Efthymiou S, Davagnanam I; SYNAPSE Study Group; Bashiri FA, Wood NW, Rothman JE, Alkuraya FS, Houlden H. Chelban V, et al. Among authors: davagnanam i. Am J Hum Genet. 2017 Jun 1;100(6):969-977. doi: 10.1016/j.ajhg.2017.05.009. Am J Hum Genet. 2017. PMID: 28575651 Free PMC article.
118 results