نتائج البحث - Justin Kinsella
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Redefining the phenotype of ALSP and <i>AARS2</i> mutation–related leukodystrophy حسب Rahul Lakshmanan, Matthew Adams, David S. Lynch, Justin Kinsella, Rahul Phadke, Jonathan M. Schott, Elaine Murphy, Jonathan D. Rohrer, Jeremy Chataway, Henry Houlden, Nick C. Fox, Indran Davagnanam
منشور في 2017Revisão -
2
Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era حسب David S. Lynch, Charles Wade, Anderson Rodrigues Brandão de Paiva, Nevin John, Justin Kinsella, Áine Merwick, Rebekah M. Ahmed, Jason D. Warren, Catherine J. Mummery, Jonathan M. Schott, Nick C. Fox, Henry Houlden, Matthew Adams, Indran Davagnanam, Elaine Murphy, Jeremy Chataway
منشور في 2018Revisão -
3
Analysis of Mutations in <i>AARS2</i> in a Series of <i>CSF1R</i>-Negative Patients With Adult-Onset Leukoencephalopathy With Axonal Spheroids and Pigmented Glia حسب David S. Lynch, Wei Jia Zhang, Rahul Lakshmanan, Justin Kinsella, Güneş Altıokka Uzun, Merih Karbay, Zeynep Tüfekçıoğlu, Haşmet Hanağası, Georgina Burke, Nicola Foulds, Simon Hammans, Anupam Bhattacharjee, Heather Wilson, Matthew Adams, Mark Walker, James A. R. Nicoll, Jeremy Chataway, Nick C. Fox, Indran Davagnanam, Rahul Phadke, Henry Houlden
منشور في 2016Artigo -
4
Clinical and genetic characterization of leukoencephalopathies in adults حسب David S. Lynch, Anderson Rodrigues Brandão de Paiva, Wei Jia Zhang, Enrico Bugiardini, Fernando Freua, Leandro Tavares Lucato, Lúcia Inês Macedo‐Souza, Rahul Lakshmanan, Justin Kinsella, Áine Merwick, Alexander M. Rossor, Nin Bajaj, Brian Herron, Paul McMonagle, Patrick J. Morrison, Deborah Hughes, Alan Pittman, Matilde Laurá, Mary M. Reilly, Jason D. Warren, Catherine J. Mummery, Jonathan M. Schott, Matthew Adams, Nick C. Fox, Elaine Murphy, Indran Davagnanam, Fernando Kok, Jeremy Chataway, Henry Houlden
منشور في 2017Artigo
أدوات البحث:
موضوعات ذات صلة
Disease
Leukoencephalopathy
Medicine
Pathology
Leukodystrophy
Biology
Exome sequencing
Gene
Genetic testing
Genetics
Internal medicine
Magnetic resonance imaging
Mutation
Radiology
White matter
Ataxia
Atrophy
Bioinformatics
CADASIL
Corpus callosum
Diffusion MRI
Exome
Movement disorders
Neurodegeneration
Neuroscience
Pediatrics
Psychiatry
Psychology