Kết quả tìm kiếm - Justin Kinsella
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1
Redefining the phenotype of ALSP and <i>AARS2</i> mutation–related leukodystrophy Bằng 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
Được phát hành 2017Revisão -
2
Practical approach to the diagnosis of adult-onset leukodystrophies: an updated guide in the genomic era Bằng 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
Được phát hành 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 Bằng 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
Được phát hành 2016Artigo -
4
Clinical and genetic characterization of leukoencephalopathies in adults Bằng 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
Được phát hành 2017Artigo
Công cụ tìm kiếm:
Các môn học liên quan
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