Iron stores and cerebral veins in MS studied by susceptibility weighted imaging
HAACKE, E. M, GARBERN, J, MIAO, Y, HABIB, C, LIU, M
Published in International angiology (01.04.2010)
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Published in International angiology (01.04.2010)
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Assessing Abnormal Iron Content in the Deep Gray Matter of Patients with Multiple Sclerosis versus Healthy Controls
HABIB, C. A, LIU, M, BAWANY, N, GARBERN, J, KRUMBEIN, I, MENTZEL, H.-J, REICHENBACH, J, MAGNANO, C, ZIVADINOV, R, HAACKE, E. M
Published in American journal of neuroradiology : AJNR (01.02.2012)
Published in American journal of neuroradiology : AJNR (01.02.2012)
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Patients lacking the major CNS myelin protein, proteolipid protein 1, develop length-dependent axonal degeneration in the absence of demyelination and inflammation
GARBERN, James Y, YOOL, Donald A, SHY, Michael E, KAMHOLZ, John A, GRIFFITHS, Ian R, MOORE, Gregory J, WILDS, Ian B, FAULK, Michael W, KLUGMANN, Matthias, NAVE, Klaus-Amin, SISTERMANS, Erik A, VAN DER KNAAP, Marjo S, BIRD, Thomas D
Published in Brain (London, England : 1878) (01.03.2002)
Published in Brain (London, England : 1878) (01.03.2002)
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Journal Article
Neurological dysfunction and axonal degeneration in Charcot–Marie–Tooth disease type 1A
Krajewski, Karen M., Lewis, Richard A., Fuerst, Darren R., Turansky, Cheryl, Hinderer, Steven R., Garbern, James, Kamholz, John, Shy, Michael E.
Published in Brain (London, England : 1878) (01.07.2000)
Published in Brain (London, England : 1878) (01.07.2000)
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Journal Article
Cerebellar leukoencephalopathy: most likely histiocytosis-related
van der Knaap, M S, Arts, W F M, Garbern, J Y, Hedlund, G, Winkler, F, Barbosa, C, King, M D, Bjørnstad, A, Hussain, N, Beyer, M K, Gomez, C, Patterson, M C, Grattan-Smith, P, Timmons, M, van der Valk, P
Published in Neurology (21.10.2008)
Published in Neurology (21.10.2008)
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Steroid-responsive neurologic relapses in a child with a proteolipid protein-1 mutation
Gorman, M P, Golomb, M R, Walsh, L E, Hobson, G M, Garbern, J Y, Kinkel, R P, Darras, B T, Urion, D K, Eksioglu, Y Z
Published in Neurology (17.04.2007)
Published in Neurology (17.04.2007)
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Evaluation of loss of function as an explanation for SPG4-based hereditary spastic paraplegia
Solowska, Joanna M., Garbern, James Y., Baas, Peter W.
Published in Human molecular genetics (15.07.2010)
Published in Human molecular genetics (15.07.2010)
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Journal Article
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21
Kennerson, M, Nicholson, G, Kowalski, B, Krajewski, K, El-Khechen, D, Feely, S, Chu, S, Shy, M, Garbern, J
Published in Neurology (20.01.2009)
Published in Neurology (20.01.2009)
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Journal Article
17p11.2p12 triplication and del(17)q11.2q12 in a severely affected child with dup(17)p11.2p12 syndrome
Girirajan, S, Williams, SR, Garbern, JY, Nowak, N, Hatchwell, E, Elsea, SH
Published in Clinical genetics (01.07.2007)
Published in Clinical genetics (01.07.2007)
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Journal Article
Juvenile onset Huntington disease resulting from a very large maternal expansion
Nahhas, F.A., Garbern, J., Krajewski, K.M., Roa, B.B., Feldman, G.L.
Published in American journal of medical genetics. Part A (01.09.2005)
Published in American journal of medical genetics. Part A (01.09.2005)
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Journal Article
Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene
Edgar, J M, McLaughlin, M, Barrie, J A, McCulloch, M C, Garbern, J, Griffiths, I R
Published in Acta neuropathologica (01.04.2004)
Published in Acta neuropathologica (01.04.2004)
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Journal Article
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus–Merzbacher disease
Wolf, Nicole I., Sistermans, Erik A., Cundall, Maria, Hobson, Grace M., Davis-Williams, Angelique P., Palmer, Rodger, Stubbs, Paula, Davies, Sally, Endziniene, Milda, Wu, Yvonne, Chong, Wui K., Malcolm, Sue, Surtees, Robert, Garbern, James Y., Woodward, Karen J.
Published in Brain (London, England : 1878) (01.04.2005)
Published in Brain (London, England : 1878) (01.04.2005)
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Journal Article
Prion disease (PrP-A117V) presenting with ataxia instead of dementia
Mastrianni, J A, Curtis, M T, Oberholtzer, J C, Da Costa, M M, DeArmond, S, Prusiner, S B, Garbern, J Y
Published in Neurology (01.11.1995)
Published in Neurology (01.11.1995)
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228 DEVELOPMENT OF AN INJECTABLE PH- AND TEMPERATURE-RESPONSIVE HYDROGEL DRUG DELIVERY SYSTEM
Garbern, J. C., Hoffman, A. S., Stayton, P. S.
Published in Journal of investigative medicine (01.01.2007)
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Published in Journal of investigative medicine (01.01.2007)
Journal Article
α-Amino-3-hydroxy-5-methylisoxazole-4-propionic acid-mediated excitotoxic axonal damage is attenuated in the absence of myelin proteolipid protein
Fowler, J.H., Edgar, J.M., Pringle, A., McLaughlin, M., McCulloch, J., Griffiths, I.R., Garbern, J.Y., Nave, K.A., Dewar, D.
Published in Journal of neuroscience research (01.07.2006)
Published in Journal of neuroscience research (01.07.2006)
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Journal Article
Phenotypic clustering in MPZ mutations
Shy, Michael E., Jáni, Agnes, Krajewski, Karen, Grandis, Marina, Lewis, Richard A., Li, Jun, Shy, Rosemary R., Balsamo, Janne, Lilien, Jack, Garbern, James Y., Kamholz, John
Published in Brain (London, England : 1878) (01.02.2004)
Published in Brain (London, England : 1878) (01.02.2004)
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Journal Article
Evidence That the Homeodomain Protein Gtx Is Involved in the Regulation of Oligodendrocyte Myelination
Awatramani, Raj, Scherer, Steven, Grinspan, Judith, Collarini, Ellen, Skoff, Robert, O'Hagan, David, Garbern, James, Kamholz, John
Published in The Journal of neuroscience (01.09.1997)
Published in The Journal of neuroscience (01.09.1997)
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