Keith Van Haren
Keith Van Haren
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Acute disseminated encephalomyelitis: updates on an inflammatory CNS syndrome
D Pohl, G Alper, K Van Haren, AJ Kornberg, CF Lucchinetti, ...
Neurology 87 (9 Supplement 2), S38-S45, 2016
A novel outbreak enterovirus D68 strain associated with acute flaccid myelitis cases in the USA (2012–14): a retrospective cohort study
AL Greninger, SN Naccache, K Messacar, A Clayton, G Yu, S Somasekar, ...
The Lancet Infectious Diseases 15 (6), 671-682, 2015
Clinical approach to the diagnosis of autoimmune encephalitis in the pediatric patient
T Cellucci, H Van Mater, F Graus, E Muscal, W Gallentine, ...
Neurology-Neuroimmunology Neuroinflammation 7 (2), 2020
Acute flaccid myelitis: a clinical review of US cases 2012–2015
K Messacar, TL Schreiner, K Van Haren, M Yang, CA Glaser, KL Tyler, ...
Annals of neurology 80 (3), 326-338, 2016
Safety and immunologic effects of high-vs low-dose cholecalciferol in multiple sclerosis
ES Sotirchos, P Bhargava, C Eckstein, K Van Haren, M Baynes, A Ntranos, ...
Neurology 86 (4), 382-390, 2016
Acute flaccid myelitis of unknown etiology in California, 2012-2015
K Van Haren, P Ayscue, E Waubant, A Clayton, H Sheriff, S Yagi, ...
Jama 314 (24), 2663-2671, 2015
De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy
JR Lee, M Srour, D Kim, FF Hamdan, SH Lim, C Brunel‐Guitton, ...
Human mutation 36 (1), 69-78, 2015
Acute flaccid paralysis with anterior myelitis—California, June 2012–June 2014
P Ayscue, K Van Haren, H Sheriff, E Waubant, P Waldron, S Yagi, C Yen, ...
Morbidity and Mortality Weekly Report 63 (40), 903, 2014
The unfolded protein response in vanishing white matter disease
JP Van Der Voorn, B Van Kollenburg, G Bertrand, K Van Haren, ...
Journal of Neuropathology & Experimental Neurology 64 (9), 770-775, 2005
Acute flaccid myelitis: cause, diagnosis, and management
OC Murphy, K Messacar, L Benson, R Bove, JL Carpenter, T Crawford, ...
The Lancet 397 (10271), 334-346, 2021
Natural history of vanishing white matter
EMC Hamilton, HDW van der Lei, G Vermeulen, JAM Gerver, ...
Annals of neurology 84 (2), 274-288, 2018
The life and death of oligodendrocytes in vanishing white matter disease
K Van Haren, JP Van Der Voorn, DR Peterson, MS Van Der Knaap, ...
Journal of Neuropathology & Experimental Neurology 63 (6), 618-630, 2004
Identification of naturally occurring fatty acids of the myelin sheath that resolve neuroinflammation
PP Ho, JL Kanter, AM Johnson, HK Srinagesh, EJ Chang, TM Purdy, ...
Science translational medicine 4 (137), 137ra73-137ra73, 2012
Genetic and phenotypic spectrum associated with IFIH1 gain‐of‐function
GI Rice, S Park, F Gavazzi, LA Adang, LA Ayuk, L Van Eyck, L Seabra, ...
Human mutation 41 (4), 837-849, 2020
Safety, tolerability, and efficacy of fluoxetine as an antiviral for acute flaccid myelitis
K Messacar, S Sillau, SE Hopkins, C Otten, M Wilson-Murphy, B Wong, ...
Neurology 92 (18), e2118-e2126, 2019
Revised consensus statement on the preventive and symptomatic care of patients with leukodystrophies
LA Adang, O Sherbini, L Ball, M Bloom, A Darbari, H Amartino, D DiVito, ...
Molecular genetics and metabolism 122 (1-2), 18-32, 2017
Clinical subpopulations in a sample of North American children diagnosed with acute flaccid myelitis, 2012-2016
MJ Elrick, E Gordon-Lipkin, TO Crawford, K Van Haren, K Messacar, ...
JAMA pediatrics 173 (2), 134-139, 2019
Disease specific therapies in leukodystrophies and leukoencephalopathies
G Helman, K Van Haren, JL Bonkowsky, G Bernard, A Pizzino, ...
Molecular genetics and metabolism 114 (4), 527-536, 2015
Serum autoantibodies to myelin peptides distinguish acute disseminated encephalomyelitis from relapsing–remitting multiple sclerosis
K Van Haren, BH Tomooka, BA Kidd, B Banwell, A Bar-Or, T Chitnis, ...
Multiple Sclerosis Journal 19 (13), 1726-1733, 2013
MRI surveillance of boys with X‐linked adrenoleukodystrophy identified by newborn screening: meta‐analysis and consensus guidelines
EJ Mallack, BR Turk, H Yan, C Price, M Demetres, AB Moser, C Becker, ...
Journal of inherited metabolic disease 44 (3), 728-739, 2021
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