Consensus Paper: Neuroimmune Mechanisms of Cerebellar Ataxias
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Shinji Kakei | Makoto Yoneda | Hiroshi Mitoma | Mario Manto | Jérôme Honnorat | H. Mitoma | S. Kakei | J. Honnorat | M. Manto | D. Aeschlimann | C. Hampe | N. Yuki | H. Mizusawa | M. Hadjivassiliou | Jongho Lee | Hidehiro Mizusawa | P. Shanmugarajah | B. Joubert | M. Yoneda | Jongho Lee | Akiko Matsunaga | Daniel Aeschlimann | Keya Adhikari | Partha Chattopadhyay | Marios Hadjivassiliou | Christiane S. Hampe | Bastien Joubert | Kazunori Nanri | Priya Shanmugarajah | Nobuhiro Yuki | K. Nanri | A. Matsunaga | P. Chattopadhyay | J. Honnorat | Bastien Joubert | Keya Adhikari
[1] Xinqing Zhang,et al. Hashimoto’s encephalopathy mimicking spinocerebellar ataxia , 2011, Journal of Neurology.
[2] MR spectroscopy in paraneoplastic cerebellar degeneration. , 2013, Journal of neuroradiology. Journal de neuroradiologie.
[3] I. Kanazawa,et al. Anti‐GQ1b IgG antibody is associated with ataxia as well as ophthalmoplegia , 1999, Muscle & nerve.
[4] G. Davies-Jones,et al. Cerebellar ataxia as a possible organ‐specific autoimmune disease , 2008, Movement disorders : official journal of the Movement Disorder Society.
[5] J. Honnorat,et al. Paraneoplastic neurologic syndrome in the PNS Euronetwork database: a European study from 20 centers. , 2010, Archives of neurology.
[6] A. García-Zarza,et al. Cerebellar ataxia associated with neuroendocrine thymic carcinoma and GAD antibodies , 2009, Journal of Neurology, Neurosurgery, and Psychiatry.
[7] E. Tongiorgi,et al. Anti Transglutaminase Antibodies Cause Ataxia in Mice , 2010, PloS one.
[8] Ikuo Tsunoda,et al. Purkinje Cell Death After Uptake of Anti-Yo Antibodies in Cerebellar Slice Cultures , 2010, Journal of neuropathology and experimental neurology.
[9] H. Mitoma,et al. Presynaptic dysfunction caused by cerebrospinal fluid from a patient with the ataxic form of Hashimoto's encephalopathy , 2014 .
[10] R. Vandenberghe,et al. Orchiectomy for suspected microscopic tumor in patients with anti-Ma2-associated encephalitis , 2007, Neurology.
[11] M. Rowley,et al. Stiff-person syndrome (SPS) and anti-GAD-related CNS degenerations: protean additions to the autoimmune central neuropathies. , 2011, Journal of autoimmunity.
[12] A. Vighetto,et al. Cerebellar ataxia with anti-glutamic acid decarboxylase antibodies: study of 14 patients. , 2001, Archives of neurology.
[13] M. Dalakas,et al. Immunology of stiff person syndrome and other GAD-associated neurological disorders , 2013, Expert review of clinical immunology.
[14] H. Urbach,et al. Antibodies to glutamic acid decarboxylase define a form of limbic encephalitis , 2010, Annals of neurology.
[15] B. Giometto,et al. Homer 3 autoimmunity in subacute idiopathic cerebellar ataxia , 2007, Neurology.
[16] M. Yoneda,et al. High prevalence of serum autoantibodies against the amino terminal of α-enolase in Hashimoto's encephalopathy , 2007, Journal of Neuroimmunology.
[17] D. Friedman,et al. Antibodies to the GABAB receptor in limbic encephalitis with seizures: case series and characterisation of the antigen , 2010, The Lancet Neurology.
[18] M. Fisher. An unusual variant of acute idiopathic polyneuritis (syndrome of ophthalmoplegia, ataxia and areflexia). , 1956, The New England journal of medicine.
[19] S. Kusunoki,et al. Serum IgG antibody to ganglioside GQ1b is a possible marker of Miller Fisher syndrome , 1992, Annals of neurology.
[20] M. Dalakas,et al. Brain γ-Aminobutyric Acid Changes in Stiff-Person Syndrome , 2005 .
[21] T. Walls,et al. Hashirnoto's encephalopathy , 1991, Neurology.
[22] B. Sharrack,et al. Gluten ataxia in perspective: epidemiology, genetic susceptibility and clinical characteristics. , 2003, Brain : a journal of neurology.
[23] M. Pani,et al. Familial clustering of juvenile thyroid autoimmunity: higher risk is conferred by human leukocyte antigen DR3-DQ2 and thyroid peroxidase antibody status in fathers. , 2002, The Journal of clinical endocrinology and metabolism.
[24] K. Ikeda,et al. Antineuronal antibodies in acute cerebellar ataxia following Epstein‐Barr virus infection , 1994, Neurology.
[25] J. Dichgans,et al. Cerebellar ataxia with glutamic acid decarboxylase autoantibodies , 1999, Neurology.
[26] M. Manto,et al. [Cerebellar syndrome associated with Hashimoto's encephalopathy]. , 1996, Revue neurologique.
[27] Loise M. Francisco,et al. Tumor-specific killer cells in paraneoplastic cerebellar degeneration , 1998, Nature Medicine.
[28] B. Hart,et al. Magnetic resonance imaging and brain histopathology in neuropsychiatric systemic lupus erythematosus. , 2010, Seminars in arthritis and rheumatism.
[29] J. Rose,et al. Journal of Neuroinflammation Cerebellar Purkinje Cells Incorporate Immunoglobulins and Immunotoxins in Vitro: Implications for Human Neurological Disease and Immunotherapeutics , 2022 .
[30] F. Udaka,et al. Miller Fisher-Guillain-Barré overlap syndrome with enhancing lesions in the spinocerebellar tracts. , 1995, Journal of neurology, neurosurgery, and psychiatry.
[31] D. Sanders,et al. Autoantibody targeting of brain and intestinal transglutaminase in gluten ataxia , 2006, Neurology.
[32] A. Malaviya,et al. Cerebellar ataxia in systemic lupus erythematosus: three case reports. , 1988, Annals of the rheumatic diseases.
[33] D. Drachman,et al. Ataxia associated with Hashimoto's disease: progressive non-familial adult onset cerebellar degeneration with autoimmune thyroiditis , 2001, Journal of neurology, neurosurgery, and psychiatry.
[34] L. Ramió-Torrentá,et al. Spectrum of neurological syndromes associated with glutamic acid decarboxylase antibodies: diagnostic clues for this association. , 2008, Brain : a journal of neurology.
[35] J. Dichgans,et al. The humoral response in the pathogenesis of gluten ataxia , 2002, Neurology.
[36] G. E. Newman,et al. Incidence and significance , 1988 .
[37] P. Chattopadhyay,et al. Acute cerebellar ataxia in lupus , 2011, Lupus.
[38] R. Darnell,et al. Paraneoplastic syndromes involving the nervous system. , 2003, The New England journal of medicine.
[39] J. Hunter,et al. Cerebral and Cerebellar Volume Loss in Children and Adolescents with Systemic Lupus Erythematosus: A Review of Clinically Acquired Brain Magnetic Resonance Imaging , 2010, The Journal of Rheumatology.
[40] M. Dalakas,et al. Stiff person syndrome with cerebellar disease and high-titer anti-GAD antibodies , 2006, Neurology.
[41] E. Richardson,et al. The neurological manifestations of systemic lupus erythematosus. , 1968, Medicine.
[42] J. Bobholz,et al. Multiple Sclerosis and Other Demyelinating Disorders , 2011 .
[43] M. Manto,et al. Syndrome cérébelleux associé à une encéphalopathie d'hashimoto. , 1996 .
[44] L. Cinotti,et al. FDG-PET improves tumour detection in patients with paraneoplastic neurological syndromes. , 2004, Brain : a journal of neurology.
[45] C. Almonte,et al. [Acute cerebellitis]. , 1962, Revista chilena de pediatria.
[46] D. Jacobowitz,et al. Stiff person syndrome: Advances in pathogenesis and therapeutic interventions , 2001, Neurology.
[47] L. Borges,et al. Intraneuronal accumulation of myeloma proteins. , 1985, Archives of neurology.
[48] A. Vincent,et al. Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia , 2010, Brain : a journal of neurology.
[49] J. J. Stagnone,et al. Small bowel changes in dermatitis herpetiformis. , 1969, Southern medical journal.
[50] M. Rosenblum,et al. Paraneoplastic cerebellar degeneration. , 1992, Neurology.
[51] G. Davies-Jones,et al. Clinical, radiological, neurophysiological, and neuropathological characteristics of gluten ataxia , 1998, The Lancet.
[52] H. Meinck,et al. Two new cases of anti-Ca (anti-ARHGAP26/GRAF) autoantibody-associated cerebellar ataxia , 2013, Journal of Neuroinflammation.
[53] J. Honnorat,et al. Spectrum of paraneoplastic disease associated with lymphoma , 2011, Neurology.
[54] F. Ducray,et al. Seronegative paraneoplastic cerebellar degeneration: the PNS Euronetwork experience , 2014, European journal of neurology.
[55] R. Casamitjana,et al. T‐cell reactivity to glutamic acid decarboxylase in stiff‐man syndrome and cerebellar ataxia associated with polyendocrine autoimmunity , 2002, Clinical and experimental immunology.
[56] Yasuhiro Kagamihara,et al. Quantitative evaluation of movement disorders in neurological diseases based on EMG signals , 2008, 2008 30th Annual International Conference of the IEEE Engineering in Medicine and Biology Society.
[57] B. Dan,et al. Opsoclonus-myoclonus associated with celiac disease. , 2006, Pediatric neurology.
[58] I. Korponay-Szabó,et al. Deamidated Gliadin Peptides Form Epitopes That Transglutaminase Antibodies Recognize , 2008, Journal of pediatric gastroenterology and nutrition.
[59] J. Honnorat,et al. Monoclonal antibodies to 65kDa glutamate decarboxylase induce epitope specific effects on motor and cognitive functions in rats , 2013, Orphanet Journal of Rare Diseases.
[60] R. Balice-Gordon,et al. Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series , 2010, The Lancet Neurology.
[61] P. Ranganathan,et al. An unusual case of cerebellar hemorrhage in a patient with systemic lupus erythematosus , 2010, Arthritis care & research.
[62] H. Mitoma,et al. Reversibility of cerebellar GABAergic synapse impairment induced by anti-glutamic acid decarboxylase autoantibodies , 2008, Journal of the Neurological Sciences.
[63] E. Anghileri,et al. Novel autoantigens recognized by CSF IgG from Hashimoto's encephalitis revealed by a proteomic approach , 2008, Journal of Neuroimmunology.
[64] Xiaoyu Peng,et al. Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies , 2008, The Lancet Neurology.
[65] J. Dichgans,et al. Cerebellar encephalitis in adults , 2004, Journal of Neurology.
[66] W. Paulus,et al. Hashimoto encephalopathy: A brainstem vasculitis? , 2000, Neurology.
[67] M. Suenaga,et al. Acute cerebellar ataxia of a patient with SLE , 2000, Clinical neurology and neurosurgery (Dutch-Flemish ed. Print).
[68] C. Wessig,et al. Stiff person syndrome-associated autoantibodies to amphiphysin mediate reduced GABAergic inhibition. , 2010, Brain : a journal of neurology.
[69] D. Ellison,et al. Cerebellum and brainstem vasculopathy in systemic lupus erythematosus: two clinico-pathological cases. , 1994, Annals of the rheumatic diseases.
[70] S. Tsuji,et al. Passive transfer and active immunization with the recombinant leucine-zipper (Yo) protein as an attempt to establish an animal model of paraneoplastic cerebellar degeneration , 1994, Journal of the Neurological Sciences.
[71] M. Yoneda,et al. Hashimoto’s encephalopathy presenting with progressive cerebellar ataxia , 2007, Journal of Neurology, Neurosurgery & Psychiatry.
[72] S. Baekkeskov,et al. Increased anxiety and altered responses to anxiolytics in mice deficient in the 65-kDa isoform of glutamic acid decarboxylase. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[73] R. Kalb,et al. AMPA receptor antibodies in limbic encephalitis alter synaptic receptor location , 2009, Annals of neurology.
[74] W. Cooke,et al. Neurological disorders associated with adult coeliac disease. , 1966, Brain : a journal of neurology.
[75] R. Griffey,et al. Magnetic resonance and computed tomographic imaging in the evaluation of acute neuropsychiatric disease in systemic lupus erythematosus. , 1989, Annals of the rheumatic diseases.
[76] D. Copenhagen,et al. The role of the synthetic enzyme GAD65 in the control of neuronal gamma-aminobutyric acid release. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[77] P. De Camilli,et al. Association of HLA-DQB1*0201 with stiff-man syndrome. , 1993, The Journal of clinical endocrinology and metabolism.
[78] J. Li,et al. Antecedent infections in Fisher syndrome , 2005, Neurology.
[79] R. Richter. PRESIDENTIAL ADDRESS: The Ataxic Form of Polyradiculoneuritis (Landry‐Guillain‐Barré Syndrome) Clinical and Pathologic Observations , 1962, Journal of neuropathology and experimental neurology.
[80] L. Trandafir,et al. Celiac disease with neurologic manifestations in children. , 2013, Revista medico-chirurgicala a Societatii de Medici si Naturalisti din Iasi.
[81] D. Perani,et al. Human Stiff-Person Syndrome IgG Induces Anxious Behavior in Rats , 2011, PloS one.
[82] A. Vincent,et al. Stiff, twitchy or wobbly: are GAD antibodies pathogenic? , 2008, Brain : a journal of neurology.
[83] I. Kanazawa,et al. Serum anti-GQ1b IgG antibody is associated with ophthalmoplegia in Miller Fisher syndrome and Guillain-Barré syndrome: Clinical and immunohistochemical studies , 2011, Neurology.
[84] J. Whisstock,et al. GABA production by glutamic acid decarboxylase is regulated by a dynamic catalytic loop , 2007, Nature Structural &Molecular Biology.
[85] M. Dalakas,et al. The clinical spectrum of anti-GAD antibody-positive patients with stiff-person syndrome , 2000, Neurology.
[86] D. Aeschlimann,et al. Protein Crosslinking in Assembly and Remodelling of Extracellular Matrices: The Role of Transglutaminases , 2000, Connective tissue research.
[87] S. Rogers,et al. Glutamate receptor antibodies activate a subset of receptors and reveal an agonist binding site , 1995, Neuron.
[88] G. Davies-Jones,et al. The humoral response in the pathogenesis of gluten ataxia , 2002, Neurology.
[89] Jianning Wei,et al. Demonstration of functional coupling between γ-aminobutyric acid (GABA) synthesis and vesicular GABA transport into synaptic vesicles , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[90] D. Sanders,et al. Transglutaminase 6 antibodies in the diagnosis of gluten ataxia , 2013, Neurology.
[91] M. Ikawa,et al. Hashimoto’s Encephalopathy as a Treatable Adult-Onset Cerebellar Ataxia Mimicking Spinocerebellar Degeneration , 2012, European Neurology.
[92] S. Tsuji,et al. Trial to establish an animal model of paraneoplastic cerebellar degeneration with anti-Yo antibody 1. Mouse strains bearing different MHC molecules produce antibodies on immunization with recombinant Yo protein, but do not cause Purkinje cell loss , 1995, Clinical Neurology and Neurosurgery.
[93] A. Vincent,et al. Autoimmune encephalitis -- new awareness, challenging questions. , 2011, Discovery medicine.
[94] L. Lagae,et al. MRI findings in acute cerebellitis , 2004, European Radiology.
[95] I. N. Reid,et al. Hashimoto’s encephalopathy , 2003, Neurology.
[96] D. Sanders,et al. Autoantibodies in gluten ataxia recognize a novel neuronal transglutaminase , 2008, Annals of neurology.
[97] H. Willison,et al. Antiganglioside antibodies in acute self-limiting ataxic neuropathy: incidence and significance , 2001, Journal of Neuroimmunology.
[98] M. Erlander,et al. Two genes encode distinct glutamate decarboxylases , 1991, Neuron.
[99] H. Greenberg. Paraneoplastic cerebellar degeneration , 2004, Journal of Neuro-Oncology.
[100] L. Brain,et al. Hashimoto's disease and encephalopathy. , 1966, Lancet.
[101] E. Tolosa,et al. Autoantibodies to glutamic acid decarboxylase in three patients with cerebellar ataxia, late-onset insulin-dependent diabetes mellitus, and polyendocrine autoimmunity , 1997, Neurology.
[102] A. Connolly,et al. Course and outcome of acute cerebellar ataxia , 1994, Annals of neurology.
[103] S. Nakanishi,et al. Paraneoplastic cerebellar ataxia due to autoantibodies against a glutamate receptor. , 2000, The New England journal of medicine.
[104] P. Shaw,et al. Hashimoto's encephalopathy: a steroid-responsive disorder associated with high anti-thyroid antibody titers--report of 5 cases. , 1991, Neurology.
[105] H. Mitoma,et al. Dual impairment of GABAA- and GABAB-receptor-mediated synaptic responses by autoantibodies to glutamic acid decarboxylase , 2003, Journal of the Neurological Sciences.
[106] C. Geis,et al. Human Stiff person syndrome IgG-containing high-titer anti-GAD65 autoantibodies induce motor dysfunction in rats , 2013, Experimental Neurology.
[107] H. Mitoma,et al. Classification of cerebellar atrophy using voxel-based morphometry and SPECT with an easy Z-score imaging system. , 2010, Internal medicine.
[108] S. Maekawa,et al. Interaction of NAP-22 with brain glutamic acid decarboxylase (GAD) , 2013, Neuroscience Letters.
[109] H. Willison,et al. Immunolocalization of GQ1b and related gangliosides in human extraocular neuromuscular junctions and muscle spindles. , 2009, Investigative ophthalmology & visual science.
[110] Xiaoyu Peng,et al. Cellular and Synaptic Mechanisms of Anti-NMDA Receptor Encephalitis , 2010, The Journal of Neuroscience.
[111] A. Feinstein,et al. I. Incidence and Significance ‡ , 1961, The Yale journal of biology and medicine.
[112] Jianjun Li,et al. A Haemophilus influenzae strain associated with Fisher syndrome expresses a novel disialylated ganglioside mimic. , 2007, Biochemistry.
[113] M. Daras,et al. Cerebellar ataxia in systemic lupus erythematosus. , 1983, New York state journal of medicine.
[114] M. Rowley,et al. HLA-DQ genotypes are associated with autoimmunity to glutamic acid decarboxylase in insulin-dependent diabetes mellitus patients. , 1993, Human immunology.
[115] J. Honnorat,et al. Human epidermal growth factor receptor 2 overexpression in breast cancer of patients with anti-Yo--associated paraneoplastic cerebellar degeneration. , 2012, Neuro-oncology.
[116] A. Draguhn,et al. GABA Metabolism and Transport: Effects on Synaptic Efficacy , 2012, Neural plasticity.
[117] S. Tsuji,et al. Trial to establish an animal model of paraneoplastic cerebellar degeneration with anti-Yo antibody 2. Passive transfer of murine mononuclear cells activated with recombinant Yo protein to paraneoplastic cerebellar degeneration lymphocytes in severe combined immunodeficiency mice , 1995, Clinical Neurology and Neurosurgery.
[118] I. Wilkinson,et al. Should we be ‘nervous’ about coeliac disease? Brain abnormalities in patients with coeliac disease referred for neurological opinion , 2012, Journal of Neurology, Neurosurgery & Psychiatry.
[119] H. Mitoma,et al. Low-Titer Anti-GAD-Antibody-Positive Cerebellar Ataxia , 2013, The Cerebellum.
[120] T. Miyatake,et al. Association of IgG anti‐GD1a antibody with severe Guillain–Barré syndrome , 1993, Muscle & nerve.
[121] H. Brashear,et al. Antibodies to cerebellar Purkinje cells in patients with paraneoplastic cerebellar degeneration and ovarian carcinoma , 1983, Annals of neurology.
[122] H. Mitoma,et al. Selective loss of Purkinje cells in a patient with anti-glutamic acid decarboxylase antibody-associated cerebellar ataxia , 2006, Journal of Neurology, Neurosurgery & Psychiatry.
[123] K. Hirata,et al. Ataxic Guillain‐Barré syndrome with anti‐GQ1b antibody: Relation to Miller Fisher syndrome , 2000, Neurology.
[124] S. Currie,et al. Progressive ataxia with palatal tremor due to gluten sensitivity , 2012, Movement disorders : official journal of the Movement Disorder Society.
[125] Josep Dalmau,et al. Paraneoplastic anti–N‐methyl‐D‐aspartate receptor encephalitis associated with ovarian teratoma , 2007, Annals of neurology.
[126] J. Delgado-García,et al. The GABAergic septohippocampal pathway is directly involved in internal processes related to operant reward learning. , 2014, Cerebral cortex.
[127] B. Passarella,et al. Cerebellar subacute syndrome due to corticosteroid-responsive encephalopathy associated with autoimmune thyroiditis (also called "Hashimoto's encephalopathy"). , 2005, La Clinica terapeutica.
[128] N. Kokubun,et al. Non-demyelinating, reversible conduction failure in Fisher syndrome and related disorders , 2012, Journal of Neurology, Neurosurgery & Psychiatry.
[129] J. Dichgans,et al. Effectiveness of intravenous immunoglobin therapy in cerebellar ataxia associated with gluten sensitivity , 2001, Annals of neurology.
[130] S. Baekkeskov,et al. Membrane anchoring of the autoantigen GAD65 to microvesicles in pancreatic beta-cells by palmitoylation in the NH2-terminal domain , 1992, The Journal of cell biology.
[131] M. Paulsson,et al. Epidermal Transglutaminase (TGase 3) Is the Autoantigen of Dermatitis Herpetiformis , 2002, The Journal of experimental medicine.
[132] David W. Franklin,et al. Computational Mechanisms of Sensorimotor Control , 2011, Neuron.
[133] K. Hirata,et al. Ataxic Guillain–Barré syndrome and acute sensory ataxic neuropathy form a continuous spectrum , 2011, Journal of Neurology, Neurosurgery & Psychiatry.
[134] P. De Camilli,et al. GABA and pancreatic beta‐cells: colocalization of glutamic acid decarboxylase (GAD) and GABA with synaptic‐like microvesicles suggests their role in GABA storage and secretion. , 1991, The EMBO journal.
[135] M. Yamashita,et al. Autoantibodies against the amino terminal of α-enolase are a useful diagnostic marker of Hashimoto's encephalopathy , 2005, Journal of Neuroimmunology.
[136] H. Meinck,et al. Inhibition of γ‐aminobutyric acid synthesis by glutamic acid decarboxylase autoantibodies in stiff‐man syndrome , 1998 .
[137] T. Miyatake,et al. Beneficial effect of plasmapheresis on Fisher's syndrome. , 1993, Muscle & nerve.
[138] A. Vincent,et al. Immunization against GAD Induces Antibody Binding to GAD-Independent Antigens and Brainstem GABAergic Neuronal Loss , 2013, PloS one.
[139] N. Yuki,et al. Special sensory ataxia in Miller Fisher syndrome detected by postural body sway analysis , 1999, Annals of neurology.
[140] C. Vedeler,et al. Morphological and immunohistochemical characterization of paraneoplastic cerebellar degeneration associated with Yo antibodies , 2009, Acta neurologica Scandinavica.
[141] N. Yuki,et al. IgG anti-GQ1b positive acute ataxia without ophthalmoplegia , 1999, Journal of neurology, neurosurgery, and psychiatry.
[142] D. Copenhagen,et al. The role of the synthetic enzyme GAD65 in the control of neuronal γ-aminobutyric acid release , 1999 .
[143] M. J. van den Bent,et al. Paraneoplastic cerebellar degeneration associated with antineuronal antibodies: analysis of 50 patients. , 2003, Brain : a journal of neurology.
[144] D. Sanders,et al. Myoclonus ataxia and refractory coeliac disease , 2014, Cerebellum & Ataxias.
[145] L. Velloso,et al. GAD Autoantibodies in IDDM, Stiff-Man Syndrome, and Autoimmune Polyendocrine Syndrome Type I Recognize Different Epitopes , 1994, Diabetes.
[146] J. McNamara,et al. Autoantibodies to glutamate receptor GluR3 in Rasmussen's encephalitis. , 1994, Science.
[147] M. Molinari,et al. Cerebellar contribution to feedforward control of locomotion , 2014, Front. Hum. Neurosci..
[148] Winfried Stöcker,et al. Antibodies to the inositol 1,4,5-trisphosphate receptor type 1 (ITPR1) in cerebellar ataxia , 2014, Journal of Neuroinflammation.
[149] Yasuhiro Kagamihara,et al. The Functional Role of the Cerebellum in Visually Guided Tracking Movement , 2012, The Cerebellum.
[150] G. Davies-Jones,et al. Dietary treatment of gluten ataxia , 2003, Journal of neurology, neurosurgery, and psychiatry.
[151] J. Dalmau,et al. Cerebellar ataxia and glutamic acid decarboxylase antibodies: immunologic profile and long-term effect of immunotherapy. , 2014, JAMA neurology.
[152] J. Hildebrand,et al. Subacute pancerebellar syndrome associated with systemic lupus erythematosus , 1996, Clinical Neurology and Neurosurgery.
[153] Adam Possner,et al. Cerebellum , 2012, Neurology.
[154] L. Sollid,et al. Role of tissue transglutaminase in celiac disease. , 2000, Journal of pediatric gastroenterology and nutrition.
[155] J. Dichgans,et al. Manifestation of Hashimoto’s Encephalopathy Years before Onset of Thyroid Disease , 1999, European Neurology.
[156] J. Murray. Gluten sensitivity: from gut to brain , 2011 .
[157] J. Honnorat,et al. Effects of anti–glutamic acid decarboxylase antibodies associated with neurological diseases , 2007, Annals of neurology.
[158] H. Mitoma,et al. Intravenous immunoglobulin therapy for autoantibody-positive cerebellar ataxia. , 2009, Internal medicine.
[159] J. Honnorat,et al. Respective implications of glutamate decarboxylase antibodies in stiff person syndrome and cerebellar ataxia , 2011, Orphanet journal of rare diseases.