Population-based perspective of anti-neuronal autoantibodies in patients with idiopathic late onset cerebellar ataxia (ILOCA)

Population-based perspective of anti-neuronal autoantibodies in patients with idiopathic late onset cerebellar ataxia (ILOCA)

ग्रंथसूची विवरण
मुख्य लेखकों:	Muzaimi, M, Clover, L, Lang, B, Vincent, A, Wiles, M, Robertson, N
स्वरूप:	Conference item
प्रकाशित:	2004

समान संसाधन

Role of antineuronal autoantibodies in population based samples of apparently idiopathic late onset cerebellar ataxia (ILOCA)
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The role of anti-glutamic acid decarboxylase autoantibodies (GAD-Ab) in idiopathic late onset cerebellar ataxia (ILOCA)
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Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxia.
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Contactin-associated protein-2 antibodies in non-paraneoplastic cerebellar ataxia.
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Associative learning in patients with cerebellar ataxia.
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Idiopathic pulmonary fibrosis: a paradigm of late-onset, single-gene human disease?
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Co-occurrence of acute ophthalmoplegia (without ataxia) and idiopathic intracranial hypertension
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Clinical features which predict neuronal surface autoantibodies in new-onset focal epilepsy: implications for immunotherapies
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The growing recognition of immunotherapy-responsive seizure disorders with autoantibodies to specific neuronal proteins.
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The Moonwalker mouse: new insights into TRPC3 function, cerebellar development, and ataxia.
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Recent advances in modelling of cerebellar ataxia using induced pluripotent stem cells
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Autoantibodies in epilepsy
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Pathogenic autoantibodies to neuronal proteins in neurological disorders.
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Autoantibodies in patients with gut motility disorders and enteric neuropathy.
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Idiopathic aneurysms of distal cerebellar arteries: endovascular treatment after rupture.
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MAPPING THE GENE FOR ACETAZOLAMIDE-RESPONSIVE HEREDITARY PAROXYSMAL CEREBELLAR-ATAXIA TO CHROMOSOME-19P
द्वारा: Bulman, D, और अन्य
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Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p.
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A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.
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A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse
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An apparently non-maternally inherited syndrome of seizures, ataxia and ophthalmoplegia, with distinctive cerebellar lesions, in an Irish pedigree
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