Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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im August 2018 veröffentlichter wissenschaftlicher Artikel

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wetenschappelijk artikel

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наукова стаття, опублікована в серпні 2018

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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P1476

Glutamate receptor δ2 serum antibodies in pediatric opsoclonus myoclonus ataxia syndrome

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P2093

A Radu Aricescu

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Bethan Lang

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David A Menassa

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Georgina Berridge

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Imogen Welding

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Michael Pike

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Ming Lim

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Roman Fischer

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Russell C Dale

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Sameer Zuberi

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A homozygous deletion in GRID2 causes a human phenotype with cerebellar ataxia and atrophy.

The Laboratory Rat: Relating Its Age With Human's.

Neuroepidemiologic trends in 105 US cases of pediatric opsoclonus-myoclonus syndrome.

Antibodies to dendritic neuronal surface antigens in opsoclonus myoclonus ataxia syndrome.

Multiple sequential antibody-associated syndromes with a recurrent mutated neuroblastoma.

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e714-e723

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P31

scholarly article

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10.1212/WNL.0000000000006035

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English

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P478

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Benedikt M. Kessler

Angela Vincent

Patrick Waters

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2018-08-21T00:00:00Z

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30045961

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6107266

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