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September 10, 2002

P/Q type calcium-channel antibodies in paraneoplastic cerebellar degeneration with lung cancer

September 10, 2002 issue
59 (5) 764-766

Abstract

Raised levels of P/Q type voltage-gated calcium-channel (VGCC) antibodies were found in 16 (41%) of 39 patients with paraneoplastic cerebellar degeneration (PCD) and Hu antibodies were found in nine (23%). Seven of the 16 VGCC antibody-positive patients had Lambert–Eaton myasthenic syndrome (LEMS). Seven of 15 CSF samples had VGCC antibodies, with evidence of intrathecal synthesis in four. VGCC antibodies should be looked for in PCD, even if there are no symptoms of LEMS, and may be related to the cerebellar dysfunction.

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Information & Authors

Information

Published In

Neurology®
Volume 59Number 5September 10, 2002
Pages: 764-766
PubMed: 12221175

Publication History

Received: February 20, 2002
Accepted: May 3, 2002
Published online: September 10, 2002
Published in print: September 10, 2002

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Authors

Affiliations & Disclosures

F. Graus, MD
From the Services of Neurology (Drs. Graus, Pozo-Rosich, and Saiz) and Hormonal Laboratory (Dr. Casamitjana), Hospital Clínic, Universitat de Barcelona and Institut d’Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain; and Neurosciences Group (Drs. Lang and Vincent), Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.
B. Lang, PhD
From the Services of Neurology (Drs. Graus, Pozo-Rosich, and Saiz) and Hormonal Laboratory (Dr. Casamitjana), Hospital Clínic, Universitat de Barcelona and Institut d’Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain; and Neurosciences Group (Drs. Lang and Vincent), Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.
P. Pozo-Rosich, MD
From the Services of Neurology (Drs. Graus, Pozo-Rosich, and Saiz) and Hormonal Laboratory (Dr. Casamitjana), Hospital Clínic, Universitat de Barcelona and Institut d’Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain; and Neurosciences Group (Drs. Lang and Vincent), Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.
A. Saiz, MD
From the Services of Neurology (Drs. Graus, Pozo-Rosich, and Saiz) and Hormonal Laboratory (Dr. Casamitjana), Hospital Clínic, Universitat de Barcelona and Institut d’Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain; and Neurosciences Group (Drs. Lang and Vincent), Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.
R. Casamitjana, MD
From the Services of Neurology (Drs. Graus, Pozo-Rosich, and Saiz) and Hormonal Laboratory (Dr. Casamitjana), Hospital Clínic, Universitat de Barcelona and Institut d’Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain; and Neurosciences Group (Drs. Lang and Vincent), Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.
A. Vincent, FRCPath
From the Services of Neurology (Drs. Graus, Pozo-Rosich, and Saiz) and Hormonal Laboratory (Dr. Casamitjana), Hospital Clínic, Universitat de Barcelona and Institut d’Investigació Biomèdica August Pi i Sunyer (IDIBAPS), Barcelona, Spain; and Neurosciences Group (Drs. Lang and Vincent), Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, United Kingdom.

Notes

Address correspondence and reprint requests to Dr. Francesc Graus, Servei de Neurologia, Hospital Clínic. Villarroel 170, Barcelona 08036. Spain; e-mail: [email protected]

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