Autoimmune parkinsonism with faciobrachiocrural dystonic seizures: a new phenotype of leucine-rich glioma-inactivated 1 (LGI1) autoimmunity-Reference-Cited by-同舟云学术

Autoimmune parkinsonism with faciobrachiocrural dystonic seizures: a new phenotype of leucine-rich glioma-inactivated 1 (LGI1) autoimmunity

Published:2022-07-18 Issue:5 Volume:122 Page:1323-1328
ISSN:0300-9009
Container-title:Acta Neurologica Belgica
language:en
Short-container-title:Acta Neurol Belg

Author:

Sasikumar Sruthi,Vincent Jino,Gopinath Siby,Nambiar Vivek,Umesh Saraf Udit,Kannoth Sudheeran^ORCID,Antony Dayana,Mathai Annamma,Anandakuttan Anandkumar

Funder

None

Publisher

Springer Science and Business Media LLC

Subject

Neurology (clinical),General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s13760-022-02018-8.pdf

Reference15 articles.

1. Lai M, Huijbers M, Lancaster E, Graus F, Bataller L, Balice-Gordon R, Cowell J, Dalmau J (2010) Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series. Lancet Neurol 9(8):776–785

2. Irani S, Alexander S, Waters P, Kleopa K, Pettingill P, Zuliani L, Peles E, Buckley C, Lang B, Vincent A (2010) 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. Brain 133(9):2734–2748

3. Irani S, Michell A, Lang B, Pettingill P, Waters P, Johnson M, Schott J, Armstrong R, Zagami S, Bleasel A, Somerville E, Smith S, Vincent A (2011) Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis. Ann Neurol 69(5):892–900

4. Maramattom B, Jeevanagi S, George C (2013) Facio-brachio-crural dystonic episodes and drop attacks due to leucine rich glioma inactivated 1 encephalitis in two elderly Indian women. Ann Indian Acad Neurol 16(4):590

5. Gadoth A, Pittock S, Dubey D, McKeon A, Britton J, Schmeling J, Smith A, Kotsenas A, Watson R, Lachance D, Flanagan E, Lennon V, Klein C (2017) Expanded phenotypes and outcomes among 256 LGI1/CASPR2-IgG-positive patients. Ann Neurol 82(1):79–92

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