A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom

Yumi YamadaDepartment of Neurology, Niigata Prefectural Shibata Hospital, Shibata, JapanView further author information

Takao FukushimaDepartment of Neurology, Niigata Prefectural Shibata Hospital, Shibata, JapanView further author information

Satoshi KodamaDepartment of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, JapanView further author information

Hiroshi ShimizuDepartment of Pathology, Brain Research Institute, Niigata University, Niigata, JapanView further author information

Akiyoshi KakitaDepartment of Pathology, Brain Research Institute, Niigata University, Niigata, JapanView further author information

Kunihiko MakinoDepartment of Neurology, Niigata Prefectural Shibata Hospital, Shibata, JapanView further author information

Yoshiki SekijimaDepartment of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Matsumoto, JapanCorrespondence[email protected]
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References

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A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom

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A case of cerebral amyloid angiopathy-type hereditary ATTR amyloidosis with Y69H (p.Y89H) variant displaying transient focal neurological episodes as the main symptom

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