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Search Results - Mikasa, Michitaka
Search Results - Mikasa, Michitaka
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COQ2 variants in Parkinson’s disease and multiple system atrophy
by
Mikasa, Michitaka
,
Kanai, Kazuaki
,
Li, Yuanzhe
,
Yoshino, Hiroyo
,
Mogushi, Kaoru
,
Hayashida, Arisa
,
Ikeda, Aya
,
Kawajiri, Sumihiro
,
Okuma, Yasuyuki
,
Kashihara, Kenichi
,
Sato, Tatsuya
,
Kondo, Hiroshi
,
Funayama, Manabu
,
Nishioka, Kenya
,
Hattori, Nobutaka
Published in
Journal of Neural Transmission
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A TREX1 mutation causing cerebral vasculopathy in a patient with familial chilblain lupus
by
Yamashiro, Kazuo
,
Tanaka, Ryota
,
Li, Yuanzhe
,
Mikasa, Michitaka
,
Hattori, Nobutaka
Published in
Journal of neurology
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A case of encephalitis lethargica associated with relapsing polychondritis
by
Fujioka, Shinsuke
,
Tsuboi, Yoshio
,
Mikasa, Michitaka
,
Onozawa, Rieko
,
Saitoh, Nobuhiro
,
Baba, Yasuhiko
,
Yamada, Tatsuo
Published in
Movement disorders
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A TREX1 mutation causing cerebral vasculopathy in a patient with familial chilblain lupus
by
Yamashiro, Kazuo
,
Tanaka, Ryota
,
Li, Yuanzhe
,
Mikasa, Michitaka
,
Hattori, Nobutaka
Published in
Journal of neurology
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A case of encephalitis lethargica associated with relapsing polychondritis
by
Fujioka, Shinsuke
,
Tsuboi, Yoshio
,
Mikasa, Michitaka
,
Onozawa, Rieko
,
Saitoh, Nobuhiro
,
Baba, Yasuhiko
,
Yamada, Tatsuo
Published in
Movement disorders : official journal of the Movement Disorder Society
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Journal Of Neural Transmission
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Journal Of Neurology
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Movement Disorders
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Clinical Neurology
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Life Sciences & Biomedicine
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Chilblains - Complications
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Coq2
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Exodeoxyribonucleases - Genetics
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Familial Parkinson’s Disease
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