Mitochondrial <i>UQCRC1</i> mutations cause autosomal dominant parkinsonism with polyneuropathy

Chin‐Hsien Lin, Pei-I Tsai, Han‐Yi Lin, +28

Brain

Sporadic ParkinsonGeneticsGenetic EpidemiologyMolecular BiologyMolecular Genetics +14

High frequency of beta-propeller protein-associated neurodegeneration (BPAN) among patients with intellectual disability and young-onset parkinsonism

Kenya Nishioka, Genko Oyama, Hiroyo Yoshino, +16

Neurobiology of Aging

Neurodegenerative DiseasesAmyotrophic Lateral SclerosisAlzheimer's DiseaseNeurochemical BiomarkersNeurology +5

PLA2G6 variant in Parkinson's disease

Hiroyuki Tomiyama, Hiroyo Yoshino, Kotaro Ogaki, +8

Journal of Human Genetics

Mendelian DisorderParkinson DiseasePathologyNeurologyNeurodegeneration +2

Altered brain network functional connectivity patterns in patients with vestibular migraine diagnosed according to the diagnostic criteria of the Bárány Society and the International Headache Society

Yuanzhe Li, Lihong Si, Bo Shen, +1

Journal of Neurology

Altered functional activity in the right superior temporal gyrus in patients with definite vestibular migraine

Yuanzhe Li, Lihong Si, Bo Shen, +2

Neurological Sciences

Cluster HeadacheNeuropsychologyVestibular SystemDefinite Vestibular MigraineNeurophysiology +9

Clinical Characteristics of Patients With Benign Paroxysmal Positional Vertigo Diagnosed Based on the Diagnostic Criteria of the Bárány Society

Xia Ling, Danhua Zhao, Bo Shen, +5

Frontiers in Neurology

PLA2G6 variants associated with the number of affected alleles in Parkinson’s disease in Japan

Kensuke Daida, Kenya Nishioka, Yuanzhe Li, +36

Neurobiology of Aging

Neurodegenerative DiseasesAllelic VariantMendelian DisorderGenetic DisorderGenetics +7

Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonism

Chikara Yamashita, Manabu Funayama, Yuanzhe Li, +5

Journal of Neural Transmission

Neurodegenerative DiseasesGenetic DisorderParkinson DiseaseGeneticsDegenerative Disease +7

Prevalence of GJB2 causing recessive profound non-syndromic deafness in Japanese children

Chieri Hayashi, Manabu Funayama, Yuanzhe Li, +5

International Journal of Pediatric Otorhinolaryngology

Japanese ChildrenMendelian DisorderGenetic DisorderGeneticsGenetic Epidemiology +4

&lt;i&gt;CSF1R&lt;/i&gt; Mutation p.G589R and the Distribution Pattern of Brain Calcification

Kensuke Daida, Kenya Nishioka, Yuanzhe Li, +3

Internal Medicine

Brain DevelopmentNeurological DisorderGeneticsCorticobasal DegenerationWhite Matter +20