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Itaru Toyoshima

Showing results (1-10 of 43) with videos related to

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Brain and Nerve = Shinkei Kenkyu No Shinpo|April 22, 2009
[Causative gene and its associated gene for Parkinson disease and dystonia]Kazuko Hasegawa, Itaru Toyoshima
Molecular Syndromology|September 26, 2022
Dyggve-Melchior-Clausen Syndrome Caused by a Novel Frameshift Variant in a Japanese PatientKoji Obara, Erika Abe, Itaru Toyoshima
Case Reports in Neurology|May 12, 2021
Frontal Hypoperfusion and the Effectiveness of Perampanel in Long-Lived Patient with Lafora DiseaseKoji Obara, Erika Abe, Itaru Toyoshima
Movement Disorders : Official Journal of the Movement Disorder Society|April 8, 2006
Prevalence of dystonia in Akita Prefecture in Northern JapanMasashiro Sugawara, Sumio Watanabe, Itaru Toyoshima
Cureus|January 11, 2023
Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7Koji Obara, Erika Abe, Itaru Toyoshima
Cureus|June 29, 2026
Intellectual Disability and Microcephaly With Pontine and Cerebellar Hypoplasia in Adults: Severity Spectrum and Diversity of the CASK Gene AberrationsKoji Obara, Erika Abe, Itaru Toyoshima
Case Reports in Neurology|February 22, 2021
Anti-N-Methyl-D-Aspartate Receptor Encephalitis with Decrease in Blood Flow in CerebellumKoji Obara, Tomoko Ono, Itaru Toyoshima
Journal of General and Family Medicine|August 4, 2020
A case of female adrenoleukodystrophy carrier with insidious neurogenic bladderKoji Obara, Erika Abe, Nobuyuki Shimozawa, et al.
Case Reports in Neurology|October 21, 2020
The Effectiveness of Perampanel for Myoclonic Seizures in Down Syndrome with Isodicentric Chromosome 21Koji Obara, Tsuyoshi Imota, Shigeo Mamiya, et al.
Molecular Syndromology|February 13, 2023
Cerebellar Hypoperfusion in Two Patients with Cornelia de Lange Syndrome with Novel <i>NIPBL</i> VariantsKoji Obara, Erika Abe, Shigeo Mamiya, et al.
Pageof 5

Showing results (1-10 of 43) with videos related to

Sort By:
Pageof 5
Brain and Nerve = Shinkei Kenkyu No Shinpo|April 22, 2009
[Causative gene and its associated gene for Parkinson disease and dystonia]Kazuko Hasegawa, Itaru Toyoshima
Molecular Syndromology|September 26, 2022
Dyggve-Melchior-Clausen Syndrome Caused by a Novel Frameshift Variant in a Japanese PatientKoji Obara, Erika Abe, Itaru Toyoshima
Case Reports in Neurology|May 12, 2021
Frontal Hypoperfusion and the Effectiveness of Perampanel in Long-Lived Patient with Lafora DiseaseKoji Obara, Erika Abe, Itaru Toyoshima
Movement Disorders : Official Journal of the Movement Disorder Society|April 8, 2006
Prevalence of dystonia in Akita Prefecture in Northern JapanMasashiro Sugawara, Sumio Watanabe, Itaru Toyoshima
Cureus|January 11, 2023
Whole-Exome Sequencing Identified a Novel DYRK1A Variant in a Patient With Intellectual Developmental Disorder, Autosomal Dominant 7Koji Obara, Erika Abe, Itaru Toyoshima
Cureus|June 29, 2026
Intellectual Disability and Microcephaly With Pontine and Cerebellar Hypoplasia in Adults: Severity Spectrum and Diversity of the CASK Gene AberrationsKoji Obara, Erika Abe, Itaru Toyoshima
Case Reports in Neurology|February 22, 2021
Anti-N-Methyl-D-Aspartate Receptor Encephalitis with Decrease in Blood Flow in CerebellumKoji Obara, Tomoko Ono, Itaru Toyoshima
Journal of General and Family Medicine|August 4, 2020
A case of female adrenoleukodystrophy carrier with insidious neurogenic bladderKoji Obara, Erika Abe, Nobuyuki Shimozawa, et al.
Case Reports in Neurology|October 21, 2020
The Effectiveness of Perampanel for Myoclonic Seizures in Down Syndrome with Isodicentric Chromosome 21Koji Obara, Tsuyoshi Imota, Shigeo Mamiya, et al.
Molecular Syndromology|February 13, 2023
Cerebellar Hypoperfusion in Two Patients with Cornelia de Lange Syndrome with Novel <i>NIPBL</i> VariantsKoji Obara, Erika Abe, Shigeo Mamiya, et al.
Pageof 5