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Molecular Biology of Pediatric Hydrocephalus and Hydrocephalus-related Diseases

Neurologia medico-chirurgica, 2015, Vol.55(8), pp.640-646

2015

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Visualization of migration of human cortical neurons generated from induced pluripotent stem cells

Journal of neuroscience methods, 2017-09, Vol.289, p.57-63

2017

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KIF1A mutation in a patient with progressive neurodegeneration

Journal of human genetics, 2014-11, Vol.59 (11), p.639-641

2014

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Detection of Transient Increase of Cerebral Blood Flow and Reversible Neuronal Dysfunction by Iodine-123-Iomazenil Single Photon Emission Computed Tomography After Cerebral Hyperperfusion Syndrome After Revascularization Surgery for Moyamoya Disease

World neurosurgery, 2020-09, Vol.141, p.335-338

2020

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Working Conditions and Lifestyle of Female Surgeons Affiliated to the Japan Neurosurgical Society: Findings of Individual and Institutional Surveys

Neurologia medico-chirurgica, 2016, Vol.56(11), pp.704-708

2016

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A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate

Journal of human genetics, 2017-09, Vol.62 (9), p.861-863

2017

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Significance of molecular classification of ependymomas: C11orf95-RELA fusion-negative supratentorial ependymomas are a heterogeneous group of tumors

Acta neuropathologica communications, 2018-12, Vol.6 (1), p.134-134, Article 134

2018

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Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

Scientific reports, 2017-06, Vol.7 (1), p.3552-11, Article 3552

2017

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A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome

Journal of human genetics, 2018-09, Vol.63 (9), p.957-963

2018

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Drifting algae and fish: Implications of tropical Sargassum invasion due to ocean warming in western Japan

Estuarine, coastal and shelf science, 2014-06, Vol.147, p.32-41

2014

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Siblings with optic neuropathy and RTN4IP1 mutation

Journal of human genetics, 2017-10, Vol.62 (10), p.927-929

2017

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Role of a heterotrimeric G‐protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability

Journal of neurochemistry, 2017-01, Vol.140 (1), p.82-95

2017

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Isolation and cellular properties of mesenchymal cells derived from the decidua of human term placenta

Differentiation (London), 2011-09, Vol.82 (2), p.77-88

2011

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Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome

American journal of medical genetics. Part A, 2016-07, Vol.170A (7), p.1863-1867

2016

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Feeder-free generation and long-term culture of human induced pluripotent stem cells using pericellular matrix of decidua derived mesenchymal cells

PloS one, 2013-01, Vol.8 (1), p.e55226-e55226

2013

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Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate

Journal of human genetics, 2019-07, Vol.64 (7), p.701-702

2019

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TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis

Scientific reports, 2015-10, Vol.5 (1), p.15165-15165, Article 15165

2015

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Human neural stem/progenitor cells, expanded in long-term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils

Journal of neuroscience research, 2004-10, Vol.78 (2), p.215-223

2004

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Effect of neurosphere size on the growth rate of human neural stem/progenitor cells

Journal of neuroscience research, 2006-12, Vol.84 (8), p.1682-1691

2006

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Brain malformation with loss of normal FGFR3 expression in thanatophoric dysplasia type I

Neuropathology, 2013-12, Vol.33 (6), p.663-666

2013

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Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

Scientific reports, 2018-07, Vol.8 (1), p.10367-2, Article 10367

2018

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A method for efficiently generating neurospheres from human-induced pluripotent stem cells using microsphere arrays

Neuroreport, 2013-01, Vol.24 (2), p.84-90

2013

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A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations

Scientific reports, 2015-03, Vol.5 (1), p.9331-9331, Article 9331

2015

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Diagnosis, treatment, and long-term outcomes of fetal hydrocephalus

Seminars in fetal & neonatal medicine, 2012-12, Vol.17 (6), p.330-335

2012

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Three-Dimensional Reconstructed Computed Tomography-Magnetic Resonance Fusion Image-Based Preoperative Planning for Surgical Procedures for Spinal Lipoma or Tethered Spinal Cord After Myelomeningocele Repair: Technical Note

Neurologia medico-chirurgica, 2011, Vol.51(5), pp.397-402

2011

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Molecular Biology of Pediatric Hydrocephalus and Hydrocephalus-related Diseases

Visualization of migration of human cortical neurons generated from induced pluripotent stem cells

KIF1A mutation in a patient with progressive neurodegeneration

Detection of Transient Increase of Cerebral Blood Flow and Reversible Neuronal Dysfunction by Iodine-123-Iomazenil Single Photon Emission Computed Tomography After Cerebral Hyperperfusion Syndrome After Revascularization Surgery for Moyamoya Disease

Working Conditions and Lifestyle of Female Surgeons Affiliated to the Japan Neurosurgical Society: Findings of Individual and Institutional Surveys

A novel missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria and cleft palate

Significance of molecular classification of ependymomas: C11orf95-RELA fusion-negative supratentorial ependymomas are a heterogeneous group of tumors

Defects in autophagosome-lysosome fusion underlie Vici syndrome, a neurodevelopmental disorder with multisystem involvement

A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome

Drifting algae and fish: Implications of tropical Sargassum invasion due to ocean warming in western Japan

Siblings with optic neuropathy and RTN4IP1 mutation

Role of a heterotrimeric G‐protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability

Isolation and cellular properties of mesenchymal cells derived from the decidua of human term placenta

Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome

Feeder-free generation and long-term culture of human induced pluripotent stem cells using pericellular matrix of decidua derived mesenchymal cells

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate

TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis

Human neural stem/progenitor cells, expanded in long-term neurosphere culture, promote functional recovery after focal ischemia in Mongolian gerbils

Effect of neurosphere size on the growth rate of human neural stem/progenitor cells

Brain malformation with loss of normal FGFR3 expression in thanatophoric dysplasia type I

Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis

A method for efficiently generating neurospheres from human-induced pluripotent stem cells using microsphere arrays

A combination of targeted enrichment methodologies for whole-exome sequencing reveals novel pathogenic mutations

Diagnosis, treatment, and long-term outcomes of fetal hydrocephalus

Three-Dimensional Reconstructed Computed Tomography-Magnetic Resonance Fusion Image-Based Preoperative Planning for Surgical Procedures for Spinal Lipoma or Tethered Spinal Cord After Myelomeningocele Repair: Technical Note

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