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Lhermitte's Sign in a Patient with Thoracic Myelitis

Internal Medicine, 2020/07/15, Vol.59(14), pp.1787-1788

2020

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Progressive Supranuclear Palsy with Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome: Authors’ Second Case

Case reports in neurology, 2019-05, Vol.11 (2), p.205-208

2019

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Gait improvement after levofloxacin administration in a progressive supranuclear palsy patient

Clinical parkinsonism & related disorders, 2020-01, Vol.3, p.100080-100080, Article 100080

2020

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Severe visual impairment and subclinical encephalitis preceding clinical signs of chondritis in relapsing polychondritis

Neurology and clinical neuroscience, 2019-03, Vol.7 (2), p.75-77

2019

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Lhermitte's Sign in a Patient with Thoracic Myelitis

Internal Medicine, 2020, pp.4411-20

2020

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Symmetrical Interhemispheric Subdural Hematoma

Curēus (Palo Alto, CA), 2021-03

2021

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A Case of Multiple Cerebral Infarction Preceding Acute Exacerbation of Idiopathic Thrombocytopenic Purpura

Journal of stroke and cerebrovascular diseases, 2019-03, Vol.28 (3), p.789-791

2019

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Progressive Supranuclear Palsy with Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome: Authors' Second Case

Case reports in neurology, 2019, Vol.11 (2), p.205-208

2019

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ACTN1 Mutations Cause Congenital Macrothrombocytopenia

American journal of human genetics, 2013-03, Vol.92 (3), p.431-438

2013

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Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

Nature communications, 2015-07, Vol.6 (1), p.7557-7557, Article 7557

2015

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Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

Haematologica (Roma), 2019-10, Vol.104 (10), p.1962-1973

2019

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Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese biliary atresia registry

Journal of pediatric surgery, 2003-07, Vol.38 (7), p.997-1000

2003

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Biallelic DICER1 Mutations in Sporadic Pleuropulmonary Blastoma

Cancer research (Chicago, Ill.), 2014-05, Vol.74 (10), p.2742-2749

2014

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Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

Haematologica (Roma), 2020-04, Vol.105 (4), p.1166-1167

2020

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Loss of DNA Damage Response in Neuroblastoma and Utility of a PARP Inhibitor

JNCI : Journal of the National Cancer Institute, 2017-11, Vol.109 (11)

2017

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Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis

Oncotarget, 2017-12, Vol.8 (64), p.107513-107529

2017

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Distribution and Clinical Features of NOTCH1 Signaling Activating Alterations in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL)

BLOOD, 2018-11, Vol.132 (Supplement 1), p.4089-4089

2018

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Functional Characterization of a Novel GFI1B Mutation Causing Congenital Macrothrombocytopenia

Blood, 2015-12, Vol.126 (23), p.75-75

2015

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Whole Exome and Transcriptome Analyses in Pediatric T-Cell Acute Lymphoblastic Leukemia

Blood, 2014-12, Vol.124 (21), p.3527-3527

2014

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TAL1 and MYB Abnormalities in Childhood T-Cell Acute Lymphoblastic Leukemia

Blood, 2015-12, Vol.126 (23), p.2628-2628

2015

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TAL1 Super Enhancer Aberration and Stil-TAL1 Fusion in Pediatric T Cell Acute Lymphoblastic Leukemia

Blood, 2016-12, Vol.128 (22), p.1734-1734

2016

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Lhermitte's Sign in a Patient with Thoracic Myelitis

Progressive Supranuclear Palsy with Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome: Authors’ Second Case

Gait improvement after levofloxacin administration in a progressive supranuclear palsy patient

Severe visual impairment and subclinical encephalitis preceding clinical signs of chondritis in relapsing polychondritis

Lhermitte's Sign in a Patient with Thoracic Myelitis

Symmetrical Interhemispheric Subdural Hematoma

A Case of Multiple Cerebral Infarction Preceding Acute Exacerbation of Idiopathic Thrombocytopenic Purpura

Progressive Supranuclear Palsy with Wall-Eyed Bilateral Internuclear Ophthalmoplegia Syndrome: Authors' Second Case

ACTN1 Mutations Cause Congenital Macrothrombocytopenia

Integrated genetic and epigenetic analysis defines novel molecular subgroups in rhabdomyosarcoma

Recurrent SPI1 (PU.1) fusions in high-risk pediatric T cell acute lymphoblastic leukemia

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

Five- and 10-year survival rates after surgery for biliary atresia: a report from the Japanese biliary atresia registry

Biallelic DICER1 Mutations in Sporadic Pleuropulmonary Blastoma

DNA methylation-based classification reveals difference between pediatric T-cell acute lymphoblastic leukemia and normal thymocytes

Pathogenic mutations identified by a multimodality approach in 117 Japanese Fanconi anemia patients

Loss of DNA Damage Response in Neuroblastoma and Utility of a PARP Inhibitor

Identification of the genetic and clinical characteristics of neuroblastomas using genome-wide analysis

The Epigenetic and Genetic Landscapes of Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL)

Distribution and Clinical Features of NOTCH1 Signaling Activating Alterations in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL)

Identifications of Highly Aggressive Phenotype with SPI1 Overexpression in Pediatric T Cell Acute Lymphoblastic Leukemia/Lymphoma

Functional Characterization of a Novel GFI1B Mutation Causing Congenital Macrothrombocytopenia

Whole Exome and Transcriptome Analyses in Pediatric T-Cell Acute Lymphoblastic Leukemia

TAL1 and MYB Abnormalities in Childhood T-Cell Acute Lymphoblastic Leukemia

TAL1 Super Enhancer Aberration and Stil-TAL1 Fusion in Pediatric T Cell Acute Lymphoblastic Leukemia

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