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Myalgic encephalomyelitis/chronic fatigue syndrome post coronavirus disease 2019

Pediatric investigation, 2022-01, Vol.64 (1), p.e14976-n/a

2022

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A metastatic malignancy of unknown primary origin in a 12‐year‐old girl with anti‐N‐methyl‐d‐aspartate encephalitis

Pediatrics international, 2020-02, Vol.62 (2), p.238-240

2020

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Rapid progressive destruction of the cochleae in an infant due to pneumococcal meningitis

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2022-06, Vol.28 (6), p.806-809

2022

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Clinical Characteristics of Fragile X Syndrome Patients in Japan

YONAGO ACTA MEDICA, 2021, Vol.64 (1), p.30-33

2021

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Hematological manifestation of scurvy

EJHaem, 2023-08, Vol.4 (3), p.852-853

2023

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Transient extreme spindles in a young child with anti-NMDAR encephalitis: A case report

Brain & development (Tokyo. 1979), 2019-02, Vol.41 (2), p.210-213

2019

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Rhabdomyosarcoma with premature chromatid separation–mosaic variegated aneuploidy syndrome: Reduced‐intensity chemotherapy

Pediatrics international, 2019-06, Vol.61 (6), p.613-616

2019

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Diffusion-weighted MRI for early diagnosis of neonatal herpes simplex encephalitis

Brain & development (Tokyo. 1979), 2015-04, Vol.37 (4), p.423-431

2015

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Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia

Journal of clinical immunology, 2015-07, Vol.35 (5), p.512-516

2015

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Trends in Dietary Micronutrient Adequacy in Young Adults Over the Latest 25 Years in Japan

Food and nutrition bulletin, 2023-12, Vol.44 (4), p.265-267

2023

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Two Japanese Patients With SMA Type 1 Suggest that Axonal-SMN May Not Modify the Disease Severity

Pediatric neurology, 2015-06, Vol.52 (6), p.638-641

2015

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Accumulation of N‐Acetyl‐L‐Aspartate in the Brain of the Tremor Rat, a Mutant Exhibiting Absence‐Like Seizure and Spongiform Degeneration in the Central Nervous System

Journal of neurochemistry, 2000-06, Vol.74 (6), p.2512-2519

2000

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Low-level germline 48,XYY,+21 mosaicism associated with transient abnormal myelopoiesis in a phenotypically normal neonate

Cytogenetic and genome research, 2023-05, Vol.162 (11-12), p.625-631

2023

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Cell-free DNA Oncogene Copy Number as a Surrogate Molecular Biomarker in ALK/MYCN-coamplified Neuroblastoma

Journal of pediatric hematology/oncology, 2021-03, Vol.43 (2), p.e165

2021

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Difficulty of morphological diagnosis in Gram staining

BMJ case reports, 2021-08, Vol.14 (8), p.e245349

2021

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Atypical eosinophils as a biomarker of idiopathic pericardial effusion associated with transient abnormal myelopoiesis in Down syndrome

Pediatric blood & cancer, 2024-02, Vol.71 (2), p.e30763-n/a

2024

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Cerebral Sinovenous Thrombosis and Subdural Hematoma as Treatment-Related Complications in Suprasellar Germ Cell Tumor Associated with Adipsic Diabetes Insipidus

Pediatric neurosurgery, 2019-01, Vol.54 (4), p.288-292

2019

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Leigh syndrome associated with West syndrome

Brain & development (Tokyo. 1979), 2003-06, Vol.25 (4), p.245-250

2003

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Ultra-late-onset Meningitis Caused by Serotype IX Group B Streptococcus

The Pediatric infectious disease journal, 2015-07, Vol.34 (7), p.801-801

2015

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Paraneoplastic hypereosinophilic syndrome associated with IL3‐IgH positive acute lymphoblastic leukemia

Pediatric blood & cancer, 2019-01, Vol.66 (1), p.e27449-n/a

2019

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Sensitive detection of GATA1 mutations using complementary DNA‐based analysis for transient abnormal myelopoiesis associated with the Down syndrome

International journal of laboratory hematology, 2022-04, Vol.44 (2), p.349-355

2022

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Role of monocyte chemoattractant protein‐1 in liver fibrosis with transient myeloproliferative disorder in down syndrome

Hepatology communications, 2018-03, Vol.2 (3), p.230-236

2018

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Epilepsy in children with trisomy 18

American journal of medical genetics. Part A, 2013-04, Vol.161A (4), p.696-701

2013

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NER Rat Strain: A New Type of Genetic Model in Epilepsy Research

Epilepsia (Copenhagen), 1998-01, Vol.39 (1), p.99-107

1998

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Myalgic encephalomyelitis/chronic fatigue syndrome post coronavirus disease 2019

A metastatic malignancy of unknown primary origin in a 12‐year‐old girl with anti‐N‐methyl‐d‐aspartate encephalitis

Rapid progressive destruction of the cochleae in an infant due to pneumococcal meningitis

Clinical Characteristics of Fragile X Syndrome Patients in Japan

Hematological manifestation of scurvy

Transient extreme spindles in a young child with anti-NMDAR encephalitis: A case report

Rhabdomyosarcoma with premature chromatid separation–mosaic variegated aneuploidy syndrome: Reduced‐intensity chemotherapy

Diffusion-weighted MRI for early diagnosis of neonatal herpes simplex encephalitis

Mosaicism of an ELANE Mutation in an Asymptomatic Mother in a Familial Case of Cyclic Neutropenia

Trends in Dietary Micronutrient Adequacy in Young Adults Over the Latest 25 Years in Japan

Two Japanese Patients With SMA Type 1 Suggest that Axonal-SMN May Not Modify the Disease Severity

Accumulation of N‐Acetyl‐L‐Aspartate in the Brain of the Tremor Rat, a Mutant Exhibiting Absence‐Like Seizure and Spongiform Degeneration in the Central Nervous System

Low-level germline 48,XYY,+21 mosaicism associated with transient abnormal myelopoiesis in a phenotypically normal neonate

Cell-free DNA Oncogene Copy Number as a Surrogate Molecular Biomarker in ALK/MYCN-coamplified Neuroblastoma

Difficulty of morphological diagnosis in Gram staining

Atypical eosinophils as a biomarker of idiopathic pericardial effusion associated with transient abnormal myelopoiesis in Down syndrome

Cerebral Sinovenous Thrombosis and Subdural Hematoma as Treatment-Related Complications in Suprasellar Germ Cell Tumor Associated with Adipsic Diabetes Insipidus

Leigh syndrome associated with West syndrome

Ultra-late-onset Meningitis Caused by Serotype IX Group B Streptococcus

Paraneoplastic hypereosinophilic syndrome associated with IL3‐IgH positive acute lymphoblastic leukemia

Sensitive detection of GATA1 mutations using complementary DNA‐based analysis for transient abnormal myelopoiesis associated with the Down syndrome

Role of monocyte chemoattractant protein‐1 in liver fibrosis with transient myeloproliferative disorder in down syndrome

Epilepsy in children with trisomy 18

NER Rat Strain: A New Type of Genetic Model in Epilepsy Research

Monocyte Chemoattractant Protein-1 (MCP-1) as a Potential Therapeutic Target and a Noninvasive Biomarker of Liver Fibrosis Associated With Transient Myeloproliferative Disorder in Down Syndrome

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