238 results on '"Shiohama, Tadashi"'
Search Results
2. Japanese guidelines for treatment of pediatric status epilepticus – 2023
3. Clinical characteristics and management of plexiform neurofibromas in children with neurofibromatosis 1: A Japanese nationwide survey
4. Infantile Epileptic Spasms Syndrome Complicated by Leigh Syndrome and Leigh-Like Syndrome: A Retrospective, Nationwide, Multicenter Case Series
5. Oval Pupils in a Child with Acute Autonomic and Sensory Neuropathy
6. Generation of human induced pluripotent stem cell lines derived from four Rett syndrome patients with MECP2 mutations
7. Comprehensive genetic analysis confers high diagnostic yield in 16 Japanese patients with corpus callosum anomalies
8. Structural magnetic resonance imaging demonstrates volumetric brain abnormalities in down syndrome: Newborns to young adults
9. Comprehensive High-Depth Proteomic Analysis of Plasma Extracellular Vesicles Containing Preparations in Rett Syndrome.
10. Structural Magnetic Resonance Imaging-Based Surface Morphometry Analysis of Pediatric Down Syndrome.
11. A case report of a child with pulmonary hypertension associated with SARS-CoV-2 infection
12. Decreased head circumference at birth associated with maternal tobacco smoke exposure during pregnancy on the Japanese prospective birth cohort study
13. Structural Magnetic Resonance Imaging-Based Brain Morphology Study in Infants and Toddlers With Down Syndrome: The Effect of Comorbidities
14. Ex vivo fetal brain MRI: Recent advances, challenges, and future directions
15. Drastic fall of growth differentiation factor 15 in influenza encephalopathy
16. Structural magnetic resonance imaging demonstrates abnormal cortical thickness in Down syndrome: Newborns to young adults
17. Quantitative brain morphological analysis in CHARGE syndrome
18. Brain Pathways in LIS1-Associated Lissencephaly Revealed by Diffusion MRI Tractography
19. Lipid Peroxidation via Regulating the Metabolism of Docosahexaenoic Acid and Arachidonic Acid in Autistic Behavioral Symptoms
20. MicroRNAs profiling in fibroblasts derived from patients with Gorlin syndrome
21. Senescence-associated inflammation and inhibition of adipogenesis in subcutaneous fat in Werner syndrome
22. Lipid Peroxidation of the Docosahexaenoic Acid/Arachidonic Acid Ratio Relating to the Social Behaviors of Individuals with Autism Spectrum Disorder: The Relationship with Ferroptosis
23. A Brain Morphometry Study with Across-Site Harmonization Using a ComBat-Generalized Additive Model in Children and Adolescents
24. Case report: Progressive pulmonary artery hypertension in a case of megalencephaly-capillary malformation syndrome
25. Brain structure alterations in girls with central precocious puberty
26. Nationwide survey of childhood Guillain-Barré syndrome, Fisher syndrome, and Bickerstaff brainstem encephalitis in Japan
27. Acute myelitis associated with human herpesvirus 7 infection
28. A novel CUL7 mutation in a Japanese patient with 3M syndrome
29. microRNA Biology on Brain Development and Neuroimaging Approach
30. Identification of association fibers using ex vivo diffusion tractography in Alexander disease brains
31. Severe neuroglycopenic symptoms due to nonketotic hypoglycemia in children with cardio‐facio‐cutaneous syndrome
32. Cortical thickness abnormalities in attention deficit hyperactivity disorder revealed by structural magnetic resonance imaging: Newborns to young adults
33. Magnetic resonance imaging demonstrates gyral abnormalities in Tourette syndrome
34. 147-OR: Glucose Intolerance of Hereditary Progeria Werner Syndrome and Cellular Senescence in Their Adipose Tissue
35. Comprehensive Volumetric Analysis of Mecp2-Null Mouse Model for Rett Syndrome by T2-Weighted 3D Magnetic Resonance Imaging
36. Quantitative Structural Brain Magnetic Resonance Imaging Analyses: Methodological Overview and Application to Rett Syndrome
37. Focal Coxsackie virus B5 encephalitis with synchronous seizure cluster and eruption: Infantile case
38. Subtle infantile spasms presenting as hyperirritability in CK syndrome
39. Structural Abnormalities in Pediatric Moyamoya Disease Revealed by Clinical Magnetic Resonance Imaging, Regionally Distributed Relative Signal Intensities and Volumes
40. Frameshift mutation in the PTCH2 gene can cause nevoid basal cell carcinoma syndrome
41. Small Nucleus Accumbens and Large Cerebral Ventricles in Infants and Toddlers Prior to Receiving Diagnoses of Autism Spectrum Disorder
42. Remitting and exacerbating white matter lesions in leukoencephalopathy with thalamus and brainstem involvement and high lactate
43. Coexistence of neuroblastoma detected on staging of Langerhans cell histiocytosis
44. Symptom-Related Differential Neuroimaging Biomarkers in Children with Corpus Callosum Abnormalities
45. Specific temperament in patients with nevoid basal cell carcinoma syndrome
46. Magnetic resonance neurography in diagnosing childhood chronic inflammatory demyelinating polyradiculoneuropathy
47. Nationwide Survey of Childhood Guillain-Barré Syndrome, Fisher Syndrome, and Bickerstaff Brainstem Encephalitis in Japan
48. Intravenous immune globulin plus corticosteroids in refractory Kawasaki disease
49. Quantitative analyses of high‐angular resolution diffusion imaging (HARDI)‐derived long association fibers in children with sensorineural hearing loss
50. Fulminant myocarditis following recurrent generalized erythrokeratoderma in a child with a heterozygousGJA1variant
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