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藤田医科大学 ホーム
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研究部門
研究成果
専門知識、名前、または所属機関で検索
Scopus著者プロファイル
石原 尚子
小児科学
h-index
672
被引用数
13
h 指数
Pureの文献数とScopusの被引用数に基づいて算出されます
2000
2023
年別の研究成果
概要
フィンガープリント
ネットワーク
研究成果
(36)
類似のプロファイル
(6)
フィンガープリント
Naoko Ishiharaが活動している研究トピックを掘り下げます。このトピックラベルは、この研究者の研究成果に基づきます。これらがまとまってユニークなフィンガープリントを構成します。
並べ替え順
重み付け
アルファベット順
Keyphrases
Segment Length
50%
Aganglionic
50%
Mowat-Wilson Syndrome
50%
GLUT1 Deficiency Syndrome
50%
Glucose Transporter Type 1 Deficiency Syndrome
50%
Hypocarbia
50%
Focal Cortical Dysplasia
50%
Benign Convulsions
50%
Paroxysmal Kinesigenic Dyskinesia
50%
Rett Syndrome
50%
Pathological Gait
50%
Lacosamide
50%
Deep Brain Structures
50%
Splenic Lesions
50%
Benign Convulsions with Mild Gastroenteritis
50%
Academic Society
50%
Cerebrospinal Fluid Glucose
50%
Seizure Characteristics
50%
Developmental Status
50%
Medical Academics
50%
Post-traumatic Epilepsy
50%
Temporal Lobe Epilepsy
50%
Smad Interacting Protein 1
50%
SARS-CoV-2 Vaccine
50%
Cryptogenic West Syndrome
50%
PRRT2 mutations
50%
ZEB2
50%
SLC19A3 Gene
50%
SLC19A3
50%
Surfer's Myelopathy
50%
Hydranencephaly
50%
Conus Medullaris
50%
Developmental Outcomes
50%
Seizure Outcome
50%
Severe Neurocognitive Disorder
50%
THOC2
50%
Cortical Dysplasia
50%
Severe Disease
50%
TUBA1A
50%
Neuroimaging Findings
50%
Posterior Reversible Encephalopathy Syndrome
50%
Nuclear RNA Export
50%
Growth Disorders
50%
ATP1A3 Gene
50%
Convulsions with Mild Gastroenteritis
50%
Childhood Epilepsy
50%
Cytotoxic Edema
50%
Longitudinal Diffusion
50%
Co-medication
50%
Gait Pathology
40%
Biochemistry, Genetics and Molecular Biology
Messenger RNA
100%
Human Herpesvirus 6
100%
Genetics
50%
Liquid
50%
Titer
50%
Glucose Transporter
50%
SARS Coronavirus
50%
SLC19A3
50%
PRRT2
50%
Exome
50%
ZEB2
50%
TUBA1A
50%
Homeobox
50%
ATP1A3
50%
Exome Sequencing
50%
Missense
41%
Uniparental Disomy
33%
Normal Human
33%
Glucose Blood Level
21%
Depolymerization
20%
Single-Nucleotide Polymorphism
16%
Medical Genetics
16%
Medical Genomics
16%
Thiamine
16%
Epigenetics
16%
Vitamin B1
16%
Angelman Syndrome
16%
Exon
16%
Gene Expression
14%
Messenger RNA
14%
Zinc Finger E Box Binding Homeobox 2
14%
Intellectual Disability
12%
Protein Stability
12%
Tachyarrhythmia
12%
Tachycardia
12%
Amino Acids
12%
Tubulin
10%
Dynamics
10%
Mutant Protein
10%
Thiamine Transporter
8%
Monocyte
7%
Real-Time Polymerase Chain Reaction
7%
Gene Expression Profiling
7%
DNA RNA Hybridization
7%
Reverse Transcription Polymerase Chain Reaction
7%
Synapsin I
7%
Glial Fibrillary Acidic Protein
7%
Genotyping
7%
Medical Record
7%
TaqMan
7%
Medicine and Dentistry
Clinical Feature
58%
Hypocapnia
50%
Human Herpesvirus 6
50%
Rotavirus Infection
50%
Gastroenteritis
50%
Psychosomatic Medicine
50%
Benign Childhood Epilepsy
50%
Febrile Seizure
50%
COVID-19 Vaccine
50%
Neurofibromatosis Type I
50%
Acetylcholine
50%
Infection
50%
Posterior Reversible Encephalopathy Syndrome
50%
Zonisamide
50%
Alternating Hemiplegia of Childhood
50%
Epileptic Discharge
37%
Gliosis
30%
False Positive Result
25%
Intelligence Test
25%
Conus medullaris
25%
Disease
25%
Phenobarbital
25%
Epileptic Seizure
21%
Diffusion MRI
20%
Thalamus Nucleus
18%
Epileptic Spasms
18%
Plexiform Neurofibroma
16%
Zinc Finger E Box Binding Homeobox 2
16%
Medical Care
16%
Magnetic Resonance Imaging
15%
Default Mode Network
12%
Epilepsy in Children
12%
Ictal
12%
Provocation Test
12%
Mean Airway Pressure
11%
Myenteric Plexus
10%
Cortical Malformation
10%
Rotavirus
10%
Vision Disorder
10%
Partial Seizure
10%
Corpus Callosum
10%
Malignant Neoplasm
8%
Systemic Disease
8%
Arm
8%
Tibia
8%
Scoliosis
8%
Orthopedics
8%
Agenesis
8%
Clinician
8%
Phosphorus Deficiency
8%