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藤田医科大学 ホーム
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プロファイル
研究部門
研究成果
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Scopus著者プロファイル
伊藤 哲哉
小児科学
h-index
1548
被引用数
21
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
1985 …
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
(109)
類似のプロファイル
(6)
フィンガープリント
Tetsuya Ito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
Medicine and Dentistry
Neonatal Sepsis
100%
Antioxidant
90%
Neonatal Infant
86%
Liver Transplantation
70%
Endothelin Receptor Antagonist
66%
Glycogen Storage Disease
66%
Interleukin 8
66%
Newborn Screening
66%
Cerebrospinal Fluid
66%
Complement Component C5a
53%
Oxidative Stress
48%
Hydroperoxide
43%
Hypoglycemia
38%
Hypoxic Ischemic Encephalopathy
37%
Philadelphia 1 Chromosome
37%
Aspartate Aminotransferase
34%
Brain Imaging
33%
Chylous Ascites
33%
Protein Restriction
33%
Maple Syrup Urine Disease
33%
Blood Glucose
33%
Citrullinemia
33%
Allopurinol
33%
Succinyl-CoA
33%
Methylmalonyl Coenzyme A Mutase
33%
Steroid 21 Monooxygenase Deficiency
33%
Virilization
33%
Salt Wasting
33%
Propionic Acidemia
33%
Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
33%
Pegvaliase
33%
Propionyl Coenzyme A Carboxylase
33%
Lymphocyte
33%
Inborn Error of Metabolism
33%
Mass Screening
33%
Galactosemia
33%
Donor Lymphocyte Infusion
33%
Dried Blood Spot
33%
Hydroxyl Radical
33%
Encephalomalacia
33%
Hyperammonemia
33%
Ornithine Transcarbamylase Deficiency
33%
Severe Combined Immunodeficiency
33%
Complement Factor I
33%
Spastic Diplegia
33%
Adrenal Cortex
33%
Next Generation Sequencing
33%
Cord Blood Stem Cell Transplantation
33%
Hypothermia
33%
Sex Difference
33%
Biochemistry, Genetics and Molecular Biology
Arginase
66%
RNA Splicing
66%
Inosine
66%
Exon
61%
Genetics
56%
Metabolic Pathway
55%
Liquid Chromatography-Mass Spectrometry
50%
Ornithine Transcarbamylase Deficiency
44%
Intron
42%
Uracil
40%
Minigene
37%
Beta Oxidation
36%
Dehydrogenase
33%
T-Cell Receptor Excision Circles
33%
Transient Expression
33%
Amino Acid Metabolism
33%
G6PC
33%
Medical Biology
33%
Methylmalonyl-CoA Mutase
33%
Phenylalanine
33%
Preimplantation
33%
Fluorescence in Situ Hybridization
33%
Leigh's Disease
33%
Homoplasmy
33%
Digital Positive Youth Development
33%
Synthase
33%
Histocompatibility
33%
21-Hydroxylase
33%
Propionyl-CoA Carboxylase
33%
Citrin
33%
Propionic Acidemia
33%
Virilization
33%
Coenzyme A
33%
Autosomal Recessive Inheritance
33%
Ultra High Performance Liquid Chromatography-Tandem Mass Spectrometry
33%
Sphingomyelin Phosphodiesterase 1
33%
Humidity
33%
Electrospray Ionization
33%
Directed Differentiation
33%
Whole Genome Sequencing
33%
Philadelphia Chromosome
33%
Dried Blood Spot
33%
Dihydropyrimidine Dehydrogenase
33%
Haplotype Map
33%
Purine Metabolism
33%
Isovaleryl-CoA
33%
Dihydropyrimidinase
33%
Tandem Mass Spectrometry
33%
CYP2C19
33%
Inorganic Pyrophosphatase
33%
Keyphrases
Ornithine Transcarbamylase Deficiency
66%
Inosine Triphosphate
66%
Hyperammonemia
52%
Uracil
40%
White Blood Cells
40%
Kappa-deleting Recombination Excision Circles
33%
BCKDH
33%
Maple Syrup Urine Disease
33%
Endothelin Receptor Antagonist
33%
Living Donor Liver Transplantation
33%
Leigh Syndrome
33%
Homoplasmy
33%
Citrullinemia
33%
Challenge Test
33%
Mutanase
33%
Citrin
33%
Citrin Deficiency
33%
Human Urine
33%
Pivalic Acid
33%
Carnitine Metabolism
33%
Virilization
33%
Salt Wasting
33%
Piglet Model
33%
Adaptation
33%
Prader
33%
21-Hydroxylase Deficiency (21OHD)
33%
From Bench to Bed
33%
External Genitalia
33%
Drug-induced
33%
Pegvaliase
33%
Carboxylase
33%
Neonatal Respiratory Support
33%
Mass Screening
33%
Lipase Gene
33%
Structural Integrity
33%
Coenzyme A
33%
Propionic Acidemia
33%
Toxicology
33%
Endotracheal Tube
33%
Inborn Errors of Metabolism
33%
Filter Paper Strips
33%
Genotype-phenotype
33%
Epileptic children
33%
Directed Differentiation
33%
Sphingomyelin Phosphodiesterase 1
33%
Acid Sphingomyelinase Deficiency
33%
Saposin
33%
Female Donors
33%
Neuronopathy
33%
Electrospray Tandem Mass Spectrometry
33%
