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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
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
水野 晴夫
小児科学
h-index
674
被引用数
16
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
1995 …
2024
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
(46)
類似のプロファイル
(6)
フィンガープリント
Haruo Mizuno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
Diabetes
100%
Pediatrics Patient
91%
Endothelin Receptor Antagonist
85%
Steroid 21 Monooxygenase Deficiency
85%
Patient with Diabetes
85%
Hypoglycemia
85%
Pediatrics
83%
Insulin Dependent Diabetes Mellitus
47%
Hypovitaminosis D
42%
Vitamin D Deficiency
42%
Oxidative Stress
42%
Thiazide Diuretic Agent
42%
Adrenal Cortex
42%
ABC Transporter Subfamily G
42%
Insulin Detemir
42%
Histidine Ammonialyase
42%
Neonatal Diabetes Mellitus
42%
Virilization
42%
Salt Wasting
42%
Laparoendoscopic Single Site Surgery
42%
Chromosome Mosaicism
42%
Turner Syndrome
42%
Gonadectomy
42%
Adolescent
42%
Monocarboxylate Transporter 8
42%
Congenital Hypothyroidism
42%
Kallmann Syndrome
42%
Nephrogenic Diabetes Insipidus
42%
Karyotype 45,X
42%
Mixed Gonadal Dysgenesis
42%
Hydroxyl Radical
42%
Fulminant
42%
Neonatal Sepsis
42%
Bartter Syndrome
42%
Insulin Treatment
42%
Shwachman Syndrome
42%
Syndrome CHARGE
42%
Kabuki Syndrome
42%
Desmopressin
42%
Pediatric Endocrinology
35%
Disease
32%
Hydroperoxide
26%
Sitosterol
21%
Campesterol
21%
Interleukin 6
21%
Mass Screening
21%
Leydig Cell
21%
Trichlormethiazide
21%
Symptom
16%
Antioxidant
16%
Keyphrases
TSH Receptor
42%
Longitudinal Assessment
42%
Adrenal Cortex
42%
Fetal Adrenal
42%
Graves' Disease
42%
Endothelin Receptor Antagonist
42%
Insulin Detemir
42%
Detemir
42%
Joint Research
42%
Parental Diabetes
42%
Adolescent Diabetes
42%
Tall Stature
42%
Histidase
42%
Serum Creatine Kinase
42%
Medical Treatment
42%
Neonatal Diabetes Mellitus
42%
Familial Glucocorticoid Deficiency
42%
Maturity-onset Diabetes of the Young
42%
Children with Type 1 Diabetes
42%
Virilization
42%
Analogue Insulin
42%
Salt Wasting
42%
Piglet Model
42%
Adolescents with Type 1 Diabetes
42%
Insulin Delivery Systems
42%
Prader
42%
21-Hydroxylase Deficiency (21OHD)
42%
External Genitalia
42%
Laparoendoscopic Single-site Surgery
42%
Laparoendoscopic Single-site
42%
Gonadectomy
42%
Testicular Morphology
42%
Hydroxyl Radical Scavengers
42%
Gonadal Dysgenesis
42%
Idic(Y)
42%
SLC26A7
42%
Diagnostic Potential
42%
SLC26A4
42%
TSHR Gene
42%
Thyrotropin Receptor
42%
Hereditary Orotic Aciduria
42%
KMT2D
42%
Uridine Monophosphate
42%
Shwachman-Diamond Syndrome
42%
Lipocortin-1
42%
Kabuki Syndrome
42%
Pediatric Diabetes
42%
Renal Tubular Function
42%
Factor Mobility
32%
ACTH Receptor
28%
Biochemistry, Genetics and Molecular Biology
Mouse
53%
Exon
50%
Glucokinase
42%
Thyroid Function
42%
Insulin Analog
42%
Monospecific Antibody
42%
ABCC8
42%
Testis Development
42%
Selected Ion Monitoring
42%
Aldosterone
42%
Thyrotropin Receptor
42%
Molecular Cloning
42%
21-Hydroxylase
42%
Virilization
42%
Molecular Genetics
42%
Annexin
42%
Glycemic Control
42%
Amnion Fluid
42%
Bartter Syndrome
42%
Genetic Disorder
42%
CHD7
42%
Thyroid Hormone Synthesis
42%
Receptor Gene
42%
Pendrin
42%
Uridine Monophosphate
42%
Desmopressin
42%
Shwachman-Diamond Syndrome
42%
Genetics
30%
Proband
28%
Genotype Phenotype Correlation
28%
ACTH Receptor
24%
Steroid Urine Level
21%
Drug Dose
21%
Recessive Gene
21%
Hemoglobin A
21%
Campesterol
18%
Infancy
17%
Thyroid Hormone
17%
SBDS
16%
Autosomal Recessive Disorder
14%
Next Generation Sequencing
14%
Pregnancy
14%
Autosomal Dominant Inheritance
14%
Gingiva
14%
Hypercalciuria
14%
Hyponatremia
14%
Enzyme Inactivation
14%
Hypomagnesemia
14%
Autosomal Recessive Inheritance
14%
Sanger Sequencing
14%
