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Department Of Pediatrics Graduate School Of Medicine Chiba University | 論文
- Respiratory Symptoms Correlating to Smoking Prevalence : The National Nutrition Survey and the National Life-style Survey in Japan
- A case of 6-pyruvoyl-tetrahydropterin synthase deficiency demonstrates a more significant correlation of L-Dopa dosage with serum prolactin levels than CSF homovanillic acid leyels
- Magnetic resonance imaging in late-onset ornithine transcarbamylase deficiency
- Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
- Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population
- Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiency
- An Ile/Val polymorphism at codon 1464 of the ATP7A gene
- Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease
- Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism : Comparison between Type 1a and Type 1b
- Transient Central Hypothyroidisim Due to Pituitary Suppression in a Premature Neonate Born to a Mother with Three-Year-Untreated Graves' Disease
- A Girl with Prolactinoma Presenting Cessation of Pubertal Development and Growth
- The Standard Ratio of Upper Segment Length to Lower Segment Length According to Spina Malleolar Distance in Japanese Children
- A 9-Year-Old Girl Presenting Central Precocious Puberty with Polycystic Ovary Syndrome
- Genital Bleeding in a 2-Month-Old Infant with Congenital Adrenal Hyperplasia
- Estrogen Secreting Adrenal Adenocarcinoma in an 18-Month-old Boy: Aromatase Activity, Protein Expression, mRNA and Utilization of Gonadal Type Promoter
- Characterization of Genes Encoding the Pancreatic β-cell ATP-sensitive K^+ Channel in Persistent Hyperinsulinemic Hypoglycemia of Infancy in Japanese Patients
- Analyses of Fatal Cases of Kawasaki Disease in Japan Using Vital Statistical Data over 27 Years
- 41 Pseudohypoparathyroidism type Ib with atypical features : the relationship with DNA methylation pattern in XLαs region of GNAS1 gene
- Clinical Utility of Thyroid Ultrasonography in the Diagnosis of Congenital Hypothyroidism
- Guidelines for Diagnosis and Management of Pediatric Food Allergy in Japan