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Department of Pediatrics, Keio University School of Medicine | 論文
- 49 THE CROSS-SECTIONAL BMI GROWTH CURVES FOR JAPANESE FROM BIRTH TO 17 YEARS OF AGE : THE 2000-2001 NATIONAL SURVEY DATA : the comparison with the 1990-1994 data and the 1978-1981 data
- Association of Micropenis with Pro185Ala Polymorphism of the Gene for Aryl Hydrocarbon Receptor Repressor Involved in Dioxin Signaling
- Evalution of serodiagnosis of toxoplasmosis by using the recombinant nucleoside triphosphate hydrolase isoforms expressed in Escherichia coli
- 小児科領域における精神保健疾患 : 日本の医療における新たな課題
- Clinical Utility of Insulin-Like Growth Factor-l(IGF-I)and IGF Binding Protein-3 Levels in the Diagnosis of GH Deficiency(GHD)During Childhood
- Timing for Discontinuation of Treatment with a Long-Acting Gonadotropin-Releasing Hormone Analog in Girls with Central Precocious Puberty
- A major influence of CYP2C19 genotype on the steady-state concentration of N-desmethylclobazam
- Mutational Analysis of Androgen Receptor (AR) Gene in 46, XY Patients with Ambiguous Genitalia and Normal Testosterone Secretion : Endocrinological Characteristics of Three Patients with AR Gene Mutations
- Development of Growth Hormone and Adrenocorticotropic Hormone Deficiencies in Patients with Prenatal or Perinatal-Onset Hypothalamic Hypopituitarism Having Invisible or Thin Pituitary Stalk on Magnetic Resonance Imaging
- Genome-wide screening of dioxin-responsive genes in fetal brain : bioinformatic and experimental approaches
- Setting Up an Automated System for Evaluation of Bone Age
- Large fontanelles are a shared feature of haploinsufficiency of RUNX2 and its co-activator CBFB
- A Two-year-old Female with Methylmalonic Acidemia and Progressive Low Density Lesions in the Basal Ganglia on CT Scans
- Deletion involving the TWIST locus and the HOXA cluster : A contiguous gene syndrome on 7p?
- Auxological and Radiological Manifestations of Patients with Hypochondroplasia Negative for N540K Mutation in Fibroblast Growth Factor Receptor 3 Gene
- Joint laxity, vitreoretinal degeneration, facial abnormalities, and generalized skeletal alterations : A new syndrome?
- Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
- Discrepancies in cytogenetic results between amniocytes and postnatally obtained blood : trisomy 9 mosaicism
- Recurrence of seizures in childhood epilepsy after discontinuation of antiepileptic drugs
- A novel nonsense mutation of the PEPD gene in a Japanese patient with prolidase deficiency