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Department Of Pediatrics Nagasaki University School Of Medicine | 論文
- Case with Small Testes Associated with Skeletal Dysplasia
- PROP1 Abnormality
- P-MN-03 NANOFABRICATION OF SILICON BY MECHANO-CHEMICAL PROCESSING AND ITS APPLICATION TO ETCHING MASK FOR POTASSIUM HYDROXIDE SOLUTION
- ^Sn NMR Studies of the Heavy-Electron Compound U_3Au_3Sn_4
- Early detection of cutaneous microcirculatory change during hemorrhage using a laser Doppler flowmetry
- Neonatal behavioral assessment scale as a predictor of later developmental disabilities of low birth-weight and/or premature infants
- Sigmoid Colon Perforation Induced by the Vascular Type of Ehlers-Danlos Syndrome : Report of a Case
- Response of skin blood volume, velocity and flow to local warming in newborns, measured by laser Doppler flowmetry
- 長崎県妊婦におけるサイトメガロウイルス感染の血清疫学的調査
- 168 A frameshift mutation and a familial deletion mutation of the DAX1 gene in patients with X-linked adrenal hypoplasia congenita
- Miller syndrome with novel dihydroorotate dehydrogenase gene mutations
- 40 A NOVEL MUTATION OF 25-HYDROXY VITAMIN D3 1α-HYDROXYLASE GENE IN A JAPANESE FAMILY WITH VITAMIN D DEPENDENT RICKETS TYPE1
- 53 PITUITARY MAGNETIC RESONANCE IMAGING IN CHILDREN WITH GROWTH HORMONE DEFICIENCY
- 66 Conventional detection of somatic GNAS1 mutation utilizing peripheral blood leukocyte in McCune-Albright syndrome
- 64 GNAS1 mutation in a Japanese boy with progressive osseous heteroplasia.
- 98 A male-raised 46, XX case of congenital adrenal hyperplasia due to 21 hydroxylase deficiency
- 101 A female case of classical 3β-hydroxysteroid dehydrogenase deficiency with multicystic ovary and anovulatory menstruation : Evaluation of ovarian function after puberty
- 109 A case of allergy to gelatin included in the gonadotropin-releasing hormone analog "depot leuprorelin acetate"
- Mutations in PRRT2 responsible for paroxysmal kinesigenic dyskinesias also cause benign familial infantile convulsions