スポンサーリンク
Department of Pediatrics, Hokkaido University, School of Medicine | 論文
- Reply to Dr Mussa A et al.
- A Novel V2 Vasopressin Receptor Mutation with X-Linked Nephrogenic Diabetes Insipidus
- Two Japanese Patients with Gitelman Syndrome
- Molecular Analysis of the CLCNKB Gene in Japanese Patients with Classic Bartter Syndrome
- Two Novel Mutations in the Thyroid Peroxidase Gene with Goitrous Hypothyroidism
- A Pseudohypoparathyroidism Type Ia Patient with Normocalcemia
- A Novel Heterozygous Mutation of Steroidogenic Factor-1 (SF-1/Ad4BP) Gene (NR5A1) in a 46, XY Disorders of Sex Development (DSD) Patient without Adrenal Failure
- Recurrent pneumococcal meningitis in a patient with transient IgG subclass deficiency
- 21-Hydroxylase Deficiency Presenting as Massive Bilateral Adrenal Masses in the Seventh Decade of Life
- Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
- Measles encephalomyelitis in a patient with a history of vaccination
- Epidemiology of influenza-associated encephalitis-encephalopathy in Hokkaido, the northernmost island of Japan