スポンサーリンク
Department Of Pediatrics Hokkaido University Graduate School Of Medicine | 論文
- Epitope mapping of anti-α-fodrin antibody in a case of early-onset multiple sclerosis
- Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism
- Laparoscopic liver biopsy using cup-shaped punch biopsy forceps and argon beam coagulator in children
- MAGNIFYING ENDOSCOPIC OBSERVATION OF THE UPPER GASTROINTESTINAL TRACT
- A Novel PAX4 Mutation in a Japanese Patient with Maturity-Onset Diabetes of the Young
- Postoperative portal and splenic vein thrombosis in children : Identification of risk factors
- ENDOCYTOSCOPIC OBSERVATION OF ESOPHAGEAL SQUAMOUS CELL CARCINOMA
- Vaccine-associated paralytic poliomyelitis in a non-immunocompromised infant
- A Novel Missense Mutation (p.P52R) in Amelogenin Gene Causing X-linked Amelogenesis Imperfecta
- The first report of a novel mutation in the amelogenin gene in a Japanese family affected with X-linked amelogenesis imperfecta (Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- Identification of a novel mutation in the enamelin gene in a Japanese family affected with autosomal dominant amelogenesis imperfecta(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
- Autosomal-dominant Hypoplastic Form of Amelogenesis Imperfecta Caused by an Enamelin Gene Mutation at the Exon-Intron Boundary
- Gitelmans Syndrome with Mental Retardation
- Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome
- Curative Resection of a Huge Malignant Pancreatic Endocrine Tumor by Pancreatoduodenectomy with Portal and Superior Mesenteric Vein Resection and Reconstruction Using the Right Ovarian Vein : Report of a Case
- Source localization in magnetoencephalography to identify epileptogenic foci
- Successful reduced-intensity SCT from unrelated cord blood in three patients with X-linked SCID
- Identification and functional analysis of novel calcium-sensing receptor gene mutation in familial hypocalciuric hypercalcemia
- Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
- Detection of Human Bocaviruses 1 to 4 from Nasopharyngeal Swab Samples Collected from Patients with Respiratory Tract Infections