スポンサーリンク
Shinshu Univ. School Of Medicine Matsumoto Jpn | 論文
- Seroepidemiological study of hepatitis E virus infection in Japan using a newly developed antibody assay
- Transmission of and liver injury by TT virus in patients on maintenance hemodialysis
- Prevalence and disease association of TT virus infection in Japanese Patients With viral hepatitis
- TT virus infection in an area of high-endemicity for hepatitis C
- Long-term Follow-up of Patients with Multiple Endocrine Neoplasia Type 1
- Budd-Chiari Syndrome Caused by Hepatic Vein Thrombosis in a Patient with Myeloproliferative Disorder
- X-Ray Microanalysis at High Accelerating Voltage Detecting Aluminum Accumulation in Mouse Kidney after Short-Term Aluminum Administration
- P4-47 Energy dispersive X-ray microanalysis of Al in mouse kidney after short period oral administration
- Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1
- Efficacy of preoperative endoscopic nasobiliary drainage for hilar cholangiocarcinoma
- Abscess of the Round Ligament of the Liver Associated with Acute Obstructive Cholangitis and Septic Thrombosis
- Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan
- Regional features of autosomal-dominant cerebellar ataxia in Nagano : clinical and molecular genetic analysis of 86 families
- Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss
- Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification
- Neurotransmission in the vestibular endorgans : Glutamatergic transmission in the afferent synapses of hair cells
- Genetic features of hearing loss associated with ear anomalies : PDS and EYA1 mutation analysis
- Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss : KCNQ4 is a gene responsible in Japanese
- Rapid mass screening method and counseling for the 1555A'G mitochondrial mutation
- EYA1 nonsense mutation in a Japanese branchio-oto-renal syndrome family