スポンサーリンク
Department of Pediatrics, Akita University School of Medicine | 論文
- In Situ Morphometric Analysis of Left and Right Ventricles in Fetal Rats : Changes in Ventricular Volume, Mass, Wall Thickness, and Valvular Size
- Enzyme Therapy in Gaucher Disease Type 2 : An Autopsy Case
- Identification and Expression of a Missense Mutation (Y446C) in the Acid Sphingomyelinase Gene from a Japanese Patient with Type A Niemann-Pick Disease
- Prolonged hypothermia protects neonatal rat brain against hypoxic-ischemia by reducing both apoptosis and necrosis
- Numerous Hypopigmented Patches Associated with Atopic Dermatitis
- Successful Treatment of Vitiligo with a Sex Steroid-Thyroid Hormone Mixture
- Mass screening for Wilson's disease : Results and recommendations
- Periaxin mutation causes early-onset but slow-progressive Charcot-Marie-Tooth disease
- Specific Adsorption of Clostridium stercorarium Xylanase to Amorphous Cellulose and Its Desorption by Cellobiose
- II D11 Diffusion tensor MR imaging of cerebral axonal tracts in patients with cortical malformations
- Liver Fibrosis in an Extremely Small Infant for Gestational Age
- Niemann-Pick Disease Type C : Cataplexy and Hypocretin in Cerebrospinal Fluid
- A molecular lesion in a Japanese patient with severe phenotype of 3-methylglutaconic aciduria type I
- Osteopontin expression in the liver with severe perisinusoidal fibrosis : Autopsy case of Down syndrome with transient myeloproliferative disorder
- Using Transthoracic Doppler Echocardiography to Diagnose Reduced Coronary Flow Velocity Reserve in the Posterior Descending Coronary Artery in Children With Elevated Right Ventricular Pressure
- Left Ventricular Systolic and Diastolic Function During Early Neonatal Period Using Transthoracic Echocardiography
- Cloning and Sequencing of an Endoglucanase Gene from Scopulariopsis brevicaulis TOF-1212,and Its Expression in Saccharomyces cerevisiae
- Role of insulin resistance in nondipper essential hypertensive patients
- Polysplenia Syndrome with Common Atrioventricular Canal and Persistent Truncus Arteriosus
- Partial 6p Trisomy with Abnormal ABR and Hypogenesis of the Corpus Callosum