Adult combined GH, prolactin, and TSH deficiency associated with circulating PIT-1 antibody in humans
スポンサーリンク
概要
著者
-
Iida Keiji
神戸大学 医学研究科内科学講座糖尿病代謝内分泌内科学
-
Iguchi Genzo
Division Of Diabetes Metabolism And Endocrinology Department Of Internal Medicine Kobe University Gr
-
Okimura Yasuhiko
Department Of Basic Allied Medicine Kobe University School Of Medicine
-
Takeno Ryoko
Division Of Diabetes Metabolism And Endocrinology Department Of Internal Medicine Kobe University Gr
-
Fukuoka Hidenori
Division Of Diabetes Metabolism And Endocrinology Department Of Internal Medicine Kobe University Gr
-
Iida Keiji
Division Of Diabetes Metabolism And Endocrinology Department Of Internal Medicine Kobe University Gr
関連論文
- An Observation of Plasma Cell Dyscrasia Developing to Multiple Myeloma With a Rare Association of Pituitary Adenoma and Pituitary Apoplexy
- Hepatic Failure and Enhanced Oxidative Stress in Mitochondrial Diabetes
- Growth Hormone Stimulates Mechano Growth Factor Expression and Activates Myoblast Transformation in C2C12 cells
- Hormone Replacement Therapy and Vascular Risk Disorders in Adult Hypopituitarism
- The N131S Mutation in the von Hippel-Lindau Gene in a Japanese Family with Pheochromocytoma and Hemangioblastomas
- Mutations of the Growth Hormone Receptor Found in Japanese Short Children
- Multifocal Fibrosclerosis as a Possible Cause of Panhypopituitarism with Central Diabetes Insipidus
- Short Stature Caused by a Mutant Growth Hormone with an Antagonistic Effect
- Expression of mPOU Protein in the Human Pituitary Adenomas
- Adult Growth Hormone Deficiency in Japan : Results of Investigation by Questionnaire
- A Novel Mutation in the von HippelLindau Tumor Suppressor Gene Identified in a Japanese Family with Pheochromocytoma and Hepatic Hemangioma
- Unresponsiveness of GH and Cortisol to Insulin-Hypoglycemia in a Patient with Sub-total Pancreatectomy
- W194XProp1 and S156insTProp1, both of which have intact DNA-binding domain, show a different DNA-binding activity to the Prop1-binding element in human Pit-1 gene
- Adult combined GH, prolactin, and TSH deficiency associated with circulating PIT-1 antibody in humans
- McCune-Albright Syndrome with Acromegaly and Fibrous Dysplasia Associated with the GNAS Gene Mutation Identified by Sensitive PNA-clamping Method