スポンサーリンク
Department of Aging Medicine and Geriatrics, Shinshu University | 論文
- Frequency of Facial Angiofibromas in Japanese Patients with Multiple Endocrine Neoplasia Type 1
- Administration of Recombinant Human Growth Hormone Normalizes GH-IGF1 Axis and Improves Malnutrition-related Disorders in Patients with Anorexia Nervosa
- Pheochromocytoma Arising from an Accessory Adrenal Gland in a Patient with Multiple Endocrine Neoplasia Type 2A: Transient Development of Clinical Manifestations after Hemorrhagic Necrosis
- Duodenal Somatostatinoma and Erythrocytosis in a Patient with Von Hippel-Lindau Disease Type 2A
- An Ectopic ACTH-Producing Carcinoid Tumor Localized by the Measurement of ACTH in the Bronchial Lavage
- Octreotide as a Rapid and Effective Painkiller for Metastatic Carcinoid Tumor
- JunD-Menin Interaction Regulates c-Jun-mediated AP-1 Transactivation
- A Case of Familial Isolated Hyperparathyroidism with Ectopic Parathyroid Cancer
- Characterization of the MEN1 Gene Product, Menin, by Site-specific Polyclonal Antibodies
- Multiple Endocrine Neoplasia Type 1 Is Not Rare in Japan
- Unusual Clinical and Pathological Presentation of a Neuroendocrine Tumor in a Patient with Multiple Endocrine Neoplasia Type 1
- Characterization of Two Novel Retinoic Acid-resistant Cell Lines Derived from HL-60 Cells Following Long-term Culture with all-trans-Retinoic Acid
- Long-term Follow-up of Patients with Multiple Endocrine Neoplasia Type 1
- Chromogranin A Expression in Hepatocellular Carcinoma in a Patient with Germline MEN1 Gene Mutation
- Novel MEN1 gene mutations in familial multiple endocrine neoplasia type 1
- Hyperfunctioning Thyroid Adenoma Concomitant with Papillary Thyroid Carcinoma, Follicullar Thyroid Adenoma and Primary Hyperparathyroidism
- Pituitary Adenomas in Adolescent Patients with Multiple Endocrine Neoplasia Type 1
- Carbachol-Induced Secretion and Homologous Desensitization in Rat Basophilic Leukemia (RBL-2H3) Cells Transfected With Human m2 Muscarinic Acetylcholine Receptors
- Genetic Screening in Hereditary Multiple Endocrine Neoplasia Type 1: Absence of a Founder Effect among Japanese Families