Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Munehiro Honda"'
Autor:
Munehiro Honda
Publikováno v:
ISRN Endocrinology
A 52-year-old Japanese woman was examined because of general malaise, weight loss and a lump in her left breast. She was diagnosed with cancer of the left breast and Graves' disease, and was administered methimazole (MMI). A left mastectomy was perfo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38166e7e6d7595b415ee0bbf0c6c2bfe
https://doi.org/10.5402/2011/732623
https://doi.org/10.5402/2011/732623
Autor:
Tomoyuki Yoshizaki, Takahiro Fujioka, Koutaro Shimokawa, Kazunori Koyama, Hisako Matsuno, Munehiro Honda, Momoko Ogawa
Publikováno v:
Internal Medicine. 49:1987-1990
We report a case of type 1 diabetes onset and recurrence of Graves' disease during pegylated interferon (PEG-IFN)-alpha plus ribavirin treatment for chronic hepatitis C. The patient was a 55-year-old woman diagnosed with chronic hepatitis at age 46 y
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f47e149d588bd986874b2a519d997791
https://doi.org/10.2169/internalmedicine.49.3831
https://doi.org/10.2169/internalmedicine.49.3831
Publikováno v:
Internal Medicine. 46:1573-1576
We report a case of diabetic mastopathy in an elderly woman with type 2 diabetes. The patient was a 69-year-old woman diagnosed with type 2 diabetes at the age of 33 years. She had been treated with insulin for 25 years, however, her blood glucose ha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9ecd4a929c7e23ae8559542a7acfd447
https://doi.org/10.2169/internalmedicine.46.6191
https://doi.org/10.2169/internalmedicine.46.6191
Autor:
Hiroshi Ohashi, Kentaro Kikuchi, Hiroko Kawamura, Hirotoshi Fujikawa, Miyuki Ishibashi, Munehiro Honda, Hiroshi Miyakawa, Yasumichi Mori, Yumi Kawashima
Publikováno v:
Internal Medicine. 45:1225-1229
Here, we report a case of acute liver dysfunction complicated with uncontrollable glycemia due to insulin antibody. The patient was admitted to our hospital due to diabetic ketoacidosis. He was administered insulin immediately, however, his fasting p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b6375c5bbff5f9744c7e625fde16b10
https://doi.org/10.2169/internalmedicine.45.6009
https://doi.org/10.2169/internalmedicine.45.6009
Autor:
Toshimitsu Horiuchi, Miyuki Ishibashi, Ken Yamaguchi, Hiroshi Miyakawa, Toshihiko Tsukada, Takao Obara, Reiko Tanaka, Munehiro Honda, Tohru Yamaji
Publikováno v:
Internal Medicine. 43:310-314
A rare case of primary hyperparathyroidism associated with primary aldosteronism and breast cancer is reported. A 44-year-old woman was admitted to our hospital to undergo surgical removal of breast cancer. She had hypertension with low serum potassi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5bdd1191d3e614181938cfe7064996
https://doi.org/10.2169/internalmedicine.43.310
https://doi.org/10.2169/internalmedicine.43.310
Autor:
Tohru Yamaji, K Maruyama, H Tanaka, K Yamaguchi, Toshihiko Tsukada, Takao Obara, Miyuki Ishibashi, Munehiro Honda
Publikováno v:
European Journal of Endocrinology. :138-143
OBJECTIVE: To determine whether familial isolated hyperparathyroidism (FIHP) is a variant of multiple endocrine neoplasia type 1 (MEN1) we analyzed the MEN1 gene in such a kindred. DESIGN AND METHODS: The study included the 70-year-old proband and ni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de4440ea164a4896f5077cdcee7e8ed1
https://doi.org/10.1530/eje.0.1420138
https://doi.org/10.1530/eje.0.1420138
Autor:
Ken Yamaguchi, Munehiro Honda, Toshihiko Tsukada, Noriko Nara-Ashizawa, Tetsuji Hosono, Mari Kishi, Koichi Nagasaki, Kouji Maruyama, Naganari Ohkura
Publikováno v:
Molecular and Cellular Endocrinology. 156:25-33
Menin is a protein product of a tumor supressor gene MEN1, mutations of which are responsible for multiple endocrine neoplasia type 1, an autosomal dominant familial cancer syndrome. We isolated rat menin cDNA clones from a fetal rat brain cDNA libra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2501b9bc76e09b90b7fa40771c7ff56
https://doi.org/10.1016/s0303-7207(99)00150-1
https://doi.org/10.1016/s0303-7207(99)00150-1
Autor:
Yuko Nagamura, Munehiro Honda, Dong Yu, Satoko Shimazu, Toshihiko Tsukada, Seiki Wada, Hiroshi Kaji, Junko Naito, Lian Xue
Publikováno v:
Endocrine journal. 57(9)
Menin is lost by the sequential inactivation of both MEN1 alleles in subsets of non-hereditary endocrine tumors as well as those associated with multiple endocrine neoplasia type 1 (MEN1), an autosomal dominant hereditary cancer syndrome characterize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4504adde777bf458e9ef403648b49593
https://pubmed.ncbi.nlm.nih.gov/20616437
https://pubmed.ncbi.nlm.nih.gov/20616437
Autor:
Munehiro, Honda, Miyuki, Ishibashi
Publikováno v:
Nihon rinsho. Japanese journal of clinical medicine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2ee061c0acfdf7fb0004e036e10c0b5b
https://pubmed.ncbi.nlm.nih.gov/17022545
https://pubmed.ncbi.nlm.nih.gov/17022545
Autor:
Munehiro, Honda, Miyuki, Ishibashi
Publikováno v:
Gan to kagaku ryoho. Cancerchemotherapy. 31(3)
The gastroenteropancreatic endocrine tumor is relatively rare tumor that originate from pancreas, duodenum, and a variety of neuroendocrine cells. The differential diagnosis and preoperative localization of the tumor are important, because surgical r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::20aa44a2c3837d2b68094757a08a6302
https://pubmed.ncbi.nlm.nih.gov/15045936
https://pubmed.ncbi.nlm.nih.gov/15045936