Akihiro Sakurai

Author PubWeight™ 22.02‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1). J Clin Endocrinol Metab 2012 2.87
2 Fitz-Hugh and Curtis syndrome-like diaphragmatic endometriosis. Fertil Steril 2005 1.42
3 High prevalence of hypothyroidism in patients with autoimmune pancreatitis. Dig Dis Sci 2005 1.10
4 Genetic basis of inter-individual variability in the effects of exercise on the alleviation of lifestyle-related diseases. J Physiol 2009 1.02
5 A novel technique using magnetic resonance imaging jelly for evaluation of rectovaginal endometriosis. Fertil Steril 2005 0.95
6 Vasopressin V1a receptor polymorphism and interval walking training effects in middle-aged and older people. Hypertension 2010 0.93
7 Genetic analyses in patients with familial isolated hyperparathyroidism and hyperparathyroidism-jaw tumour syndrome. Clin Endocrinol (Oxf) 2006 0.90
8 Suppression of insulin-induced AP-1 transactivation by menin accompanies inhibition of c-Fos induction. Int J Cancer 2003 0.90
9 Octreotide as a rapid and effective painkiller for metastatic carcinoid tumor. Endocr J 2005 0.89
10 High penetrance of pheochromocytoma in multiple endocrine neoplasia 2 caused by germ line RET codon 634 mutation in Japanese patients. Eur J Endocrinol 2013 0.89
11 Mandibuloacral dysplasia and a novel LMNA mutation in a woman with severe progressive skeletal changes. Am J Med Genet A 2007 0.84
12 Surgery for a gastroenteropancreatic neuroendocrine tumor (GEPNET) in multiple endocrine neoplasia type 1. Surg Today 2012 0.80
13 Pituitary adenomas in adolescent patients with multiple endocrine neoplasia type 1. Endocr J 2002 0.78
14 A newly identified missense mutation in RET codon 666 is associated with the development of medullary thyroid carcinoma. Endocr J 2014 0.77
15 Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan. J Hum Genet 2013 0.77
16 Parasitic myomas after laparoscopic-assisted myomectomy in multiple endocrine neoplasia type 1. J Obstet Gynaecol Res 2013 0.77
17 Application of an intracellular stability test of a novel missense menin mutant to the diagnosis of multiple endocrine neoplasia type 1. Endocr J 2012 0.77
18 [Basic information on medical genetics for internists (2)]. Nihon Naika Gakkai Zasshi 2008 0.77
19 JunD-menin interaction regulates c-Jun-mediated AP-1 transactivation. Endocr J 2004 0.76
20 A novel splice site mutation of the MEN1 gene identified in a patient with primary hyperparathyroidism. Endocr J 2012 0.75
21 Mediastinal seminoma in a patient with multiple endocrine neoplasia type 1. Intern Med 2008 0.75
22 Early-onset, severe, and recurrent primary hyperparathyroidism associated with a novel CDC73 mutation. Endocr J 2015 0.75
23 Effective perioperative management of multiple endocrine neoplasia type 1-associated insulinomas. Arch Surg 2012 0.75
24 Multiple endocrine neoplasia type 1 with unusual concomitance of various neoplastic disorders. Endocr J 2004 0.75
25 Delay in the diagnosis of multiple endocrine neoplasia type 1: typical symptoms are frequently overlooked. Endocr J 2012 0.75
26 Plasma free metanephrines in the diagnosis of pheochromocytoma: diagnostic accuracy and strategies for Japanese patients. Endocr J 2014 0.75
27 Comprehensive genetics clinic for familial tumors: proposal for a suitable system in Japan. Int J Clin Oncol 2004 0.75
28 Novel 14 base-pair deletion of the MEN1 gene in a patient with recurrent primary hyperparathyroidism. Jpn J Clin Oncol 2006 0.75
29 Carbachol-induced secretion and homologous desensitization in rat basophilic leukemia (RBL-2H3) cells transfected with human m2 muscarinic acetylcholine receptors. J Pharmacol Sci 2004 0.75
30 [Genetic testing and counseling for familial tumor syndromes]. Gan To Kagaku Ryoho 2002 0.75
31 [Endocrine diseases: progress in diagnosis and treatments. Topics: IX. Recent topics; 3. Multiple endocrine neoplasia]. Nihon Naika Gakkai Zasshi 2014 0.75
32 [Basic knowledge in medical genetics for internists (1)]. Nihon Naika Gakkai Zasshi 2008 0.75
33 Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan. J Hum Genet 2007 0.75
34 Diagnosis of fucosidosis through a skin rash. Intern Med 2005 0.75