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Akihiro Sakurai
Author PubWeight™ 22.02
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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