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Takeshi Usui

International Institute of Minnesota

14

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356

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Familial congenital choanal atresia with GATA3 associated hypoparathyroidism-deafness-renal dysplasia syndrome unidentified on auditory brainstem response

2018 Auris Nasus Larynx
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A Novel Truncation Mutation of the PRRT2 Gene Resulting in a 16‐Amino‐Acid Protein Causes Self‐inducible Paroxysmal Kinesigenic Dyskinesia

2017 Movement Disorders Clinical Practice
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Pheochromocytoma complicated by cyanotic congenital heart disease: a case report

2016 Clinical Pediatric Endocrinology
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Effects of natural S‐equol supplements on overweight or obesity and metabolic syndrome in the Japanese, based on sex and equol status

2013 Clinical Endocrinology
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Two rare TSH receptor amino acid substitutions in toxic thyroid adenomas

2012 Endocrine Journal
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Salivary cortisol levels are associated with outcomes of weight reduction therapy in obese Japanese patients

2012 Metabolism-clinical and Experimental
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Successful treatment of Cushing’s disease caused by ectopic intracavernous microadenoma

2011 Pituitary
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Prevention of type 2 diabetes in a primary healthcare setting: three-year results of lifestyle intervention in Japanese subjects with impaired glucose tolerance.

2011 BMC Public Health
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H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency

2009 Clinical Pediatric Endocrinology
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Characterization of Prophet of Pit-1 Gene Expression in Normal Pituitary and Pituitary Adenomas in Humans

1999 The Journal of Clinical Endocrinology and Metabolism
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Citations (29)