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Toshihiro Tajima

Jichi Medical University

10

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35

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The progression of salt wasting and the body weight change during the first two weeks of life in classical 21-hydroxylase deficiency patients.

2020 Clinical Endocrinology
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Clinical features of 57 patients with lipoid congenital adrenal hyperplasia: criteria for nonclassic form revisited.

2020 The Journal of Clinical Endocrinology and Metabolism
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Health problems of adolescent and adult patients with 21-hydroxylase deficiency

2018 Clinical Pediatric Endocrinology
- Toshihiro Tajima
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Sulfonylurea treatment in an infant with transient neonatal diabetes mellitus caused by an adenosine triphosphate binding cassette subfamily C member 8 gene mutation

2017 Clinical Pediatric Endocrinology
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A Novel Mutation of wfs1 Gene in a Japanese Infant of Diabetes Mellitus, Deafness, and Congenital Cataract

2014
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