Nishihara Eijun | Kuma Hospital

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著作論文

A Case of Adrenal Insufficiency Due to Acquired Hypothalamic CRH Deficiency
Prevalence of TSH Receptor and Gsα Mutations in 45 Autonomously Functioning Thyroid Nodules in Japan
Sporadic Congenital Hyperthyroidism due to a Germline Mutation in the Thyrotropin Receptor Gene (Leu 512 Gln) in a Japanese Patient
Two-day Thionamide Withdrawal prior to Radioiodine Uptake Sufficiently Increases Uptake and does not Exacerbate Hyperthyroidism Compared to 7-day Withdrawal in Graves' Disease
A Case of Hypothyroid Graves' Disease Following External Radiation Therapy to the Cervical Region
Effect of High Dose Methylprednisolone Pulse Therapy Followed by Oral Prednisolone Administration on the Production of Anti-TSH Receptor Antibodies and Clinical Outcome in Graves' Disease
A Novel Thyrotropin Receptor Germline Mutation (Asp617Tyr) Causing Hereditary Hyperthyroidism
Pathologic features of polycystic thyroid disease : Comparison with benign nodular goiter
Clinical Characteristics of 852 Patients with Subacute Thyroiditis before Treatment
Effect of L-thyroxine replacement on apolipoprotein B-48 in overt and subclinical hypothyroid patients

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