Search Results - Hanae Hagiwara

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  1. 1
    Successful treatment of Cushing’s disease caused by ectopic intracavernous microadenoma

    Successful treatment of Cushing’s disease caused by ectopic intracavernous microadenoma by Koizumi, Mitsuteru, Usui, Takeshi, Yamada, Shozo, Fujisawa, Ichiro, Tsuru, Tsunehisa, Nanba, Kazutaka, Hagiwara, Hanae, Kimura, Takashi, Tamanaha, Tamiko, Tagami, Tetsuya, Naruse, Mitsuhide, Shimatsu, Akira

    Published in Pituitary
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  2. 2
    P15-3-9 A case of multiple lung metastases from adrenocortical carcinoma

    P15-3-9 A case of multiple lung metastases from adrenocortical carcinoma by Hanae Hagiwara

    Published in ENDOCRINE JOURNAL
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  3. 3
    P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease

    P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease by Kawashima, Sachiko-Tsukamoto, Usui, Takeshi, Sano, Toshiaki, Iogawa, Hitomi, Hagiwara, Hanae, Tamanaha, Tamiko, Tagami, Tetsuya, Naruse, Mitsuhide, Hojo, Masato, Takahashi, June A., Shimatsu, Akira

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  4. 4
    Pheochromocytoma with Subclinical Cushing’s Syndrome Caused by Corticomedullary Mixed Tumor of the Adrenal Gland

    Pheochromocytoma with Subclinical Cushing’s Syndrome Caused by Corticomedullary Mixed Tumor of the Adrenal Gland by Kimura, Takashi, Usui, Takeshi, Inamoto, Susumu, Minamiguchi, Sachiko, Okuno, Hiroshi, Sasano, Hironobu, Hagiwara, Hanae, Nagata, Daisuke, Tagami, Tetsuya, Naruse, Mitsuhide, Shimatsu, Akira

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  5. 5
    Lack of ACTH and Androgen Receptor Expression in a Giant Adrenal Myelolipoma Associated with 21-hydroxylase Deficiency

    Lack of ACTH and Androgen Receptor Expression in a Giant Adrenal Myelolipoma Associated with 21-hydroxylase Deficiency by Hagiwara, Hanae, Usui, Takeshi, Kimura, Takashi, Tagami, Tetsuya, Naruse, Mitsuhide, Minamiguchi, Sachiko, Kato, Takuma, Okuno, Hiroshi, Shimatsu, Akira

    Published in Endocrine pathology
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  6. 6
    R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma

    R27X nonsense mutation of the SDHB gene in a patient with sporadic malignant paraganglioma by Naito, Masaki, Usui, Takeshi, Tamanaha, Tamiko, Kawashima, Sachiko-Tsukamoto, Iogawa, Hitomi, Hagiwara, Hanae, Kimura, Takashi, Tagami, Tetsuya, Kurosawa, Manabu, Shimatsu, Akira, Naruse, Mitsuhide

    Published in Endocrine
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  7. 7
    Meningioma in an acromegalic patient treated with long-term octreotide therapy

    Meningioma in an acromegalic patient treated with long-term octreotide therapy by Shimatsu, Akira, Nakakuki, Takuya, Kimura, Takashi, Hagiwara, Hanae, Usui, Takeshi, Nagata, Daisuke, Tagami, Teatsuya, Naruse, Mitsuhide, Tsukahara, Tetsuya

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  8. 8
    P4-11-1 The prevalence of polycystic thyroid disease in the hypothyroid patients with negative thyroid auto-antibodies

    P4-11-1 The prevalence of polycystic thyroid disease in the hypothyroid patients with negative thyroid auto-antibodies by Sumihisa Kubota, Mako Fujiwara, Hanae Hagiwara, Naoyuki Tsujimoto, Kazuna Takata, Takumi Kudo, Eijun Nishihara, Mitsuru Ito, Nobuyuki Amino, Akira Miyauchi

    Published in ENDOCRINE JOURNAL
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  9. 9
    Image in endocrinology. Pheochromocytoma with subclinical Cushing's syndrome caused by corticomedullary mixed tumor of the adrenal gland

    Image in endocrinology. Pheochromocytoma with subclinical Cushing's syndrome caused by corticomedullary mixed tumor of the adrenal gland by Kimura, Takashi, Usui, Takeshi, Inamoto, Susumu, Minamiguchi, Sachiko, Okuno, Hiroshi, Sasano, Hironobu, Hagiwara, Hanae, Nagata, Daisuke, Tagami, Tetsuya, Naruse, Mitsuhide, Shimatsu, Akira

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  10. 10
    P7-5-2 Usefulness of MR imaging in multiple endocinopathies due to primary hemochoromocytosis

    P7-5-2 Usefulness of MR imaging in multiple endocinopathies due to primary hemochoromocytosis by Tamiko Tamanaha, Takeshi Usui, Ichiro Fujisawa, Yoshiaki Okuno, Sachiko Minamiguchi, Toshiki Komeda, Hitomi Iogawa, Hanae Hagiwara, Tetsuya Tagami, Mitsuhide Naruse, Akira Shimatsu

    Published in ENDOCRINE JOURNAL
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  11. 11
    P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease

    P53 gene mutation in an atypical corticotroph adenoma with Cushing's disease by Kawashima, Sachiko-Tsukamoto, Usui, Takeshi, Sano, Toshiaki, Iogawa, Hitomi, Hagiwara, Hanae, Tamanaha, Tamiko, Tagami, Tetsuya, Naruse, Mitsuhide, Hojo, Masato, Takahashi, June A, Shimatsu, Akira

    Published in Clinical endocrinology
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  12. 12
    M3 muscarinic acetylcholine receptor-reactive Th17 cells in primary Sjögren's syndrome

    M3 muscarinic acetylcholine receptor-reactive Th17 cells in primary Sjögren's syndrome by Abe, Saori, Tsuboi, Hiroto, Kudo, Hanae, Asashima, Hiromitsu, Ono, Yuko, Honda, Fumika, Takahashi, Hiroyuki, Yagishita, Mizuki, Hagiwara, Shinya, Kondo, Yuya, Matsumoto, Isao, Sumida, Takayuki

    Published in JCI insight
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