Search Results - "Ujiie, H"

IgE autoantibodies in bullous pemphigoid by Ujiie, H.

“…Linked Article: Freire et al. Br J Dermatol 2017; 177:1644–1653…”
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Atypical manifestations of hemangiomas in epidermolysis bullosa by Itamoto, S, Natsuga, K, Takashima, S, Ujiie, H

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Clinical and immunological features of pemphigus relapse by Ujiie, I., Ujiie, H., Iwata, H., Shimizu, H.

“…Summary Background More than half of patients with pemphigus experience relapse during the disease course. The risk factors and clinical and immunological…”
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Acquired perforating dermatosis induced by necitumumab by Kimura, A., Kosumi, H., Natsuga, K., Goda, T., Ujiie, H.

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Clinical and immunological features of pemphigus relapse by Ujiie, I., Ujiie, H., Iwata, H., Shimizu, H.

“…Summary Pemphigus is a potentially fatal blistering skin disease. It is an autoimmune disease, meaning that the body's immune system, which normally fights off…”
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Detection of anti‐BP180 NC16A autoantibodies after the onset of dipeptidyl peptidase‐IV inhibitor‐associated bullous pemphigoid: a report of three patients by Mai, Y., Nishie, W., Izumi, K., Yoshimoto, N., Morita, Y., Watanabe, M., Toyonaga, E., Ujiie, H., Iwata, H., Fujita, Y., Nomura, T., Sato‐Matsumura, K.C., Shimizu, S., Shimizu, H.

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Linear IgA/IgG bullous dermatosis with autoantibodies directing the native and processed forms of BP180 by Inamura, E., Nishie, W., Yamaguchi, Y., Fujimura, Y., Ujiie, H., Natsuga, K., Shimizu, H.

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A case of non‐bullous pemphigoid induced by IgG4 autoantibodies targeting BP230 by Yoshimoto, N., Takashima, S., Kawamura, T., Inamura, E., Sugai, T., Ujiie, I., Izumi, K., Natsuga, K., Nishie, W., Shimizu, H., Ujiie, H.

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Bullous pemphigoid suggestive of complement-independent blister formation with anti-BP180 IgG4 autoantibodies by Dainichi, T., Nishie, W., Yamagami, Y., Sonobe, H., Ujiie, H., Kaku, Y., Kabashima, K.

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Native collagen XVII complex ELISA: An approach for diagnosis and monitoring of anti‐integrin β4 mucous membrane pemphigoid by Mai, S., Izumi, K., Itamoto, S., Kurosawa, S., Nagata, Y., Hikichi, S., Miyazawa, H., Tokuchi, K., Imafuku, K., Yanagi, T., Tsutsui, M., Ujiie, H.

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Palmoplantar keratoderma with deafness due to GJB2 mutation can develop ichthyosiform symptoms: a case report by Kimura, A., Miyauchi, T., Peh, J.T., Yanagi, T., Hasegawa, S., Morita, S., Ujiie, H.

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Autoantibodies undetectable by chemiluminescent enzyme immunoassay require extended antigen–antibody reaction time for detection by Mai, Y., Ujiie, H., Higashi, T., Yamagami, J., Iwata, H., Shimizu, H.

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Characteristics of IgG subclasses and complement deposition in BP230‐type bullous pemphigoid by Zheng, M., Ujiie, H., Iwata, H., Muramatsu, K., Yoshimoto, N., Ito, T., Ujiie, I., Shimizu, S., Sato‐Matsumura, K.C., Shimizu, H.

“…Background Bullous pemphigoid (BP) is the most common autoimmune blistering disease. BP180 is the primary autoantigen of BP, and in a portion of BP cases,…”
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Oral mucosa is a useful substrate for detecting autoantibodies of mucous membrane pemphigoid by Kamaguchi, M., Iwata, H., Ujiie, H., Izumi, K., Natsuga, K., Nishie, W., Asaka, T., Kitagawa, Y., Shimizu, H.

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Linagliptin‐associated bullous pemphigoid that was most likely caused by IgG autoantibodies against the midportion of BP180 by Sakai, A., Shimomura, Y., Ansai, O., Saito, Y., Tomii, K., Tsuchida, Y., Iwata, H., Ujiie, H., Shimizu, H., Abe, R.

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Linear immunoglobulin A/immunoglobulin G bullous dermatosis with autoantibodies to LAD‐1 and laminin‐γ1 by Matsudate, Y., Yamasaki, K., Ujiie, H., Iwata, H., Kubo, Y.

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A case of subepidermal autoimmune bullous disease with autoantibodies against 200 and 290‐kDa antigens by Sawada, M., Hida, T., Ujiie, H., Iwata, H., Uhara, H.

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Lichenoid drug eruption caused by clonazepam by Muramatsu, K., Ujiie, H., Natsuga, K., Nishie, W., Shimizu, H.

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Bullous pemphigoid developed in a patient with prurigo nodularis by Yoshimoto, N., Ujiie, H., Hirata, Y., Izumi, K., Nishie, W., Shimizu, H.

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A possible association between BP230‐type bullous pemphigoid and dementia: a report of two cases in elderly patients by Zheng, M., Ujiie, H., Muramatsu, K., Sato‐Matsumura, K.C., Maeda, T., Ujiie, I., Iwata, H., Izumi, K., Nishie, W., Shimizu, H.

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