Kwesi Teye

KRT10-nEDD-superficial: A novel phenotype characterized by vesicles and skin peeling

Norito Ishii, Kwesi Teye, Masahiro Tsutsumi, Takahiro Hamada et autres

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Immunological and genetic characterizations of pemphigoid diseases associated with immune checkpoint inhibitors: Supplementary data

Hiroshi Koga, Masahiro Tsutsumi, Kwesi Teye, Norito Ishii et autres

This dataset includes: Supplementary Materials and Methods, Supplementary Table I: The clinical information and results in each case, Supplementary Table II: Summary of clinical characteristics in ICI-pemphigoid, Supplementary Table III: Summary of histological and immunological characteristics in ICI-pemphigoid, and Supplementary table IV: …

Immunological and genetic characterizations of pemphigoid diseases associated with immune checkpoint inhibitors: Supplementary data

Hiroshi Koga, Masahiro Tsutsumi, Kwesi Teye, Norito Ishii et autres

This dataset includes: Supplementary Materials and Methods, Supplementary Table I: The clinical information and results in each case, Supplementary Table II: Summary of clinical characteristics in ICI-pemphigoid, Supplementary Table III: Summary of histological and immunological characteristics in ICI-pemphigoid, and Supplementary table IV: …

Paraneoplastic Pemphigus Mimicking Pemphigus Herpetiformis – Overlap of Two Diseases

Sakura Maeda, M. Tsutsumi, Kwesi Teye, Norito Ishii et autres

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Susceptibility to Dermatophytosis in SDR9C7 ‐Nonsyndromic Epidermal Differentiation Disorder: Observation of Cutaneous Inflammation Involving IRF4 and IL ‐17

Takuya Takeichi, Kwesi Teye, Ryo Fukaura, Takumi Sugiyama et autres

ABSTRACT SDR9C7 ‐nonsyndromic epidermal differentiation disorder (nEDD) is a form of ceramide synthesis disorder that is known to confer susceptibility to dermatophytosis. Recurrent widespread tinea corporis developed in a SDR9C7 ‐nEDD patient with homozygosity for the Japanese founder variant (c.826C>T, p.Arg276Cys) during …

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A new pathogenic variant of the SASH1 gene in a Japanese patient with a lentiginous phenotype successfully treated with Q-switched ruby laser

Eri Katsumura, Miyuki Kawamura, Kwesi Teye, Sayumi Yamamoto et autres

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Epitope Spreading in Immune Checkpoint Inhibitor–Associated Bullous Pemphigoid

Hiroshi Koga, Masahiro Tsutsumi, Kwesi Teye, Toshihiro Shirahama et autres

This case report describes a patient with immune checkpoint inhibitor–associated bullous pemphigoid and preexisting anti-BP180–C-terminus antibodies.

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Diagnostic methods and strategies for autoimmune bullous diseases

Hua Qian, Norito Ishii, Hiroshi Koga, Kwesi Teye et autres

INTRODUCTION: Autoimmune bullous disease (AIBD), showing blistering lesions on the skin and/or mucous membranes, is characterized by autoantibodies against various structural molecules present in keratinocyte cell surfaces and epidermal basement membrane zone. In addition to the clinical and pathological features, identification of …

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Correlation of BP180 , BP230 , and type VII collagen antibody titers in serum, blister fluid, erosion, and saliva in pemphigoid diseases

Hiroshi Koga, Norito Ishii, Masahiro Tsutsumi, Kwesi Teye et autres

Autoantibodies, including anti-BP180 and anti-BP230 antibodies in bullous pemphigoid (BP) and mucous membrane pemphigoid (MMP), and anti-type VII collagen (COL7) antibodies in epidermolysis bullosa acquisita (EBA), are well characterized. Enzyme-linked immunosorbent assays (ELISAs) for the detection of these antibodies in the serum …

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Improvement of immunological tests for detecting autoantibodies in patients with lamina lucida-type linear IgA bullous dermatosis

Masahiro Tsutsumi, Hiroshi Koga, Kwesi Teye, Norito Ishii et autres

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Eccrine syringofibroadenoma as a manifestation of ichthyosis follicularis‐atrichia‐photophobia syndrome‐1

Norito Ishii, Hiroshi Koga, Kwesi Teye, Takahiro Hamada et autres

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First report of ATP2A2 somatic mosaicism occurring during embryogenesis in transient acantholytic dermatosis

Emi Hiromatsu, Toshifumi Abe, Kwesi Teye, Hiroshi Koga et autres

Abstract Transient acantholytic dermatosis (TAD) is a relatively common skin disease that typically affects older individuals, which shows clinical and histologic similarities to autosomal dominant Darier disease. TAD was recently shown to be caused by somatic ATP2A2 damaging variants. In this study, …

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