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Dermatologica|January 1, 1984
Facial hemiatrophy in a patient with systemic sclerodermaK Nomura, Y Yagihashi, S Chiyoya, et al.Dermatology (Basel, Switzerland)|January 1, 1997
Eccrine syringofibroadenomatosis in two patients with bullous pemphigoidK Nomura, I HashimotoJournal of Maxillofacial Surgery|June 1, 1986
Lentigo maligna melanoma with deep invasion along the mental nerveY Sawada, K Nomura, I HashimotoJournal of Dermatological Science|October 1, 1993
Gene expression of collagenase and stromelysin in skin fibroblasts derived from dystrophic epidermolysis bullosaT Sugawara, K Nomura, I HashimotoArchives of Dermatological Research|January 1, 1995
Expression of collagenase and stromelysin in skin fibroblasts from recessive dystrophic epidermolysis bullosaT Sato, K Nomura, I HashimotoDermatologica|January 1, 1983
Genetic counseling for skin diseases. A statistical analysis of 182 casesI Hashimoto, Y Katabira, M Sugawara, et al.Clinical Physiology and Biochemistry|January 1, 1990
Interleukin-1 levels in blister fluids of some skin diseases with blister formationT Imaizumi, K Nomura, I Hashimoto, et al.The American Journal of Dermatopathology|June 8, 2001
Atrichia with papular lesions: electron microscopic observations of cystic lesionsK Nomura, I Hashimoto, G Takahashi, et al.Acta Dermato-Venereologica|July 1, 1997
Dominant dystrophic epidermolysis bullosa albopapuloidea Pasini -- ultrastructural observations of albopapuloid lesions and a type VII collagen DNA polymorphism study of a familyK Nomura, K Umeki, D Sawamura, et al.The Journal of Dermatology|May 1, 1993
Clinical criteria for differentiating between recessive and dominant forms of dystrophic epidermolysis bullosa, elaborated from an analysis of 119 casesK Nomura, T Imaizumi, T Sato, et al.Pageof 415