Published in Case Rep Dermatol on June 14, 2017
Discoid lupus erythematosus with dystrophic calcinosis cutis. JAAD Case Rep (2015) 0.81
Case of pachydermoperiostosis with solute carrier organic anion transporter family, member 2A1 (SLCO2A1) mutations. J Dermatol (2015) 0.77
A novel deletion mutation of the ATP2C1 gene in a family with Hailey-Hailey disease. Eur J Dermatol (2016) 0.76
Diaminodiphenyl Sulfone-Induced Hemolytic Anemia and Alopecia in a Case of Linear IgA Bullous Dermatosis. Case Rep Dermatol (2015) 0.75
Elderly-Onset Generalized Pustular Psoriasis without a Previous History of Psoriasis Vulgaris. Case Rep Dermatol (2015) 0.75
A palindromic motif in the -2084 to -2078 upstream region is essential for ABCA12 promoter function in cultured human keratinocytes. Sci Rep (2014) 0.75
Blue Rubber Bleb Nevus Syndrome Showing Vascular Skin Lesions Predominantly on the Face. Case Rep Dermatol (2015) 0.75
Generalized verrucosis caused by various human papillomaviruses in a patient with GATA2 deficiency. J Dermatol (2017) 0.75
Cimetidine/lactulose therapy ameliorates erythropoietic protoporphyria-related liver injury. Clin J Gastroenterol (2017) 0.75
Translucent basal cell carcinoma with a single cyst of the upper eyelid. J Dermatol (2017) 0.75
Immunosuppressive effect of adipose-derived stromal cells on imiquimod-induced psoriasis in mice. J Dermatol Sci (2015) 0.75
Successful epithelialization of perianal infantile hemangioma, presenting as intractable ulcers, with application of protective colostomy powder. J Dermatol (2017) 0.75
Multiple Milia as an Isolated Skin Manifestation of Dominant Dystrophic Epidermolysis Bullosa: Evidence of Phenotypic Variability. Pediatr Dermatol (2016) 0.75
Crouzon syndrome with acanthosis nigricans and prominent diffuse hyperpigmentation associated with gain-of-function A391E mutation in FGFR3 gene. J Dermatol (2020) 0.75
CARD14 Glu138 mutation in familial pityriasis rubra pilaris does not warrant differentiation from familial psoriasis. J Dermatol (2015) 0.75
Juvenile temporal arteritis with eosinophilia associated with systemic sclerosis. J Dermatol (2016) 0.75
Psoriasis Area and Severity Index is closely related to serum C-reactive protein level and neutrophil to lymphocyte ratio in Japanese patients. J Dermatol (2017) 0.75
External chalazion as reddish and intractable lower eyelid nodules in a child. J Dermatol (2016) 0.75
Successful treatment of low-dose methotrexate in combination with systemic steroids for juvenile multiple and symmetrical circumscribed morphea. J Dermatol (2017) 0.75
Subcutaneous histiocytoid Sweet's syndrome followed by acute myelocytic leukemia. J Dermatol (2016) 0.75
Mycosis fungoides bullosa associated with bullous pemphigoid. Int J Dermatol (2015) 0.75
Superficial epidermolytic ichthyosis caused by a novel KRT2 mutation. J Dermatol Sci (2015) 0.75
Incontinentia pigmenti in a male (XY) infant with long-term follow up over 8 years. J Dermatol (2017) 0.75
Two Japanese familial cases of punctate palmoplantar keratoderma caused by a novel AAGAB mutation, c.191_194delCAAA. J Dermatol Sci (2015) 0.75