I. Nemoto-Hasebe

发表

Clinical effect of delgocitinib 0.5% ointment on atopic dermatitis eczema intensity and skin barrier function

K. Kabashima, M. Abe, O. Nemoto, 2021, Journal of Cutaneous Immunology and Allergy.

Japanese-specific filaggrin gene mutations in Japanese patients suffering from atopic eczema and asthma.

M. Nishimura, M. Akiyama, H. Shimizu, 2010, The Journal of investigative dermatology.

Specific filaggrin mutations cause ichthyosis vulgaris and are significantly associated with atopic dermatitis in Japan.

M. Akiyama, H. Shimizu, C. Palmer, 2008, The Journal of investigative dermatology.

A novel PTPN11 missense mutation in a patient with LEOPARD syndrome

M. Akiyama, H. Shimizu, H. Ujiie, 2009, The British journal of dermatology.

FLG mutation p.Lys4021X in the C‐terminal imperfect filaggrin repeat in Japanese patients with atopic eczema

M. Akiyama, H. Shimizu, T. Nomura, 2009, The British journal of dermatology.

Analysis of Taiwanese ichthyosis vulgaris families further demonstrates differences in FLG mutations between European and Asian populations

M. Akiyama, H. Shimizu, T. Nomura, 2009, The British journal of dermatology.

Prevalent and rare mutations in the gene encoding filaggrin in Japanese patients with ichthyosis vulgaris and atopic dermatitis.

M. Akiyama, H. Shimizu, C. Palmer, 2009, The Journal of investigative dermatology.

Desmoglein1 and BP 180 ELISA indexes correlating with disease activity in a patient with coexisting pemphigus foliaceus and bullous pemphigoid

T. Hashimoto, B. Ohyama, K. Sato-Matsumura, 2009, Clinical and experimental dermatology.

CD30‐positive primary cutaneous anaplastic large‐cell lymphoma and definite squamous cell carcinoma

H. Shimizu, T. Shimizu, T. Yanagi, 2009, Clinical and experimental dermatology.

Diagnosis of Hailey-Hailey disease facilitated by DNA testing: a novel mutation in ATP2C1.

M. Akiyama, H. Shimizu, Hiroyuki Nakamura, 2008, Acta dermato-venereologica.

Clinical severity correlates with impaired barrier in filaggrin-related eczema.

M. Akiyama, H. Shimizu, T. Nomura, 2009, The Journal of investigative dermatology.

Novel mutation p.Gly59Arg in GJB6 encoding connexin 30 underlies palmoplantar keratoderma with pseudoainhum, knuckle pads and hearing loss

M. Akiyama, H. Shimizu, A. Ishiko, 2009, The British journal of dermatology.

Chromosome 11q13.5 variant: No association with atopic eczema in the Japanese population.

M. Akiyama, H. Shimizu, T. Nomura, 2010, Journal of dermatological science.

Circumscribed palmar hypokeratosis: correlation between histopathological patterns and dermoscopic findings

H. Shimizu, Y. Fujita, W. Nishie, 2012, The British journal of dermatology.

Extremely severe palmoplantar hyperkeratosis in a generalized epidermolytic hyperkeratosis patient with a keratin 1 gene mutation.

M. Akiyama, H. Shimizu, K. Izumi, 2011, Journal of the American Academy of Dermatology.

Wells' syndrome associated with chronic myeloid leukaemia.

H. Shimizu, Y. Fujita, W. Nishie, 2013, Acta dermato-venereologica.