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Research 30 of 241
- NEMO syndrome (incontinentia pigmenti) and systemic lupus erythematosus: A new disease association
- Nemolizumab Treatment for Severe Atopic Dermatitis Led to the Simultaneous Improvement of Coexisting Refractory Alopecia Areata: A Case Report
- A case of atopic dermatitis with self‐healing acute diffuse and total alopecia during nemolizumab treatment
- Farmácia do Lago, Porto e nos Serviços Farmacêuticos do Nemocnica Akademika Ladislava Dérera (Kramáre Hospital), Eslováquia
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Biologics in the management of childhood atopic dermatitis
- 1430 Modeling the onset of senescence associated secretory phenotype predicts therapeutic targets
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- The patient journey in prurigo nodularis: what lies ahead
- Three-Dimensional Analysis of Cell Division Orientation in Epidermal Basal Layer Using Intravital Two-Photon Microscopy
- Selective Androgen Receptor Modulator, YK11, Up-Regulates Osteoblastic Proliferation and Differentiation in MC3T3-E1 Cells
- Five-year efficacy of finasteride in 801 Japanese men with androgenetic alopecia
- Differentiation and Apoptosis in Pilomatrixoma
- Long-term (10-year) efficacy of finasteride in 523 Japanese men with androgenetic alopecia
- Minoxidil-induced lung disease, masquerading as hypersensitivity pneumonitis
- Aggressive squamous cell carcinoma developing in a giant epidermal cyst of the abdomen
- Hair loss due to treatment of multiple sclerosis
- Dermatological Issues in a Child with Diabetes Mellitus
- Alopecia - overview, causes and current treatment options
- Differential diagnosis of alopetia in children and adolescents
- 公表学術論文等リスト 2018
- New possibilities extemporaneous preparation in dermatology - innovative foam base Espumil
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- XEDAR activates the non-canonical NF-κB pathway
- A new mutation resulting in the truncation of the TRAF6-interacting domain of XEDAR: a possible novel cause of hypohidrotic ectodermal dysplasia: Figure 1
- Human hair follicle and interfollicular keratinocyte reactivity to mouse HPV16-transformed cells: An in vitro study
- A Case of Familial Male-limited Precocious Puberty with a Novel Mutation
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Mister XX