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Research 121–150 of 1000+
- Guidelines for the diagnosis and treatment of male-pattern and female-pattern hair loss, 2017 version
- Severe form of keratitis–ichthyosis–deafness (KID) syndrome associated with septic complications
- Biotin deficiency in an infant fed with amino acid formula and hypoallergenic rice
- A case of monilethrix caused by novel compound heterozygous mutations in the desmoglein 4 (DSG4) gene
- Alopecia Areata Associated with Myasthenia Gravis and Thymoma: A Case of Alopecia with Marked Improvement Following Thymectomy and High Level Prednisolone Administration
- Severe dermographism after topical therapy with diphenylcyclopropenone for alopecia universalis
- Alopecia Universalis Following Two Sequential Traffic Accidents : Possible Association with Increased Th1 and Th17 Cells and Decreased Th2 Cells
- Neurosarcoidosis Occurring 6 Years after Onset of Vogt-Koyanagi-Harada Disease
- A case of refractory alopecia areata successfully treated by combining delgocitinib ointment with excimer laser
- Influence of Scalp Problems on Physical Properties of Hair and Their Prevention by Plant Extracts
- Case of follicular mucinosis: Nestin‐expression in mucin‐producing cells
- Infiltrative Erythemas and Nodules on a Unilateral Cheek Following Inappropriate Use of a Topical Steroid
- Characterization of the lipid composition at the proximal root regions of human hair
- Long-term safety and efficacy of dutasteride in the treatment of male patients with androgenetic alopecia
- Changes in structure and geometric properties of human hair by aging
- Age‐dependent changes in damage processes of hair cuticle
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Characterization of hair lipid images by argon sputter etching-scanning electron microscopy
- Alopecia universalis after injection of messenger RNA COVID-19 vaccine. A case report
- Rehabilitation therapy for a severe case of coronavirus disease 2019: a case report
- Clinical features of non‐classical 21‐hydroxylase deficiency after normal newborn mass screening
- Case 22
- Ethanol Patch Test—A Simple and Sensitive Method for Identifying ALDH Phenotype
- Hair Regeneration Therapy: Application of Adipose-Derived Stem Cells
- Biotin Deficiency in an Infant Fed with Amino Acid Formula
- Cervical cancer metastasis to the scalp presenting as alopecia neoplastica
- Evaluation of the quality of life of lupus erythematosus patients with cutaneous lesions in Japan
- Trichoscopic Findings of Erosive Pustular Dermatosis of the Scalp Associated with Gefitinib
- Folliculosebaceous cystic hamartoma with hair shaft fragments.
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation