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Research 31–60 of 1000+
- Swastyayanam of Bhela indriya Sthana - an explorative study
- Inherited Epidermolysis Bullosa: A Clinical Case
- MECHANISM OF PROTEINURIA
- Biology and Genetics of Hair
- Congenital hair loss disorders: Rare, but not too rare
- Severe Physical Complications among Survivors of Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis
- The Pathogenesis of Alopecia Areata in Rodent Models
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Inherited Disorders of the Hair
- Case Report: Successful treatment of pediatric alopecia universalis with ritlecitinib after failure of baricitinib
- Lupus erythematosus: systemic and cutaneous manifestations
- BMP-FGF Signaling Axis Mediates Wnt-Induced Epidermal Stratification in Developing Mammalian Skin
- Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations
- Alopecia.
- Targeted expression of SV40 T antigen in the hair follicle of transgenic mice produces an aberrant hair phenotype
- The eye and the skin in endocrine metabolic diseases
- Diseases of Periocular Hair
- The spectrum of nephrocutaneous diseases and associations
- Cosmetic Surgery Considerations in the Female Patient
- Interpretation of Laboratory Data and General Physical Examination by Pharmacists
- Cutaneous drug reactions
- Geriatric Dermatologic Therapy
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Survey on Alopecia Areata Patients’ Reported Factors that Determine Severity of Alopecia Areata: A Nationwide Multicenter Study
- Skin Disorders in Athletes: Professional and Recreational Sports
- Secondary cicatricial and other permanent alopecias
- Olympic and Board Game Dermatology: Exploring Eponyms Linking Skin Conditions to Sports and Strategy Games
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review