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Research 181–210 of 1000+
- Olympic and Board Game Dermatology: Exploring Eponyms Linking Skin Conditions to Sports and Strategy Games
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Skin manifestations among<i>GATA2</i>-deficient patients
- Congenital atrichia and hypotrichosis
- Alopecia - the search for novel agents continues
- Acne and acneiform eruptions
- The Skin and Subcutaneous Tissues
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Do you know this syndrome? * Você conhece esta síndrome? *
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- Ischemic onycholysis of the hands
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- The Genetics of Human Skin Disease
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Diseases of Periocular Hair
- Benefit-Risk Assessment of GLP-1 Receptor Agonists: Implications for Dermatologists and Plastic Surgeons
- Melanocytes and Vitiligo (and Hair Graying)
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Skin Manifestations in Primary Immunodeficient Children
- Hair Loss in Children
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Cutaneous findings and systemic associations in women with polycystic ovary syndrome
- Dermatology consultations significantly contribute to efficient care of hospitalized patients: A prospective study of dermatology inpatient consults at a tertiary care center
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Hair Growth Cycle Is Arrested in SCD1 Deficiency by Impaired Wnt3a-Palmitoleoylation and Retrieved by the Artificial Lipid Barrier
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome