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Research 61–90 of 367
- Management of congenital ichthyoses: European guidelines of care, part two
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Secondary cicatricial and other permanent alopecias
- Hair loss in children.
- The spectrum of nephrocutaneous diseases and associations
- Marie-unna hereditary hypotrichosis
- Progeroide Syndrome
- Dermatology
- A survey study to assess prevalence rate of premature grey hair in school-going children aged between 5 to 15 years
- Grand challenges in dermatologic drug discovery: four priorities to transform skin disease treatment
- Breaking the biofilm- A persistent case of deep pyoderma in a Bullykutta dog
- Fatores nutricionais e resistência da haste capilar: estudo clínico piloto
- Retinoids - new uses and new synthetic agents
- The human keratins: biology and pathology
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Nutrition and hair
- Dermatoscopy of hair shaft disorders
- The Spectrum of Skin Disease Among Indian Children
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Congenital hair loss disorders: Rare, but not too rare
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Consensus on the use of oral isotretinoin in dermatology - Brazilian Society of Dermatology
- Change of the diagnostic distribution in applicants to dermatology after COVID ‐19 pandemic: What it whispers to us?
- Ashy Dermatosis
- Treatment of frontal fibrosing alopecia and lichen planopilaris
- Molecular Genetics of Alopecias
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients