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Research 31–60 of 326
- Eruptive Vellus Hair Cysts: Report of a New Case with Immunohistochemical Study and Literature Review
- Oral retinoids-present status
- Cicatricial (Scarring) Alopecias
- Dermatopathology and molecular genetics
- Pluripotent Stem Cell Technology: A Promising Remedy for Hypopigmentation Disorders
- Congenital Atrichia: A Case Report
- Sjogren-Larsson syndrome
- Biology and Genetics of Hair
- 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
- The Genetics of Human Skin Disease
- Secondary cicatricial and other permanent alopecias
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Hair loss in children.
- Progeroide Syndrome
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- 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
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Breaking the biofilm- A persistent case of deep pyoderma in a Bullykutta dog
- Inherited Epidermolysis Bullosa: A Clinical Case
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Fatores nutricionais e resistência da haste capilar: estudo clínico piloto
- Retinoids - new uses and new synthetic agents
- Congenital atrichia and hypotrichosis
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot