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Research 61–90 of 386
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Oral retinoids-present status
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- 878 Individual variation in balance between platelet-secreted growth factors causing contradictory effects on hair follicle could potentially impact response to PRP therapy in patients with scalp hair loss
- 876 Imaging nanoscale changes in desmosome protein organization
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- 874 Elevated expression of osteopontin splice variants in nonmelanoma skin cancer compared to normal skin and adult keratinocytes
- Retinoids - new uses and new synthetic agents
- Hair growth promoting effects of adipose tissue-derived stem cells
- Frontal fibrosing alopecia: treatment with oral dutasteride and topical pimecrolimus
- The non-neuronal and nonmuscular effects of botulinum toxin: an opportunity for a deadly molecule to treat disease in the skin and beyond
- Dermatopathology and molecular genetics
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Thyroid Autoimmunity in Patients with Skin Disorders
- Dermatological manifestations and associated factors in patients with Graves\' disease in Dakar
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- 892 Behavior of the two circulating androgens testosterone and DHEA and their main intracellular metabolites in an androgen-sensitive sebocyte cell line
- Circumferential acute limited exanthematous pustulosis
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- The human keratins: biology and pathology
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Keratin disorders: from gene to therapy
- Biology and Genetics of Hair
- Clinical and biological impact of the exposome on the skin
- Beyond Expectations
- New Activators and Inhibitors in the Hair Cycle Clock: Targeting Stem Cells’ State of Competence