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Research 61–90 of 430
- Woolly Hair in Two Siblings
- Olmsted syndrome
- Dysfunction of keratinocyte adhesion
- P029 A case of atypical bullous pemphigoid
- Pityriasis rubra pilaris: a rare inflammatory dermatosis
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- [Acitretine].
- 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
- 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
- 879 IL-9 mediated human primary keratinocytes invasion is dependent on MLC controlled contractility and independent of MMP activity
- 874 Elevated expression of osteopontin splice variants in nonmelanoma skin cancer compared to normal skin and adult keratinocytes
- 893 Low-level laser therapy for the treatment of male and female-pattern hair loss: A review of literature
- Dermoscopy in General Dermatology: A Practical Overview
- 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
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- Dermatopathology and molecular genetics
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Inherited Disorders of the Hair
- Thyroid Autoimmunity in Patients with Skin Disorders
- Dermatological manifestations and associated factors in patients with Graves\' disease in Dakar