Search
for
Sort by
Research 271–300 of 649
- PA05 A rare case of cardiocutaneous syndrome in a young child
- LB1671 Large-scale skin scRNA-seq profiling highlights distinct body site-specific ligand-receptor interactions and pathways in keratinocytes
- 413 DC-HIL+ myeloid-derived suppressor cells are elevated in the peripheral blood and lesional skin of cutaneous lupus patients
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Scorbut atypique associé à une anorexie mentale
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- Efficacy and safety of systemic monotherapy in the management of generalized pustular psoriasis: A systematic review
- 415 IL-17C: Checkpoint in innate skin immunology
- [Acitretine].
- [Oral treatment of severe psoriasis with a new aromatic retinoid (Ro 10-9359) (author's transl)].
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A Clinicopathological and Immunofluorescence study of Lichen Planus
- Antipsoriatic Activity of a New Synthetic Retinoid
- 414 A fitst-in-human study of BLZ-100 (tozuleristide) demonstrates tolerability and fluorescence contrast in skin cancer
- 412 High amphiregulin expression is a high-risk feature of acute graft-versus-host disease of the skin
- Role of caffeine in the management of androgenetic alopecia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- 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
- PLAU and SerpinB2 role in apoptosis in leprosy
- Pityriasis rubra pilaris unveiling a case of a new onset hepatitis C infection
- Decades of progressive red and yellow nodules
- Hair growth promoting effects of adipose tissue-derived stem cells
- Psoriatic Skin Lesions Induced by Certolizumab Pegol
- Dermatopathology and molecular genetics
- Granulation Tissue that Developed after a Minor Trauma in a Psoriatic Patient on Long-term Etretinate Therapy