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Research 751–780 of 1000+
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Impact of different mating and surgical protocols on the establishment of a mouse model for fetal scarless skin healing
- BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Chronic Overlapping Pain Conditions and Nociplastic Pain
- Novel insights into cardiocutaneous syndromes
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- Síndrome de ovario poliquístico: la distancia anogenital como marcador del entorno androgénico prenatal y revisión y comparación de los criterios diagnósticos
- The role of skin macrophages under conditions of stress and injury: ultraviolet irradiation and wound healing
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- Il-10 family members as novel responders to genotoxic stress
- The Cutaneous Epidermal Growth Factor Network: Can it be Translated Clinically to Stimulate Hair Growth? - eScholarship
- Unravelling the Genetics of Physical Appearance Variation in Modern Humans
- Reprogramming the wound microenvironment: identity remodeling strategies for fibroblasts, keratinocytes, and macrophages
- Author response: scRNA+TCR-seq reveals the proportion and characteristics of dual TCR Treg cells in mouse lymphoid and non-lymphoid tissues
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Finding Long-COVID: Temporal Topic Modeling of Electronic Health Records from the N3C and RECOVER Programs
- From hair colour to diagnosis
- Dumhetens rum i bildningens mitt
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Solidariedade e plasticidade fenotípica entre indivíduos de Thunbergia grandiflora Roxb. e Russelia equisetiformis Schltdl. & Cham.
- 304 Sephardic Ancestry in Recessive Dystrophic Epidermolysis Bullosa Individuals Carrying the Prevalent c.6527insC Mutation
- Laser-Induced Koebner-Related Skin Reactions: A Clinical Overview
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Systemic testosterone induces structural, immunological, and sex steroid receptor changes in human XX skin
- Ivarmacitinib in atopic dermatitis presenting with prurigo nodularis-like lesions and alopecia areata: a case report
- Impaired turnover of autophagolysosomes in cathepsin L deficiency
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Testosterone enantate