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Research 271–300 of 1000+
- A study on common clinical pattern of presentation of skin and hair changes in nutritional deficiencies associated with dietary fallacies in children 1 to 5 years of age
- PREVALENCE OF SKIN DISEASES IN A DERMATOLOGY OUTPATIENT CLINIC IN RIMS, KADAPA, A CROSS - SECTIONAL, RETROSPECTIVE STUDY
- Lymphomatoid granulomatosis
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Epidermis-specific ablation of claudin-1 in adult mice demonstrates the essential role of a tight junction barrier in skin homeostasis
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Off-label dermatologic uses of IL-23 inhibitors
- A case of acquired trichorrhexis nodosa after applying new hair spray
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- Topical corticosteroid in foam vehicle offers comparable coverage compared with traditional vehicles
- “Structural imprinting” of the cutaneous immune effector function
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- The molecular basis of human keratin disorders
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Porokeratotic eccrine ostial and dermal duct nevus and porokeratotic eccrine and hair follicle nevus: Is nomenclature “porokeratotic adnexal ostial nevus” more appropriate?
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- Positive Impact of Fish Oil on Diabetic and Hypercholestrolemic Skin Disorders