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Research 721–750 of 1000+
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Dermatology Patient Support Groups
- Phenotypic Characterization of Patients with Polycystic Ovary Syndrome in a Population from the Ecuadorian Andes: A Cross-Sectional Study
- Melanocytes in regenerative medicine applications and disease modeling
- Conference 2022, The Sequel
- Efficacy of platelet-rich plasma in the treatment of thin endometrium: a meta-analysis of randomized controlled trials
- Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation
- Presentations of Cutaneous Disease in Various Skin Pigmentations: Keratosis Pilaris
- Isolated patchy heterochromia with pili annulati features on light and electron microscopy
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- A Clinical Review of Trichorrhexis Nodosa
- Pigmented Epithelioid Melanocytoma (PEM)/Animal Type Melanoma (ATM): Quest for an Origin. Report of One Unusual Case Indicating Follicular Origin and Another Arising in an Intradermal Nevus
- Cellular Senescence and Aging in Myotonic Dystrophy
- The distribution of melanocytes and the degradation of melanosomes in fetal hair follicles
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Bubble Hair Deformity Induced by Bathroom Heating Lamp: A Report of Two Cases
- Understanding Polycystic Ovary Syndrome: A Comprehensive Guide
- Fibrodysplasia Ossificans Progressiva (FOP): A Segmental Progeroid Syndrome
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma
- Analogs of human genetic skin disease in domesticated animals
- Current Genetics in Hair Diseases
- Clinical and dermoscopic patterns of childhood alopecia areata in a tertiary care centre in North India
- Mining and analysis of adverse event signals of isotretinoin based on the real-world data of FAERS database
- Ichthyosis hystrix
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Endocrinology
- Novel insights into the pathways regulating the canine hair cycle and their deregulation in alopecia X