Search
for
Sort by
Research 391–420 of 1000+
- Spontaneous hair hyperpigmentation in response to vitamin intake in pregnancy—A clue for homocystinuria
- Melanotrichoblastoma: A Histopathological Case Report of a Rare Pigmented Variant of Trichoblastoma
- Clinical Features and Treatment Options of Vogt-Koyanagi-Harada Disease
- Photobiomodulation for Skin Pigmentation Disorders: A Dual-Function Treatment
- Apoptosis in Hair and Skin: A Review
- Segmental Vitiligo
- Disorders of pigmentation in infants and children
- Langerhans' cells in hair follicles of the depigmenting C57Bl/Ler-vit.vit mouse. A model for human vitiligo
- The Role of Mast Cells in Skin Aging: Mechanisms and Therapeutic Advances
- Neurological Mechanisms Exploration and Therapeutic Targets in Segmental Vitiligo Accompanied by White Hair
- Editorial: Advances and novel intervention in photodermatology
- Performance exploration of multi-gene panels of alopecia areata susceptibility and drug-binding targets
- Particularidades dermatológicas, fisiológicas e as dermatoses na pele negra
- Developmental characteristics of cutaneous telocytes in late embryos of the silky fowl
- Nearly complete hair re-pigmentation in an older patient treated with hydroxyurea for essential thrombocytosis
- Applications of Human Pluripotent Stem Cell–Derived Skin Organoids in Dermatology
- Perinevoid Alopecia: Report of Two Cases and Literature Review
- Determining the Secondary Role of UV Light in Swimmers Melanoma Genesis
- Anatomy of the Integumentary System
- LB1053 Dysregulation of antioxidant enzyme PRDX5 in alopecia areata
- The secondary role of UV light in swimmers melanoma genesis
- Pluripotent Stem Cell Technology: A Promising Remedy for Hypopigmentation Disorders
- Structure and Development of the Skin and Cutaneous Appendages
- Lentiginous melanoma. A clinically malignant entity that histopathologically seems benign. Case study harbouring BRAF V 600R mutation
- Resident Stem Cell in Skin
- Woolly Antics between the Sheaths
- Colourless side of the <i>nude</i> mutation: Foxn1 and hair pigmentation
- The Hair Follicle Stem Cell as the Paradigm Multipotent Adult Stem Cell
- Models for Skin Cancer
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature