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Research 481–510 of 932
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- Alopecias in lupus erythematosus
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Evaluation of serum level of biotin and effect of biotin replacement therapy in patients with telegon effluvium
- Dissolving microneedles: Applications and growing therapeutic potential
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Generalized atrophic benign epidermolysis bullosa.
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Primary hypothyroidism with exuberant dermatological manifestations
- A Novel Device to Insert FU Grafts into Premade Sites
- Redefining the “crown”: Approaching chemotherapy‐induced alopecia among Black patients with breast cancer
- Kerion Celsi in a Nepalese Boy: An Underdiagnosed Cause of Scalp Swelling
- Differentiating central centrifugal cicatricial alopecia and androgenetic alopecia in african american men: report of three cases.
- Nanogenerators in Biomedical Frontiers: Revolutionizing Self-Powered Healthcare Systems
- Persistent scurvy after vitamin C supplementation in a high-risk patient: a case report
- Indigenous Women in North Africa: Amazigh Women and Argan Oil
- Cutaneous manifestations of endocrine diseases in children
- Cutaneous manifestations in patients attending the hematology clinic at King Fahd Hospital of the University during a 13 week-period
- Successful management of a large feline skin defect using xenogeneic bovine amniotic membrane: a case report
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Impact of different mating and surgical protocols on the establishment of a mouse model for fetal scarless skin healing
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Bioactives in Nutricosmetics: A Focus on Caffeine from Tea to Coffee
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa