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Research 841–870 of 1000+
- Diagnostic challenges in determining alopecia areata
- Efficacy, Safety, and Real-World Aspects of Janus Kinase Inhibitors to Treat Patients With Alopecia Areata
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Simultaneous Alopecia Areata in Identical Twins: First Case Reported in Saudi Arabia
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- TỔNG QUAN VỀ SINH HỌC CỦA TÓC, MÔ HÌNH NGHIÊN CỨU VÀ ĐÁNH GIÁ KHẢ NĂNG MỌC LẠI TÓC TRÊN IN-VITRO VÀ IN-VIVO
- Novel immune mechanisms in androgenetic alopecia
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Cancer risk in polycystic ovary syndrome patients: Common treatments and future perspectives
- Acne Keloidalis Nuchae
- Spectrum of clinical manifestations of SLE patients from India and its correlation with KIR gene polymorphism
- Uloga folikularnih matičnih stanica u patofiziologiji alopecije areate
- Trichothiodystrophy in a child with occult learning disorder
- Mechanisms of Hair Graying: Incomplete Melanocyte Stem Cell Maintenance in the Niche
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Patologías dermatológicas de origen nutricional en los pequeños animales: una revisión
- Diagnosis and treatment of trichotillomania
- Current and future pharmacotherapy for alopecia areata
- Keratinocyte Stem Cells: Role in Aging
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome
- A Comprehensive Review On: Polycystic Ovarian Disease and It’s Impact on Health Care of Female
- Central Centrifugal Cicatricial Alopecia
- Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death
- Targeted Skin Overexpression of the Mineralocorticoid Receptor in Mice Causes Epidermal Atrophy, Premature Skin Barrier Formation, Eye Abnormalities, and Alopecia
- Taiwanese Dermatological Association consensus on the diagnosis and management of alopecia areata
- Parental Uveitis Influences Offspring With an Increased Susceptibility to the Experimental Autoimmune Uveitis
- Copper Deficiency a New Reason of Androgenetic Alopecia?
- Phenotypic Heterogeneity in 5 Japanese Patients with an Identical Point Mutation in the Vitamin D Receptor Gene
- A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man