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Research 931–960 of 1000+
- Clinical and dermatoscopic features of temporal triangular alopecia in infants
- 7745 Hirsutism in young girls: Beyond PCOS
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Telogen Effluvium
- A study on the clinical and hormonal profile of patients with hirsutism
- Expert consensus recommendations on appropriate serological testing for the chief complaint of alopecia
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- [Trichothiodystrophy: a morphological and biochemical study].
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Evaluating 5 alpha reductase inhibitors for the treatment of male androgenic alopecia
- Common causes of paediatric alopecia
- Trichoscopic Findings in Androgenetic Alopecia
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Severe Hyperandrogenism in A Premenopausal Woman With An Imaging-Negative Leydig Cell Tumor
- AAPS and PSRC 2016 Abstract Supplement
- Low-dose oral minoxidil in a case of short anagen syndrome
- 861 Frontal fibrosing alopecia (FFA) under dynamic optical coherence tomography (D-OCT)
- Hypertrichosis Induced by Minoxidil: A Case of Systemic Absorption from Scalp Occlusion
- Discrimination of Dysplastic Nevi from Common Melanocytic Nevi by Cellular and Molecular Criteria
- Comparative dermatology—canine endocrine dermatoses
- A rational approach to the diagnosis of polycystic ovarian syndrome during adolescence
- Trichoscopic Evaluation of Focal Non-Cicatricial Alopecia in Egyptian Children
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Sebaceous immunobiology - skin homeostasis, pathophysiology, coordination of innate immunity and inflammatory response and disease associations
- A Systemic Review on Topical Marketed Formulations, Natural Products, and Oral Supplements to Prevent Androgenic Alopecia: A Review