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Research 631–660 of 1000+
- When one size does not fit all: Reconsidering PCOS etiology, diagnosis, clinical subgroups, and subgroup-specific treatments
- E-Poster
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Endocrinology
- Association of Acne Tarda with Endocrinological Disorders
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Hair & Cutaneous Development
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Werewolf, There Wolf: Variants in Hairless Associated with Hypotrichia and Roaning in the Lykoi Cat Breed
- A rare cutis verticis gyrata secondary to cerebriform intradermal nevus: case report and literature review
- Association between PITX2 polymorphism and androgenetic alopecia in the Indian population
- Development of Hair Fibres
- Blank Spots in the Map of Human Skin: The Challenge for Xenotransplantation
- TRP Channels in Skin Biology and Pathophysiology
- Aging of the hair follicle pigmentation system
- Melanoma: Genetic Abnormalities, Tumor Progression, Clonal Evolution and Tumor Initiating Cells
- A Comprehensive Review of Acne Vulgaris
- Abstracts
- Trailing the Path to Preventive Oncology
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Toward Elucidating Epigenetic and Metabolic Regulation of Stem Cell Lineage Plasticity in Skin Aging
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Cell-free fat extract improves embryo development and clinical outcomes in older women with previous in-vitro fertilization failure
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- A homozygous missense variant in type I keratin <i>KRT25</i> causes autosomal recessive woolly hair
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation