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Research 151–180 of 1000+
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Roles of tumor suppressors in regulating tumor-associated inflammation
- What may be the markers of the male equivalent of polycystic ovary syndrome?
- Trichoscopy in Hair Shaft Disorders
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Physiology and Medical Treatments for Alopecia
- Polycystic Ovarian Syndrome: The Androgenized Adolescent
- Treatment of Hair Loss
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Approach to the adult female patient with diffuse nonscarring alopecia
- <i>WNT10A</i> , dermatology and dentistry
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Disease causing homozygous variants in the human hairless gene
- An Ayurvedic Approach to Palitya (Premature Greying of Hair)
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Inherited Epidermolysis Bullosa: A Clinical Case
- Oral Presentations
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment