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Research 151–180 of 1000+
- Pathology in Practice
- Alopecia Areata: A Comprehensive Review of Pathogenesis, Diagnosis, and Emerging Therapeutics
- No genetic support for a contribution of prostaglandins to the aetiology of androgenetic alopecia
- Androgenetic alopecia in men and women
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Role of genetics and sex steroid hormones in male androgenetic alopecia and female pattern hair loss: An update of what we now know
- Meta-analysis identifies novel risk loci and yields systematic insights into the biology of male-pattern baldness
- The Noggin null mouse phenotype is strain dependent and haploinsufficiency leads to skeletal defects
- Skin diseases associated with atopic dermatitis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- HAIR LOSS IN WOMEN
- Turner's syndrome associated with psoriasis and alopecia areata
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- Safe Selection of Genetically Manipulated Human Primary Keratinocytes with Very High Growth Potential Using CD24
- Genetics of Structural Hair Disorders
- Research Relevant Conditions and Pathology in Nonhuman Primates
- Update on the Genetics of Androgenetic Alopecia, Female Pattern Hair Loss, and Alopecia Areata: Implications for Molecular Diagnostic Testing
- Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Genetic Basis of Pigmentation and Its Disorders
- Pediatric dermatoses pattern at a Brazilian reference center
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Dramatic Clinical Improvement With Biotin Mega‐Dose Therapy in a Neonate With Holocarboxylase Synthetase Deficiency
- High-throughput Sequencing to Identify Monogenic Etiologies in a Preselected Polycystic Ovary Syndrome Cohort
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle
- Lipedematous Alopecia: Clinical, Histopathological, and Trichoscopic Findings of a Single Case and Review of the Literature
- Clinical Impact of Molecular Diagnostics in Endocrinology
- Management and Genetics of Alopecia Areata within the USA: A Cross-Sectional Study of All of Us