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Research 61–90 of 524
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- Evidence for two independent functional variants for androgenetic alopecia around the androgen receptor gene
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Disease causing homozygous variants in the human hairless gene
- The oestrogen receptor 2 (<i>ESR2</i>) gene in female-pattern hair loss: replication of association with rs10137185 in German patients
- Serum sickness–like reaction in children: A retrospective review
- Genome-Wide Association Study of Alopecia Areata in Taiwan: The Conflict Between Individuals and Hair Follicles
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- The alopecia areata phenotype is induced by the water avoidance stress test in <i>cchcr1</i>-deficient mice
- Measuring the impact on quality of life of infants with atopic dermatitis in a dedicated clinic
- Treatment of frontal fibrosing alopecia: literature review 2020-2025
- The Rotterdam Study: 2018 update on objectives, design and main results
- The Rotterdam Study: 2016 objectives and design update
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- COVID-19 and Sex Differences
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Alopecia areata
- An Update of Congenital Adrenal Hyperplasia
- Clinical manifestations of cutaneous lupus erythematosus
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Genetic prediction of male pattern baldness
- Cryptic Patterning of Avian Skin Confers a Developmental Facility for Loss of Neck Feathering
- Congenital Adrenal Hyperplasia
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Dermatoses of Pregnancy - Clues to Diagnosis, Fetal Risk and Therapy
- Dermatologic manifestations of endocrine disorders