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Research 751–780 of 1000+
- Diagnoseverzögerung, komorbide Hidradenitis suppurativa und die prognostische Bedeutung bakterieller Kulturen bei Folliculitis decalvans: eine Kohortenstudie
- Medications
- Gene expression patterns during palatal shelf fusion
- Melanocytes: The new Black
- Malignant epithelial tumors: Part II. Therapy and prevention
- Efficacy and safety of systemic monotherapy in the management of generalized pustular psoriasis: A systematic review
- Dermatological drugs and topical agents
- A Combinatorial Tweet Clustering Methodology Utilizing Inter and Intra Cosine Similarity
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- The Effect of Finasteride on the Risk of Acute Urinary Retention and the Need for Surgical Treatment among Men with Benign Prostatic Hyperplasia
- The Effect of Finasteride in Men with Benign Prostatic Hyperplasia
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Susceptibility variants for male-pattern baldness on chromosome 20p11
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Urinary Retention in Patients with BPH Treated with Finasteride or Placebo over 4 Years
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Androgenetic Alopecia: Identification of Four Genetic Risk Loci and Evidence for the Contribution of WNT Signaling to Its Etiology
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Genome-wide Scan and Fine-Mapping Linkage Study of Androgenetic Alopecia Reveals a Locus on Chromosome 3q26
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Genetics and other factors in the aetiology of female pattern hair loss
- Traction alopecia: 2% topical minoxidil shows promise. Report of two cases
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i>
- Acute ‘relaxer’-associated scarring alopecia: a report of five cases
- Continued improvement in pressure-flow parameters in men receiving finasteride for 2 years
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Investigation of six novel susceptibility loci for male androgenetic alopecia in women with female pattern hair loss