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Research 721–750 of 1000+
- Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Frontal Fibrosing Alopecia: A Review
- New developments in the molecular treatment of ichthyosis: review of the literature
- Report from the Cicatricial Alopecia Colloquium
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Pathophysiology of Alopecia Areata in the Pediatric Patient
- A Genome-Wide Association Study and Machine-Learning Algorithm Analysis on the Prediction of Facial Phenotypes by Genotypes in Korean Women
- Intraethnic variation in steroid-5-alpha-reductase polymorphisms in prostate cancer patients: a potential factor implicated in 5-alpha-reductase inhibitor treatment
- Celiac disease associated with alopecia areata: A multicenter case-control study
- The Association Between Polycystic Ovary Syndrome and Its Dermatological Manifestations
- Frontal Fibrosing Alopecia and the Role of Cosmeceuticals in Its Pathogenesis
- Männlicher Haarausfall – was uns unsere Gene verraten
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- The First Visit: Consult and Workup Before Sperm Banking
- Андрогенетическая алопеция: патогенетические механизмы и подходы к лечению
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Frontal fibrosing alopecia: a disease that remains enigmatic
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Case Report: Androgen-secreting pediatric adrenocortical tumor of uncertain malignant potential presenting with virilization in a 19-month-old girl
- BH28 Breaking the pattern: frontal fibrosing alopecia in men, a case series
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Paxbp1 is Indispensable for the Maintenance of Hair Follicle Homeostasis
- Advantages of Incomplete Digestion in Human Hair Shaft Proteomics, a Focus on Cuticular Keratins
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- The Rotterdam Study: 2012 objectives and design update
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- A PAX1 enhancer locus is associated with susceptibility to idiopathic scoliosis in females