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Research 241–270 of 1000+
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Ptosis in childhood
- Hairless Suppresses Vitamin D Receptor Transactivation in Human Keratinocytes
- TRP Channels in Skin Biology and Pathophysiology
- Skin Manifestations in Primary Immunodeficient Children
- Diseases of the Hair and Nails
- Clinical dermatoendocrinology: saving lives by looking at the skin.
- Hypotrichosis in a child with olmsted syndrome
- Depo-Provera: an injectable contraceptive.
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Stem-cell therapy in dermatology – Challenges and opportunities
- A rare hair loss in children: Monilethrix
- Alopecia and Thyroid Disease
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Madarosis: A marker of many Maladies
- Neonatal lupus syndrome in a Nigerian child
- Sexual Dysfunction in Alopecia Areata: A Systematic Review
- Innovative Reports on the Effects of Anabolic Androgenic Steroid Abuse—How to Lose Your Mind for the Love of Sport
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Erosive pustular dermatosis of the scalp: challenges and solutions
- Utility of trichoscopy
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- A case of unilateral congenital triangular alopecia
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- T-Cell Reconstitution after Thymus Xenotransplantation Induces Hair Depigmentation and Loss
- Current understanding and treatment of sex hormone-related hair diseases
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Systematic review of mesotherapy: a novel avenue for the treatment of hair loss
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
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