Search
for
Sort by
Research 781–810 of 1000+
- Hair loss and its management in children
- Cutaneous Manifestations of Endocrine Disease
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- Tricorrexis nodosa localizada
- An unusual case of quadruple polyorchidism in a human cadaver mimicking bilateral lipoma
- Delayed Puberty
- P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases
- Pesticides Exposure and Risk of Hypospadias
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Unruly hair
- Sjogren-Larsson syndrome
- Short anagen syndrome: Case series and literature review
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- A rare case of woolly hair with unusual associations
- An inherited nail dystrophy principally affecting the great toenails
- Hair loss
- Breast Embryology, Anatomy, and Physiology
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome
- Syphilis: today
- Two Cases of Hypertrichosis Cubiti
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- A Clinical Review of Trichorrhexis Nodosa
- Hyperpigmentation in a child as a clue to chikungunya
- Pallister-Killian Syndrome
- Introducción a la cirugía plástica reconstructiva conceptos básicos y aplicaciones
- Solitary Basaloid Follicular Hamartoma: A Report of Two Cases.