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Research 31–60 of 367
- Eruptive Vellus Hair Cysts: Report of a New Case with Immunohistochemical Study and Literature Review
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Sjogren-Larsson syndrome
- Severe Hypernatremia as Presentation of Netherton Syndrome
- Oral retinoids-present status
- Cicatricial (Scarring) Alopecias
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Keratosis follicularis spinulosa decalvans in a female
- Dermatopathology and molecular genetics
- Pluripotent Stem Cell Technology: A Promising Remedy for Hypopigmentation Disorders
- Congenital Atrichia: A Case Report
- Biology and Genetics of Hair
- The Genetics of Human Skin Disease
- Trias of keratosis pilaris, ulerythema ophryogenes and 18p monosomy: Zouboulis syndrome
- Congenital atrichia and hypotrichosis
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Adalimumab improves health-related quality of life (HRQoL) in patients with moderate to severe hidradenitis suppurativa (HS): Results from the first 12 weeks of PIONEER II
- Androgenic pattern presentation of scarring and inflammatory alopecia
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- A Newborn With Hair Loss
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report
- Inherited Epidermolysis Bullosa: A Clinical Case
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Acquired epidermodysplasia verruciformis in a heart transplant patient
- Accident by a rare wild animal with skin injury
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin