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Research 691–720 of 1000+
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- Spiny keratoderma ‐ a demonstration of hair keratin and hair type keratinization
- Ulerythema ophryogenes with multiple congenital anomalies
- Yellow dots in trichoscopy: relevance, clinical significance and peculiarities
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- The Link Between Obesity and the Skin
- A rare case of woolly hair with unusual associations
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Punctate Follicular Porokeratosis
- Atrichia with papular lesions
- Follicular porokeratosis: four new cases
- [Basal cell carcinomas of the scalp. Review of 77 patients with 81 tumors].
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in <i> KRT 5 </i>
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- Discreet monilethrix: De novo mutation on the example of polish families
- Atrichia with papular lesions in Syrian siblings exposing global diagnostic challenges in genetic alopecia: A rare case report
- Multiple facial atrophic scars in childhood
- Atrichia With Papular Lesions Confirmed via Genetic Testing: A Case Report
- Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity
- Trichoscopy I: Non-Cicatricial Alopecia
- Sparse Hair on the Scalp
- Hypotrichosis in a child with olmsted syndrome
- A rare hair loss in children: Monilethrix
- Moniletherix
- The Effect of Hairless Mutant Gene on The Thymus and Skin Under The C_(57)BL/6 Genetic Background
- BRITISH ASSOCIATION OF DERMATOLOGY.
- CENTRAL STATES DERMATOLOGICAL SOCIETY
- Avian-Inspired Analogies in Dermatology
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Ichthyosis