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Research 61–90 of 1000+
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Unruly hair
- Hair loss and its management in children
- 860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Diseases of Periocular Hair
- Dermatoscopy of hair shaft disorders
- Management of congenital ichthyoses: European guidelines of care, part two
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Acquired Uncombable Hair
- Psychotrichology: psychosomatic aspects of hair diseases
- Effect of Oral Minoxidil on Monilethrix
- Superficial temporal artery flap for reconstruction of complex facial defects: A new algorithm
- Ectrodactyly, Soft‐Tissue Syndactyly, and Nodulocystic Acne: Coincidence or Association?
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Madarosis
- Alopecias
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- From the Elephant Man to Barbie Girl: Dissecting the Freak from the Margins to the Mainstream
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Alopecia Areata with Renal Dysgenesis
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- A Case of IFAP Syndrome with Severe Atopic Dermatitis