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Research 211–240 of 1000+
- Alopecia in Epidermolysis Bullosa
- The clinical spectrum of parathyroid disease
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Inconsolable Crying in Infants: Differential Diagnosis in the Pediatric Emergency Department
- Alopecia and Its homoeopathic treatment
- Overexpression of HE4/WFDC2 gene in mice leads to keratitis and corneal opacity
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Disorders of the skin appendages
- Australasian Society for Dermatology Research Meeting, May 2006
- Australasian Society for Dermatology Research Meeting, May 2007
- Syndromes of Severe Insulin Resistance (SSIRs)
- Dermoscopy — 4th Conference of the Section of Dermoscopy and Other Skin Imaging Techniques (DiTOS) of the Polish Dermatological Society — Abstracts
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Genetic prediction of male pattern baldness
- Atlas of Geriatric Dermatology
- Cycle pilaire et alopécie X chez le chien
- Skin melanocytes: biology and development
- Dermatoses of pregnancy
- Cutaneous reactions to recombinant cytokine therapy
- Dermoscopy Research—An Update
- Medical dermatologic conditions in transgender women
- Improving Posttraumatic Facial Scars
- A Comprehensive Review of Management of Patients with Infertility having Polycystic Ovarian Syndrome
- Poster session
- Cutaneous signals of immune system disease
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Trichoscopy in genetic hair shaft abnormalities
- High-sulfur protein deficient human hair: clinical aspects and biochemical study of two unreported cases of a variant type of trichothiodystrophy
- Low-sulfur hair syndrome associated with UVB photosensitivity and testicular failure
- An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review