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Research 181–210 of 1000+
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Amino Acid Content of Damaged Human Hair
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Management of congenital ichthyoses: European guidelines of care, part two
- Congenital Adrenal Hyperplasia
- Congenital hair loss disorders: Rare, but not too rare
- A case of androgen-secreting adrenal carcinoma with non-classical congenital adrenal hyperplasia
- The Distribution of Preputial Vessels in Different Severity of Rat Congenital Hypospadias Model: Imaging study using Micro-Computerized Tomograph
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- Hypothyroidism in Dogs
- Keratin disorders: from gene to therapy
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Polarized microscopy in genetic hair disorders: case series
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Scalp Repair Using Tissue Expanders
- Congenital triangular alopecia: Is it always confined to fronto-temporal region?
- Congenital triangular alopecia - A case report
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Secondary cicatricial and other permanent alopecias
- Hair Loss in Children
- Cutaneous manifestations of systemic infection in children
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Position effect on <i>FGF13</i> associated with X-linked congenital generalized hypertrichosis
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Differential Diagnosis of Hyperandrogenism in Women with Polycystic Ovary Syndrome