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Research 721–750 of 1000+
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Prenatal hair development: Implications for drug exposure determination
- Trichoscopy in Hair Shaft Disorders
- Ichthyosis with confetti: clinics, molecular genetics and management
- Atrichia With Papular Lesions
- Platelet-rich plasma—an ‘Elixir’ for treatment of alopecia: personal experience on 117 patients with review of literature
- Ectodysplasin research—Where to next?
- Gastrointestinal polyposis with protein-losing enteropathy, abnormal skin pigmentation and loss of hair and nails (Cronkhite-Canada syndrome)
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Inherited disorders of the skin in human and mouse: from development to differentiation.
- Ulerythema Ophryogenes
- Genetics of Structural Hair Disorders
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Epidermal stem cell fate: what can we learn from embryonic stem cells?
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Dermatopathology and molecular genetics
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations
- Clinical Case Notes. Propecia-associated bilateral cataract
- Hair loss among a group of Egyptian children
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Transcriptional activation of a subset of hair keratin genes by the NF-κB effector p65/RelA
- Whiskers amiss, a new vibrissae and hair mutation near the Krt1 cluster on mouse Chromosome 11
- The fundamentals of WNT10A
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Disorders of the Hair and Scalp in Children
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- What Syndrome Is This?
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b