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Research 30 of 807
- Spiny Keratoderma
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Updates from the British Association of Dermatologists 91st Annual Meeting, 5-7 July 2011, London, U.K.
- Atypical Juvenile Pityriasis Rubra Pilaris: A Case Report of Early Onset With Late Diagnosis
- Molecular pathology of skin adnexal tumours
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Inherited Disorders of the Hair
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- The human keratins: biology and pathology
- Biology and Genetics of Hair
- Dermatoscopy of hair shaft disorders
- Primary cicatricial alopecia
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Hair Loss in Children
- Diseases of Periocular Hair
- Advances in Hair Diseases
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Trichodystrophies: A hair-raising differential diagnosis
- Hair loss in infancy and childhood
- Primary cicatricial alopecias
- Congenital Atrichia: A Case Report
- Hair Loss in Children
- General Dermatology