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Research 91–120 of 1000+
- New developments in the molecular treatment of ichthyosis: review of the literature
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- The developmental basis of fingerprint pattern formation and variation
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Acquired scalp alopecia. Part I: A review
- Congenital hair loss disorders: Rare, but not too rare
- Hair loss in children.
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Molecular Genetics of Alopecias
- Hair Shafts in Trichoscopy
- Alopecia in Epidermolysis Bullosa
- Dermatoscopy of hair shaft disorders
- Psychotrichology: psychosomatic aspects of hair diseases
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- LITERATURE REVIEW
- The urine as a diagnostic key for a homozygous EGFR mutation
- Evaluation of hair loss
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Clinical Approach to the Patient With Alopecia
- British Society for Dermatopathology: Summaries of Papers
- Towards a molecular understanding of hair loss and its treatment
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Evaluation of SALT score severity in correlation with trichoscopic findings in alopecia areata: a study of 303 patients