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Research 61–90 of 1000+
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Marie-unna hereditary hypotrichosis
- Woolly hair generalizado: caso clínico e revisão da literatura
- Pearly Pinna Papules in a Young Female
- Monilethrix – Case report of a rare disease
- Genetic Variant of the Canine FGF5 Gene for the Hair Length Trait in the Akita: Utility for Hair Coat Variations and Welfare in Conservation Breeding
- The systemic wrinkled skin phenotype involves aberrant expression and variation of genes related to the oxidative stress and extracellular matrix in Xiang pigs
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Diagnostic approach to low‐renin hypertension
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Whole genome sequencing analysis of alpaca suggests TRPV3 as a candidate gene for the suri phenotype
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Woolly Hair in Two Siblings
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Biology and Genetics of Hair
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex