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Research 721–750 of 1000+
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Monilethrix: Beaded hair and hypotrichosis in a child
- Assessment of scalp hair survivin in patients with premature greying of hair
- Painful thickened skin on the soles of the feet
- Dermatomyositis Disease in Dogs
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Polycystic ovarian disease in adult and perimenopausal women
- Office Diagnosis of Hair Shaft Defects
- A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Sjogren-Larsson syndrome
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- 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
- The medusa head: Dermoscopic diagnosis of woolly hair syndrome
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study
- 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
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Genetics of Inherited Ichthyoses and Related Diseases
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis