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Research 61–90 of 1000+
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- [Hirsutism].
- Disorders of hair growth : diagnosis and treatment
- Disorders of the Hair and Nails
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Congenital hypotrichosis due to short anagen
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children
- Loose anagen hair syndrome presenting as patchy hypotrichosis – clinico-trichoscopic correlation
- Generalised Gingival Fibromatosis and Hypertrichosis: A Rare Case of Syndromic Presentation
- Hypertrichosis of the pinnae in a patient using panitumumab
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- Androgenetic alopecia, hirsutism and hypertrichosis
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree
- Focal and Generalized Alopecia
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Bimatoprost in the treatment of eyelash hypotrichosis
- Isolated autosomal recessive woolly hair/hypotrichosis: genetics, pathogenesis and therapies
- Disorders of hair in children
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review