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- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- A matter of excessive hair growth
- Congenital atrichia and hypotrichosis
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Bimatoprost solution 0·03% topical application to the eyelid margin for the treatment of eyelash hypotrichosis
- Notes from the Editor Emeritus: Medical therapy for hair loss: what we know and what we need to find out
- Marie-unna hereditary hypotrichosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Safety of low-dose oral minoxidil for hair loss: A multicenter study of 1404 patients
- Hair Restoration Surgery in Patients with Pubic Atrichosis or Hypotrichosis
- The effects of minoxidil, 1% pyrithione zinc and a combination of both on hair density: a randomized controlled trial
- Hipertricose generalizada exuberante em um lactente: relato de caso
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Minoxidil oral en alopecia androgénica: estudio retrospectivo acerca de su seguridad en práctica clínica real
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Síndrome do nevo de Becker
- Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Bilateral Temporal Triangular Alopecia Associated with Phakomatosis Pigmentovascularis Type IV Successfully Treated with Follicular Unit Transplantation
- Hypertrichosis of the pinnae in a patient using panitumumab
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- Inherited Disorders of the Hair
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost