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- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hypertrichosis in Childhood
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Two Cases of Hypertrichosis Cubiti
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Faun tail nevus: A series of 15 cases and their management with Intense Pulse Light
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Current Genetics in Hair Diseases
- Marie-unna hereditary hypotrichosis
- Hipertricose generalizada exuberante em um lactente: relato de caso
- Biology and Genetics of Hair
- Cutaneous Side Effects of Chemotherapy and Radiotherapy
- Case Report: Diffuse Hypertrichosis in the Course of Hepatitis C Treatment by IFN-<i>α</i> and Ribavirin
- Bimatoprost solution 0·03% topical application to the eyelid margin for the treatment of eyelash hypotrichosis
- Congenital atrichia and hypotrichosis
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- 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
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- What Do We Know About Hair Growth Induced by Wounding and Its Therapeutic Applications?
- Genital Dermatology
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Acquired Localized Hypertrichosis Induced by Rivastigmine
- Bimatoprost for the treatment of eyelash, eyebrow and scalp alopecia
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Diseases of Periocular Hair
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil