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Research 91–120 of 1000+
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- Hair follicles and their role in skin health
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- Hair Disorders
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- 882 Syndactyly type III and hypotrichosis in oculodentodigital syndrome with GJA1 mutation
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Causes and Management of Hypertrichosis
- Congenital atrichia associated with situs inversus and mesocardia
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Hypotrichosis in a child with olmsted syndrome
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves
- Congenital atrichia associated with nevus flammeus: A rare association
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- In Silico Characterization and Analysis of Clinically Significant Variants of Lipase-H (LIPH Gene) Protein Associated with Hypotrichosis
- Hair Shaft Dysplasias
- Hair loss and its management in children
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Solitary Basaloid Follicular Hamartoma: A Report of Two Cases.
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- A rare hair loss in children: Monilethrix
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Ectodermal Dysplasia: Variable Expressions
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Genetic Hair Disorders: A Review
- Acne Syndromes and Mosaicism