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Research 241–270 of 1000+
- Human Hair Growth Deficiency Is Linked to a Genetic Defect in the Phospholipase Gene <i>LIPH</i>
- Genetic Hair Disorders: A Review
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Ectodermal Dysplasia: Variable Expressions
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Current Genetics in Hair Diseases
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Clinical report of a Holstein's calf with ichthyosis.
- Hair and Nail Relationship
- Hair Shaft Dysplasias
- Hirsutism
- Hair loss and its management in children
- Primary Hypothyroidism and Thyroid Goiter in an Adult Cat
- The stem cell quiescence and niche signaling is disturbed in the hair follicle of the hairpoor mouse, an MUHH model mouse
- Madarosis
- Short anagen syndrome: Case series and literature review
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Skin Development and Disease: A Molecular Perspective
- Solitary Basaloid Follicular Hamartoma: A Report of Two Cases.
- Acquired Uncombable Hair
- The Role of Histone Demethylases in Disease
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report
- Hair Loss in Children, Etiologies, and Treatment
- The Requirement to Monitor Low-dose Oral Minoxidil in the Management of Hair Loss
- Hair Growth on Nude Mice Due to Cyclosporin A
- Eyelash Trichomegaly: A Rare Presenting Feature of Systemic Lupus Erythematosus.