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Research 151–180 of 363
- Eyebrow Loss
- TONGUE, RED
- Alopecia: possible causes and treatments, particularly in captive nonhuman primates.
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Bioactive Compound-Loaded Nanocarriers for Hair Growth Promotion: Current Status and Future Perspectives
- Recent Advances in Understanding of the Etiopathogenesis, Diagnosis, and Management of Hair Loss Diseases
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation
- Molecular basis of congenital atrichia in humans and mice.
- Assessing the Efficacy of Follicular Unit Extraction (FUE) in Beard and Moustache Transplants: A Comprehensive Analysis of 300 Cases
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Genetic Variation in the Human Androgen Receptor Gene Is the Major Determinant of Common Early-Onset Androgenetic Alopecia
- Androgenetic Alopecia: In Vivo Models
- Methods of hair loss evaluation: a comparison of TrichoScan<sup>®</sup>with the modified wash test
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Keratoma Hereditaria Mutilans (Vohwinkel's Disease) with Congenital Alopecia Universalis (Atrichia Congenita)
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Congenital atrichia and hypotrichosis
- CONGENITAL ATRICHIA.*
- Focal atrichia: A diagnostic clue in female pattern hair loss
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- Premature termination of hair follicle morphogenesis and accelerated hair follicle cycling in Iasi congenital atrichia (fz<sup>ica</sup>) mice points to <i>fuzzy</i> as a key element of hair cycle control
- Effects of Dehydroepiandrosterone Therapy on Pubic Hair Growth and Psychological Well-Being in Adolescent Girls and Young Women with Central Adrenal Insufficiency: A Double-Blind, Randomized, Placebo-Controlled Phase III Trial
- Inherited ichthyosis: Syndromic forms
- Hair physiology and its disorders
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Alopezien und Hypotrichosen im Kindesalter