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Research 541–570 of 1000+
- Clinical and molecular genetic studies in hereditary hair loss
- Quantitative image analysis for hereditary hair disorders
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Hair Loss, Insulin Resistance, and Heredity in Middle-aged Women. a Population-based Study
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Central hair loss in African American women: Incidence and potential risk factors
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- hKAP1.6 and hKAP1.7, Two Novel Human High Sulfur Keratin-Associated Proteins are Expressed in the Hair Follicle Cortex
- AN UPDATE OF HAIR SHAFT DISORDERS
- Hair science and technology
- Trichodystrophies: A hair-raising differential diagnosis
- A Precis of the alopecia (Hair loss) associated with therapies based on nanotechnology and its impact on quality of Life (QoL)
- Hair loss (alopecia or baldness)
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Hair Loss and It’s Homeopathic Approach
- Microscopic Study concerning Hair Form of One Family in the Mixed Blood between European and Ponapean
- Alopecia: Hair loss what is it indicating and role of homeopathy
- Genetics of Structural Hair Disorders
- Topical minoxidil therapy for hereditary male pattern alopecia.
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Hereditary, Congenital, and Acquired Alopecias
- Disorders of the hair and scalp.
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Gene that causes woolly hair revealed
- Hereditary Androgenetic Alopecia and Minoxidil
- Keratins of the Human Hair Follicle
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Hair follicle group and skin follicle population of Australian Merino sheep