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Research 91–120 of 1000+
- Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA
- Myotonic dystrophy type 1
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Nonscarring hair loss disorders
- Nucleating agent solves a packaging problem
- Hague (<i>Hag</i>): A New Mouse Hair Mutation With an Unstable Semidominant Allele
- Vitamin D dependent rickets type 2: a case-based review of patient with alopecia and rickets
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Studies of normal moult and of artifically induced regeneration of pelage in peromyscus
- The Near-Naked Hairless (Hr) Mutation Disrupts Hair Formation but Is Not Due to a Mutation in the Hairless Coding Region
- Novel <i>ABCD1</i> Gene Mutation in Adrenomyeloneuropathy with Hypoplasia and Agenesis of the Corpus Callosum
- Alopezien und Hypotrichosen im Kindesalter
- Androgenic alopecia and differential diagnoses of alopecia
- Clinical cases of Darier-White follicular dyskeratosis
- Study on Antioxidants and Growth Factors in the Treatment of Alopecia with Injectables
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- The genetics of androgenetic alopecia
- Keratosis follicularis spinulosa decalvans in a family
- An overview on congenital alopecia in domestic animals
- Crystalline Cataract and Uncombable Hair
- The Genetics of Human Skin Disease
- Sebaceous adenitis in Swedish dogs, a retrospective study of 104 cases
- Delayed Puberty
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- The Annual Changes of Clinical Manifestation of Androgenetic Alopecia Clinic in Korean Males and Females: A Outpatient-Based Study
- Two familial cases of Olmsted-like syndrome with a G573V mutation of the<i>TRPV3</i>gene
- AN UPDATE OF HAIR SHAFT DISORDERS
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings