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Research 30 of 1000+
- Monilethrix: A rare hereditary condition
- Distinct Conditions Support a Novel Classification for Bradykinin-Mediated Angio-Oedema
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Iron Screening in Alopecia Areata Patients May Catch Hereditary Hemochromatosis Early
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2%
- Hereditary, Congenital, and Acquired Alopecias
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Focal and Generalized Alopecia
- Androgenetic Alopecia (AGA)
- A Practitioner's Guide to Hair Loss Part 1—History, Biology, Genetics, Prevention, Conventional Treatments, and Herbals
- Hair loss (alopecia or baldness)
- Secondary Cicatricial and other Permanent Alopecias
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Hereditary Chorea Associated With and Aggravated by Systemic Lupus Erythematosus
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Congenital and Hereditary Skin Diseases
- Dyschromatosis Universalis Hereditaria: Report of a case and Review of the Literature
- 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Coat Problems
- A Kaleidoscope of Keratin Gene Expression and the Mosaic of Its Regulatory Mechanisms
- Knowledge, Beliefs, and Perceptions among Alopecia Areata Patients: A Cross-Sectional Study in CMH Kharian