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Research 61–90 of 1000+
- Sudden whitening of the hair in an 82-year-old woman: the ‘overnight greying’ phenomenon
- Changes in Color of Hair and Feathers
- Unusual forms of alopecia areata in a Trichology Unit
- Stress, Hair Growth Control, and the Neuro-Endocrine-Immune Connection
- Effects of Cooling Micrografts in Hair Transplantation Surgery
- Targetoid Polycyclic Concentric Hair Regrowth Pattern Is a Sign of Immunological Recovery in Alopecia Areata
- Targetoid Hair Regrowth Pattern in Alopecia Areata: A Case Series
- Natural Compound Isoliensinine Inhibits Stress-Induced Hair Greying by Blocking β2-Adrenoceptor
- Bacterial Diseases of the Skin
- The ethical foundations of patient-centered care in aesthetic medicine
- Immunohistochemical demonstration of keratins in the epidermal layers of the Malayan pangolin (Manis javanica), with remarks on the evolution of the integumental scale armour
- Skin and Scalp Health Benefits of a Specific Botanical Extract Blend: Results from a Double-Blind Placebo-Controlled Study in Urban Outdoor Workers
- Sterilization and low temperature effects on regenerative potential of hyaluronic acid
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Marie Unna hereditary hypotrichosis: Identification of a U2HR mutation in the family from the original 1925 report
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- 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
- Marie-unna hereditary hypotrichosis
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Marie Krogh's contributions to the study of thyroid physiology and pathophysiology
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Marie‐Unna Hereditary Hypotrichosis: Case Report and Review of the Literature