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Research 91–120 of 1000+
- Hair Loss: A Harbinger of the Morbidities to Come!
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Nonscarring hair loss disorders
- Trichodystrophies: A hair-raising differential diagnosis
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Gender aspects in skin diseases
- Graft versus host disease presenting as fibrosing alopecia in a pattern distribution: A model for pathophysiological understanding of cicatricial pattern hair loss
- Congenital hair loss disorders: Rare, but not too rare
- Hair and Nail Relationship
- Anaemia and skin disease
- Pinnal Diseases
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Cutaneous signals of immune system disease
- Metabolic Syndrome, Cardiovascular Disease and the Hair Growth Cycle: Addressing hair growth disruptions using Nourkrin® with Marilex® as a proteoglycan replacement therapy: A concise review
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- Hair follicles, their disorders and their opportunities
- The Genetics of Human Skin Disease
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Metabolism and skin diseases
- Drug-Induced Skin, Nail and Hair Disorders
- Polarized microscopy in genetic hair disorders: case series
- Diseases of Hair
- Diseases of Hair
- Current understanding and treatment of sex hormone-related hair diseases
- The clinical spectrum of parathyroid disease
- Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease
- 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: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation