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Research 151–180 of 1000+
- Molecular and functional aspects of the hairless (<i>hr</i>) gene in laboratory rodents and humans
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Genetic hair and nail disorders
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- A Review on-Types and Treatment of Alopecia
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Genetics of Inherited Ichthyoses and Related Diseases
- Short anagen syndrome: Case series and literature review
- Psychotrichology: psychosomatic aspects of hair diseases
- Telogen Effluvium: A Review
- Diagnosis and management of hair loss in children
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Dermatoscopic findings of syphilitic alopecia
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Trichoscopy and Trichogram
- Approach to the adult female patient with diffuse nonscarring alopecia
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Biology of the Hair Follicle: The Basics
- The cycling hair follicle as an ideal systems biology research model
- Alopecia Areata
- Therapeutic strategies for treating hair loss
- Electron paramagnetic resonance (EPR) spectroscopy for investigating murine telogen skin after spontaneous or depilation-induced hair growth
- A non-invasive study of alopecia in Japanese macaques Macaca fuscata
- Alopecia: Association with Resistance to Thyroid Hormones
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- The Stem Cell Quiescence and Niche Signaling is Disturbed in the Hair Follicle of the Hairpoor Mouse, an MUHH Model Mouse.
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Disorders of the skin appendages