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Research 91–120 of 1000+
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- Hair Loss and It’s Homeopathic Approach
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Common Causes of Hair Loss
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Clinical relevance of hair microscopy in alopecia
- Hair Today
- Dermatologic manifestations of endocrine disorders
- Effects of Hormones and Endocrine Disorders on Hair Growth
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Society's Knowledge About Physiological Causes of Hair Loss: A Cross-Sectional Study at The University of Basrah
- A CLINICAL STUDY OF CUTANEOUS MANIFESTATIONS IN PATIENTS WITH THYROID DISORDERS
- Evaluation of Dermatoscopic (Trichoscopic) Patterns in Hair and Scalp Disorders: A Clinical Observational Study
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Canine alopecia X-Like disorder
- Hair and scalp disorders
- Identification of tpo, tg, tshr and ana antibodies associated with thyroid disorders
- Hair in health and disease: an introduction
- Hair loss in children in South-East Nigeria: common and uncommon cases
- Clinical Evaluation of Cactus (Cereus Grandiflorus) Enriched Hair Oil for Hair Fall Disorders
- Hair Disorders
- Clinical Role of Oral Vitamin C and E Therapy in Skin and Hair Disorders
- Congenital atrichia and hypotrichosis
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings
- Histopathology of non-scarring alopecia
- Hairless is a nuclear receptor corepressor essential for skin function
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Loss of epidermal Evi/Wls results in a phenotype resembling psoriasiform dermatitis