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Research 121–150 of 1000+
- COMPREHENSIVE OVERVIEW ON THE PROBLEMS OF HAIR AND THE VARIOUS HERBAL APPROACHES TO TREAT THEM
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- 9 Role of 5α-reductase in health and disease
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- The Role of Vitamin D and Testosterone Levels with Hair Loss among Females with Coronavirus Disease
- Application of Ultraviolet-Induced Fluorescence Trichoscopy (UVFT) in Hair and Scalp Diseases
- Hair Loss, Insulin Resistance, and Heredity in Middle-aged Women. a Population-based Study
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor
- A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia
- A frameshift mutation in HTRA1 expands CARASIL syndrome and peripheral small arterial disease to the Chinese population
- Congenital atrichia and hypotrichosis
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Editors' Picks
- A Precis of the alopecia (Hair loss) associated with therapies based on nanotechnology and its impact on quality of Life (QoL)
- Hair Loss and It’s Homeopathic Approach
- Common Causes of Hair Loss
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- Dermatologic manifestations of endocrine disorders
- Focal and Generalized Alopecia
- Alopecia in Cronkhite-Canada syndrome
- Zebrafish Model of Hereditary Pigmentary Disorders
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Iron Screening in Alopecia Areata Patients May Catch Hereditary Hemochromatosis Early