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Research 91–120 of 784
- Hair and Nail Relationship
- The inconsistent regulation of HOXC13 on different keratins and the regulation mechanism on HOXC13 in cashmere goat (Capra hircus)
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Hair loss and its management in children
- Advances in Hair Diseases
- Darier Sign: A Historical Note
- Trichodystrophies: A hair-raising differential diagnosis
- Ingestion of topical steroid triggering pustular psoriasis?
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Hair Loss in Children
- Learning from nudity: lessons from the nude phenotype
- Cutaneous and Mucosal Manifestations Associated with Celiac Disease
- Dermatologic Manifestations of Human Immunodeficiency Virus Infection
- Endocrine-skin interactions
- Adolescent hair loss
- Change of the diagnostic distribution in applicants to dermatology after COVID ‐19 pandemic: What it whispers to us?
- Hair loss
- Non‐infective mucocutaneous presentations of human immunodeficiency virus infection
- Skin changes in pediatric transplant patients
- Dermatological Manifestations of Celiac Disease: a Literature Review
- Tricotiodistrofia. Reporte de un caso
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Spink5-deficient mice mimic Netherton syndrome through degradation of desmoglein 1 by epidermal protease hyperactivity
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Diagnosis of Hair Loss: Clinical features of common causes of hair loss.
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Hair and Scalp Disorders in a Tuscan Pediatric Dermatological Outpatient Clinic: A Clinical and Epidemiological Evaluation
- An autosomal recessive nonsense variant in the EGFR gene induces perinatal lethality in “Blonde d'Aquitaine” calves