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Research 601–630 of 1000+
- Solitary pedunculated multicystic viral plaque associated with canine papillomavirus 18 in a British Bulldog
- A histological study of the effect of panax ginseng versus finasteride on induced benign prostatic hyperplasia in rats with potentiality of spontaneous recovery
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Reversible hypopigmentation of hair secondary to Vitamin B12 deficiency
- Clinical Snippets
- Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review
- Ectodermal Dysplasia: Variable Expressions
- Drug-associated gingival disorders: a retrospective pharmacovigilance assessment using disproportionality analysis
- Surgical Treatment Combined With Concentrated Growth Factor Injection for a Case of Pseudopelade of Brocq
- Olympic and Board Game Dermatology: Exploring Eponyms Linking Skin Conditions to Sports and Strategy Games
- Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation
- 671 Impaired follicular Nrf2 signaling: Potential early therapeutic target in hidradenitis suppurativa
- Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism
- SUN-287 A Case of Ectopic Neurohypophysis
- P095 The Very Interesting Small Bowel Lesions of Cronkhite-Canada Syndrome
- Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
- O que sabemos sobre os inibidores da 5 alfa redutase?
- A Rare Case of Cronkhite-Canada Syndrome
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
- Early Onset Werner Syndrome
- Nitrogen Mustard Induces DNA Damage and Structural Changes in Mouse Skin Hair Follicles
- A Very Unusual Cause of Diarrhea in a 60-Year-Old Man
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Preliminary studies on the phytochemistry and efficacy of extracts of the bark of <i>Spondias mombin</i> l. on induced cancer in rats
- This Month in the Journal