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Research 361–390 of 1000+
- Comment on Malloy (2008) “James Watson tells the inconvenient truth: Faces the consequences”
- Are sex discordant outcomes in COVID-19 related to sex hormones?
- GYNECOMASTIA AFTER FINASTERIDE THERAPY
- A perfusable vascularized full-thickness skin model for potential topical and systemic applications
- Induced pluripotent stem cells: Generation methods and a new perspective in COVID-19 research
- Case 21-2012
- Misdiagnosis as asphyxiating thoracic dystrophy and CMV-associated haemophagocytic lymphohistiocytosis in Shwachman-Diamond syndrome
- Pemphigus Vulgaris Lacking Mucosal Involvement in a German Shepherd Dog: Possible Response to Heparin Therapy
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Congenital atrichia and hypotrichosis
- Advances in precise cell manipulation
- Disappearance of Tramadol and THC-COOH in Hair After Discontinuation of Abuse. Two Different Profiles
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- On Photo-Stability of Oxybenzone
- Successful management of minoxidil toxicosis in a dog
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Biomarkers in alopecia Areata: A systematic review and meta-analysis.
- Patterns of Care for Newly Diagnosed Benign Prostatic Hyperplasia in the United States
- Marie-unna hereditary hypotrichosis
- A 13-Year-Old Boy from Thailand with Hutchinson-Gilford Progeria Syndrome with Coronary Artery and Aortic Calcification and Non-ST-Segment Elevation Myocardial Infarction (NSTEMI)
- First Case of Degenerative Mucinotic Mural Folliculitis in Brazil
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Mixed-pattern, essential syphilitic alopecia, uveitis, and papillitis in an immunocompetent patient with neurosyphilis
- Comprehensive Insight into Cutaneous Application of Hemp
- Hereditary Chorea Associated With and Aggravated by Systemic Lupus Erythematosus
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Werner's syndrome: incidental finding during pregnancy
- Multi-target evaluation of Korean herbal compounds against the SRD5A2 / AR / beta-catenin axis for androgenetic alopecia: Boltz-2 cofold, ChEMBL-anchored ranking, ADMET-AI 107-endpoint safety panel, and pilosebaceous single-cell atlas-constrained prioritization of Saponin Re, Emodin, and Biochanin A
- Exploring the efficacy evaluation model for androgenic alopecia using hair organoids: Transcending conventional hair research
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant