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Research 451–480 of 1000+
- Prevalence Of Male Balding Pattern In Patient From Saveetha Dental College- Retrospective Comparative Evaluation Study
- Polikistik Over Sendromu ve Obezite: FTO ve MC4R Gen Polimorfizmlerinin Rolü
- An Assessment on Impact of COVID-19 Infection in a Gender Specific Manner
- Hypothyroidism in Dogs
- CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico
- Childhood Alopecia Areata: An Overview of Treatment and Recent Patents
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- Unveiling the Effect of Age and IgE Level on Alopecia Areata: Insights from Comparative RNAseq Analysis
- [Hormonal interaction and hair growth].
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Red Blood Cells Folate Level in Patients with Alopecia Areata
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Androgenetic alopecia: An update
- Regulatory pathways implicated in male androgenetic alopecia pathogenesis
- Six novel susceptibility Loci for early-onset androgenetic alopecia and their unexpected association with common diseases
- Osteopontin Gene Polymorphisms rs1126616 C>T and rs1126772 A>G are Associated with Atopic Dermatitis in Polish Population
- Common Variants in the Trichohyalin Gene Are Associated with Straight Hair in Europeans
- Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023)
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Tracing the cellular origin of cancer
- Uveodermatological syndrome in dogs: A review of diagnosis, management, and ophthalmic patient needs
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Exploring Hirsutism: Epidemiology, Associated Endocrinal Abnormalities, and Societal Challenges in GCC—A Narrative Review
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Metabolic dysfunction in female mice with disruption of 5α-reductase 1
- Hair Loss: Pathogenesis and Prevention: A Literature Review