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Research 931–960 of 1000+
- Increasing of PCOs among Young Females
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- Cicatricial Alopecia
- The Interplay between Finasteride-Induced Androgen Imbalance, Endoplasmic Reticulum Stress, Oxidative Stress, and Liver Disorders in Paternal and Filial Generation
- Genetics of polycystic ovary syndrome: searching for the way out of the labyrinth
- Seborrheic keratosis
- A Technique for Reconstruction of Eyebrows and Eyelashes
- AYURVEDIC COSMETOLOGY APPROACHES TO PREMATURE HAIR GREYING (AKĀLAPĀLITYA): A LITERATURE REVIEW
- Predictive Modeling of Hair Fall using Random Forest Algorithms
- Bir ikinci sağlık kuruluşunun dermatoloji polikliniğine başvuran hastaların klinik tanılarının, yaş, cinsiyet ve mevsimsel farklılıklarının aile hekimliği bakış açısı ile değerlendirilmesi
- 410 NON-INVASIVE DIAGNOSIS OF PROSTATE CANCER FROM BODY FLUIDS USING A PANEL OF TUMOR SUPPRESSOR GENES
- Noninflammatory, Nonpruritic Alopecia of Horses
- How Do You Treat Premature Hair Loss in Women in Your Practice
- National scientific medical meeting 1996 abstracts
- Regulatory pathway analysis of coat color genes in Mongolian horses
- <i>Hoxc13</i> and the development of hair follicle
- Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6
- Four Independent Mutations in the Feline Fibroblast Growth Factor 5 Gene Determine the Long-Haired Phenotype in Domestic Cats
- Zinc metabolism in lethal-milk mice
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- Itpr3 Is Responsible for the Mouse Tufted (tf) Locus
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The character “hairless” in the mouse
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Biotinidase deficiency characterized by skin and hair findings
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Hair loss in infancy and childhood
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Metabolic Syndrome in Androgenetic Alopecia in a Tertiary Care Centre in Goa: A Case Control Study During COVID-19 Pandemic