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Research 721–750 of 1000+
- Ulerythema ophryogenes (keratosis pilaris atrophicans faciei).
- Cicatricial Alopecia
- Dermatologic therapy: December 1984 through December 1985
- The Interplay between Finasteride-Induced Androgen Imbalance, Endoplasmic Reticulum Stress, Oxidative Stress, and Liver Disorders in Paternal and Filial Generation
- Male Androgenetic Alopecia — Endotext
- 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
- Scalp Reduction
- Fibrosing Alopecia in a Pattern Distribution
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- The character “hairless” in the mouse
- Hair growth promoting effect of white wax and policosanol from white wax on the mouse model of testosterone-induced hair loss
- Juri Flap Procedure for the Treatment of Baldness: Two-Year Experience
- 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