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Research 631–660 of 1000+
- Contents
- Manual of chemical peels: Superficial and medium depth
- Low level of high-density lipoprotein cholesterol is solely associated with greater severity of male androgenetic alopecia: A cross-sectional study of Thai population
- Cutaneous manifestations of HIV infection other than Kaposi's sarcoma: Clinical and histologic aspects
- Endocrine-skin interactions
- p53‐dependent transcriptional regulation of EDA2R and its involvement in chemotherapy‐induced hair loss
- Hair-Thread Tourniquet Syndrome: A Case Report and Literature Review
- Secondary cicatricial and other permanent alopecias
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- 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
- Hair loss
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Symmetrical alopecia in the dog
- Hair loss in children.
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome
- A small scale study to evaluate the efficacy of microneedling in the presence or absence of platelet‐rich plasma in the treatment of post‐clipping alopecia in dogs
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Breaking the biofilm- A persistent case of deep pyoderma in a Bullykutta dog
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Bioregenerative Applications of the Human Mesenchymal Stem Cell- Derived Secretome: Part-II
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- Expression of COX-2 and Bcl-2 in 50 patients of Lichen Planus
- Case of Cronkhite Canada Syndrome - A Non-Inherited Gastrointestinal Polyposis Syndrome
- Abnormal fingerprints and immigration delay disease
- Canine alopecia X
- Trilostane Treatment of Canine Alopecia X in an American Pit Bull Terrier