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Research 691–720 of 1000+
- Progression of Pseudolymphoma to true Cutaneous lymphoma, possible role of Platelet-rich plasma (PRP), a case report.
- Sparse Hair on the Scalp
- Clinical Profile of Pediatric Alopecia Areata in Faisalabad City
- Zdravstvena njega bolesnika oboljelih od hipertireoze
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- SUN-208 Rare Case of 47XXY/46XX Mosaic Klinefelter Syndrome
- 012 A Case Report of Central Centrifugal Cicatricial Alopecia in Two Generations
- 미녹시딜 도포로 호전을 보인 청소년기 여아에서 발생한 안드로겐 탈모증 1예
- From Past to Present
- Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes
- Associations between semen quality and lower urinary tract symptoms in ageing male
- Frequency of Hirsutism among females students in Babol University of Medical Sciences, 1999
- Assessment of The Influence of Non-Genetic Risk Factors on The Disease Onset and Progression of Androgenetic Alopecia in Egyptian Males
- Prevalence and clinical correlates of impaired glucose tolerance in young women with polycystic ovary syndrome.
- Atrichia with papular lesions in Syrian siblings exposing global diagnostic challenges in genetic alopecia: A rare case report
- Multifocal alopecia of the scalp, axillae, and body
- Factors associated with the prevalence of diseases in the scalp: a prospective study in Mugdha Medical College and Hospital, Dhaka, Bangladesh
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- The COVID-19 pandemic and its skin effects
- Knowledge, Attitude and Perceptions of the population towards Vitamin D in Jeddah, Saudi Arabia
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Itchy scalp with scale
- Philological Obfuscation
- TOC
- 1,25-dihydroxyvitamin D resistance, rickets, and alopecia
- Human tissue kallikreins as promiscuous modulators of homeostatic skin barrier functions
- Calcitriol-Resistant Rickets With Alopecia
- Highly Prevalent LIPH Founder Mutations Causing Autosomal Recessive Woolly Hair/Hypotrichosis in Japan and the Genotype/Phenotype Correlations
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- A Clinical Study of Androgenetic Alopecia (V)