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Research 631–660 of 1000+
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- A Genetically Defined Male Counterpart of Polycystic Ovary Syndrome: Evidence for Ovarian-Independent Pathogenesis
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Potential Sequels of Undiagnosed Marfan Syndrome: A Case Report
- 10-Year-Old Female with an Irregularly Shaped Patch of Hair Loss
- Frontal Fibrosing Alopecia
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Familial patterns of alopecia areata: A systematic review and meta-analysis
- Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report
- Joint study of the associations of HLA‐B and the transmembrane short tandem repeat polymorphism of MICA protein with alopecia areata shows independent associations of both with the disease
- The impact of obesity: a narrative review
- Partial Reversal of Canities in a 22-Year-Old Normal Chinese Male
- Abstracts of 42nd National Conference of Association of Clinical Biochemists of India (ACBICON 2015)
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- Gray Hair: From Preventive to Treatment
- Painful thickened skin on the soles of the feet
- How Many Sessions Does It Take For Scalp Micropigmentation
- 420 Severe thiopurine-induced myelotoxicity and hair loss in Japanese patients with NUDT15 gene variant: A retrospective case-control study
- Metabolic disease with autoimmune phenomena: 2 cases of SLE-like disease in young children diagnosed with lysinuric protein intolerance
- Androgenetic alopecia in children: report of 20 cases
- Familial scarring alopecia associated with scalp psoriasis
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Berardinelli–Seip syndrome
- BG02 A case of Werner syndrome: undiagnosed progeroid syndrome presenting as female pattern hair loss
- Light Microscopic Hair Abnormalities in Children: Retrospective Review of 119 Cases in a 10-Year Period
- 8242 A Case of Ayme Gripp Syndrome
- CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma
- Clinical case of alopecia totalis in pediatric practice