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Research 841–870 of 1000+
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- <i>WNT10A</i> , dermatology and dentistry
- Riboflavin-responsive glutaryl CoA dehydrogenase deficiency
- Signal transducer and activator of transcription 5B deficiency due to a novel missense mutation in the coiled-coil domain
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Hemoglobinopathy and Systemic Lupus: A Rare Association
- 5-Alpha-reductase deficiency in a Saudi "girl"
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- A Rare Presentation of Biotinidase Deficiency Mimicking Acrodermatitis Enteropathica in a Toddler
- Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- SEBACEOUS ADENITIS IN AKITA DOG – CASE REPORT
- Decades of progressive red and yellow nodules
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- Insulin resistance is increased in alopecia areata patients
- CLINICAL UPDATES IN HAIR
- Recent Advances in Drug Design and Drug Discovery for Androgen- Dependent Diseases
- Evidence based homoeopathy: A case report on androgenic alopecia in 23 year old male
- Health Utility of Facial Angiofibroma associated with Tuberous Sclerosis Complex
- A Review on Ayurvedic Niadanatmak Concept of Khalityavyadhi
- Review Article - Changing trends in hair restoration surgery
- SELF-CARE OF MALE PATTERN HAIR LOSS – Selfcare Journal
- Gestational diabetes mellitus and COVID-19, clinical characteristics and review of the literature
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Plakophilin 1 suppresses keratinocyte innate immune responses through DExD/H helicases
- Scarring Alopecia in Localized Dystrophic Epidermolysis Bullosa: A Case Report and a Scoping Review