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Research 301–330 of 1000+
- Regional Dermatology
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Use of Induced Pluripotent Stem Cells in Dermatological Research
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Supplementary Material for: Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- Case report - Hair shaft normalization and hair growth in SPINK5-syndromic epidermal differentiation disorder (Netherton syndrome) while on treatment with dupilumab: a novel therapeutic approach for Trichorrhexis invaginata
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Congenital Atrichia: A Case Report
- Ichthyosis with confetti: clinics, molecular genetics and management
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Precocious puberty: the unlikely herald of Familial adenomatous polyposis in a young girl
- ST Premature Graying Hair in Seven Years Old Children
- Fetal Programming of Polycystic Ovary Syndrome by Androgen Excess: Evidence from Experimental, Clinical, and Genetic Association Studies
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Acne as a chronic systemic disease
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- HAIR LOSS IN WOMEN
- The Implication of Neuroactive Steroids in Tourette's Syndrome Pathogenesis: A Role for 5α‐Reductase?
- Aetiology and Pathophysiology of Hair Loss
- A “hair‐raising” history of alopecia areata
- 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
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Lipin 1 Gene Polymorphisms in Polycystic Ovary Syndrome
- Formation of the cornified envelope
- Interleukins gene polymorphism in alopecia areata patients: a systematic review
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- Trichotillomania Across Circuits: Neurobiology, Sensory Processing, and Genetic Insights
- Correlation between Pilomatrixoma and Polycystic Ovary Syndrome (PCOS)