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Research 361–390 of 363
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Junctional Epidermolysis Bullosa, Generalized Intermediate Type
- Proceedings of the Inaugural Pediatric Dermatology Research Alliance (PeDRA) Conference
- Molecular Genetics of the PI3K-AKT-mTOR Pathway in Genodermatoses: Diagnostic Implications and Treatment Opportunities
- Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region
- Unveiling the Roots of Monogenic Genodermatoses: Genotrichoses as a Paradigm
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Corneodesmosomes and corneodesmosin: from the stratum corneum cohesion to the pathophysiology of genodermatoses
- Male fertility and skin diseases
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Generalized Congenital Hypotrichosis in a Female Rottweiler
- A 40-Year-Old Woman With Facial Papules and Flank Pain
- Vulvovaginal involvement in Netherton syndrome: A case report
- Rothmund‐Thomson syndrome type 2 – a rare cause of chronic wounds
- Painful thickened skin on the soles of the feet
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Overexpression of human keratin 16 produces a distinct skin phenotype in transgenic mouse skin
- Spectrum of skin diseases in Yemen (Hajjah and adjacent region)
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Pediatric dermatoses pattern at a Brazilian reference center
- Case Report: A case of Rothmund–Thomson syndrome-like phenotype with an ANAPC1 variant of uncertain significance and observed hair improvement
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Clouston’s syndrome: a rare case report
- Keratin gene mutations in disorders of human skin and its appendages
- The Human Type II Keratin Gene Cluster on Chromosome 12q13.13: Final Count or Hidden Secrets?
- Treatment of monilethrix with oral minoxidil
- Generalized multiple eruptive milia in an infant – An unusual presentation
- Keratosis Follicularis Spinulosa Decalvans: Diagnosis and Therapeutic Evaluation.