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Research 151–180 of 189
- TONGUE, RED
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Trichoscopy in genetic hair shaft abnormalities
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Advancements and challenges in stem cell transplantation for regenerative medicine
- Myotonic Dystrophy—A Progeroid Disease?
- Progress in Topical and Transdermal Drug Delivery Research—Focus on Nanoformulations
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- Strategies for High-Efficiency Mutation Using the CRISPR/Cas System
- The role of platelet-rich plasma in biomedicine: A comprehensive overview
- Efficacy and safety of the oral Janus kinase 3/tyrosine kinase expressed in hepatocellular carcinoma family kinase inhibitor ritlecitinib over 24 months: integrated analysis of the ALLEGRO phase IIb/III and long-term phase III clinical studies in alopecia areata
- New developments in the molecular treatment of ichthyosis: review of the literature
- Ptosis in childhood
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Making the head: Caspases in life and death
- The color of skin: white diseases of the skin, nails, and mucosa
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Differential Expression of MITF, WNT3A, SLC7A11, and EDN3 in the Shoulder ‘Bider Marking’ of Dun Mongolian Horses
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Uncombable hair in a case of Zellweger syndrome – A new association
- First Symposium of Ichthyosis Experts
- Selected abstracts from the 47th meeting of the Irish Endocrine Society Sligo, 24th & 25th November 2023
- Short- and mid-term outcomes of multisystem inflammatory syndrome in children: a longitudinal prospective single-center cohort study
- Transport of Biotin in Human Keratinocytes
- Carotid Body Tumor: Review of the Literature and Report of a Case With a Rare Sensorineural Symptomatology
- The Clinical Presentation of Systemic Lupus Erythematosus
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- The urine as a diagnostic key for a homozygous EGFR mutation
- Melanocytes and Vitiligo (and Hair Graying)
- The Skin and Subcutaneous Tissues