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Research 31–60 of 194
- Positional Vertigo and Unilateral Gradual Hearing Loss Following Sleeve Gastrectomy: A Case Report
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- 8242 A Case of Ayme Gripp Syndrome
- Telogen Effluvium Following Orthognathic Surgery
- Large Scale Gene Expression Profiles of Regenerating Inner Ear Sensory Epithelia
- Hearing impairment in patients with alopecia areata
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Use of chemotherapy during human pregnancy
- Crafting Polymeric and Peptidic Hydrogels for Improved Wound Healing
- Management of congenital ichthyoses: European guidelines of care, part two
- A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice
- HAIR AND SYSTEMATIC DISEASE
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- The Clinical Presentation of Systemic Lupus Erythematosus
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Clinical relevance of hair microscopy in alopecia
- Male fertility and skin diseases
- Cardiodermatology: the heart of the connection between the skin and cardiovascular disease
- Vogt-Koyanagi-Harada Disease: A Narrative Review
- Umbilical Cord Mesenchymal Stromal Cell-Derived Exosomes Rescue the Loss of Outer Hair Cells and Repair Cochlear Damage in Cisplatin-Injected Mice
- Symptom management in inflammatory bowel disease
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- A Case of Rhupus with Rowell Syndrome
- Evaluation of Animal Models Suitable for Hair Research and Regeneration
- The urine as a diagnostic key for a homozygous EGFR mutation
- Premature Greying of Hair (Premature Canities): A Concern for Parent and Child