19 results on '"Wei-Ting Tu"'
Search Results
2. Complexity of Transcriptional and Translational Interference of Laminin-332 Subunits in Junctional Epidermolysis Bullosa with LAMB3 Mutations
3. Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex
4. Exertional plantar blistering as an easily overlooked clue for epidermolysis bullosa simplex
5. Concurrence of recurrent Wells syndrome and flares of systemic lupus erythematosus
6. Folliculotropic non‐alopecic secondary syphilis presenting with rosary beads‐like annular plaques
7. Autosomal dominant epidermolysis bullosa simplex exacerbated by hyperkeratotic scabies
8. Novel compound heterozygous ITGB4 mutations underlie lethal junctional epidermolysis bullosa with pyloric atresia and aplasia cutis congenita
9. A de novo COL17A1 splice-site mutation causing a 7-bp deletion in a Taiwanese patient with junctional epidermolysis bullosa
10. Complexity of Transcriptional and Translational Interference of Laminin-332 Subunits in Junctional Epidermolysis Bullosa with LAMB3 Mutations
11. Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex
12. LB732 Intravenous gentamicin therapy in adult junctional and recessive dystrophic Epidermolysis Bullosa with nonsense mutations does not result in sustained clinical improvement
13. Utility of Gram staining for diagnosis of Malassezia folliculitis
14. Semidominant GPNMB Mutations in Amyloidosis Cutis Dyschromica
15. The efficacy of adjuvant radiotherapy in dermatofibrosarcoma protuberans: a systemic review and meta‐analysis
16. Exertional plantar blistering as an easily overlooked clue for epidermolysis bullosa simplex
17. 276 Exome sequencing identifies semi-dominant GPNMB mutations in amyloidosis cutis dyschromica
18. LB1541 GPNMB mutations and skin pathology in amyloidosis cutis dyschromica
19. Concurrence of recurrent Wells syndrome and flares of systemic lupus erythematosus
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