13 results on '"Sargolzaeiaval, Forough"'
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2. Development of an automated estimation of foot process width using deep learning in kidney biopsies from patients with Fabry, minimal change, and diabetic kidney diseases.
3. Uncommon cause of cirrhosis—A case of Werner syndrome with a novel WRN mutation
4. Automated estimation of foot process width using deep learning in kidney biopsies from patients with Fabry disease
5. Podocyte globotriaosylceramide (GL-3) content in female adult patients with Fabry disease and amenable mutations reduces following 6 months of treatment with migalastat
6. Reconstruction of mandibular defects using synthetic octacalcium phosphate combined with bone matrix gelatin in rat model
7. Inactivating Mutations in Exonuclease and Polymerase Domains in DNA Polymerase Delta Alter Sensitivities to Inhibitors of dNTP Synthesis
8. CTC1 mutations in a Brazilian family with progeroid features and recurrent bone fractures
9. Histological Assessment of Bone Regeneration by Octacalcium Phosphate and Bone Matrix Gelatin Composites in a Rat Mandibular Defect Model
10. Biallelic WRN Mutations in Newly Identified Japanese Werner Syndrome Patients
11. Biallelic <bold>WRN</bold> Mutations in Newly Identified Japanese Werner Syndrome Patients.
12. Biallelic WRNMutations in Newly Identified Japanese Werner Syndrome Patients
13. Histomorphometric Analysis of Newly-formed Bone Using Octacalcium Phosphate and Bone Matrix Gelatin in Rat Tibial Defects.
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