18 results on '"Di Blasi, Francesco Domenico"'
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2. The 9 bp Deletion between the Mitochondrial COII and Lysine tRNA Genes in a Caucasian Population with Cognitive Disorders: An Observational Study.
3. Aromatic L-Amino Acid Decarboxylase Deficiency: A Genetic Screening in Sicilian Patients with Neurological Disorders
4. Academic Skills in Students with Autism Spectrum Disorder and Intellectual Disability: A Systematic Review and Meta-Analysis
5. Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex Families
6. A Next-Generation Sequencing Study in a Cohort of Sicilian Patients with Parkinson's Disease.
7. The Mitochondrial tRNASer(UCN) Gene: A Novel m.7484A>G Mutation Associated with Mitochondrial Encephalomyopathy and Literature Review
8. Spelling deficits in children with intellectual disabilities: Evidence from a regular orthography
9. Reading decoding and comprehension in children with autism spectrum disorders: Evidence from a language with regular orthography
10. The in cis T251I and P587L POLG1 base changes: Description of a new family and literature review
11. Dyslexia and Attention Deficit Hyperactivity Disorder Associated to a De Novo 1p34.3 Microdeletion
12. The Mitochondrial tRNA Ser(UCN) Gene: A Novel m.7484A>G Mutation Associated with Mitochondrial Encephalomyopathy and Literature Review.
13. Reading and spelling disorders in a school‐based population screening in Sicily (Italy)
14. Stile attributivo, rappresentazione dell'intelligenza e obiettivi di apprendimento in ragazzi con Funzionamento Intellettivo Borderline
15. Reading Deficits in Intellectual Disability Are still an Open Question: A Narrative Review.
16. A case of savant syndrome in a child with autism spectrum disorder
17. The Mitochondrial tRNASer(UCN) Gene: A Novel m.7484A>G Mutation Associated with Mitochondrial Encephalomyopathy and Literature Review
18. Coexistence of mitochondrial and nuclear DNA mutations in a woman with mitochondrial encephalomyopathy and double cortex.
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