17 results on '"Pellissier, Jean-François"'
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2. Reply: MFN2, a new gene responsible for mitochondrial DNA depletion
3. Reply: MFN2 mutations cause compensatory mitochondrial DNA proliferation
4. The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy ‘plus’ phenotype
5. NON-LETHAL NEONATAL NEUROMUSCULAR VARIANT OF GLYCOGENOSIS TYPE IV WITH NOVEL GBE1 MUTATIONS
6. Analysis of the DYSF Mutational Spectrum in a Large Cohort of Patients
7. Type 2 Myotonic Dystrophy Can Be Predicted by the Combination of Type 2 Muscle Fiber Central Nucleation and Scattered Atrophy
8. Biological Effects of Four PSEN1 Gene Mutations Causing Alzheimer Disease With Spastic Paraparesis and Cotton Wool Plaques
9. Progressive multifocal leukoencephalopathy in HIV-2-infected patient
10. Lewis–Sumner syndrome and multifocal motor neuropathy
11. Pellagra: A Rare Disease Observed in a Victim of Mental and Physical Abuse
12. Multiminicore Disease in a Family Susceptible to Malignant Hyperthermia: Histology, In Vitro Contracture Tests, and Genetic Characterization
13. HLA–DRB1*01 and macrophagic myofasciitis
14. CD44H is expressed by cells of the oligodendrocyte lineage and by oligodendrogliomas in humans
15. Human synemin gene generates splice variants encoding two distinct intermediate filament proteins
16. Tubular lesions and tubular cell adhesion molecules for the prognosis of lupus nephritis
17. Chronic hepatitis C virus infection associated with a generalized granuloma annulare
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