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4. miR-376a-3p and miR-376b-3p overexpression in Hutchinson-Gilford progeria fibroblasts inhibits cell proliferation and induces premature senescence

9. Leukocytes containing lipid inclusions in congenital ichthyosis without classical Chanarin‐Dorfman mutations.

10. Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

12. A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities

13. miR-140-5p and miR-140-3p: Key Actors in Aging-Related Diseases?

23. An overview of treatment strategies for Hutchinson-Gilford Progeria syndrome

38. Detection of ALK and ROS1 rearrangements by immunocytochemistry on cytological samples

39. SRPX2 mutations in disorders of language cortex and cognition

40. Large-scale expression study of human mesial temporal lobe epilepsy: evidence for dysregulation of the neurotransmission and complement systems in the entorhinal cortex

44. A rare case of pleural localisation of both metastatic Merkel cell carcinoma and chronic lymphocytic leukaemia.

45. Molecular evolution of the human SRPX2 gene that causes brain disorders of the Rolandic and Sylvian speech areas

46. Pleural effusion in a patient with Ewing sarcoma.

48. Detection of EGFR, KRAS and BRAF mutations in metastatic cells from cerebrospinal fluid

50. Chest ultrasonography to assess the kinetics and efficacy of talc pleurodesis in a model of pneumothorax: an experimental animal study

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