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1. Inhibiting glycolysis rescues memory impairment in an intellectual disability Gdi1-null mouse

2. A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome

11. La Mano in Movimento. Anticipazione del Gesto Grafico

15. Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly

32. A quantitative comparison between a navigated Cartesian and a self‐navigated radial protocol from clinical studies for free‐breathing 3D whole‐heart bSSFP coronary MRA.

33. A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome

35. Altered fronto-striatal functions in the Gdi1 -null mouse model of X-linked Intellectual Disability

37. Alterations in the brain adenosine metabolism cause behavioral and neurological impairment in ADA-deficient mice and patients

38. A Novel Mecp2Y120D Knock-in Model Displays Similar Behavioral Traits But Distinct Molecular Features Compared to the Mecp2-Null Mouse Implying Precision Medicine for the Treatment of Rett Syndrome.

39. Accelerated and high‐resolution cardiac T2 mapping through peripheral k‐space sharing.

40. Disruption of ArhGAP15 results in hyperactive Rac1, affects the architecture and function of hippocampal inhibitory neurons and causes cognitive deficits

44. Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks

45. Managing of dredged sediments applying a non conventional technique

47. Loss of Either Rac1 or Rac3 GTPase Differentially Affects the Behavior of Mutant Mice and the Development of Functional GABAergic Networks

48. 2-Deoxy-d-Glucose Ameliorates PKD Progression

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