640 results on '"Blouin, J."'
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2. Vestibular control of deep and superficial lumbar muscles
3. CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells
4. Detection of TPSAB1 copy number variation for the diagnosis of hereditary alpha‐tryptasemia by quantitative PCR.
5. Vers une quantification de la dominance oculaire pour une meilleure prise en charge des pathologies de l’œil
6. Caractéristiques cliniques et biochimiques des lithiases urinaires de l’enfant
7. Cortical involvement in the StartReact effect
8. A Holistic Approach for Integrated Requirements Modeling in the Product Development Process
9. Online control of anticipated postural adjustments in step initiation: Evidence from behavioral and computational approaches
10. Identification d'un agrégat inhabituel d'anaplasmose granulocytaire humaine dans la région de l'Estrie, Québec, Canada en 2021
11. Age-related decline in sensory processing for locomotion and interception
12. Reply from J. S. Blouin, H. J. Brown, M. E. Héroux, J. T. Inglis and G. P. Siegmund
13. Observational study of the effect of μ-opioid receptor genetic polymorphism on intrathecal opioid labor analgesia and post-cesarean delivery analgesia
14. Visual Guidance of Pointing Movements: Kinematic Evidence for Static and Kinetic Feedback Channels
15. Down syndrome: a model for the study of Alzheimer’s disease and aging
16. Contributions to enhanced activity in rectus femoris in response to Lokomat-applied resistance
17. Can prepared anticipatory postural adjustments be updated by proprioception?
18. Multiple mantleomas: an unusual clinical presentation of an intriguing tumour
19. Multiplex targeted high-throughput sequencing for Mendelian cardiac disorders
20. Comparison of direct health care costs related to the pharmacological treatment of osteoporosis and to the management of osteoporotic fractures among compliant and noncompliant users of alendronate and risedronate: a population-based study
21. Acute and selective regulation of glyceroneogenesis and cytosolic phosphoenolpyruvate carboxykinase in adipose tissue by thiazolidinediones in type 2 diabetes
22. A task-relevant experimental pain model to target motor adaptation
23. Accuracy of spatial localization depending on head posture in a perturbed gravitoinertial force field
24. Telesonography: Virtual 3D Image Processing of Remotely Acquired Abdominal, Vascular, and Fetal Sonograms
25. Recurrent posterior reversible encephalopathy syndrome in a patient with acute intermittent porphyria
26. Therapeutic Potential of Proteasome Inhibitors in Congenital Erythropoietic Porphyria: OC22
27. Genetic Background Affects Anemia, Iron Metabolism, Hepatic and Renal Function in a Mouse Model of Congenital Erythropoietic Porphyria (CEP): OC20
28. Genetic heterogeneity in schizophrenia: stratification of genome scan data using co-segregating related phenotypes
29. Online corrective responses following target jump in altered gravitoinertial force field point to nested feedforward and feedback control
30. Molecular characterization and clinical history of a homozygous functional C1q abnormality: P179
31. Double-Step Paradigm in Microgravity: Preservation of Sensorimotor Flexibility in Altered Gravitational Force Field
32. Disseminated Tuberculosis in a Patient with Hereditary C1-inhibitor Deficiency
33. Updating visual space during passive and voluntary head-in-space movements
34. The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
35. Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia
36. Infection par Neisseria meningitidis: Critères cliniques orientant vers un déficit en protéines du complement
37. A method for the extraction of genomic DNA from human brain tissue fixed and stored in formalin for many years
38. Local subcutaneous and muscle pain impairs detection of passive movements at the human thumb
39. A DNA resequencing array for pathogenic mutation detection in hypertrophic cardiomyopathy: 203
40. Epistatic Interactions With a Common Hypomorphic Ret Allele in Syndromic Hirschsprung Disease
41. Posterpräsentation
42. Reference systems for coding spatial information in normal subjects and a deafferented patient
43. Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome
44. Pre-eclampsia and peripartum cardiomyopathy in molar pregnancy: clinical implication for maternally imprinted genes
45. A balanced complex chromosomal rearrangement (BCCR) in a family with reproductive failure
46. Restricted genetic defects underlie human complement C6 deficiency
47. Directional control of rapid arm movements: the role of the kinetic visual feedback system
48. Lack of evidence of a specific role for C4A gene deficiency in determining disease susceptibility among C4-deficient patients with systemic lupus erythematosus (SLE)
49. Development of a conversion model between mechanical and electrical vestibular stimuli
50. Coding Spatial Information Through Retinal and Labyrinthine Signals
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