Over the last decade there has been an enormous increase in basic neuroscience research in a variety of areas including systems neuroscience, developmental neuroscience, molecular neuroscience, and cellular neurophysiology/neuropharmacology. While clinical neuroscientists have managed to keep pace with the information and technology that most directly impacts upon the daily practice of medicine, they have been unable to appreciate the full implications of much of this basic research. Moreover, they have not been able to actively participate in the actual acquisition of new neurobiological data because the research technology is beyond the scope of medical school and neurology residency education. The NSADA institutional award represents a creative new mechanism to bring potential young academic pediatric neurologists into fundamental neuroscience research. The five year award allows motivated individuals to get sufficient didactic and laboratory experience to begin sophisticated independent investigation in the neurosciences. We expect to admit pediatric neurology residents into the NSADA program for two research years prior to the start of their core clinical neurology residency. After completion of clinical neurology training, they will have three additional years of intense laboratory exposure. This is the equivalent of two standard postdoctoral fellowships and should provide the NSADA fellows with a substantial research background. The Division of Pediatric Neurology and Program in Neurosciences at Washington University have extensive intellectual and physical resources that will be available to NSADA trainees. The 18 mentors identified for this grant have been selected from over 75 full-time faculty members with neuro-science labs. They represent a group with superb teaching skills and proven interest in the research development of clinicians. They should insure our ability to educate these pediatric neuroscientists for the next millennium. This research immersion should translate into better care for children with neurological disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Physician Scientist Award (Program) (PSA) (K12)
Project #
5K12NS001690-03
Application #
2259765
Study Section
NST-2 Subcommittee (NST)
Project Start
1993-07-01
Project End
1998-06-30
Budget Start
1995-07-01
Budget End
1996-06-30
Support Year
3
Fiscal Year
1995
Total Cost
Indirect Cost
Name
Washington University
Department
Neurology
Type
Schools of Medicine
DUNS #
062761671
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
El Ters, Nathalie M; Mathur, Amit M; Jain, Siddharth et al. (2018) Long term electroencephalography in preterm neonates: Safety and quality of electrode types. Clin Neurophysiol 129:1366-1371
McGill, Bryan E; Barve, Ruteja A; Maloney, Susan E et al. (2018) Abnormal Microglia and Enhanced Inflammation-Related Gene Transcription in Mice with Conditional Deletion of Ctcf in Camk2a-Cre-Expressing Neurons. J Neurosci 38:200-219
Morris, Stephanie M; Gutmann, David H (2018) A genotype-phenotype correlation for quantitative autistic trait burden in neurofibromatosis 1. Neurology 90:377-379
Ryckman, Justin; Hilton, Claudia; Rogers, Cynthia et al. (2017) Sensory processing disorder in preterm infants during early childhood and relationships to early neurobehavior. Early Hum Dev 113:18-22
Anastasaki, Corina; Morris, Stephanie M; Gao, Feng et al. (2017) Children with 5'-end NF1 gene mutations are more likely to have glioma. Neurol Genet 3:e192
Smyser, Christopher D; Snyder, Abraham Z; Shimony, Joshua S et al. (2016) Resting-State Network Complexity and Magnitude Are Reduced in Prematurely Born Infants. Cereb Cortex 26:322-333
Morris, Stephanie M; Acosta, Maria T; Garg, Shruti et al. (2016) Disease Burden and Symptom Structure of Autism in Neurofibromatosis Type 1: A Study of the International NF1-ASD Consortium Team (INFACT). JAMA Psychiatry 73:1276-1284
Dietz, Alexander R; Bucelli, Robert C; Pestronk, Alan et al. (2016) Nerve ultrasound identifies abnormalities in the posterior interosseous nerve in patients with proximal radial neuropathies. Muscle Nerve 53:379-83
Zaidman, Craig M; Malkus, Elizabeth C; Connolly, Anne M (2015) Muscle ultrasound quantifies disease progression over time in infants and young boys with duchenne muscular dystrophy. Muscle Nerve 52:334-8
Ng, Kay W; Connolly, Anne M; Zaidman, Craig M (2015) Quantitative muscle ultrasound measures rapid declines over time in children with SMA type 1. J Neurol Sci 358:178-82

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