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Annals of Neurology
|
August 28, 2023
Early Treatment with Vigabatrin Does Not Decrease Focal Seizures or Improve Cognition in Tuberous Sclerosis Complex: The PREVeNT Trial
Elizabeth Martina Bebin, Jurriaan M Peters, Brenda E Porter, et al.
JCI Insight
|
February 28, 2020
FPR-1 is an important regulator of neutrophil recruitment and a tissue-specific driver of pulmonary fibrosis
Jack Leslie, Ben Jm Millar, Alicia Del Carpio Pons, et al.
Pediatric Neurology
|
August 14, 2024
Drug-Resistant Epilepsy in Tuberous Sclerosis Complex Is Associated With TSC2 Genotype: More Findings From the Preventing Epilepsy Using Vigatrin (PREVeNT) Trial
Laura S Farach, Melissa A Richard, Aynara C Wulsin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 12, 2000
Augmentation of immune responses to HIV-1 and simian immunodeficiency virus DNA vaccines by IL-2/Ig plasmid administration in rhesus monkeys
D H Barouch, A Craiu, M J Kuroda, et al.
Pediatric Neurology
|
October 8, 2025
Neurodevelopmental Outcomes From the PREVeNT Trial
Sarah E O'Kelley, Jamie K Capal, Tarrant O McPherson, et al.
Pediatric Neurology
|
March 29, 2026
Early Vigabatrin Treatment Before Seizure Onset Decreased Interictal Epileptiform Discharges Over the Duration of the PREVeNT Study
Tarrant O McPherson, E Martina Bebin, Laura S Farach, et al.
Pediatric Neurology
|
August 16, 2021
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations
Hope Northrup, Mary E Aronow, E Martina Bebin, et al.
British Journal of Cancer
|
March 24, 2011
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
A Osorio, R L Milne, R Alonso, et al.
British Journal of Cancer
|
June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
A Jakubowska, D Rozkrut, A Antoniou, et al.
British Journal of Cancer
|
November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)
A Osorio, R L Milne, G Pita, et al.
Page
of 30
Search research articles
Search
Showing results (291-300 of 300) with videos related to
Sort By:
Page
of 30
You have reached the last page of results.
This site can display upto 300 results.
Annals of Neurology
|
August 28, 2023
Early Treatment with Vigabatrin Does Not Decrease Focal Seizures or Improve Cognition in Tuberous Sclerosis Complex: The PREVeNT Trial
Elizabeth Martina Bebin, Jurriaan M Peters, Brenda E Porter, et al.
JCI Insight
|
February 28, 2020
FPR-1 is an important regulator of neutrophil recruitment and a tissue-specific driver of pulmonary fibrosis
Jack Leslie, Ben Jm Millar, Alicia Del Carpio Pons, et al.
Pediatric Neurology
|
August 14, 2024
Drug-Resistant Epilepsy in Tuberous Sclerosis Complex Is Associated With TSC2 Genotype: More Findings From the Preventing Epilepsy Using Vigatrin (PREVeNT) Trial
Laura S Farach, Melissa A Richard, Aynara C Wulsin, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 12, 2000
Augmentation of immune responses to HIV-1 and simian immunodeficiency virus DNA vaccines by IL-2/Ig plasmid administration in rhesus monkeys
D H Barouch, A Craiu, M J Kuroda, et al.
Pediatric Neurology
|
October 8, 2025
Neurodevelopmental Outcomes From the PREVeNT Trial
Sarah E O'Kelley, Jamie K Capal, Tarrant O McPherson, et al.
Pediatric Neurology
|
March 29, 2026
Early Vigabatrin Treatment Before Seizure Onset Decreased Interictal Epileptiform Discharges Over the Duration of the PREVeNT Study
Tarrant O McPherson, E Martina Bebin, Laura S Farach, et al.
Pediatric Neurology
|
August 16, 2021
Updated International Tuberous Sclerosis Complex Diagnostic Criteria and Surveillance and Management Recommendations
Hope Northrup, Mary E Aronow, E Martina Bebin, et al.
British Journal of Cancer
|
March 24, 2011
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
A Osorio, R L Milne, R Alonso, et al.
British Journal of Cancer
|
June 7, 2012
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
A Jakubowska, D Rozkrut, A Antoniou, et al.
British Journal of Cancer
|
November 19, 2009
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)
A Osorio, R L Milne, G Pita, et al.
Page
of 30