Annapurna Poduri

Affiliations: 
Neurology Boston Children's Hospital, Harvard Medical School 
Google:
"Annapurna Poduri"
Mean distance: (not calculated yet)
 
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

Ernst ME, Baugh EH, Thomas A, et al. (2021) CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity. Epilepsia
Ernst ME, Baugh EH, Thomas A, et al. (2021) CSNK2B: A broad spectrum of neurodevelopmental disability and epilepsy severity. Epilepsia
Olson HE, Costantini JG, Swanson LC, et al. (2021) Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure. Developmental Medicine and Child Neurology
Olson HE, Costantini JG, Swanson LC, et al. (2021) Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure. Developmental Medicine and Child Neurology
Keywan C, Poduri AH, Goldstein RD, et al. (2021) Genetic Factors Underlying Sudden Infant Death Syndrome. The Application of Clinical Genetics. 14: 61-76
Berg AT, Mahida S, Poduri A. (2021) KCNQ2-DEE: developmental or epileptic encephalopathy? Annals of Clinical and Translational Neurology. 8: 666-676
McGraw CM, Mahida S, Jayakar P, et al. (2021) Uridine-responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings. Annals of Clinical and Translational Neurology
Ni M, Afroze B, Xing C, et al. (2021) A pathogenic UFSP2 variant in an autosomal recessive form of pediatric neurodevelopmental anomalies and epilepsy. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Dentici ML, Alesi V, Quinodoz M, et al. (2021) Biallelic variants in cause a severe neurodevelopmental disorder with microcephaly, bilateral cataract, epilepsy and simplified gyration. Journal of Medical Genetics
Moufawad El Achkar C, Harrer M, Smith L, et al. (2020) Characterization of the GABRB2 associated neurodevelopmental disorders. Annals of Neurology
See more...