Instructor in Neurology, Boston Children's Hospital

Neurology

Annapurna Poduri, MD works in the field of Neurology. She attended Perelman School of Medicine at the University of Pennsylvania. Dr. Annapurna Poduri is a published doctor. She has 44 publications published. The most current publication "CA3 neuronal degeneration follows chronic entorhinal cortex lesions."

Publications

---

• Disorders of Microtubule Function in Neurons: Imaging Correlates.
• Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain.
• Surgery for intractable Epilepsy due to unilateral brain disease: a retrospective study comparing hemispherectomy techniques.
• Genetic forms of epilepsies and other paroxysmal disorders.
• Copy number variation plays an important role in clinical Epilepsy.
• Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures.
• Clobazam: Effect on Frequency of Seizures and Safety Profile in Different Subgroups of Children With Epilepsy.
• Inherited mutations of SLC25A22.
• Clinical application and evaluation of the Bien diagnostic criteria for Rasmussen encephalitis.
• Witnessed sleep-related seizure and sudden unexpected death in infancy: a case report.
• Polymicrogyria-associated Epilepsy: A multicenter phenotypic study from the Epilepsy Phenome/Genome Project.
• De novo mutations in epileptic encephalopathies.
• Altered white matter connectivity and network organization in polymicrogyria revealed by individual gyral topology-based analysis.
• Somatic mutation, genomic variation, and neurological disease.
• Whole genome sequencing identifies SCN2A mutation in monozygotic twins with Ohtahara syndrome and unique neuropathologic findings.
• Location of periventricular nodular heterotopia is related to the malformation phenotype on MRI.
• Using Whole-Exome Sequencing to Identify Inherited Causes of Autism.
• Dacrystic seizures: Demographic, semiologic, and etiologic insights from a multicenter study in long-term video-EEG monitoring units.
• Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy.
• Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations.
• Inheritance of febrile seizures in sudden unexplained death in toddlers.
• Effect of ACE inhibitors and beta-blockers on homocysteine levels in essential hypertension.
• Apolipoprotein E4 and beta amyloid in senile plaques and cerebral blood vessels of aged rhesus monkeys.
• CA3 neuronal degeneration follows chronic entorhinal cortex lesions.
• Congenital microcephaly with a simplified gyral pattern: associated findings and their significance.
• Micro-duplications of 1q32.1 associated with neurodevelopmental delay.
• Rufinamide for the treatment of epileptic spasms.
• Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.
• Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.
• Expect the unexpected in Epilepsy genetics: Mutations in an Epilepsy gene considered to be benign result in a severe phenotype.
• Trends in resource utilization by children with neurological impairment in the United States inpatient health care system: a repeat cross-sectional study.
• Treatment of malignant migrating partial Epilepsy of infancy with rufinamide: report of five cases.
• Epilepsy genetics--past, present, and future.
• The syndrome of perisylvian polymicrogyria with congenital arthrogryposis.
• Cerebral volumetric analysis over time in children with malformations of cortical development: a quantitative investigation.
• Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort.
• Nocturnal choking episodes: under-recognized and misdiagnosed.
• Experience with rufinamide in a pediatric population: a single center's experience.
• Ethnically diverse causes of Walker-Warburg syndrome (WWS): FCMD mutations are a more common cause of WWS outside of the Middle East.
• Oxcarbazepine in children with nocturnal frontal-lobe Epilepsy.
• Focal cortical malformations can show asymmetrically higher uptake on interictal fluorine-18 fluorodeoxyglucose positron emission tomography (PET).
• Does albendazole affect seizure remission and computed tomography response in children with neurocysticercosis? A Systematic review and meta-analysis.
• A distinct asymmetrical pattern of cortical malformation: large unilateral malformation of cortical development with contralateral periventricular nodular heterotopia ...

Schools

---

• Perelman School of Medicine University of Pennsylvania

• Chldrns Hospital Boston

• Boston Combined Peds

• University Of Pennsylvania

Procedures Preformed

---

• EEG (Electroencephalogram)

Conditions Treated

---

• Convulsions
• Epilepsy

Doctors Specialties

---

• Clinical Neurophysiology
• Neurology

Accepted Insurances

---

Education

---

• Children's Hospital of Philadelphia
• Boston Children's Hospital
• Perelman School of Medicine at the University of Pennsylvania

Hospital

---

• South Shore Hospital
• Boston Children's Hospital

Helpful Reviews

---

Give Anonymous Review

Similar Doctors

---

	Dr. Atul Maheshwari, MD This Doctor is OpenDoctor Recommended.
	Dr. Jang-Ho J. Cha, MD
	Dr. Tommy Thomas, MD This Doctor is OpenDoctor Recommended.
	Dr. Alice D. Lam, MD This Doctor is OpenDoctor Recommended.
	Dr. Oluwole O. Awosika, MD
	Dr. Elizabeth R. Gerstner, MD This Doctor is OpenDoctor Recommended.
	Dr. Jeffrey Bolton, MD This Doctor is OpenDoctor Recommended.
	Dr. Tracey A. Milligan, MD This Doctor is OpenDoctor Recommended.
	Dr. Peter R. Bergethon, MD This Doctor is OpenDoctor Recommended.

---

Doctor Directory | TOS | twitter | FB | Angel | blog