A sample of some of our resident publications in peer reviewed journals completed with our faculty during residency over the last 5 years.

Bach I, Surathi P, Montealegre N, Abu-Hadid O, Rubenstein S, Redko S, Gupta S, Hillen M, Patel P, Khandelwal P, Kamel A.   Stroke in COVID-19: a single-centre initial experience in a hotspot of the pandemic.  Stroke Vasc Neurol. 2020 Sep 24 Online ahead of print. PMID: 32973116 

Oh DM, Johnson J, Shah B, Bhat S, Nuoman R, Ming X.  Treatment of vagus nerve stimulator-induced sleep-disordered breathing: A case series.
  Epilepsy Behav Rep. 2019 Jun 22;12:100325. PMID: 31497754 

Silverstein S, Veerapandiyan A, Hayes-Rosen C, Ming X, Kornitzer J.  A novel intronic homozygous mutation in the AMT gene of a patient with nonketotic hyperglycinemia and hyperammonemia.
   Metab Brain Dis. 2019 Feb;34(1):373-376. PMID: 30350008

Aravindhan A, Shah K, Pak J, Veerapandiyan A.  Early-onset epileptic encephalopathy with myoclonic seizures related to 9q33.3-q34.11 deletion involving STXBP1 and SPTAN1 genes.
     Epileptic Disord. 2018 Jun 1;20(3):214-218. PMID: 29897043 

Aravindhan A, Shah K, Pak J, Veerapandiyan A.   Early-onset epileptic encephalopathy with myoclonic seizures related to 9q33.3-q34.11 deletion involving STXBP1 and SPTAN1 genes.
  Epileptic Disord. 2018 Jun 1;20(3):214-218. PMID: 29897043 

Mulvey MA, Veerapandiyan A, Marks DA, Ming X.  Electronic health record cue identifies epilepsy patients at risk for obstructive sleep apnea.
   Neurol Clin Pract. 2018 Dec;8(6):468-471. PMID: 30588375

Aravindhan A, Veerapandiyan A, Earley C, Thulasi V, Kresge C, Kornitzer J.    Child Neurology: Type 1 sialidosis due to a novel mutation in NEU1 gene.

Neurology. 2018 Mar 27;90(13):622-624. PMID: 29581327 

Veerapandiyan A, Aravindhan A, Takahashi JH, Segal D, Pecor K, Ming X.   Use of Head Computed Tomography (CT) in the Pediatric Emergency Department in Evaluation of Children With New-Onset Afebrile Seizure.
   J Child Neurol. 2018 Oct;33(11):708-712. PMID: 29987971

Veerapandiyan A, Enner S, Thulasi V, Ming X.   A Rare Syndrome of GRID2 Deletion in 2 Siblings.
    Child Neurol Open. 2017 Aug 22;4 PMID: 28856174 

Al-Mufti F, Alkanaq A, Amuluru K, Nuoman R, Abdulrazzaq A, Sami T, Nuoaman H, Hayes-Rosen C, Prestigiacomo CJ, Gandhi CD.Genetic Insights into Cerebrovascular Disorders: A Comprehensive Review.
   J Vasc Interv Neurol. 2017 Oct;9(5):21-32.  PMID: 29163746 

Al-Mufti F, Amuluru K, Changa A, Lander M, Patel N, Wajswol E, Al-Marsoummi S, Alzubaidi B, Singh IP, Nuoman R, Gandhi C.   Traumatic brain injury and intracranial hemorrhage-induced cerebral vasospasm: a systematic review.
   Neurosurg Focus. 2017 Nov;43(5) PMID: 29088959 

Thulasi V, Veerapandiyan A, Pletcher BA, Tong CM, Ming X.  A Case of Brown- Vialetto-Van Laere Sydrome Due To a Novel Mutaion in SLC52A3 Gene: Clinical Course and Rsponse to Riboflavin.  Child Neurology Open. 2017 Aug 22;4: 2329048X17725610  PMID: 28856173

Veerapandiyan A, Chaudhari A, Deo P, Ming X.   Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS): A pediatric case report with six year follow-up.
   Mult Scler Relat Disord. 2017 Oct;17:95-98. PMID: 29055484

Veerapandiyan A, Chaudhari A, Traba CM, Ming X.   Novel mutation in mitochondrial DNA in 2 siblings with Leigh syndrome.
   Neurol Genet. 2016 Aug 16;2(5):e99. PMID: 27574709 

Segal D, Heary RF, Sabharwal S, Barry MT, Ming X.   Severe holocord syrinx in a child with megalencephaly-capillary malformation syndrome.
   J Neurosurg Pediatr. 2016 Jul;18(1):79-82.  PMID: 27035547

Philip M, Kornitzer J, Marks D, Lee HJ, Souayah N.   Alice in Wonderland Syndrome associated with a temporo-parietal cavernoma.
  Brain Imaging Behav. 2015 Dec;9(4):910-2. PMID: 25663031

American Academy of Neurology Annual Meeting Abstracts & Posters
A sample of resident abstracts and posters over the last 5 years.

2020 AAN
Rubenstein S, Gupta S, Mulvey M, Marks D.   Symptomatic Ictal Bradycardia, An Important Consideration in the Workup of Syncope in Temporal Lobe Epilepsy   
Rubenstein S, Hilmi A, Ming X.   Atypical Presentation of Lebers Hereditary Optic Neuropathy    

2019 AAN
Gupta S, Toor F, You B, Kornitzer J.   Novel Mutation in ACSL4 Gene Leading to X-linked Intellectual Disability, Autism and ADHD  

2018 AAN
Gupta S, Pecor K, Agarwal S, Oh D, Kornitzer J.   Micronutrient Levels in Patients with ADHD  
Gupta S, Mulvey M, Veerapandiyan A, Ming X.   The Effects of Assessing Obstructive Sleep Apnea Using a Prompt in the Electronic Health Record in Adult Patients with Epilepsy  

2017 AAN

Kornitzer J, Veerapandiyan A, Jakubowski L, Hayes-Rosen C, Ming X.   Homozygous AMT Mutation in a Patient with Neonatal Onset Nonketotic Hyperglycinemia and Hyperammonemia     

2015 AAN

Kornitzer J, Hillen M, Hayes-Rosen C, Hidalgo A.   Is Clinical Neurology Exposure Increasing In Medical Schools Throughout The United States?

Kornitzer J, Phillips M, Souayah N, Marks D, Lee H.  Alice in Wonderland Syndrome associated with temporo-parietal cavernoma. 

Segal D, Sheikh Z, Shahbahrami K, Garikparthy J, Monserrate A, Tentler A, Hillen M, Shih L, Pletcher B.   An Adult Presenting with Neurological Symptoms Attributed to Hyperhomocysteinemia that Resolved with Treatment.