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Last Name

Schreiber, John

TitleAssistant Professor
InstitutionChildrens National Medical Center
DepartmentNeurophysiology, Epilepsy and Neuro-ICU
Address111 Michigan Ave NW
Washington DC 20010
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    Collapse Bibliographic 
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Bartolini L, Whitehead MT, Ho CY, Sepeta LN, Oluigbo CO, Havens K, Freilich ER, Schreiber JM, Gaillard WD. Temporal lobe epilepsy and focal cortical dysplasia in children: A tip to find the abnormality. Epilepsia. 2017 Jan; 58(1):113-122. PMID: 27864929.
      View in: PubMed
    2. Lam C, Ferreira C, Krasnewich D, Toro C, Latham L, Zein WM, Lehky T, Brewer C, Baker EH, Thurm A, Farmer CA, Rosenzweig SD, Lyons JJ, Schreiber JM, Gropman A, Lingala S, Ghany MG, Solomon B, Macnamara E, Davids M, Stratakis CA, Kimonis V, Gahl WA, Wolfe L. Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylation. Genet Med. 2017 Feb; 19(2):160-168. PMID: 27388694.
      View in: PubMed
    3. Schreiber JM, Pearl PL, Dustin I, Wiggs E, Barrios E, Wassermann EM, Gibson KM, Theodore WH. Biomarkers in a Taurine Trial for Succinic Semialdehyde Dehydrogenase Deficiency. JIMD Rep. 2016; 30:81-87. PMID: 27338723.
      View in: PubMed
    4. Simons C, Griffin LB, Helman G, Golas G, Pizzino A, Bloom M, Murphy JL, Crawford J, Evans SH, Topper S, Whitehead MT, Schreiber JM, Chapman KA, Tifft C, Lu KB, Gamper H, Shigematsu M, Taft RJ, Antonellis A, Hou YM, Vanderver A. Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defect. Am J Hum Genet. 2015 Apr 02; 96(4):675-81. PMID: 25817015; PMCID: PMC4385183.
    5. Benbadis SR, Ewen JB, Schreiber JM, Trescher WH. Variations in EEG discharges predict ADHD severity within individual Smith-Lemli-Opitz patients. Neurology. 2015 Jan 27; 84(4):436. PMID: 25628433.
      View in: PubMed
    6. Ewen JB, Schreiber JM, Trescher WH. Author response. Neurology. 2015 Jan 27; 84(4):436. PMID: 25789389.
      View in: PubMed
    7. Freilich ER, Schreiber JM, Zelleke T, Gaillard WD. Pediatric status epilepticus: identification and evaluation. Curr Opin Pediatr. 2014 Dec; 26(6):655-61. PMID: 25313971.
      View in: PubMed
    8. Schreiber JM, Lanham DC, Trescher WH, Sparks SE, Wassif CA, Caffo BS, Porter FD, Tierney E, Gropman AL, Ewen JB. Variations in EEG discharges predict ADHD severity within individual Smith-Lemli-Opitz patients. Neurology. 2014 Jul 08; 83(2):151-9. PMID: 24920862; PMCID: PMC4117167.
    9. Pierson TM, Yuan H, Marsh ED, Fuentes-Fajardo K, Adams DR, Markello T, Golas G, Simeonov DR, Holloman C, Tankovic A, Karamchandani MM, Schreiber JM, Mullikin JC. GRIN2A mutation and early-onset epileptic encephalopathy: personalized therapy with memantine. Ann Clin Transl Neurol. 2014 Mar 01; 1(3):190-198. PMID: 24839611.
      View in: PubMed
    10. Pearl PL, Schreiber J, Theodore WH, McCarter R, Barrios ES, Yu J, Wiggs E, He J, Gibson KM. Taurine trial in succinic semialdehyde dehydrogenase deficiency and elevated CNS GABA. Neurology. 2014 Mar 18; 82(11):940-4. PMID: 24523482; PMCID: PMC3963004.
    11. Schreiber JM, Zelleke T, Gaillard WD, Kaulas H, Dean N, Carpenter JL. Continuous video EEG for patients with acute encephalopathy in a pediatric intensive care unit. Neurocrit Care. 2012 Aug; 17(1):31-8. PMID: 22565632.
      View in: PubMed
    12. Schreiber J, Chapman KA, Summar ML, Ah Mew N, Sutton VR, MacLeod E, Stagni K, Ueda K, Franks J, Island E, Matern D, Peña L, Smith B, Urv T, Venditti C, Chakarapani A, Gropman AL. Neurologic considerations in propionic acidemia. Mol Genet Metab. 2012 Jan; 105(1):10-5. PMID: 22078457.
      View in: PubMed
    13. Schreiber JM, Gaillard WD. Treatment of refractory status epilepticus in childhood. Curr Neurol Neurosci Rep. 2011 Apr; 11(2):195-204. PMID: 21174176.
      View in: PubMed
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