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JOHN CAREY

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Pediatrics
DivisionPediatrics-Emergency Medicine
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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. Carey JM, Studnek JR, Browne LR, Ostermayer DG, Grawey T, Schroter S, Lerner EB, Shah MI. Paramedic-Identified Enablers of and Barriers to Pediatric Seizure Management: A Multicenter, Qualitative Study. Prehosp Emerg Care. 2019 Nov-Dec; 23(6):870-881. PMID: 30917730.
      View in: PubMed
    2. Peron A, Vignoli A, Briola F, Morenghi E, Tansini L, Alfano RM, Bulfamante G, Terraneo S, Ghelma F, Banderali G, Viskochil DH, Carey JC, Canevini MP. Deep phenotyping of patients with Tuberous Sclerosis Complex and no mutation identified in TSC1 and TSC2. Eur J Med Genet. 2018 Jul; 61(7):403-410. PMID: 29432982.
      View in: PubMed
    3. Clements CC, Wenger TL, Zoltowski AR, Bertollo JR, Miller JS, de Marchena AB, Mitteer LM, Carey JC, Yerys BE, Zackai EH, Emanuel BS, McDonald-McGinn DM, Schultz RT. Critical region within 22q11.2 linked to higher rate of autism spectrum disorder. Mol Autism. 2017; 8:58. PMID: 29090080.
      View in: PubMed
    4. Shah MI, Carey JM, Rapp SE, Masciale M, Alcanter WB, Mondragon JA, Camp EA, Prater SJ, Doughty CB. Impact of High-Fidelity Pediatric Simulation on Paramedic Seizure Management. Prehosp Emerg Care. 2016 Jul-Aug; 20(4):499-507. PMID: 26953677.
      View in: PubMed
    5. John M. Carey, M.D., and Manish I. Shah, M.D. Pediatric Prehospital Seizure Management. Clinical Pediatric Emergency Medicine. 2014; 15(1):59-66.
    6. Battaglia A, Filippi T, Carey JC. Update on the clinical features and natural history of Wolf-Hirschhorn (4p-) syndrome: experience with 87 patients and recommendations for routine health supervision. Am J Med Genet C Semin Med Genet. 2008 Nov 15; 148C(4):246-51. PMID: 18932224.
      View in: PubMed
    7. Battaglia A, Hoyme HE, Dallapiccola B, Zackai E, Hudgins L, McDonald-McGinn D, Bahi-Buisson N, Romano C, Williams CA, Brailey LL, Braley LL, Zuberi SM, Carey JC. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation. Pediatrics. 2008 Feb; 121(2):404-10. PMID: 18245432.
      View in: PubMed
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