Dimitri P Agamanolis

Dimitri P Agamanolis

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Dimitri P Agamanolis

Dimitri P Agamanolis

Publications by authors named "Dimitri P Agamanolis"

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7Publications

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Neuropathological Findings in Susac Syndrome: An Autopsy Report.

J Neuropathol Exp Neurol 2019 Jun;78(6):515-519

Formerly of the Department of Pediatric Rheumatology of the Cleveland Clinic Foundation, Cleveland, Ohio.

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https://academic.oup.com/jnen/article/78/6/515/5477334
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http://dx.doi.org/10.1093/jnen/nlz031DOI Listing
June 2019

Use of next-generation sequencing as a diagnostic tool for congenital myasthenic syndrome.

Pediatr Neurol 2014 Nov 6;51(5):717-20. Epub 2014 Aug 6.

Division of Neurology, NeuroDevelopmental Science Center, Akron Children's Hospital, Akron, Ohio; Department of Pediatrics, Northeast Ohio Medical University, Rootstown, Ohio. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S08878994140046
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http://dx.doi.org/10.1016/j.pediatrneurol.2014.07.032DOI Listing
November 2014

An unusual form of superficially disseminated glioma in children: report of 3 cases.

J Child Neurol 2012 Jun;27(6):727-33

Department of Pathology, Akron Children's Hospital and Northeastern Ohio Universities College of Medicine, Akron, OH 44308, USA.

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http://dx.doi.org/10.1177/0883073811426500DOI Listing
June 2012

Differential expression and cellular distribution of gamma-tubulin and betaIII-tubulin in medulloblastomas and human medulloblastoma cell lines.

J Cell Physiol 2010 May;223(2):519-29

Sbarro Institute for Cancer Research and Molecular Medicine, Center for Biotechnology, College of Science and Technology, Temple University, Philadelphia, Pennsylvania, USA.

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http://dx.doi.org/10.1002/jcp.22077DOI Listing
May 2010

Neuropathological findings in West Nile virus encephalitis: a case report.

Ann Neurol 2003 Oct;54(4):547-51

Department of Pathology, Children's Hospital Medical Center of Akron, OH 44308, USA.

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http://dx.doi.org/10.1002/ana.10731DOI Listing
October 2003

Congenital hypomyelinating neuropathy, central dysmyelination, and Waardenburg-Hirschsprung disease: phenotypes linked by SOX10 mutation.

Ann Neurol 2002 Dec;52(6):836-42

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.

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http://dx.doi.org/10.1002/ana.10404DOI Listing
December 2002