Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Jerome A, Rusin"'
Autor:
Hira, Ahmad, Devin R, Halleran, Joseph R, Stanek, Benjamin P, Thompson, D Gregory, Bates, Jerome A, Rusin, Peter C, Minneci, Marc A, Levitt, Richard J, Wood
Publikováno v:
Pediatric radiology. 51(10)
The sacral ratio has been used as a tool for evaluating sacral development in patients with anorectal malformations. Sacral ratios can be calculated by obtaining sacral radiographs in the anteroposterior (AP) and lateral planes.The objective of the s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ab98a3fa8c2b02be6863e936dfa08bda
https://pubmed.ncbi.nlm.nih.gov/33991195
https://pubmed.ncbi.nlm.nih.gov/33991195
BACKGROUND AND PURPOSE: Advanced imaging techniques have allowed earlier and more accurate detection of cerebral deep medullary vein thrombosis and infarction. Our objective was to develop an MR imaging scoring system to evaluate the severity of whit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8edf4608dd034a6f1dd86282810315dd
https://europepmc.org/articles/PMC6375778/
https://europepmc.org/articles/PMC6375778/
Autor:
Jeffery J. Auletta, Jerome A. Rusin, Jeffrey R. Leonard, Christopher R. Pierson, Mohamed S. AbdelBaki, Lisa Martin, Daniel R. Boue, Joshua D. Palmer, Margaret Shatara, Jonathan L. Finlay, Mohammad H Abu-Arja, Diana S Osorio, Ralph E. Vatner, Rolla Abu-Arja, Jeremy Jones, Annie I. Drapeau, Eric A. Sribnick, Suzanne Conley
Publikováno v:
Neuro-Oncology
BACKGROUND About one-third of children with primary CNS MMGCT experience incomplete responses to initial induction chemotherapy prior to irradiation, many of whom will subsequently relapse. Such high-risk patients are variably defined as having initi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa0ed141ad47be0d5e8f2e9338e728e0
https://doi.org/10.1093/neuonc/noaa222.245
https://doi.org/10.1093/neuonc/noaa222.245
Publikováno v:
Journal of Pediatric Neuroradiology. :169-173
Citrullinemia is a rare inborn error of urea cycle metabolism causing hyperammonemia. In the classic form, a newborn presents with poor feeding, vomiting, progressive lethargy and signs of increasing intracranial pressure 3–7 d after birth, rapidly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8599031d097e090481904fe28940f5a7
https://doi.org/10.3233/pnr-13061
https://doi.org/10.3233/pnr-13061
Publikováno v:
Pediatric Radiology. 45:872-881
Excessive cervical flexion-extension accompanying mild to severe impact injuries can lead to C2 synchondrosal fractures in young children. To characterize and classify C2 synchondrosal fracture patterns. We retrospectively reviewed imaging and medica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aeb4bfedde4aafb81ba63f18a8b6bf43
https://doi.org/10.1007/s00247-014-3224-5
https://doi.org/10.1007/s00247-014-3224-5
Publikováno v:
Pediatric Radiology. 44:1393-1402
Deep white matter hemorrhagic venous infarction with subsequent cavitation due to necrosis and liquefaction has been described in neonates and may be associated with infection and meningitis. In our experience, the MRI pattern of these lesions is con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea5fecbeb5fc9e7a1e9c86e2921be879
https://doi.org/10.1007/s00247-014-3006-0
https://doi.org/10.1007/s00247-014-3006-0
Autor:
E. Steve Roach, Jeffrey R. Leonard, Carl P. Boesel, Fahd Al Sufiani, Christopher R. Pierson, Mohamed S. AbdelBaki, Jonathan L. Finlay, Jerome A. Rusin, Diana S Osorio, Nicholas Zumberge, Pournima Navalkele, Lisa Martin, Daniel R. Boue
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c13af8d7b2ccc65f3610c5f7bad7426
https://europepmc.org/articles/PMC4903507/
https://europepmc.org/articles/PMC4903507/
Publikováno v:
Pediatric Neurology. 51:734-736
Background Nuclear polymerase gamma ( POLG ) mutations are the most common cause of inherited mitochondrial disease. POLG mutation diseases have a broad spectrum of clinical manifestations; the lethal infantile form is myocerebrohepatopathy spectrum.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8672141813cea3ec933fc9636d6ad6ba
https://doi.org/10.1016/j.pediatrneurol.2014.06.015
https://doi.org/10.1016/j.pediatrneurol.2014.06.015
Publikováno v:
Brain and Development. 29:514-518
Sarcoidosis is uncommon in children. Although isolated neurosarcoidosis has been seen in 15% adults with sarcoidosis, pediatric neurosarcoidosis is rarely reported. Neurosarcoidosis may present with cranial neuropathy, including facial palsy, optic n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::913aebf64f35729620f7a8cd7e5906a1
https://doi.org/10.1016/j.braindev.2006.12.011
https://doi.org/10.1016/j.braindev.2006.12.011
Autor:
Jorge Vidaurre, Sharon Bout-Tabaku, Rabheh abdul Aziz, Amanda Weber, Jerome A. Rusin, Dara V.F. Albert, Kyla Driest, Charles P. Pluto, Bethanie Morgan-Followell, Fatima Barbar-Smiley, Lynne Ruess
Publikováno v:
Pediatric neurology. 55
Background Autoimmune encephalitis is currently a clinical diagnosis without widely accepted diagnostic criteria, often leading to a delay in diagnosis. The utility of magnetic resonance imaging (MRI) and electroencephalography (EEG) in this disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::001210cee6bc542ea70f6822ae40f13a
https://pubmed.ncbi.nlm.nih.gov/26724889
https://pubmed.ncbi.nlm.nih.gov/26724889