Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Austin J. Sumner"'
Autor:
Rima El-Abassi, Joaquin S. Maury, Randall D. Craver, Lenay Santana-Gould, Austin J. Sumner, Enrique Segura-Palacios, Edward C. Mader Jr
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 2012, Iss 5, Pp 49-55 (2012)
Externí odkaz:
https://doaj.org/article/b073751896fe42dd85ab55bc349aaf28
Autor:
Edward C. Mader, Joaquin S. Maury, Lenay Santana-Gould, Randall D. Craver, Rima El-Abassi, Enrique Segura-Palacios, Austin J. Sumner
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 5 (2012)
Introduction Human rabies can be overlooked in places where this disease is now rare. Its diagnosis is further confused by a negative history of exposure (cryptogenic rabies), by a Guillain-Barré syndrome (GBS) type of presentation, or by symptoms i
Externí odkaz:
https://doaj.org/article/89eb72d2c3c340aeae901380addf6cff
Autor:
David R, Cornblath, Matthew C, Kiernan, Jun, Kimura, Martin, Koltzenburg, Richard A, Lewis, Gareth J, Parry, John D, Pollard, Austin J, Sumner
Publikováno v:
Annals of Plastic Surgery. 89:343-343
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81bebd4490c91b5d16b1204867a2821
https://doi.org/10.1097/sap.0000000000003245
https://doi.org/10.1097/sap.0000000000003245
Autor:
Austin J. Sumner, Charlotte J. Sumner
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 92:6-6
Over the last 5 years, three gene-targeting therapeutics have been approved for spinal muscular atrophy (SMA) including the splice switching oligonucleotide nusinersen in 2016, the gene therapy onasemnogene abepavovec in 2019 and the splice switching
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67daa107e12ec3daa988f2ec1274f5ba
https://doi.org/10.1136/jnnp-2020-325022
https://doi.org/10.1136/jnnp-2020-325022
Autor:
Austin J. Sumner, Joaquin S. Maury, Enrique Segura-Palacios, Rima El-Abassi, Edward C. Mader, Randall D. Craver, Lenay Santana-Gould
Publikováno v:
Clinical Medicine Insights: Case Reports, Vol 2012, Iss 5, Pp 49-55 (2012)
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights: Case Reports, Vol 5 (2012)
Clinical Medicine Insights. Case Reports
Clinical Medicine Insights: Case Reports, Vol 5 (2012)
Introduction Human rabies can be overlooked in places where this disease is now rare. Its diagnosis is further confused by a negative history of exposure (cryptogenic rabies), by a Guillain-Barré syndrome (GBS) type of presentation, or by symptoms i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93e3443139c60459f8df7fc322ae7d22
http://la-press.com/human-rabies-with-initial-manifestations-that-mimic-acute-brachial-neu-a3164
http://la-press.com/human-rabies-with-initial-manifestations-that-mimic-acute-brachial-neu-a3164
Autor:
Kinga Szigeti, James R. Lupski, Michael Polydefkis, Norman Latov, David N. Herrmann, Phillip A. Low, Robert G. Miller, Austin J. Sumner, Laurence J. Kinsella, Gary S. Gronseth, Gary M. Franklin, Giuseppe Lauria, Richard A. Lewis, Jeffrey A. Cohen, Morris A. Fisher, James F. Howard, Gregory T. Carter, Arthur K. Asbury, John D. England
Publikováno v:
PM&R. 1:5-13
Background Distal symmetric polyneuropathy (DSP) is the most common variety of neuropathy. Since the evaluation of this disorder is not standardized, the available literature was reviewed to provide evidence-based guidelines regarding the role of lab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be101522044fbd223a2d6fb1040c56e9
https://doi.org/10.1016/j.pmrj.2008.11.010
https://doi.org/10.1016/j.pmrj.2008.11.010
Autor:
John D. England, Gary S. Gronseth, Giuseppe Lauria, Austin J. Sumner, Arthur K. Asbury, Michael Polydefkis, Kinga Szigeti, Gregory T. Carter, Norman Latov, James F. Howard, Laurence J. Kinsella, Phillip A. Low, Jeffrey A. Cohen, Richard A. Lewis, Morris A. Fisher, David N. Herrmann, Gary M. Franklin, James R. Lupski, Robert G. Miller
Publikováno v:
Neurology. 72:177-184
Background: Distal symmetric polyneuropathy (DSP) is the most common variety of neuropathy. Since the evaluation of this disorder is not standardized, the available literature was reviewed to provide evidence-based guidelines regarding the role of au
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5a6e9a4d2ddfd4a7a3c142a822cc53a
https://doi.org/10.1212/01.wnl.0000336345.70511.0f
https://doi.org/10.1212/01.wnl.0000336345.70511.0f
Publikováno v:
Muscle & Nerve. 23:1472-1487
The observation that inherited demyelinating neuropathies have uniform conduction slowing and that acquired disorders have nonuniform or multifocal slowing was made prior to the identification of mutations in myelin-specific genes which cause many of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df2d8f8eb4cfd9e76ce38d395d7ee374
https://doi.org/10.1002/1097-4598(200010)23:10<1472::aid-mus3>3.0.co
https://doi.org/10.1002/1097-4598(200010)23:10<1472::aid-mus3>3.0.co
Autor:
Laura E. Warner, John D. England, James R. Lupski, Carlos A. Garcia, Austin J. Sumner, Scott Ferer, Amparo Gutierrez
Publikováno v:
Muscle & Nerve. 23:182-188
X-linked Charcot-Marie-Tooth disease (CMTX) is the second most common form of Charcot-Marie-Tooth disease. Variable histopathological and nerve conduction velocity (NCV) results have suggested either a primary demyelinating or axonal polyneuropathy.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e208f764935410aad80c7adace9ef1e9
https://doi.org/10.1002/(sici)1097-4598(200002)23:2<182::aid-mus6>3.0.co
https://doi.org/10.1002/(sici)1097-4598(200002)23:2<182::aid-mus6>3.0.co