Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Bruce Day"'
Autor:
James Strathdee, Edrich Rodrigues, Mahima Kapoor, Wenwen Zhang, Mark Faragher, Bruce Day, Elspeth Hutton, Richard Stark
Publikováno v:
Wednesday, April 26.
Publikováno v:
Clinical Neurophysiology. 131:e1
Publikováno v:
Journal of Clinical Neuroscience. 22:951-954
This article discusses three patients with likely Hirayama disease. They have no other significant past medical history and no personal or family history of other neurological disorders. Hirayama disease is a form of cervical myelopathy attributed to
Autor:
Donald H. Johnson, Bruce Day
Publikováno v:
Sports Medicine and Arthroscopy Review. 20:225-230
Strength exercises for the knee, shoulder, and the core are essential to help prevent injuries to triathletes. This article will outline the most common exercises to strength the major joints and flexibility exercises to maintain range of motion of t
Autor:
Nigel W, Crawford, Allen, Cheng, Nick, Andrews, Patrick G, Charles, Hazel J, Clothier, Bruce, Day, Timothy, Day, Peter, Gates, Richard, Macdonell, Richard, Macdonnell, Les, Roberts, Victoria, Rodriguez-Casero, Tissa, Wijeratne, Lynette, Kiers
Publikováno v:
Medical Journal of Australia. 197:574-578
Objectives To determine the relative incidence (RI) of Guillain-Barre syndrome (GBS) in a single Australian state following pandemic (H1N1) 2009 influenza A immunisation (monovalent vaccine or seasonal trivalent influenza vaccine [TIV]) in 2009-2010.
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 89:A31.2-A31
IntroductionRecurrent Guillain-Barre syndrome (GBS) is very rare. It occurs in 2% to 5% of GBS patients. It is unclear as to why some patients have a recurrence and whether this occurs more frequently in a distinct group of patients. We report a case
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 89:A12.2-A12
IntroductionMultiple-acyl-CoA dehydrogenase deficiency or MADD is a rare autosomal recessive disorder caused by deficiency of electron transfer flavoprotein. Late onset form of MADD typically present with slowly progressive proximal weakness, myalgia
Publikováno v:
Movement Disorders. 24:422-425
Multimodal representation of peripersonal or near space has been demonstrated in the brain of the nonhuman primate through invasive electrophysiological experiments. Representation of peripersonal space in the human brain has been inferred from extin
Publikováno v:
Internal Medicine Journal. 43:1237-1239
Multifocal motor neuropathy is frequently an asymmetrical neuropathy predominantly affecting the upper limbs. Patients present with weakness, fasciculations and distal muscle wasting. Hypertrophy of muscles is very infrequently reported. We present t
Publikováno v:
Journal of Clinical Neuroscience. 13:576-578
A case of rippling muscle disease is presented and features of this rare condition, and its association with caveolin-3 are discussed.