Zobrazeno 1 - 10
of 27
pro vyhledávání: '"M. J. Strong"'
Publikováno v:
Childs Nerv Syst
INTRODUCTION: Various techniques are used for spinal cord untethering. The purpose of this study was to compare patient characteristics, post-operative course, and early complications after laminotomy versus laminoplasty for transection of the filum
Autor:
Sarah L. Whitehouse, M. J. Strong
Publikováno v:
Proceedings of the American Mathematical Society. 138:2221-2233
Autor:
B. P. He, M. J. Strong
Publikováno v:
Neuropathology and Applied Neurobiology. 26:150-160
Whether diseased motor neurones in sporadic amyotrophic lateral sclerosis (ALS) die via apoptosis is unknown. Because this relates primarily to difficulties in utilizing post-mortem tissue from end-stage disease, motor neurone degeneration in ALS spi
Publikováno v:
European journal of neurology. 19(6)
Sporadic amyotrophic lateral sclerosis (sALS) is a disease with a focal clinical onset and contiguous spread. We examined patterns of disease spread following symptoms onset in sALS and whether the pattern of spread predicted survival.Review of medic
Publikováno v:
Journal of forensic sciences. 46(5)
In recent years, there has been a notable increase in the number of reports on drug-facilitated sexual assault. Benzodiazepines are the most common so-called "date-rape" drugs, with flunitrazepam (Rohypnol) being one of the most frequently mentioned.
Publikováno v:
Journal of neurochemistry. 76(5)
The intraneuronal aggregation of phosphorylated high-molecular-weight neurofilament protein (NFH) in spinal cord motor neurons is considered to be a key pathological marker of amyotrophic lateral sclerosis (ALS). In order to determine whether this ob
Autor:
M J, Strong
Publikováno v:
Neurology. 53(8 Suppl 5)
Although it is desirable to simplify the diagnosis of amyotrophic lateral sclerosis (ALS), it is not obvious how to achieve this. Although a simplified electrophysiologic approach can be easily performed, interpretation of the results in a complex di
Publikováno v:
Musclenerve. 21(5)
Four patients with myasthenia gravis presented with severe, largely isolated, bulbar and respiratory muscles weakness. Tensilon tests were positive and antiacetylcholine receptor (anti-AChR) antibody titers were negative in all patients. Only 1 patie
Publikováno v:
Brain pathology (Zurich, Switzerland). 8(1)
A 42 yr old male presented with left facial weakness. MRI showed lesions affecting the distal seventh nerve and third division of the trigeminal nerve. The seventh nerve was biopsied and showed a malignant epithelioid schwannoma. The patient underwen
Autor:
M J, Strong, D M, Jakowec
Publikováno v:
Neurotoxicology. 15(4)
We have used time-course dephosphorylation experiments and two dimensional isoelectric focusing to assess the phosphorylation state of neurofilament (NF) proteins following the intracisternal inoculation of AlCl3. Littermates of New Zealand white rab