Status of this Memo Restart Signaling for (2008)
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A novel RAB7 mutation associated with ulcero-mutilating neuropathy (2004)
Houlden, H., King, R.H.M., Muddle, J.R., Warner, T.T., Reilly, M.M., Orrell, R.W., ...
There are two known autosomal dominant genes for the hereditary ulcero-mutilating neuropathies: SPTLC1 (hereditary sensory neuropathy type 1) and RAB7 (Charcot-Marie-Tooth disease type 2B). We report...
A novel RAB7 mutation associated with ulcero-mutilating neuropathy (2004)
Houlden, H., King, R.H.M., Muddle, J.R., Warner, T.T., Reilly, M.M., Orrel, R.W., ...
There are two known autosomal dominant genes for the hereditary ulcero-mutilating neuropathies: SPTLC1 (hereditary sensory neuropathy type 1) and RAB7 (Charcot-Marie-Tooth disease type 2B). We report...
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia (2004)
Wilkinson, P.A., Crosby, A.H., Turner, C., Bradley, L.J., Ginsberg, L., Wood, N.W., ...
Mutations in the SPG7 gene, encoding the mitochondrial protein paraplegin, were the first to be identified in autosomal recessive hereditary spastic paraplegia (ARHSP). Four different SPG7 mutations...
Coexistent hereditary and inflammatory neuropathy (2004)
Ginsberg, L., Malik, O., Kenton, A.R., Sharp, D., Muddle, J.R., Davis, M.B., ...
Classically, the course of Charcot–Marie–Tooth (CMT) disease is gradually progressive. We describe eight atypical patients who developed acute or subacute deterioration. Seven of these had...
A clinical, genetic and biochemical study of SPG7 mutations in hereditary spastic paraplegia (2004)
Wilkinson, P.A., Crosby, A.H., Turner, C., Bradley, L.J., Ginsberg, L., Wood, N.W., ...
Lifted Search Engines For Satisfiability (1999)
Andrew J. Parkes, Committee Dr, Matthew L. Ginsberg, B. Wilson, ...
There are several powerful solvers for satisfiability (SAT), such as WSAT, Davis-Putnam, and RelSAT. However, in practice, the SAT encodings often have so many clauses that we exceed physical memory...
Acute encephalopathy: diagnosis and outcome in patients at a regional neurological unit (1994)
GINSBERG, L., COMPSTON, D.A.S.
Sixty-five patients with a diagnosis of acute encephalitis or encephalopathy were discharged from a regional neurological unit over a 17-year period. Investigation during the acute illness, or...
Dispersions of dimyristoylphosphatidylcholine (DMPC) in water have been reported to form a structure at 29 degrees C at the equilibrium air/water surface with a molecular density equal to that of a...
Dispersions of dimyristoylphosphatidylcholine (DMPC) in water have been reported to form a structure at 29 degrees C at the equilibrium air/water surface with a molecular density equal to that of a...
Chronic inflammatory demyelinating polyneuropathy mimicking a lumbar spinal stenosis syndrome.
Ginsberg, L, Platts, A D, Thomas, P K
A patient with chronic inflammatory demyelinating polyneuropathy (CIDP) established by biopsy developed cauda equina symptoms due to swelling of the nerve roots in the lumbar spinal canal. Magnetic...
Independent segregation of von Hippel-Lindau disease and cerebral cavernomas
Webster, A., Fisher, R., Ginsberg, L., Maher, E.
A probable diagnosis of von Hippel-Lindau disease was made in a two generation family in which the proband had a phaeochromocytoma, renal cysts, and multiple cerebral cavernomas. His sister had...