Search Results - "Thomas, K P"

Modulation of nicotine effects on selective attention by DRD2 and CHRNA4 gene polymorphisms by Ahrens, Stefan, Markett, Sebastian, Breckel, Thomas P. K., Behler, Oliver, Reuter, Martin, Thiel, Christiane M.

“…Rationale Pharmacological and genetic modulation of cholinergic nicotinic neurotransmission influence visuospatial attention in humans. Prior studies show that…”
Get full text

Long-term effects of attentional performance on functional brain network topology by Breckel, Thomas P K, Thiel, Christiane M, Bullmore, Edward T, Zalesky, Andrew, Patel, Ameera X, Giessing, Carsten

“…Individuals differ in their cognitive resilience. Less resilient people demonstrate a greater tendency to vigilance decrements within sustained attention…”
Get full text

Nicotine reduces distraction under low perceptual load by Behler, Oliver, Breckel, Thomas P. K., Thiel, Christiane M.

“…Rationale Several studies provide evidence that nicotine alleviates the detrimental effects of distracting sensory stimuli. It is been suggested that nicotine…”
Get full text

Nicotinergic Modulation of Attention-Related Neural Activity Differentiates Polymorphisms of DRD2 and CHRNA4 Receptor Genes by Breckel, Thomas P K, Giessing, Carsten, Gieseler, Anja, Querbach, Sarah, Reuter, Martin, Thiel, Christiane M

“…Cognitive and neuronal effects of nicotine show high interindividual variability. Recent findings indicate that genetic variations that affect the cholinergic…”
Get full text

Pidotimod: In-depth review of current evidence by Mahashur, Ashok, Thomas, P, Mehta, Parthiv, Nivangune, Kundan, Muchhala, Snehal, Jain, Rishi

“…Pidotimod, an immunostimulant, is researched for over two decades. Current evidence indicates its utility in a variety of indications in children as well as in…”
Get full text

Idiopathic transverse myelitis : Corticosteroids, plasma exchange, or cyclophosphamide by GREENBERG, B. M, THOMAS, K. P, KRISHNAN, C, KAPLIN, A. I, CALABRESI, P. A, KERR, D. A

“…Transverse myelitis is a focal disorder of the spinal cord in which an immune-mediated process results in neural injury. In this large retrospective study, we…”
Get full text

Sural nerve pathology in diabetic patients with minimal but progressive neuropathy by MALIK, R. A, TESFAYE, S, WARD, J. D, NEWRICK, P. G, WALKER, D, RAJBHANDARI, S. M, SIDDIQUE, I, SHARMA, A. K, BOULTON, A. J. M, KING, R. H. M, THOMAS, P. K

“…The early pathological features of human diabetic neuropathy are not clearly defined. Therefore we quantified nerve fibre and microvascular pathology in sural…”
Get full text

Classification, differential diagnosis, and staging of diabetic peripheral neuropathy by THOMAS, P. K

“…The peripheral nerve disorders associated with diabetes are complex and probably involve a variety of causative mechanisms. This may give rise to difficulty in…”
Get full text

Variability of fMRI-response patterns at different spatial observation scales by Ball, Tonio, Breckel, Thomas P.K., Mutschler, Isabella, Aertsen, Ad, Schulze-Bonhage, Andreas, Hennig, Jürgen, Speck, Oliver

“…Functional organization units of the cerebral cortex exist over a wide range of spatial scales, from local circuits to entire cortical areas. In the last…”
Get full text

N-myc Downstream-Regulated Gene 1 Is Mutated in Hereditary Motor and Sensory Neuropathy–Lom by Kalaydjieva, Luba, Gresham, David, Gooding, Rebecca, Heather, Lisa, Baas, Frank, de Jonge, Rosalein, Blechschmidt, Karin, Angelicheva, Dora, Chandler, David, Worsley, Penelope, Rosenthal, Andre, King, Rosalind H.M., Thomas, P.K.

“…Hereditary motor and sensory neuropathies, to which Charcot-Marie-Tooth (CMT) disease belongs, are a common cause of disability in adulthood. Growing awareness…”
Get full text

Clinical, pathological and genetic characterization of hereditary sensory and autonomic neuropathy type 1 (HSAN I) by Houlden, Henry, King, Rosalind, Blake, Julian, Groves, Mike, Love, Seth, Woodward, Cathy, Hammans, Simon, Nicoll, James, Lennox, Graham, O'Donovan, Dominic G., Gabriel, Carolyn, Thomas, P. K., Reilly, Mary M.

“…Hereditary sensory and autonomic neuropathy type I (HSAN I) is the most frequent type of hereditary neuropathy that primarily affects sensory neurons. The…”
Get full text

Impact of brain networks involved in vigilance on processing irrelevant visual motion by Breckel, Thomas P.K., Giessing, Carsten, Thiel, Christiane M.

“…The ability to sustain attention over prolonged periods of time is called vigilance. Vigilance is a fundamental component of attention which impacts on…”
Get full text

Clinical, biochemical and molecular genetic correlations in Friedreich's ataxia by BRADLEY, J. L, BLAKE, J. C, CHAMBERLAIN, S, THOMAS, P. K, COOPER, J. M, SCHAPIRA, A. H. V

“…Friedreich's ataxia (FRDA) is an autosomal recessive disorder with a frequency of 1 in 50 000 live births. In 97% of patients it is caused by the abnormal…”
Get full text

A practical two-step quantitative clinical and electrophysiological assessment for the diagnosis and staging of diabetic neuropathy by FELDMAN, E. L, STEVENS, M. J, THOMAS, P. K, BROWN, M. B, CANAL, N, GREENE, D. A

“…A practical two-step quantitative clinical and electrophysiological assessment for the diagnosis and staging of diabetic neuropathy. E L Feldman , M J Stevens…”
Get full text

The clinical and laboratory features of chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies by Willison, H. J., O'Leary, C. P., Veitch, J., Blumhardt, L. D., Busby, M., Donaghy, M., Fuhr, P., Ford, H., Hahn, A., Renaud, S., Katifi, H. A., Ponsford, S., Reuber, M., Steck, A., Sutton, I., Schady, W., Thomas, P. K., Thompson, A. J., Vallat, J.-M., Winer, J.

“…The clinical and laboratory phenotype of a paraproteinaemic neuropathy syndrome termed chronic sensory ataxic neuropathy with anti-disialosyl IgM antibodies is…”
Get full text

Chronic inflammatory demyelinating polyradiculoneuropathy: a prevalence study in south east England by Lunn, M P T, Manji, H, Choudhary, P P, Hughes, R A C, Thomas, P K

“…Although there are now widely accepted diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) there are few epidemiological…”
Get full text

Partial deficiency of the C-terminal-domain phosphatase of RNA polymerase II is associated with congenital cataracts facial dysmorphism neuropathy syndrome by Kremensky, Ivo, Guerguelcheva, Velina, Swoboda, Kathryn, Baas, Frank, Kwa, Marcel, Gooding, Rebecca, Marns, Lorna, Ambrugger, Petra, Steglich, Christina, Bürger, Joachim, von Moers, Arpad, Müllner-Eidenböck, Andrea, Neumann, Luitgard, Yong, Kiau Kiun, Merlini, Luciano, Lochmüller, Hanns, Varon, Raymonda, Risch, Neil, Walter, Maggie, Morar, Bharti, Tournev, Ivailo, Kalaydjieva, Luba, Angelicheva, Dora, Tang, Hua, Reinhold, Anke, Thomas, P K

“…Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome (OMIM 604168) is an autosomal recessive developmental disorder that occurs in an endogamous…”
Get full text

The phenotypic manifestations of chromosome 17p11.2 duplication by THOMAS, P. K, MARQUES, W. JR, DAVIS, M. B, SWEENEY, M. G, KING, R. H. M, BRADLEY, J. L, MUDDLE, J. R, TYSON, J, MALCOLM, S, HARDING, A. E

“…Clinical and electrophysiological investigations and nerve biopsies were carried out on 61 patients shown to have a chromosome 17p11.2 duplication (hereditary…”
Get full text

Mutations in the 5′ region of the myotubularin-related protein 2 (MTMR2) gene in autosomal recessive hereditary neuropathy with focally folded myelin by Houlden, Henry, King, R. H. M., Wood, Nicholas W., Thomas, P. K., Reilly, Mary M.

“…Focally folded myelin has been recognized as a distinctive feature in some individuals with severe inherited demyelinating neuropathy, with an onset in…”
Get full text

Correlation Between Varying Levels of PMP22 Expression and the Degree of Demyelination and Reduction in Nerve Conduction Velocity in Transgenic Mice by Huxley, C., Passage, E., Robertson, A. M., Youl, B., Huston, S., Manson, A., Sabéran-Djoniedi, D., Figarella-Branger, D., Pellissier, J. F., Thomas, P. K., Fontés, M.

“…Charcot-Marie-Tooth disease type 1A is most commonly caused by a duplication of a 1.5 Mb region of chromosome 17 which includes the peripheral myelin protein…”
Get full text