Review: Somatic mutations in neurodegeneration von Leija‐Salazar, M., Piette, C., Proukakis, C.

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Genetics of Parkinson's disease: alpha-synuclein and other insights from Greece von Proukakis, C.

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Maspardin Is Mutated in Mast Syndrome, a Complicated Form of Hereditary Spastic Paraplegia Associated with Dementia von Simpson, Michael A., Cross, Harold, Proukakis, Christos, Pryde, Anna, Hershberger, Ruth, Chatonnet, Arnaud, Patton, Michael A., Crosby, Andrew H.

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Genetics of P arkinson's disease: alpha‐synuclein and other insights from G reece von Proukakis, C.

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Evolution and clustering of prodromal parkinsonian features in GBA1 carriers von Mullin, Stephen, Beavan, Michelle, Bestwick, Jonathan, McNeill, Alisdair, Proukakis, Christos, Cox, Timothy, Hughes, Derralynn, Mehta, Atul, Zetterberg, Henrik, Schapira, Anthony H.V.

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Modeling and estimation of ambiguities in linear arrays von Manikas, A., Proukakis, C.

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Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype von Smith, BN, Bevan, S, Vance, C, Renwick, P, Wilkinson, P, Proukakis, C, Squitieri, F, Berardelli, A, Warner, TT, Reid, E, Shaw, CE

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Screening of patients with hereditary spastic paraplegia reveals seven novel mutations in the SPG4 (Spastin) gene von Proukakis, C., Auer-Grumbach, M., Wagner, K., Wilkinson, P.A., Reid, E., Patton, M.A., Warner, T.T., Crosby, A.H.

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Infantile-onset symptomatic epilepsy syndrome caused by a homozygous loss-of-function mutation of GM3 synthase von Crosby, Andrew H, Simpson, Michael A, Cross, Harold, Proukakis, Christos, Priestman, David A, Neville, David C A, Reinkensmeier, Gabriele, Wang, Heng, Wiznitzer, Max, Gurtz, Kay, Verganelaki, Argyro, Pryde, Anna, Patton, Michael A, Dwek, Raymond A, Butters, Terry D, Platt, Frances M

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Is the Transportation Highway the Right Road for Hereditary Spastic Paraplegia? von Crosby, Andrew H., Proukakis, Christos

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Selective vulnerability in α-synucleinopathies von Alegre-Abarrategui, J, Brimblecombe, KR, Roberts, RF, Velentza-Almpani, E, Tilley, BS, Bengoa-Vergniory, N, Proukakis, C

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Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome von Dierick, Ines, Malli, Roland, Petek, Erwin, Warner, Thomas T, Jonghe, Peter De, Crosby, Andrew H, den Bergh, Peter Van, Timmerman, Vincent, Maldergem, Lionel Van, Patel, Heema, Wagner, Klaus, Hörl, Gerd, Verpoorten, Nathalie, Reed, Johanna A, Auer-Grumbach, Michaela, Proukakis, Christos, Verellen, Christine, Windpassinger, Christian, Merlini, Luciano, Irobi, Joy

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The interaction of genetic mutations in PARK2 and FA2H causes a novel phenotype in a case of childhood-onset movement disorder von Benger, M, Mankad, K, Proukakis, C, Mazarakis, ND, Kinali, M

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A large family with hereditary spastic paraparesis due to a frame shift mutation of the spastin (SPG4) gene: association with multiple sclerosis in two affected siblings and epilep... von Mead, S H, Proukakis, C, Wood, N, Crosby, A H, Plant, G T, Warner, T T

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Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brains von Mokretar, K, Pease, D, Taanman, J-W, Soenmez, A, Ejaz, A, Lashley, T, Ling, H, Gentleman, S, Houlden, H, Holton, JL, Schapira, AHV, Nacheva, E, Proukakis, C

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Investigative study of planar array ambiguities based on "hyperhelical" parameterization von Manikas, A., Proukakis, C., Lefkaditis, V.

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Somatic mutations in neurodegeneration: An update von Proukakis, C

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SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia von Crosby, Andrew H, Patel, Heema, Cross, Harold, Proukakis, Christos, Hershberger, Ruth, Bork, Peer, Ciccarelli, Francesca D, Patton, Michael A, McKusick, Victor A

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The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia von Ciccarelli, Francesca D, Proukakis, Christos, Patel, Heema, Cross, Harold, Azam, Shakil, Patton, Michael A, Bork, Peer, Crosby, Andrew H

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Investigation of somatic CNVs in brains of synucleinopathy cases using targeted SNCA analysis and single cell sequencing von Perez-Rodriguez, D, Kalyva, M, Leija-Salazar, M, Lashley, T, Tarabichi, M, Chelban, V, Gentleman, S, Schottlaender, L, Franklin, H, Vasmatzis, G, Houlden, H, Schapira, AHV, Warner, TT, Holton, JL, Jaunmuktane, Z, Proukakis, C

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