1 - 25 of 38 results for author:"Ludolph A.C." in Literature citations
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| NIPA1 polyalanine repeat expansions are associated with amyotrophic lateral sclerosis. Blauw H.M., van Rheenen W., Koppers M., Van Damme P., Waibel S., Lemmens R., van Vught P.W., Meyer T., Schulte C., Gasser T. et al. Hum. Mol. Genet. 21:2497-2502(2012) · Mapped (3) |
| Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. van Es M.A., Schelhaas H.J., van Vught P.W., Ticozzi N., Andersen P.M., Groen E.J., Schulte C., Blauw H.M., Koppers M., Diekstra F.P. et al. Ann. Neurol. 70:964-973(2011) · Mapped (3) |
| The modulation of Amyotrophic Lateral Sclerosis risk by ataxin-2 intermediate polyglutamine expansions is a specific effect. Gispert S., Kurz A., Waibel S., Bauer P., Liepelt I., Geisen C., Gitler A.D., Becker T., Weber M., Berg D. et al. Neurobiol. Dis. 45:356-361(2012) · Mapped (3) |
| Soluble beta-amyloid precursor protein is related to disease progression in amyotrophic lateral sclerosis. Steinacker P., Fang L., Kuhle J., Petzold A., Tumani H., Ludolph A.C., Otto M., Brettschneider J. PLoS ONE 6:e23600-e23600(2011) · Mapped (12) |
| Paroxysmal choreoathetosis/spasticity (DYT9) is caused by a GLUT1 defect. Weber Y.G., Kamm C., Suls A., Kempfle J., Kotschet K., Schule R., Wuttke T.V., Maljevic S., Liebrich J., Gasser T. et al. |
| The proteoglycan-dystrophin complex in genetic cardiomyopathies--lessons from three siblings with limb-girdle muscular dystrophy-2I (LGMD-2I). Yilmaz A., Gdynia H.J., Ponfick M., Ludolph A.C., Rosch S., Sechtem U. Clin Res Cardiol 100:611-615(2011) · Mapped (1) |
| The thermolabile variant of 5,10-methylenetetrahydrofolate reductase is a possible risk factor for amyotrophic lateral sclerosis. Kuhnlein P., Jung H., Farkas M., Keskitalo S., Ineichen B., Jelcic I., Petersen J., Semmler A., Weller M., Ludolph A.C. et al. Amyotroph Lateral Scler 12:136-139(2011) · Mapped (6) |
| Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue. Treiber N., Maity P., Singh K., Kohn M., Keist A.F., Ferchiu F., Sante L., Frese S., Bloch W., Kreppel F. et al. Aging Cell 10:239-254(2011) · Mapped (4) |
| Mutations in cytoplasmic dynein lead to a Huntington's disease-like defect in energy metabolism of brown and white adipose tissues. Eschbach J., Fergani A., Oudart H., Robin J.P., Rene F., Gonzalez de Aguilar J.L., Larmet Y., Zoll J., Hafezparast M., Schwalenstocker B. et al. Biochim. Biophys. Acta 1812:59-69(2011) · Mapped (9) |
| Genetic variants in PSEN2 and correlation to CSF beta-amyloid42 levels in AD. Lebedeva E., Stingl J.C., Thal D.R., Ghebremedhin E., Strauss J., Ozer E., Bertram L., von Einem B., Tumani H., Otto M. et al. Neurobiol. Aging 33:201.e9-18(2012) · Mapped (8) |
| A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons. Braunstein K.E., Eschbach J., Rona-Voros K., Soylu R., Mikrouli E., Larmet Y., Rene F., Gonzalez De Aguilar J.L., Loeffler J.P., Muller H.P. et al. Hum. Mol. Genet. 19:4385-4398(2010) · Mapped (8) |
| A large genome scan for rare CNVs in amyotrophic lateral sclerosis. Blauw H.M., Al-Chalabi A., Andersen P.M., van Vught P.W., Diekstra F.P., van Es M.A., Saris C.G., Groen E.J., van Rheenen W., Koppers M. et al. Hum. Mol. Genet. 19:4091-4099(2010) · Mapped (13) |
| Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic? Felbecker A., Camu W., Valdmanis P.N., Sperfeld A.D., Waibel S., Steinbach P., Rouleau G.A., Ludolph A.C., Andersen P.M. J. Neurol. Neurosurg. Psychiatr. 81:572-577(2010) · Mapped (2) |
| MMP-2 and MMP-9 are elevated in spinal cord and skin in a mouse model of ALS. Fang L., Teuchert M., Huber-Abel F., Schattauer D., Hendrich C., Dorst J., Zettlmeissel H., Wlaschek M., Scharffetter-Kochanek K., Kapfer T. et al. J. Neurol. Sci. 294:51-56(2010) · Mapped (4) |
| The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families. Rabe M., Felbecker A., Waibel S., Steinbach P., Winter P., Muller U., Ludolph A.C. J. Neurol. 257:1298-1302(2010) · Mapped (2) |
| Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. van Es M.A., Veldink J.H., Saris C.G., Blauw H.M., van Vught P.W., Birve A., Lemmens R., Schelhaas H.J., Groen E.J., Huisman M.H. et al. Nat. Genet. 41:1083-1087(2009) · Mapped (8) |
| Candidate biomarkers of chronic inflammatory demyelinating polyneuropathy (CIDP): proteome analysis of cerebrospinal fluid. Tumani H., Pfeifle M., Lehmensiek V., Rau D., Mogel H., Ludolph A.C., Brettschneider J. J. Neuroimmunol. 214:109-112(2009) · Mapped (2) |
| Linking neuron and skin: matrix metalloproteinases in amyotrophic lateral sclerosis (ALS). Fang L., Huber-Abel F., Teuchert M., Hendrich C., Dorst J., Schattauer D., Zettlmeissel H., Wlaschek M., Scharffetter-Kochanek K., Tumani H. et al. J. Neurol. Sci. 285:62-66(2009) · Mapped (9) |
| CSF proteome analysis in clinically isolated syndrome (CIS): candidate markers for conversion to definite multiple sclerosis. Tumani H., Lehmensiek V., Rau D., Guttmann I., Tauscher G., Mogel H., Palm C., Hirt V., Suessmuth S.D., Sapunova-Meier I. et al. Neurosci. Lett. 452:214-217(2009) · Mapped (2) |
| Altered migration and adhesion potential of pro-neurally converted human bone marrow stromal cells. Habisch H.J., Fiedler J., Ludolph A.C., Storch A., Brenner R.E. Cytotherapy 10:824-833(2008) · Mapped (4) |
| Mice with a mutation in the dynein heavy chain 1 gene display sensory neuropathy but lack motor neuron disease. Dupuis L., Fergani A., Braunstein K.E., Eschbach J., Holl N., Rene F., Gonzalez De Aguilar J.L., Zoerner B., Schwalenstocker B., Ludolph A.C. et al. Exp. Neurol. 215:146-152(2009) · Mapped (9) |
| Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations. Kuhnlein P., Sperfeld A.D., Vanmassenhove B., Van Deerlin V., Lee V.M., Trojanowski J.Q., Kretzschmar H.A., Ludolph A.C., Neumann M. Arch. Neurol. 65:1185-1189(2008) · Mapped (5) |
| Meta-analysis of vascular endothelial growth factor variations in amyotrophic lateral sclerosis: increased susceptibility in male carriers of the -2578AA genotype. Lambrechts D., Poesen K., Fernandez-Santiago R., Al-Chalabi A., Del Bo R., Van Vught P.W., Khan S., Marklund S.L., Brockington A., van Marion I. et al. J. Med. Genet. 46:840-846(2009) · Mapped (7) |
| Sporadic ALS with early-onset respiratory failure is not associated with IGHMBP2 gene mutations. Kuhnlein P., Sperfeld A.D., Endruhn S., Varon R., Ludolph A.C., Hubner C. J. Neurol. Neurosurg. Psychiatr. 79:737-738(2008) · Mapped (1) |
| Chemical hypoxia facilitates alternative splicing of EAAT2 in presymptomatic APP23 transgenic mice. Munch C., Zhu B.G., Mink A., Seefried U., Riepe M.W., Ludolph A.C., Meyer T. Neurochem. Res. 33:1005-1010(2008) · Mapped (9) |