au.\*:("ROEBER, Sigrun")
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Detection of bone marrow-derived cells expressing a neural phenotype in the human brainSOSTAK, Petra; THEIL, Diethilde; STEPP, Herbert et al.Journal of neuropathology and experimental neurology. 2007, Vol 66, Num 2, pp 110-116, issn 0022-3069, 7 p.Article
A new subtype of frontotemporal lobar degeneration with FUS pathologyNEUMANN, Manuela; RADEMAKERS, Rosa; ROEBER, Sigrun et al.Brain. 2009, Vol 132, pp 2922-2931, issn 0006-8950, 10 p., 11Article
Hereditary diffuse leukoencephalopathy with axonal spheroids (HDLS): A misdiagnosed disease entitySUNDAL, Christina; LASH, Jennifer; BRODERICK, Daniel et al.Journal of the neurological sciences. 2012, Vol 314, Num 1-2, pp 130-137, issn 0022-510X, 8 p.Article
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron AccumulationHARTIG, Monika B; IUSO, Arcangela; JOZWIAK, Sergiusz et al.American journal of human genetics. 2011, Vol 89, Num 4, pp 543-550, issn 0002-9297, 8 p.Article
FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutationsNEUMANN, Manuela; BENTMANN, Eva; YOKOTA, Osamu et al.Brain. 2011, Vol 134, pp 2595-2609, issn 0006-8950, 15 p., 9Article
α-Internexin in the Diagnosis of Oligodendroglial Tumors and Association With 1 p/19q StatusEIGENBROD, Sabina; ROEBER, Sigrun; THON, Niklas et al.Journal of neuropathology and experimental neurology. 2011, Vol 70, Num 11, pp 970-978, issn 0022-3069, 9 p.Article
Clinical Features of Rapidly Progressive Alzheimer's DiseaseSCHMIDT, Christian; REDYK, Katharina; MEISSNER, Bettina et al.Dementia and geriatric cognitive disorders. 2010, Vol 29, Num 4, pp 371-378, issn 1420-8008, 8 p.Article
MRI characteristics and scoring in HDLS due to CSF1R gene mutationsSUNDAL, Christina; VAN GERPEN, Jay A; BORJESSON-HANSON, Anne et al.Neurology. 2012, Vol 79, Num 6, pp 566-574, issn 0028-3878, 9 p.Article
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroidsRADEMAKERS, Rosa; BAKER, Matt; ADAMSON, Jennifer et al.Nature genetics. 2012, Vol 44, Num 2, pp 200-205, issn 1061-4036, 6 p.Article
Clinical findings and diagnostic tests in the MV2 subtype of sporadic CJDKRASNIANSKI, Anna; SCHULZ-SCHAEFFER, Walter J; ZERR, Inga et al.Brain. 2006, Vol 129, pp 2288-2296, issn 0006-8950, 9 p., 9Article