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HAX1 mutations causing severe congenital neuropenia and neurological disease lead to cerebral microstructural abnormalities documented by quantitative MRI.
Boztug K, Ding XQ, Hartmann H, Ziesenitz L, Schäffer AA, Diestelhorst J, Pfeifer D, Appaswamy G, Kehbel S, Simon T, Al Jefri A, Lanfermann H, Klein C. Boztug K, et al. Among authors: lanfermann h. Am J Med Genet A. 2010 Dec;152A(12):3157-63. doi: 10.1002/ajmg.a.33748. Am J Med Genet A. 2010. PMID: 21108402 Free PMC article.
Value of quantitative analysis of routine clinical MRI sequences in ALS.
Ding XQ, Kollewe K, Blum K, Körner S, Kehbel S, Dengler R, Lanfermann H, Petri S. Ding XQ, et al. Among authors: lanfermann h. Amyotroph Lateral Scler. 2011 Nov;12(6):406-13. doi: 10.3109/17482968.2011.597402. Epub 2011 Aug 3. Amyotroph Lateral Scler. 2011. PMID: 21812629
Quantitative MRI shows cerebral microstructural damage in hemolytic-uremic syndrome patients with severe neurological symptoms but no changes in conventional MRI.
Weissenborn K, Bültmann E, Donnerstag F, Giesemann AM, Götz F, Worthmann H, Heeren M, Kielstein J, Schwarz A, Lanfermann H, Ding XQ. Weissenborn K, et al. Among authors: lanfermann h. Neuroradiology. 2013 Jul;55(7):819-25. doi: 10.1007/s00234-013-1176-3. Epub 2013 Apr 5. Neuroradiology. 2013. PMID: 23559401
257 results