Knut Brockmann
Department of Pediatrics and Pediatric Neurology
Faculty of Medicine
Georg August University
Robert-Koch-Str. 40
Germany
Name/email consistency: high
- The expanding phenotype of GLUT1-deficiency syndrome. Brockmann, K. Brain Dev. (2009)
- Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia. Brockmann, K., Backes, H., Auber, B., Kriebel, T., Stellmer, F., Zoll, B. Am. J. Med. Genet. A (2009)
- Unilateral dilation of virchow-robin spaces in early childhood. Brockmann, K., Gröschel, S., Dreha-Kulaczewski, S., Reinhardt, K., Gärtner, J., Dechent, P. Neuropediatrics (2009)
- Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations. Brockmann, K., Dreha-Kulaczewski, S., Dechent, P., Bönnemann, C., Helms, G., Kyllerman, M., Brück, W., Frahm, J., Huehne, K., Gärtner, J., Rautenstrauss, B. J. Neurol. (2008)
- Monozygotic twins discordant for Proteus syndrome. Brockmann, K., Happle, R., Oeffner, F., König, A. Am. J. Med. Genet. A (2008)
- Quantitative proton MRS of cerebral metabolites in laminin alpha2 chain deficiency. Brockmann, K., Dechent, P., Bönnemann, C., Schreiber, G., Frahm, J., Hanefeld, F. Brain Dev. (2007)
- Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood. Brockmann, K., Becker, P., Schreiber, G., Neubert, K., Brunner, E., Bönnemann, C. Neuromuscul. Disord. (2007)
- X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene. Brockmann, K., Dumitrescu, A.M., Best, T.T., Hanefeld, F., Refetoff, S. J. Neurol. (2005)
- Visually self-induced seizures sensitive to round objects. Brockmann, K., Huppke, P., Karenfort, M., Gärtner, J., Höger, C. Epilepsia (2005)
- Moyamoya syndrome associated with hemolytic anemia due to Hb Alesha. Brockmann, K., Stolpe, S., Fels, C., Khan, N., Kulozik, A.E., Pekrun, A. J. Pediatr. Hematol. Oncol. (2005)
- Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onset. Brockmann, K., Simpson, M.A., Faber, A., Bönnemann, C., Crosby, A.H., Gärtner, J. Neuropediatrics (2005)
- Tarsal tunnel syndrome in a 7-year-old boy. Brockmann, K., Schneider-Sickert, F., Kolenda, H., Aden, I., Hanefeld, F. Eur. J. Pediatr. (2004)
- Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy. Brockmann, K., Finsterbusch, J., Schara, U., Wilichowski, E., Frahm, J., Hanefeld, F. Neuroradiology (2004)
- Cerebral proton magnetic resonance spectroscopy of a patient with giant axonal neuropathy. Brockmann, K., Pouwels, P.J., Dechent, P., Flanigan, K.M., Frahm, J., Hanefeld, F. Brain Dev. (2003)
- Proton MRS profile of cerebral metabolic abnormalities in Krabbe disease. Brockmann, K., Dechent, P., Wilken, B., Rusch, O., Frahm, J., Hanefeld, F. Neurology (2003)
- Megalencephalic leukoencephalopathy with subcortical cysts in an adult: quantitative proton MR spectroscopy and diffusion tensor MRI. Brockmann, K., Finsterbusch, J., Terwey, B., Frahm, J., Hanefeld, F. Neuroradiology (2003)
- A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?. Brockmann, K., Meins, M., Taubert, A., Trappe, R., Grond, M., Hanefeld, F. Eur. Neurol. (2003)
- Succinate in dystrophic white matter: a proton magnetic resonance spectroscopy finding characteristic for complex II deficiency. Brockmann, K., Bjornstad, A., Dechent, P., Korenke, C.G., Smeitink, J., Trijbels, J.M., Athanassopoulos, S., Villagran, R., Skjeldal, O.H., Wilichowski, E., Frahm, J., Hanefeld, F. Ann. Neurol. (2002)
