Author Brockmann, Knut
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2001 | Journal Article
Endocrinological study on growth retardation in Rett syndrome
Huppke, P.; Roth, C.; Christen, H.-J.; Brockmann, K. & Hanefeld, F. (2001)
Acta Paediatrica, 90(11) pp. 1257-1261.
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2001 | Journal Article
Myelinopathia centralis diffusa (vanishing white matter disease): Evidence of apoptotic oligodendrocyte degeneration in early lesion development
Bruck, W. W.; Herms, J.; Brockmann, K.; Schulz-Schaeffer, W. J. & Hanefeld, F. (2001)
Annals of Neurology, 50(4) pp. 532-536. DOI: https://doi.org/10.1002/ana.1227
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2001 | Journal Article | Letter Note
Progressive elevation of liver enzymes in a child treated with sulthiame
Brockmann, K. & Hanefeld, F. (2001)
Neuropediatrics, 32(3) pp. 165-166. DOI: https://doi.org/10.1055/s-2001-16617
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2001 | Journal Article
Autosomal dominant Glut-1 deficiency syndrome and familial epilepsy
Brockmann, K.; Wang, D.; Korenke, C. G.; von Moers, A. ; Ho, Y. Y.; Pascual, J. M. & Kuang, K. et al. (2001)
Annals of Neurology, 50(4) pp. 476-485. DOI: https://doi.org/10.1002/ana.1222
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2002 | Journal Article
Eosinophilic fasciitis leading to painless contractures
Huppke, P.; Wilken, B.; Brockmann, K.; Sattler, B. & Hanefeld, F. (2002)
European Journal of Pediatrics, 161(10) pp. 528-530. DOI: https://doi.org/10.1007/s00431-002-1038-1
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2002 | Journal Article | Letter Note
Juvenile horseplay purpura
Brockmann, K. & Diepold, K. (2002)
ARCHIVES OF DERMATOLOGY, 138(10). DOI: https://doi.org/10.1001/archderm.138.10.1384
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2002 | Journal Article
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. & Athanassopoulos, S. et al. (2002)
Annals of Neurology, 52(1) pp. 38-46. DOI: https://doi.org/10.1002/ana.10232
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2002 | Journal Article
Infantile Alexander disease: A GFAP mutation in monozygotic twins and novel mutations in two other patients
Meins, M.; Brockmann, K.; Yadav, S.; Haupt, M.; Sperner, J.; Stephani, U. & Hanefeld, F. (2002)
Neuropediatrics, 33(4) pp. 194-198. DOI: https://doi.org/10.1055/s-2002-34495
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2002 | Journal Article
EEG features of Glut-1 deficiency syndrome
von Moers, A.; Brockmann, K.; Wang, D.; Korenke, C. G.; Huppke, P.; De Vivo, D. C. & Hanefeld, F. (2002)
Epilepsia, 43(8) pp. 941-945. DOI: https://doi.org/10.1046/j.1528-1157.2002.50401.x
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2003 | Journal Article
Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation
Wilken, B.; Dechent, P.; Brockmann, K.; Finsterbusch, J.; Baumann, M.; Ebell, W. & Korenke, C. G. et al. (2003)
Neuropediatrics, 34(5) pp. 237-246.
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2003 | Journal Article
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. (2003)
Neuroradiology, 45(3) pp. 137-142. DOI: https://doi.org/10.1007/s00234-002-0931-7
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2003 | Journal Article
Progressive muscle weakness after high-dose steroids in two children with CIDP
Rostasy, K.; Diepold, K.; Buckard, J. A.; Brockmann, K.; Wilken, B. & Hanefeld, F. (2003)
Pediatric Neurology, 29(3) pp. 236-238. DOI: https://doi.org/10.1016/S0887-8994(03)00222-4
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2003 | Journal Article
Deep cerebral venous sinus thrombosis often presents with neuropsychologic symptoms
von Mering, M.; Stiefel, M.; Brockmann, K. & Nau, R. (2003)
Journal of Clinical Neuroscience, 10(3) pp. 310-312. DOI: https://doi.org/10.1016/S0967-5868(03)00017-1
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2003 | Journal Article
Haematopoietic stem cell transplantation in 12 patients with cerebral X-linked adrenoleukodystrophy
Baumann, M.; Korenke, C.; Weddige-Diedrichs, A. ; Wilichowski, E.; Hunneman, D. H.; Wilken, B. & Brockmann, K. et al. (2003)
European Journal of Pediatrics, 162(1) pp. 6-14. DOI: https://doi.org/10.1007/s00431-002-1097-3
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2003 | Journal Article
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. (2003)
Brain and Development, 25(1) pp. 45-50. DOI: https://doi.org/10.1016/s0387-7604(02)00154-7
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2003 | Journal Article
A novel GFAP mutation and disseminated white matter lesions: Adult Alexander disease?
Brockmann, K.; Meins, M.; Taubert, A.; Trappe, R.; Grond, M. & Hanefeld, F. (2003)
European Neurology, 50(2) pp. 100-105. DOI: https://doi.org/10.1159/000072507
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2004 | Journal Article | Letter Note
Tandem mass spectrometry for the direct assay of enzymes in dried blood spots: Application to newborn screening for Krabbe disease
Li, Y. J.; Brockmann, K.; Turecek, F.; Scott, C. R. & Gelb, M. H. (2004)
Clinical Chemistry, 50(3) pp. 638-640. DOI: https://doi.org/10.1373/clinchem.2003.028381
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2004 | Journal Article
Tarsal tunnel syndrome in a 7-year-old boy
Brockmann, K.; Schneider-Sickert, F.; Kolenda, H.; Aden, I. & Hanefeld, F. (2004)
European Journal of Pediatrics, 163(1) pp. 46-47. DOI: https://doi.org/10.1007/s00431-003-1360-2
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2004 | Journal Article
A novel syndrome combining thyroid and neurological abnormalities is associated with mutations in a monocarboxylate transporter gene
Dumitrescu, A. M.; Liao, X. H.; Best, T. B.; Brockmann, K. & Refetoff, S. (2004)
The American Journal of Human Genetics, 74(1) pp. 168-175. DOI: https://doi.org/10.1086/380999
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