AAAAAA
Results: 1-25/31
Authors:
Laccone, F
Huppke, P
Hanefeld, F
Meins, M
Citation: F. Laccone et al., Mutation spectrum in patients with Rett syndrome in the German population:Evidence of hot spot regions, HUM MUTAT, 17(3), 2001, pp. 183-190
Authors:
Caeic, M
Wilichowski, E
Mejaski-Bosnjak, V
Fumic, K
Lujic, L
Della Marina, BM
Hanefeld, F
Citation: M. Caeic et al., Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome, J CHILD NEU, 16(8), 2001, pp. 616-619
Authors:
Brockmann, K
Wang, D
Korenke, CG
von Moers, A
Ho, YY
Pascual, JM
Kuang, K
Yang, H
Ma, L
Kranz-Eble, P
Fischbarg, J
Hanefeld, F
De Vivo, DC
Citation: K. Brockmann et al., Autosomal dominant Glut-1 deficiency syndrome and familial epilepsy, ANN NEUROL, 50(4), 2001, pp. 476-485
Authors:
Bruck, W
Herms, J
Brockmann, K
Schulz-Schaeffer, W
Hanefeld, F
Citation: W. Bruck et al., Myelinopathia centralis diffusa (vanishing white matter disease): Evidenceof apoptotic oligodendrocyte degeneration in early lesion development, ANN NEUROL, 50(4), 2001, pp. 532-536
Authors:
Gieffers, J
Pohl, D
Treib, J
Dittmann, R
Stephan, C
Klotz, K
Hanefeld, F
Solbach, W
Haass, A
Maass, M
Citation: J. Gieffers et al., Presence of Chlamydia pneumoniae DNA in the cerebral spinal fluid is a common phenomenon in a variety of neurological diseases and not restricted to multiple sclerosis, ANN NEUROL, 49(5), 2001, pp. 585-589
Authors:
Pohl, D
Hanefeld, F
Citation: D. Pohl et F. Hanefeld, Multiple sclerosis in children and adolescents, AKT NEUROL, 28(1), 2001, pp. 8-11
Authors:
Brockmann, K
Hanefeld, F
Citation: K. Brockmann et F. Hanefeld, Progressive elevation of liver enzymes in a child treated with sulthiame, NEUROPEDIAT, 32(3), 2001, pp. 165-166
Authors:
Aksu, F
Thyen, U
Hanefeld, F
Auerswald, G
Christen, HJ
Faust, J
Gabriel, R
Genzel, O
Haas, D
Hasselmann, O
Heinen, F
Karch, D
Kirschstein, M
Kluger, G
Korn-Merker, E
Krageloh-Mann, I
Marg, W
Mayatepek, E
Meissner, T
Niemann, G
Pust, B
Schmitt, B
Schoening, M
Schulze, A
Sperner, J
Tegtmeyer, FK
Weisert, M
Wiebicke, W
Wilken, B
Zschocke, J
Bentele, K
Schinzel, A
Strassburg, M
Citation: F. Aksu et al., On being a child and having children with the changing times, MONATS KIND, 149(6), 2001, pp. 594-596
Authors:
Trappe, R
Laccone, F
Cobilanschi, J
Meins, M
Huppke, P
Hanefeld, F
Engel, W
Citation: R. Trappe et al., MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin, AM J HU GEN, 68(5), 2001, pp. 1093-1101
Authors:
Wilken, B
Ramirez, JM
Hanefeld, F
Richter, DW
Citation: B. Wilken et al., Aminophylline modulation of the mouse respiratory network changes during postnatal maturation, J APP PHYSL, 89(5), 2000, pp. 2015-2022
Authors:
Huppke, P
Laccone, F
Kramer, N
Engel, W
Hanefeld, F
Citation: P. Huppke et al., Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients, HUM MOL GEN, 9(9), 2000, pp. 1369-1375
Authors:
Huppke, P
Christen, HJ
Sattler, B
Hanefeld, F
Citation: P. Huppke et al., Two brothers with Hennekam syndrome and cerebral abnormalities, CLIN DYSMOR, 9(1), 2000, pp. 21-24
Authors:
Wilken, B
Dechent, P
Biol, D
Herms, J
Maxton, C
Markakis, E
Hanefeld, F
Frahm, J
Citation: B. Wilken et al., Quantitative proton magnetic resonance spectroscopy of focal brain lesions, PED NEUROL, 23(1), 2000, pp. 22-31
Authors:
Pohl, D
Hanefeld, F
Citation: D. Pohl et F. Hanefeld, Multiple sclerosis in childhood, NERVENHEILK, 19(6), 2000, pp. 324-329
Authors:
Hanefeld, F
Citation: F. Hanefeld, Award of the Peter Emil Pecker Prize 2000 to Prof. Bengt Hagberg, Gothenburg, NEUROPEDIAT, 31(6), 2000, pp. 282-283
Authors:
Hanefeld, F
Korner, C
Holzbach-Eberle, U
von Figura, K
Citation: F. Hanefeld et al., Congenital disorder of glycosylation-Ic: Case report and genetic defect, NEUROPEDIAT, 31(2), 2000, pp. 60-62
Authors:
Barmaki Pour, R
Stockler-Ipsiroglu, S
Hunneman, DH
Gahr, M
Korenke, GC
Pabst, W
Hanefeld, F
Peters, A
Citation: R. Barmaki Pour et al., Enhanced lymphocyte proliferation in patients with adrenoleukodystrophy treated with erucic acid (22 : 1)-rich triglycerides, J INH MET D, 23(2), 2000, pp. 113-119
Authors:
Frewer, A
Hanefeld, F
Citation: A. Frewer et F. Hanefeld, Not-so-simple minds, SCIENCE, 289(5486), 2000, pp. 1878-1878
Authors:
Herms, J
Neidt, I
Luscher, B
Sommer, A
Schurmann, P
Schroder, T
Bergmann, M
Wilken, B
Probst-Cousin, S
Hernaiz-Driever, P
Behnke, J
Hanefeld, F
Pietsch, T
Kretzschmar, HA
Citation: J. Herms et al., c-myc expression in medulloblastoma and its prognostic value, INT J CANC, 89(5), 2000, pp. 395-402
Authors:
Christen, HJ
Hanefeld, F
Kruse, E
Imhauser, S
Ernst, JP
Finkenstaedt, M
Citation: Hj. Christen et al., Foix-Chavany-Marie (anterior operculum) syndrome in childhood: a reappraisal of Worster-Drought syndrome, DEVELOP MED, 42(2), 2000, pp. 122-132
Authors:
Schauder, S
Hanefeld, F
Noske, UM
Zoll, B
Citation: S. Schauder et al., Depigmented hypertrichosis following Blaschko's lines associated with cerebral and ocular malformations: a new neurocutaneous, autosomal lethal gene syndrome from the group of epidermal naevus syndromes?, BR J DERM, 142(6), 2000, pp. 1204-1207
Authors:
Wilke, M
Eiffert, H
Christen, HJ
Hanefeld, F
Citation: M. Wilke et al., Primarily chronic and cerebrovascular course of Lyme neuroborreliosis: case reports and literature review, ARCH DIS CH, 83(1), 2000, pp. 67-71
Authors:
Wilken, B
Ramirez, JM
Probst, I
Richter, DW
Hanefeld, F
Citation: B. Wilken et al., Anoxic ATP depletion in neonatal mice brainstem is prevented by creatine supplementation, ARCH DIS CH, 82(3), 2000, pp. F224-F227
Authors:
Dechent, P
Pouwels, PJW
Wilken, B
Hanefeld, F
Frahm, J
Citation: P. Dechent et al., Increase of total creatine in human brain after oral supplementation of creatine-monohydrate, AM J P-REG, 46(3), 1999, pp. R698-R704
Authors:
Saul, B
Kuner, T
Sobetzko, D
Brune, W
Hanefeld, F
Meinck, HM
Becker, CM
Citation: B. Saul et al., Novel GLRA1 missense mutation (P250T) in dominant hyperekplexia defines anintracellular determinant of glycine receptor channel gating, J NEUROSC, 19(3), 1999, pp. 869-877