Results: 1-25 | 26-35
Results: 1-25/35

Authors: Bornemann, A Goebel, HH
Citation: A. Bornemann et Hh. Goebel, Introduction: Recent advances in hereditary neuromuscular diseases of childhood, BRAIN PATH, 11(2), 2001, pp. 190-192

Authors: Bornemann, A Goebel, HH
Citation: A. Bornemann et Hh. Goebel, Congenital myopathies, BRAIN PATH, 11(2), 2001, pp. 206-217

Authors: Goebel, HH Warlo, IAP
Citation: Hh. Goebel et Iap. Warlo, Surplus protein myopathies, NEUROMUSC D, 11(1), 2001, pp. 3-6

Authors: Kottler, U Schwenn, O Goebel, HH Urban, P Pfeiffer, N
Citation: U. Kottler et al., Keratopathy as an indication of multifocal congenital sensitive polyneuropathy, OPHTHALMOLO, 98(5), 2001, pp. 487-489

Authors: Goebel, HH Halbig, LE Goldfarb, L Schober, R Albani, M Neuen-Jacob, E Voit, T
Citation: Hh. Goebel et al., Reducing body myopathy with cytoplasmic bodies and rigid spine syndrome: Amixed congenital myopathy, NEUROPEDIAT, 32(4), 2001, pp. 196-205

Authors: Poppe, M Bruck, W Hahn, G Weissbrich, B Heubner, G Goebel, HH Todt, H
Citation: M. Poppe et al., Fulminant course in a case of diffuse myelinoclastic encephalitis - A casereport, NEUROPEDIAT, 32(1), 2001, pp. 41-44

Authors: Wheeler, RB Schlie, M Kominami, E Gerhard, L Goebel, HH
Citation: Rb. Wheeler et al., Neuronal ceroid lipofuscinosis: late infantile or Jansky Bielschowsky type- re-revisited, ACT NEUROP, 102(5), 2001, pp. 485-488

Authors: Nardocci, N Goebel, HH
Citation: N. Nardocci et Hh. Goebel, Neuronal ceroid lipofuscinoses - Current knowledge and perspectives - Introduction, NEUROL SCI, 21(3), 2000, pp. S13-S13

Authors: Goebel, HH
Citation: Hh. Goebel, Morphological aspects of the neuronal ceroid lipofuscinoses, NEUROL SCI, 21(3), 2000, pp. S27-S33

Authors: Goebel, HH Warlo, I
Citation: Hh. Goebel et I. Warlo, Gene-related protein surplus myopathies, MOL GEN MET, 71(1-2), 2000, pp. 267-275

Authors: Anderson, LVB Harrison, RM Pogue, R Vafiadaki, E Pollitt, C Davison, K Moss, JA Keers, S Pyle, A Shaw, PJ Mahjneh, I Argov, Z Greenberg, CR Wrogemann, K Bertorini, T Goebel, HH Beckmann, JS Bashir, R Bushby, KMD
Citation: Lvb. Anderson et al., Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies), NEUROMUSC D, 10(8), 2000, pp. 553-559

Authors: Goebel, HH Warlo, IAP
Citation: Hh. Goebel et Iap. Warlo, Progress in desmin-related myopathies, J CHILD NEU, 15(9), 2000, pp. 565-572

Authors: Goebel, HH
Citation: Hh. Goebel, Molecular, oncologic, and therapeutic spectrum of von Hippel-Lindau disease, NEUROSURG R, 23(1), 2000, pp. 24-24

Authors: Goebel, HH
Citation: Hh. Goebel, The new nosography of the neuronal ceroid-lipofuscinoses, ANN PATHOL, 20(5), 2000, pp. 479-491

Authors: Park, KY Dalakas, MC Goebel, HH Ferrans, VJ Semino-Mora, C Litvak, S Takeda, K Goldfarb, LG
Citation: Ky. Park et al., Desmin splice variants causing cardiac and skeletal myopathy, J MED GENET, 37(11), 2000, pp. 851-857

Authors: Goebel, HH Schochet, SS Jaynes, M Bruck, W Kohlschutter, A Hentati, F
Citation: Hh. Goebel et al., Progress in neuropathology of the neuronal ceroid lipofuscinoses, MOL GEN MET, 66(4), 1999, pp. 367-372

Authors: Williams, RE Gardiner, RM Goebel, HH
Citation: Re. Williams et al., The European Concerted Action NCL Clinical Case Registry, MOL GEN MET, 66(4), 1999, pp. 407-408

Authors: Nowak, KJ Wattanasirichaigoon, D Goebel, HH Wilce, M Pelin, K Donner, K Jacob, RL Hubner, C Oexle, K Anderson, JR Verity, CM North, KN Iannaccone, ST Muller, CR Nurnberg, P Muntoni, F Sewry, C Hughes, I Sutphen, R Lacson, AG Swoboda, KJ Vigneron, J Wallgren-Pettersson, C Beggs, AH Laing, NG
Citation: Kj. Nowak et al., Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy, NAT GENET, 23(2), 1999, pp. 208-212

Authors: Muller-Felber, W Ansevin, CF Ricker, K Muller-Jenssen, A Topfer, M Goebel, HH Pongratz, DE
Citation: W. Muller-felber et al., Immunosuppressive treatment of rippling muscles in patients with myasthenia gravis, NEUROMUSC D, 9(8), 1999, pp. 604-607

Authors: Goebel, HH Mole, SE Lake, BD
Citation: Hh. Goebel et al., The neuronal ceroid lipofuscinoses (Batten disease) - Introduction, BIOM HLTH R, 33, 1999, pp. 1-4

Authors: Elleder, M Lake, BD Goebel, HH Rapola, J Haltia, M Carpenter, S
Citation: M. Elleder et al., Definitions of the ultrastructural patterns found in NCL, BIOM HLTH R, 33, 1999, pp. 5-15

Authors: Williams, RE Gottlob, I Lake, BD Goebel, HH Winchester, BG Wheeler, RB
Citation: Re. Williams et al., Classic late infantile NCL, BIOM HLTH R, 33, 1999, pp. 37-54

Authors: Hofman, I Kohlschutter, A Santavuori, P Gottlob, I Goebel, HH Lake, BD Schutgens, RBH Greene, NDE Leung, KY Mitchison, HM Munroe, PB Taschner, PEM
Citation: I. Hofman et al., Juvenile NCL, BIOM HLTH R, 33, 1999, pp. 55-76

Authors: Martin, JJ Gottlob, I Goebel, HH Mole, SE
Citation: Jj. Martin et al., Adult NCL, BIOM HLTH R, 33, 1999, pp. 77-90

Authors: Lake, BD Goebel, HH
Citation: Bd. Lake et Hh. Goebel, Morphologic diagnostic considerations, BIOM HLTH R, 33, 1999, pp. 142-144
Risultati: 1-25 | 26-35