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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