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Results: 1-25 | 26-28
Results: 1-25/28
High mitochondrial DNA T8993G mutation (> 90%) without typical features ofLeigh's and NARP syndromes
Authors: Tsao, CY Mendell, JR Bartholomew, D
Citation: Cy. Tsao et al., High mitochondrial DNA T8993G mutation (> 90%) without typical features ofLeigh's and NARP syndromes, J CHILD NEU, 16(7), 2001, pp. 533-535
Treatment approaches for Guillian-Barre Syndrome and chronic inflammatory demyelinating polyradiculoneuropathy
Authors: Lindenbaum, Y Kissel, JT Mendell, JR
Citation: Y. Lindenbaum et al., Treatment approaches for Guillian-Barre Syndrome and chronic inflammatory demyelinating polyradiculoneuropathy, NEUROL CLIN, 19(1), 2001, pp. 187
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifussmuscular dystrophy
Authors: Brown, CA Lanning, RW McKinney, KQ Salvino, AR Cherniske, E Crowe, CA Darras, BT Gominak, S Greenberg, CR Grosmann, C Heydemann, P Mendell, JR Pober, BR Sasaki, T Shapiro, F Simpson, DA Suchowersky, O Spence, JE
Citation: Ca. Brown et al., Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifussmuscular dystrophy, AM J MED G, 102(4), 2001, pp. 359-367
Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral dystrophy
Authors: Kissel, JT McDermott, MP Mendell, JR King, WM Pandya, S Griggs, RC Tawil, R Cos, L Langsam, A Martens, B Brower, C Herr, BE Figlewicz, D Forrester, J Downing, K Holloway, RG Hubble, J Kolassa, J
Citation: Jt. Kissel et al., Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral dystrophy, NEUROLOGY, 57(8), 2001, pp. 1434-1440
Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy - Reply
Authors: Mendell, JR
Citation: Jr. Mendell, Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy - Reply, NEUROLOGY, 57(5), 2001, pp. 938-938
Diagnosis of Duchenne dystrophy by enhanced detection of small mutations
Authors: Mendell, JR Buzin, CH Feng, J Yan, J Serrano, C Sangani, DS Wall, C Prior, TW Sommer, SS
Citation: Jr. Mendell et al., Diagnosis of Duchenne dystrophy by enhanced detection of small mutations, NEUROLOGY, 57(4), 2001, pp. 645-650
Congenital muscular dystrophy - Searching for a definition after 98 years
Authors: Mendell, JR
Citation: Jr. Mendell, Congenital muscular dystrophy - Searching for a definition after 98 years, NEUROLOGY, 56(8), 2001, pp. 993-994
A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy
Authors: Fenichel, GM Griggs, RC Kissel, J Kramer, TI Mendell, JR Moxley, RT Pestronk, A Sheng, K Florence, J King, WM Pandya, S Robison, VD Wang, H
Citation: Gm. Fenichel et al., A randomized efficacy and safety trial of oxandrolone in the treatment of Duchenne dystrophy, NEUROLOGY, 56(8), 2001, pp. 1075-1079
Familial cerebellar ataxia with muscle coenzyme Q10 deficiency
Authors: Musumeci, O Naini, A Slonim, AE Skavin, N Hadjigeorgiou, GL Krawiecki, N Weissman, BM Tsao, CY Mendell, JR Shanske, S De Vivo, DC Hirano, M DiMauro, S
Citation: O. Musumeci et al., Familial cerebellar ataxia with muscle coenzyme Q10 deficiency, NEUROLOGY, 56(7), 2001, pp. 849-855
Autonomic impairment in painful neuropathy
Authors: Novak, V Freimer, ML Kissel, JT Sahenk, Z Periquet, IM Nash, SM Collins, MP Mendell, JR
Citation: V. Novak et al., Autonomic impairment in painful neuropathy, NEUROLOGY, 56(7), 2001, pp. 861-868
Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy
Authors: Mendell, JR Barohn, RJ Freimer, ML Kissel, JT King, W Nagaraja, HN Rice, R Campbell, WW Donofrio, PD Jackson, CE Lewis, RA Shy, M Simpson, DM Parry, GJ Rivner, MH Thornton, CA Bromberg, MB Tandan, R Harati, Y Giuliani, MJ
Citation: Jr. Mendell et al., Randomized controlled trial of IVIg in untreated chronic inflammatory demyelinating polyradiculoneuropathy, NEUROLOGY, 56(4), 2001, pp. 445-449
Positive neuropathic sensory symptoms as endpoints in diabetic neuropathy trials
Authors: Apfel, SC Asbury, AK Bril, V Burns, TM Campbell, JN Chalk, CH Dyck, PJ Dyck, PJB Feldman, EL Fields, HL Grant, IA Griffin, JW Klein, CJ Lindblom, U Litchy, WJ Low, PA Melanson, M Mendell, JR Merren, MD O'Brien, PC Rendell, M Rizza, RA Service, FJ Thomas, PK Walk, D Wang, AK Wessel, K Windebank, AJ Ziegler, D Zochodne, DW
Citation: Sc. Apfel et al., Positive neuropathic sensory symptoms as endpoints in diabetic neuropathy trials, J NEUR SCI, 189(1-2), 2001, pp. 3-5
Mitochondrial respiratory-chain defects presenting as nonspecific featuresin children
Authors: Tsao, CY Mendell, JR Lo, WD Luquette, M Rusin, J
Citation: Cy. Tsao et al., Mitochondrial respiratory-chain defects presenting as nonspecific featuresin children, J CHILD NEU, 15(7), 2000, pp. 445-448
Mitochondrial DNA depletion in children
Authors: Tsao, CY Mendell, JR Luquette, M Dixon, B Morrow, G
Citation: Cy. Tsao et al., Mitochondrial DNA depletion in children, J CHILD NEU, 15(12), 2000, pp. 822-824
Myasthenia gravis and associated autoimmune diseases in children
Authors: Tsao, CY Mendell, JR Lo, WD Luquette, M Rennebohm, R
Citation: Cy. Tsao et al., Myasthenia gravis and associated autoimmune diseases in children, J CHILD NEU, 15(11), 2000, pp. 767-769
Randomized trials of dichlorphenamide in the periodic paralyses
Authors: Tawil, R McDermott, MP Brown, R Shapiro, BC Ptacek, LJ McManis, PG Dalakas, MC Spector, SA Mendell, JR Hahn, AF Griggs, RC
Citation: R. Tawil et al., Randomized trials of dichlorphenamide in the periodic paralyses, ANN NEUROL, 47(1), 2000, pp. 46-53
Another approach to ventilatory failure in neuromuscular disease
Authors: Reynolds, JE Mendell, JR
Citation: Je. Reynolds et Jr. Mendell, Another approach to ventilatory failure in neuromuscular disease, NEUROLOGY, 55(5), 2000, pp. 611-612
Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathy
Authors: Collins, MP Mendell, JR Periquet, MI Sahenk, Z Amato, AA Gronseth, GS Barohn, RJ Jackson, CE Kissel, JT
Citation: Mp. Collins et al., Superficial peroneal nerve/peroneus brevis muscle biopsy in vasculitic neuropathy, NEUROLOGY, 55(5), 2000, pp. 636-643
Intracellular processing and toxicity of the truncated androgen receptor: Nuclear congophilia-associated cell death
Authors: Feng, B Chen, L Drmanovic, Z Kakabadze, I Mendell, JR Marzluf, GA Sahenk, Z
Citation: B. Feng et al., Intracellular processing and toxicity of the truncated androgen receptor: Nuclear congophilia-associated cell death, J NE EXP NE, 59(8), 2000, pp. 652-663
Expression of gamma-sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex
Authors: Barresi, R Moore, SA Stolle, CA Mendell, JR Campbell, KP Campbell, P
Citation: R. Barresi et al., Expression of gamma-sarcoglycan in smooth muscle and its interaction with the smooth muscle sarcoglycan-sarcospan complex, J BIOL CHEM, 275(49), 2000, pp. 38554-38560
Effects of PMP22 duplication and deletions on the axonal cytoskeleton
Authors: Sahenk, Z Chen, L Mendell, JR
Citation: Z. Sahenk et al., Effects of PMP22 duplication and deletions on the axonal cytoskeleton, ANN NEUROL, 45(1), 1999, pp. 16-24
Muscular dystrophy: Historical overview and classification in the genetic era
Authors: Kissel, JT Mendell, JR
Citation: Jt. Kissel et Jr. Mendell, Muscular dystrophy: Historical overview and classification in the genetic era, SEM NEUROL, 19(1), 1999, pp. 5-7
The childhood muscular dystrophies: Making order out of chaos
Authors: Tsao, CY Mendell, JR
Citation: Cy. Tsao et Jr. Mendell, The childhood muscular dystrophies: Making order out of chaos, SEM NEUROL, 19(1), 1999, pp. 9-23
Painful sensory neuropathy - Prospective evaluation using skin biopsy
Authors: Periquet, MI Novak, V Collins, MP Nagaraja, HN Erdem, S Nash, SM Freimer, ML Sahenk, Z Kissel, JT Mendell, JR
Citation: Mi. Periquet et al., Painful sensory neuropathy - Prospective evaluation using skin biopsy, NEUROLOGY, 53(8), 1999, pp. 1641-1647
Definitive molecular diagnosis of facioscapulohumeral dystrophy
Authors: Orrell, RW Tawil, R Forrester, J Kissel, JT Mendell, JR Figlewicz, DA
Citation: Rw. Orrell et al., Definitive molecular diagnosis of facioscapulohumeral dystrophy, NEUROLOGY, 52(9), 1999, pp. 1822-1826
Risultati: 1-25 | 26-28