Search Results - "Mah, J.K."

P.7.13 Whole body vibration training lowers serum creatine kinase levels in boys with Duchenne muscular dystrophy by Mah, J.K, Khan, A, Chiu, A, Ramage, B

“…Whole body vibration training (WBVT) involves the use of a low-amplitude high-frequency vibrating platform to transmit mechanical energy. It has been proposed…”
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Anti-myelin antibodies modulate clinical expression of childhood multiple sclerosis by O'Connor, K.C, Lopez-Amaya, C, Gagne, D, Lovato, L, Moore-Odom, N.H, Kennedy, J, Krupp, L, Tenembaum, S, Ness, J, Belman, A, Boyko, A, Bykova, O, Mah, J.K, Stoian, C.A, Waubant, E, Kremenchutzky, M, Ruggieri, M, Bardini, M.R, Rensel, M, Hahn, J, Weinstock-Guttman, B, Yeh, E.A, Farrell, K, Freedman, M.S, Iivanainen, M, Bhan, V, Dilenge, M, Hancock, M.A, Gano, D, Fattahie, R, Kopel, L, Fournier, A.E, Moscarello, M, Banwell, B, Bar-Or, A

“…Abstract Anti-myelin basic protein (MBP) antibodies in pediatric-onset MS and controls were characterized. Serum samples were obtained from 94 children with MS…”
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G.P.146 by Dabaj, I, Heller, F, Quijano-Roy, S, Mah, J.K, Rutkowski, A, Estournet, B, Clegg, R, Wahbi, K

“…Congenital muscular dystrophy secondary to variants in the lamin A/C gene (LMNA-CMD) typically present with hypotonia at birth, poor axial and truncal control,…”
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G.P.13 by Mah, J.K, Chen, Y.W, Duong, T, Cnaan, A, Sund, Z, Morgenroth, L.P, McDonald, C, Tulinius, M, Sparks, S, Webster, R, Connolly, A, Karachunski, P, Clemens, P.R

“…Infantile FSHD is uncommon. We aim to describe the clinical features and secondary conditions in early onset FSHD. This study was conducted at participating…”
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75. Vitamin D deficiency is common among children with neuromuscular diseases by Mah, J.K, Stoian, C.A, Liu, N, Goia, E

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76. Parents as the “Lifeline” for their children with neuromuscular disease by Mah, J.K, McNeil, D, Thannhauser, J, Kolski, H, Dewey, D

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P4.9 A phase 2, randomized, placebo-controlled, multiple ascending-dose study of ACE-031 (ActRIIB-IgG1) in Duchenne muscular dystrophy (DMD): Preliminary results by Campbell, C, Attie, K.M, Mah, J.K, Tarnopolsky, M, Selby, K, McMillan, H.J, Yang, Y, Wilson, D, Barger, R, Sherman, M.L, Escolar, D

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Longitudinal pulmonary function testing outcome measures in Duchenne muscular dystrophy: Long-term natural history with and without glucocorticoids by McDonald, Craig M., Gordish-Dressman, Heather, Henricson, Erik K., Duong, Tina, Joyce, Nanette C., Jhawar, Sanjay, Leinonen, Mika, Hsu, Fengming, Connolly, Anne M., Cnaan, Avital, Abresch, Richard T., Dubrovsky, A., Kornberg, A., Ryan, M., Webster, R., Biggar, W.D., McAdam, L.C., Mah, J.K., Kolski, H., Vishwanathan, V., Chidambaranathan, S., Nevo, Y., Gorni, K., Carlo, J., Tulinius, M., Lotze, T., Bertorini, T.E., Day, J.W., Karachunski, P., Clemens, P.R., Abdel-Hamid, H., Teasley, J., Kuntz, N., Driscoll, S., Bodensteiner, J.B., Connolly, A.M., Pestronk, A., Abresch, R.T., Henricson, E.K., Joyce, N.C., McDonald, C.M., Cnaan, A., Morgenroth, L.P., Leshner, R., Tesi-Rocha, C., Thangarajh, M., Duong, T.

“…•Natural history changes in pulmonary function tests across time in Duchenne muscular dystrophy.•Treatment with glucocorticoids (steroids) > 1 year was…”
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Expansion of the GLE1‐associated arthrogryposis multiplex congenita clinical spectrum by Smith, C., Parboosingh, J.S., Boycott, K.M., Bönnemann, C.G., Mah, J.K., Lamont, R.E., Micheil Innes, A., Bernier, F.P.

“…Mutations in GLE1 cause two recessive subtypes of arthrogryposis multiplex congenita (AMC), a condition characterized by joint contractures at birth, and all…”
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G.P.146: Cardiac manifestations and gastro-intestinal sequelae in children with LMNA-CMD by Dabaj, I., Heller, F., Quijano-Roy, S., Mah, J.K., Rutkowski, A., Estournet, B., Clegg, R., Wahbi, K.

“…Congenital muscular dystrophy secondary to variants in the lamin A/C gene (LMNA-CMD) typically present with hypotonia at birth, poor axial and truncal control,…”
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G.P.13: Baseline characteristics of the CINRG infantile facioscapulohumeral muscular dystrophy (FSHD) cohort by Mah, J.K., Chen, Y.W., Duong, T., Cnaan, A., Sund, Z., Morgenroth, L.P., McDonald, C., Tulinius, M., Sparks, S., Webster, R., Connolly, A., Karachunski, P., Clemens, P.R.

“…Infantile FSHD is uncommon. We aim to describe the clinical features and secondary conditions in early onset FSHD. This study was conducted at participating…”
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Pentoxifylline as a rescue treatment for DMD: A randomized double-blind clinical trial by ESCOLAR, D. M, ZIMMERMAN, A, NEVO, Y, TESI-ROCHA, C, NAGARAJU, K, RAYAVARAPU, S, HACHE, L. P, MAYHEW, J. E, FLORENCE, J, HU, F, ARRIETA, A, HENRICSON, E, BERTORINI, T, LESHNER, R. T, MAH, J. K, CLEMENS, P. R, CONNOLLY, A. M, MESA, L, GORNI, K, KORNBERG, A, KOLSKI, H, KUNTZ, N

“…To determine whether pentoxifylline (PTX) slows the decline of muscle strength and function in ambulatory boys with Duchenne muscular dystrophy (DMD). This was…”
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The prevalence of incidental findings in multiple sclerosis patients by Trufyn, J, Hill, M D, Scott, J N, Modi, J, Ciura, V, Frayne, R, Goyal, M, Lautner, D, Bhayana, D, Davenport, W J, Mah, J K, Burton, J M, Costello, F

“…Incidental findings arising from imaging research have important implications for patient safety. Magnetic resonance imaging is widespread in multiple…”
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Brain MR imaging findings in two patients with Alpers' syndrome by Smith, J.K., Mah, J.K., Castillo, M.

“…We describe the magnetic resonance (MR) imaging findings in two patients with the clinical diagnosis of progressive neuronal degeneration of childhood with…”
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