Search Results - "Kolski, H."

Etiology of Acute Childhood Encephalitis at The Hospital for Sick Children, Toronto, 1994–1995 by Kolski, H., Ford-Jones, E. L., Richardson, S., Petric, M., Nelson, S., Jamieson, F., Blaser, S., Gold, R., Otsubo, H., Heurter, H., MacGregor, D.

“…Of 145 patients admitted to our hospital because of encephalitis-like illness, 50 patients hospitalized for ⩾72 hours underwent standardized microbiological…”
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G.P.271 by Marttila, M, Lehtokari, V.L, Marston, S.B, Nyman, T.A, Barnerias, C, Beggs, A.H, Bertin, E, Ceyhan-Birsoy, Ö, Cintas, P, Gerard, M, Gilbert-Dussardier, B, Hogue, J.S, Longman, C, Eymard, B, Frydman, M, Kang, P.B, Klinge, L, Kolski, H, Lochmüller, H, Magy, L, Manel, V, Mayer, M, North, K.N, Peudenier-Robert, S, Pihko, H, Probst, F.J, Reisin, R, Stewart, W, Taratuto, A.L, de Visser, M, Wilichowski, E, Winer, J, Nowak, K, Lain, N.G, Winder, T.L, Monnier, N, Clarke, N.F, Pelin, K, Grönholm, M, Wallgren-Pettersson, C

“…Mutations affecting skeletal muscle isoforms of the tropomyosin genes may cause nemaline myopathy (NM), cap myopathy, core-rod myopathy, congenital fibre-type…”
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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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G.P.13.07 Paediatric females with dystrophinopathy by McAdam, L.C, Seemann, N, Shelby, K, Kolski, H, Campbell, C, Biggar, D

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Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing-like attacks in a pediatric patient found to have a pontine capillary telangiectasia and developmental venous anomaly: A case report exploring the root of the problem by Liapounova, Natalia A, VanderPluym, Juliana H, Bhargava, Ravi, Kolski, Hanna H

“…Introduction Short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing (SUNCT)-like attacks are rarely reported in the…”
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T.P.5.02 Pentoxifylline treatment fails to rescue muscle strength and function deterioration in prednisone-treated Duchenne muscular dystrophy (DMD) by Escolar, D.M, Gorni, K, Tesi-Rocha, A.C, Mah, J, Nevo, Y, Korengberg, A, Kolski, H, Bertorini, T, Connolly, A, Kuntz, N, Zimmerman, A, Morgenroth, L, Arrieta, A, Mayhew, J, Florence, J, Nei, L, Hu, F, Henricson, E, Leshner, R, Dubrovsky, A

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C.P.1.03 TPM3 is a recurrent cause of congenital fibre type disproportion and is associated with a consistent phenotype by Clarke, N, Kolski, H, Dye, D, Lim, E, Smith, R, Patel, R, Fahey, M, Laing, N, North, K

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DMD genotypes and loss of ambulation in the CINRG Duchenne Natural History Study by Bello, Luca, Morgenroth, Lauren P, Gordish-Dressman, Heather, Hoffman, Eric P, McDonald, Craig M, Cirak, Sebahattin

“…OBJECTIVE:To correlate time to loss of ambulation (LoA) and different truncating DMD gene mutations in a large, prospective natural history study of Duchenne…”
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P76 The Canadian neuromuscular disease registry: a national spinal muscular atrophy registry for real world evidence by Sobey, M., Hodgkinson, V., Westbury, G., Brais, B., Campbell, C., Castro-Codesal, M., Crone, M., Dojeiji, S., Genge, A., Gonorazky, H., Johnston, W., Kolski, H., Lochmüller, H., Mah, J., McAdam, L., O'Connell, C., O'Ferrall, E.K., Oskoui, M., Pfeffer, G., Phan, C.

“…Patient registries are an effective tool in tracking the natural history of rare diseases as well as post-marketing surveillance of novel therapies. The…”
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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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Development of a model‐based clinical trial simulation platform to optimize the design of clinical trials for Duchenne muscular dystrophy by Morales, Juan Francisco, Corey, Diane, Larkindale, Jane, Romero, Klaus, Schmidt, Stephan, Cregan, M, Johnson, L, Han, J, Joyce, N, Nicorici, A, Reddy, D, Mah, J, Haig, T, Sanchez, K, Alhander, A, Ekstrom, A, Gustafsson, A, Kroksmark, A, Wahlgren, L, Brody, N, Drogo, B, Leach, M, Tesi‐Rocha, C, Birkmeier, M, Toles, A, Carroll, K, DeValle, K, Kennedy, R, Rodriguez, V, Nevo, Y, Adani, R, BarLeve, A, Chen‐Joseph, L, Daana, M, Panteleyev‐Yitshak, V, Yaffe, D, Levi, L, Bendixen, R, Karnavas, K, Matthews, C, Niizawa, G, Weimer, J, Florence, J, Gadeken, R, Golumbak, P, Malkus, B, Pestronk, A, Schierbecker, J, Seiner, C, Wulf, C, Blair, S, Grillo, B, Bertorini, T, Barrett‐Adair, M, Benzel, C, Clift, J, Holloway, J, Igarashi, M, Kiphut, F, Parker, A, Phillips, A, Young, R, North, K, Gabriel, N, Harman, M, Rose, K, Kolski, H, Chen, L, Beneggi, M, Capone, L, Molteni, A, Morettini, V, Gupta, A, Knight, A, Lott, B, McNeil, R, Orozco, G, Chambers, G, Day, J, Dalton, J, Erickson, A, Marsh, J, Naughton, C, Hoffman, A, Korn‐Petersen, W, Deliz, B, Fuste, P, Luciano, C, Torres, J, Ahmed, M, Arrieta, A, Brown‐Caines, T, Carty, C, Duong, T, Feng, J, Hu, F, Hunegs, L, Zimmerman, A, Nuckolls, Glen, Carifi, Emily

“…Early clinical trials of therapies to treat Duchenne muscular dystrophy (DMD), a fatal genetic X‐linked pediatric disease, have been designed based on the…”
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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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A population-based study of dystrophin mutations in Canada by Mah, Jean K, Selby, Kathryn, Campbell, Craig, Nadeau, Amelie, Tarnopolsky, Mark, McCormick, Anna, Dooley, Joseph M, Kolski, Hanna, Skalsky, Andrew J, Smith, R Garth, Buckley, David, Ray, Peter N, Yoon, Grace

“…We carried out a population-based study of dystrophin mutations in patients followed by members of the Canadian Paediatric Neuromuscular Group (CPNG) over a…”
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G.P.271: Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies by Marttila, M., Lehtokari, V.L., Marston, S.B., Nyman, T.A., Barnerias, C., Beggs, A.H., Bertin, E., Ceyhan-Birsoy, Ö., Cintas, P., Gerard, M., Gilbert-Dussardier, B., Hogue, J.S., Longman, C., Eymard, B., Frydman, M., Kang, P.B., Klinge, L., Kolski, H., Lochmüller, H., Magy, L., Manel, V., Mayer, M., North, K.N., Peudenier-Robert, S., Pihko, H., Probst, F.J., Reisin, R., Stewart, W., Taratuto, A.L., de Visser, M., Wilichowski, E., Winer, J., Nowak, K., Lain, N.G., Winder, T.L., Monnier, N., Clarke, N.F., Pelin, K., Grönholm, M., Wallgren-Pettersson, C.

“…Mutations affecting skeletal muscle isoforms of the tropomyosin genes may cause nemaline myopathy (NM), cap myopathy, core-rod myopathy, congenital fibre-type…”
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Duchenne muscular dystrophy: Canadian paediatric neuromuscular physicians survey by McMillan, Hugh J, Campbell, Craig, Mah, Jean K

“…Duchenne muscular dystrophy (DMD) is the most common form of muscular dystrophy in childhood. To assess the current care of paediatric DMD patients in Canada,…”
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Authors' Reply to Dr Kumar by Vajsar, Jiri, Kolski, Hanna

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The Landau-Kleffner syndrome by Kolski, Hanna, Otsubo, Hiroshi

“…Landau-Kleffner Syndrome is a rare childhood disorder which involves seizures and acquired aphasia. Anticonvulsants, or the passage of time, may control the…”
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Thoracoscopic thymectomy in juvenile myasthenia gravis by Kolski, Hanna, Vajsar, Jiri, Kim, Peter C.W.

“…Background: Although transsternal thymectomy is an effective method in the treatment of juvenile myasthenia gravis (JMG) it is traumatic in pediatric patients…”
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Video-Assisted Thoracoscopic Thymectomy in Juvenile Myasthenia Gravis by Kolski, Hanna K., Kim, Peter C.W., Vajsar, Jiri

“…As video-assisted thoracoscopic surgery for thymectomy has been reported to be as effective as traditional open surgical approaches in predominantly adult…”
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Video-Assisted Thoracoscopic Thymectomy in Juvenile Myasthenia Gravis by Kolski, Hanna K., Kim, Peter C.W., Vajsar, Jiri

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