The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

by Knuiman, G. J., Küsters, B., Eshuis, L., Snoeck, M., Lammens, M., Heytens, L., De Ridder, W., Baets, J., Scalco, R. S., Quinlivan, R., Holton, J., Bodi, I., Wraige, E., Radunovic, A., von Landenberg, C., Reimann, J., Kamsteeg, E.-J., Sewry, C., Jungbluth, H., Voermans, N. C.
Published in Journal of neurology

A founder mutation in Anoctamin 5 is a major cause of limb girdle muscular dystrophy

by HICKS, Debbie, SARKOZY, Anna, BAILEY, Geraldine, MILLER, James, RADUNOVIC, Aleksander, HUGHES, Paul J, ROBERT, Richard, KRAUSE, Sabine, WALTER, Maggie C, LAVAL, Steven H, STRAUB, Volker, LOCHMÜLLER, Hanns, MUELAS, Nuria, BUSHBY, Kate, KÖEHLER, Katrin, HUEBNER, Angela, HUDSON, Gavin, CHINNERY, Patrick F, BARRESI, Rita, EAGLE, Michelle, POLVIKOSKI, Tuomo
Published in Brain (London, England : 1878)

Rituximab in the treatment of pembrolizumab-induced myasthenia gravis

by Crusz, S.M., Radunovic, A., Shepherd, S., Shah, S., Newey, V., Phillips, M., Lim, L., Powles, T., Szlosarek, P.W., Shamash, J., Rashid, S.
Published in European journal of cancer (1990)

Mutations in RYR1 are a common cause of exertional myalgia and rhabdomyolysis

by Dlamini, N, Voermans, N.C, Lillis, S, Stewart, K, Kamsteeg, E.-J, Drost, G, Quinlivan, R, Snoeck, M, Norwood, F, Radunovic, A, Straub, V, Roberts, M, Vrancken, A.F.J.E, van der Pol, W.L, de Coo, R.I.F.M, Manzur, A.Y, Yau, S, Abbs, S, King, A, Lammens, M, Hopkins, P.M, Mohammed, S, Treves, S, Muntoni, F, Wraige, E, Davis, M.R, van Engelen, B, Jungbluth, H
Published in Neuromuscular disorders : NMD

Mobility shift of beta-dystroglycan combined with reduced laminin alpha2 expression is a marker of genetic defects in the GMPPB gene

by Torelli, S, Sarkozy, A, Mein, R, Yau, M, Hammans, S, Radunovic, A, Henderson, M, Walker, M, Marino, S, Winder, S, Feng, L, Phadke, R, Sewry, C, Bushby, K, Muntoni, F, Barresi, R
Published in Neuromuscular disorders : NMD

P67 Characterisation of the expression of Polycomb Group Genes in human neuromuscular diseases

by Dibenedetto, S, East, M, Baithun, M, Robson, L.G, Radunovic, A, Marino, S
Published in Neuromuscular disorders : NMD

Assisted reproductive technology in Europe, 2012: results generated from European registers by ESHRE

by Calhaz-Jorge, C, de Geyter, C, Kupka, M.S, de Mouzon, J, Erb, K, Mocanu, E, Motrenko, T, Scaravelli, G, Wyns, C, Goossens, V
Published in Human reproduction (Oxford)

A novel bleeding disorder associated with RYR1 mutations

by Lopez, R, Byrne, S, Vukcevic, M, Sekulic-Jablanovic, M, Xu, L, Brink, M, Alamelu, J, Voermans, N, Snoeck, M, Clement, E, Muntoni, F, Zhou, H, Radunovic, A, Mohammed, S, Wraige, E, Zorzato, F, Treves, S, Jungbluth, H
Published in Neuromuscular disorders : NMD

A randomized, controlled double-blind study comparing the efficacy and safety of dose-ranging voclosporin with placebo in achieving remission in patients with active lupus nephriti...

by Rovin, Brad H., Solomons, Neil, Pendergraft, William F., Dooley, Mary Anne, Tumlin, James, Romero-Diaz, Juanita, Lysenko, Lidia, Navarra, Sandra V., Huizinga, Robert B., Adzerikho, Ihar, Mikhailova, Elena, Mitkovskaya, Natalya, Pimanov, Sergey, Soroka, Nikolay, Bogov, Boris Iliev, Deliyska, Boriana, Ikonomov, Valentin, Tilkiyan, Eduard, Almeida, Ruth, Jimenez, Fernando, Teran, Faud, Tchokhonelidze, Irma, Tsiskarishvili, Nino, Herrera Mendez, Maynor, Loaeza, Arturo Reyes, Gutierrez Urena, Sergio Ramon, Araiza Casillas, Rodolfo, Madero Rovalo, Magdalena, Niemczyk, Stanislaw, Sokalski, Antoni, Wiecek, Andrzej, Klinger, Marian, Bugrova, Olga V., Chernykh, Tatiana M., Kameneva, Tatiana R., Lysenko, Lidia V., Raskina, Tatiana A., ReshEtko, Olga V., Vezikova, Natalia N., Kropotina, Tatiana V., Maksudova, Adelya N., Marasaev, Vyacheslav, Gordeev, Ivan, EssAian, Ashot M., Frolov, Alexey, Jelacic, Rosa, Jovanovic, Dragan, Mitic, Branka, Pekovic, Gordana, Radovic, Milan, Radunovic, Goran, Carreira, Patricia, Diaz Gonzalez, Federico, Fulladosa, Xavier, Herath, Chula, Hewageegana, Anura, Nazar, Abdul Latiff Mohamed, Wazil, A.W.M., Dudar, Iryna, Godlevska, Olga, Korneyeva, Svitlana, Vasylets, ViktoriIa, Sydor, Nataliya, Kolesnyk, Mykola, Parikh, Samir V., Ginzler, Ellen M., Tumlin, James A., Saxena, Amit, Saxena, Ramesh, Lafayette, Richard Alan, Pendergraft, William Franklin, Podoll, Amber S., Arrey-Mensah, Annie A., Bubb, Michael, Grossman, Jennifer, Oporta, Alejandro I., Nami, Alireza, Rahman, Md. Mujibur, Haq, Syed Atiqul, Chan, Tak Mao Daniel, Temy, Mok Mo Yin, Gomez, Harold Michael P., Bermas, James, Reyes, Bernadette Heizel, Hao, Llewellyn T., Roberto, Linda Charmaine, Amante, Eric, Navarra, Sandra V., Lanzon, Allan E., Choe, Jung-Yoon, Kang, Tae Young, Kim, Yon Su, Lee, Seung-Geun, Lee, Ji Soo, Jun, Jason Choo Chon, Vasudevan, Archana, Luo, Shue-Fen, Cheng, Tien-Tsai, Satirapoj, Bancha, Noppakun, Kajohnsak
Published in Kidney international

Assisted reproductive technology in Europe, 2009: results generated from European registers by ESHRE

by Ferraretti, A.P, Goossens, V, Kupka, M, Bhattacharya, S, de Mouzon, J, Castilla, J.A, Erb, K, Korsak, V, Nyboe Andersen, A
Published in Human reproduction (Oxford)

Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease

by Radunovic, Aleksandar, Annane, Djillali, Rafiq, Muhammad K, Brassington, Ruth, Mustfa, Naveed
Published in Cochrane database of systematic reviews

Gastrostomy in patients with amyotrophic lateral sclerosis (ProGas): a prospective cohort study

by Anon
Published in Lancet neurology

P32 Polycomb group genes and the regenerative process in the aged and pathological human muscle

by Zhang, X, Bhagat, H, Di Foggia, V, Radunovic, A, Robson, L.G, Marino, S
Published in Neuromuscular disorders : NMD

ART in Europe, 2015: results generated from European registries by ESHRE

by De Geyter, C, Calhaz-Jorge, C, Kupka, M S, Wyns, C, Mocanu, E, Motrenko, T, Scaravelli, G, Smeenk, J, Vidakovic, S, Goossens, V
Published in Human reproduction open

Safety and efficacy of diaphragm pacing in patients with respiratory insufficiency due to amyotrophic lateral sclerosis (DiPALS): a multicentre, open-label, randomised controlled t...

by Anon
Published in Lancet neurology

ART in Europe, 2016: results generated from European registries by ESHRE

by Wyns, C, Bergh, C, Calhaz-Jorge, C, De Geyter, Ch, Kupka, M S, Motrenko, T, Rugescu, I, Smeenk, J, Tandler-Schneider, A, Vidakovic, S, Goossens, V
Published in Human reproduction open

Cu/Zn superoxide dismutase gene mutations in amyotrophic lateral sclerosis: correlation between genotype and clinical features

by Radunovíc, A, Leigh, P N
Published in Journal of neurology, neurosurgery and psychiatry

P.15.7 A founder mutation in the titin gene is a common cause of myofibrillar myopathy with early respiratory failure

by Pfeffer, G, Barresi, R, Wilson, I.J, Hardy, S.A, Griffin, H, Hudson, J, Elliott, H.R, Ramesh, A.V, Radunovic, A, Winer, J, Vaidya, S, Raman, A, Busby, M, Farrugia, M.E, Ming, A, Everett, C, Emsley, H.C.A, Horvath, R, Straub, V, Bushby, K, Lochmuller, H, Chinnery, P, Sarkozy, A
Published in Neuromuscular disorders : NMD

Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease

by Currò, Riccardo, Dominik, Natalia, Facchini, Stefano, Vegezzi, Elisa, Sullivan, Roisin, Galassi Deforie, Valentina, Fernández-Eulate, Gorka, Traschütz, Andreas, Rossi, Salvatore, Garibaldi, Matteo, Kwarciany, Mariusz, Taroni, Franco, Brusco, Alfredo, Good, Jean-Marc, Cavalcanti, Francesca, Hammans, Simon, Ravenscroft, Gianina, Roxburgh, Richard H, Parolin Schnekenberg, Ricardo, Rugginini, Bianca, Abati, Elena, Manini, Arianna, Quartesan, Ilaria, Ghia, Arianna, Lòpez de Munaìn, Adolfo, Manganelli, Fiore, Kennerson, Marina, Santorelli, Filippo Maria, Infante, Jon, Marques, Wilson, Jokela, Manu, Murphy, Sinéad M, Mandich, Paola, Fabrizi, Gian Maria, Briani, Chiara, Gosal, David, Pareyson, Davide, Ferrari, Alberto, Prados, Ferran, Yousry, Tarek, Khurana, Vikram, Kuo, Sheng-Han, Miller, James, Troakes, Claire, Jaunmuktane, Zane, Giunti, Paola, Hartmann, Annette, Basak, Nazli, Synofzik, Matthis, Stojkovic, Tanya, Hadjivassiliou, Marios, Reilly, Mary M, Houlden, Henry, Cortese, Andrea
Published in Brain (London, England : 1878)

Safety and efficacy of oral levosimendan in people with amyotrophic lateral sclerosis (the REFALS study): a randomised, double-blind, placebo-controlled phase 3 trial

by Cudkowicz, Merit, Maragakis, Nicholas, Petri, Susanne, van den Berg, Leonard, Aho, Valtteri V, Sarapohja, Toni, Kuoppamäki, Mikko, Garratt, Chris, Al-Chalabi, Ammar, Kiernan, Matthew, Mathers, Susan, Henderson, Robert, Needham, Merrilee, Schultz, David, Löscher, Wolfgang, Mitrovic, Nenad, Rath, Jakob, Damme, Philip Van, De Bleecker, Jan L., Delstanche, Stéphanie, Johnston, Wendy, Zinman, Lorne, O'Connell, Colleen, Matte, Genevieve, Dionne, Annie, Korngut, Lawrence, Turnbull, John, Laaksovirta, Hannu, Jokela, Manu, Tapiola, Tero, Soriani, Marie-Hélène, Couratier, Philippe, Camu, William, Corcia, Philippe, Ludolph, Albert, Großkreutz, Julian, Meyer, Thomas, Boentert, Matthias, Prudlo, Johannes, Untucht, Robert, Hardiman, Orla, Siciliano, Gabriele, Chio', Adriano, Mazzini, Letizia, Inghilleri, Maurizio, Caponnetto, Claudia, Mora, Gabriele, Mora Pardina, Jesús S, Farrero Munoz, Eva, Vázquez Costa, Juan F, Aguera Morales, Eduardo, Varona, Luis, Andersen, Peter, Ingre, Caroline, Johansson, Rune, Radunovic, Aleksandar, Young, Carolyn, Babu, Suma, Shaibani, Aziz, Staff, Nathan, Vu, Tuan, Rivner, Michael, Scelsa, Stephen, Sivakumar, Kumaraswamy, Waheed, Waqar, Heitzman, Daragh, Rana, Sandeep, Pattee, Gary, Bayat, Elham, Kasarskis, Edward, Lange, Dale J, Elliott, Michael, Harris, Brent, Felice, Kevin, Pulley, Michael T, Kwan, Justin, Brown, Martin, Ravits, John, Burford, Matthew, Karam, Chafic, Miller, Timothy, Andrews, Jinsy, Levine, Todd, Locatelli, Eduardo, Wymer, James, Bedlack, Richard, Fee, Dominic, Goyal, Namita, Oskarsson, Bjorn, McCluskey, Leo, Caress, James, Weiss, Michael, Quick, Adam, Bromberg, Mark, Lacomis, David, Goutman, Stephen, Rezania, Kourosh, Guliani, Gaurav, Goslin, Kimberly, Katz, Jonathan S
Published in Lancet neurology