A comparison of a wrist worn portable device (watchpat)™ with in-lab polysomnography for the diagnosis of obstructive sleep apnea von Mittal, S., Suri, T.M., Hadda, V., Madan, K., Mohan, A., PB, S., Tiwari, P., Guleria, R.

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Neurocognitive impairment in patients with obstructive sleep apnea before and after therapy with continuous positive airway pressure von Suri, T.M., Sharma, S.K., Kumaran, S.S., Nehra, A., Nischal, N., Kalaivani, M.

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417: Combined Organ Transplantation for Familial Amyloidosis von McGregor, C.G.A, Edwards, B.S, Daly, R.C, Heimbach, J.K, Dearani, J.A, Sundt, T.M, Burkhart, H.M, Suri, R.M, Park, S.J, Kushwaha, S.S, Frantz, R.P, Clavell, A.L, Pereira, N, Rodeheffer, R.J

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The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders von Saffari, A, Lau, T, Tajsharghi, H, Karimiani, E.G, Kariminejad, A, Efthymiou, S, Zifarelli, G, Sultan, T, Toosi, M.B, Sedighzadeh, S, Siu, V.M, Ortigoza-Escobar, J.D, AlShamsi, A.M, Ibrahim, S, Al-Sannaa, N.A, Al-Hertani, W, Sandra, W, Tarnopolsky, M, Alavi, S, Li, C, Day-Salvatore, D.-L, Martínez-González, M.J, Levandoski, K.M, Bedoukian, E, Madan-Khetarpal, S, Idleburg, M.J, Menezes, M.J, Siddharth, A, Platzer, K, Oppermann, H, Smitka, M, Collins, F, Lek, M, Shahrooei, M, Ghavideldarestani, M, Herman, I, Rendu, J, Faure, J, Baker, J, Bhambhani, V, Calderwood, L, Akhondian, J, Imannezhad, S, Mirzadeh, H.S, Hashemi, N, Doosti, M, Safi, M, Ahangari, N, Torbati, P.N, Abedini, S, Salpietro, V, Gulec, E.Y, Eshaghian, S, Ghazavi, M, Pascher, M.T, Vogel, M, Abicht, A, Bruel, A.-L, Rieubland, C, Gallati, S, Strom, T.M, Lochmüller, H, Mohammadi, M.H, Alvi, J.R, Zackai, E.H, Keena, B.A, Skraban, C.M, Berger, S.I, Andrew, E.H, Rahimian, E, Morrow, M.M, Wentzensen, I.M, Millan, F, Henderson, L.B, Dafsari, H.S, Jungbluth, H, Gomez-Ospina, N, McRae, A, Peter, M, Veltra, D, Marinakis, N.M, Sofocleous, C, Ashrafzadeh, F, Pehlivan, D, Lemke, J.R, Melki, J, Benezit, A, Bauer, P, Weis, D, Lupski, J.R, Senderek, J, Christodoulou, J, Chung, W.K, Goodchild, R, Offiah, A.C, Moreno-De-Luca, A, Suri, M, Ebrahimi-Fakhari, D, Houlden, H, Maroofian, R

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SLC35A2-related congenital disorder of glycosylation: Defining the phenotype von Yates, T.M, Suri, M, Desurkar, A, Lesca, G, Wallgren-Pettersson, C, Hammer, T.B, Raghavan, A, Poulat, A.-L, Møller, R.S, Thuresson, A.-C, Balasubramanian, M

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Epstein-Barr virus infection in children entering a paediatric unit von Kessell, I., Pollock, T.M., Edwards, J.M.B., Woodroof, M., Dodoo, E., Melita, D.H., Suri, K., Eaton, B.R., Wood, M.M.

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