Mutations in the gene encoding GlyT2 ( SLC6A5 ) define a presynaptic component of human startle disease von Harvey, Kirsten, Shiang, Rita, Rees, Mark I, Abbott, Kim J, Chung, Seo-Kyung, Graham, Gail E, Tijssen, Marina A J, Supplisson, Stéphane, Harvey, Robert J, Beatty, Sarah, Armstrong, Linlea, Duguid, Ian C, Smart, Trevor G, Pearce, Brian R, Owen, Michael J, Stephenson, John B P, Zuberi, Sameer M, van den Maagdenberg, Arn M J M, Thomas, Philip

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Paroxysmal non-epileptic motor events in childhood von STEPHENSON, JOHN BP

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When patients with epilepsy or "epilepsy" might need a pacemaker von Stephenson, John B.P.

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Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy von McLellan, Ailsa, Phillips, Hilary A., Rittey, Christopher, Kirkpatrick, Martin, Mulley, John C., Goudie, David, Stephenson, John B. P., Tolmie, John, Scheffer, Ingrid E., Berkovic, Samuel F., Zuberi, Sameer M.

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Bath-induced paroxysmal disorders in infancy von Nechay, Alla, Stephenson, John B.P

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Clinical Diagnosis of Syncopes (Including So-called Breath-Holding Spells) Without Electroencephalography or Ocular Compression von Stephenson, John B. P.

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Syncope and electroencephalography von Stephenson, John B P

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Aicardi–Goutières syndrome (AGS) von Stephenson, John B.P

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Childhood convulsive status epilepticus von Stephenson, John BP

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Stuart Green's Vignettes 15 and 16 von Deonna, Thierry, Stephenson, John B.P

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Stuart Green's vignettes 17 and 18 von Deonna, Thierry, Stephenson, John B.P

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Stuart Green's Vignettes 9 and 10 von Deonna, Thierry, Stephenson, John B.P

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Stuart Green's Vignettes 7 and 8 von Deonna, Thierry, Stephenson, John B.P

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Ocular compression a century on: time for a thumbs-off approach? von Stephenson, John B P

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Stuart Green's Vignettes 5 and 6 von Deonna, Thierry, Stephenson, John B.P

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Autonomic seizures in 18q- syndrome von Stephenson, John B.P.

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Stuart Green's Vignettes 3 and 4 von Deonna, Thierry, Stephenson, John B.P

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Compound heterozygosity and nonsense mutations in the α1-subunit of the inhibitory glycine receptor in hyperekplexia von REES, Mark I, LEWIS, Trevor M, SCHOFIELD, Peter R, OWEN, Michael J, VAFA, Behnaz, FERRIE, Colin, CORRY, Peter, MUNTONI, Fransesco, JUNGBLUTH, Heinz, STEPHENSON, John B. P, KERR, Mike, SNELL, Russell G

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In Memoriam: Professor Jean Aicardi (1926-2015) von Stephenson, John B.P

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Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus von Anderson, Beverley H, Kasher, Paul R, Mayer, Josephine, Szynkiewicz, Marcin, Jenkinson, Emma M, Bhaskar, Sanjeev S, Urquhart, Jill E, Daly, Sarah B, Dickerson, Jonathan E, O'Sullivan, James, Leibundgut, Elisabeth Oppliger, Muter, Joanne, Abdel-Salem, Ghada M H, Babul-Hirji, Riyana, Baxter, Peter, Berger, Andrea, Bonafé, Luisa, Brunstom-Hernandez, Janice E, Buckard, Johannes A, Chitayat, David, Chong, Wui K, Cordelli, Duccio M, Ferreira, Patrick, Fluss, Joel, Forrest, Ewan H, Franzoni, Emilio, Garone, Caterina, Hammans, Simon R, Houge, Gunnar, Hughes, Imelda, Jacquemont, Sebastien, Jeannet, Pierre-Yves, Jefferson, Rosalind J, Kumar, Ram, Kutschke, Georg, Lundberg, Staffan, Lourenço, Charles M, Mehta, Ramesh, Naidu, Sakkubai, Nischal, Ken K, Nunes, Luís, Õunap, Katrin, Philippart, Michel, Prabhakar, Prab, Risen, Sarah R, Schiffmann, Raphael, Soh, Calvin, Stephenson, John B P, Stewart, Helen, Stone, Jon, Tolmie, John L, van der Knaap, Marjo S, Vieira, Jose P, Vilain, Catheline N, Wakeling, Emma L, Wermenbol, Vanessa, Whitney, Andrea, Lovell, Simon C, Meyer, Stefan, Livingston, John H, Baerlocher, Gabriela M, Black, Graeme C M, Rice, Gillian I, Crow, Yanick J

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