Two patients with chromosome 22q11.2 deletion presenting with childhood obesity and hyperphagia von Bassett, J.K, Chandler, K.E, Douzgou, S

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Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome von Balikova, I, Lehesjoki, A.E, de Ravel, T.J.L, Thienpont, B, Chandler, K.E, Clayton-Smith, J, Träskelin, A.L, Fryns, J.P, Vermeesch, J.R

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Regulation and role of REST and REST4 variants in modulation of gene expression in in vivo and in vitro in epilepsy models von Spencer, E.M., Chandler, K.E., Haddley, K., Howard, M.R., Hughes, D., Belyaev, N.D., Coulson, J.M., Stewart, J.P., Buckley, N.J., Kipar, A., Walker, M.C., Quinn, J.P.

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Seizure-Like Episodes in 3 Cats with Intermittent High-Grade Atrioventricular Dysfunction von Penning, V.A, Connolly, D.J, Gajanayake, I, McMahon, L.A, Luis Fuentes, V, Chandler, K.E, Volk, H.A

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Portosystemic shunt associated with severe episodic weakness von Wessmann, A, Volk, H.A, Shelton, G.D, Chandler, K.E, Baines, S, Cappello, R

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The efficacy and tolerability of levetiracetam in pharmacoresistant epileptic dogs von Volk, Holger A., Matiasek, Lara A., Luján Feliu-Pascual, Alejandro, Platt, Simon R., Chandler, Kate E.

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Diagnostic criteria, clinical characteristics, and natural history of Cohen syndrome von Chandler, K E, Kidd, A, Al-Gazali, L, Kolehmainen, J, Lehesjoki, A-E, Black, G C M, Clayton-Smith, J

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Deletions in the VPS13B (COH1) gene as a cause of Cohen syndrome von Balikova, Irina, Lehesjoki, A.-E, de Ravel, Thomy, Thienpont, Bernard, Chandler, K.E, Clayton-Smith, J, Träskelin, A.-L, Fryns, Jean-Pierre, Vermeesch, Joris

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The ophthalmic findings in Cohen syndrome von Chandler, K E, Biswas, S, Lloyd, I C, Parry, N, Clayton-Smith, J, Black, G C M

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De novo mutations in HNRNPU result in a neurodevelopmental syndrome von Yates, T.M, Vasudevan, P.C, Chandler, K.E, Donnelly, D.E, Stark, Z, Sadedin, S, Willoughby, J, Balasubramanian, M

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Book Review von Chandler, K.E.

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A. Jaggy (Ed.), Atlas and Textbook of Small Animal Neurology, first ed., Schlutersche Verlagsgesellschaft, Hannover, 2010, ISBN978-3-89993-026-9, 580 pp.; £166.00 (hard) von Chandler, K.E.

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Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum von Keppler-Noreuil, K.M, Sapp, J.C, Lindhurst, M.J, Parker, V.E, Blumhorst, C, Darling, T, Tosi, L.L, Huson, S.M, Whitehouse, R.W, Jakkula, E, Grant, I, Balasubramanian, M, Chandler, K.E, Fraser, J.L, Gucev, Z, Crow, Y.J, Brennan, L.M, Clark, R, Sellars, E.A, Pena, L.D, Krishnamurty, V, Shuen, A, Braverman, N, Cunningham, M.L, Sutton, V.R, Tasic, V, Graham, J.M, Geer, J, Henderson, A, Semple, R.K, Biesecker, L.G

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Seizure-Like Episodes in 3 Cats with Intermittent High-Grade Atrioventricular Dysfunction von Penning, V.A., Connolly, D.J., Gajanayake, I., McMahon, L.A., Luis Fuentes, V., Chandler, K.E., Volk, H.A.

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Does a Jewish type of Cohen syndrome truly exist? von Chandler, K.E., Clayton-Smith, Jill

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Plasticity of GABA(B) receptor-mediated heterosynaptic interactions at mossy fibers after status epilepticus von Chandler, K.E, Princivalle, A.P, Fabian-Fine, R, Bowery, N.G, Kullmann, D.M, Walker, M.C

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Portosystemic Shunt Associated with Severe Episodic Weakness von Wessmann, A., Volk, H.A., Shelton, G.D., Chandler, K.E., Baines, S., Cappello, R.

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Method and device for providing power, guiding analogue measuring and communication signal von K.E. TESDAR,D.T. KRUK,K.G. CHANDLER

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British Association of Dermatologists' guidelines for biologic interventions for psoriasis 2009 von Smith, C.H., Anstey, A.V., Barker, J.N.W.N., Burden, A.D., Chalmers, R.J.G., Chandler, D.A., Finlay, A.Y., Griffiths, C.E.M., Jackson, K., McHugh, N.J., McKenna, K.E., Reynolds, N.J., Ormerod, A.D.

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Distinguishing craniomorphometric characteristics and severity in metopic synostosis patients von Chandler, L., Park, K.E., Allam, O., Mozaffari, M.A., Khetpal, S., Smetona, J., Pourtaheri, N., Lu, X., Persing, J.A., Alperovich, M.

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