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In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.
Published in:
2016
By:
- Tomlinson, Susan E.;
- Tan, S. Veronica;
- Burke, David;
- Labrum, Robyn W.;
- Haworth, Andrea;
- Gibbons, Vaneesha S.;
- Sweeney, Mary G.;
- Griggs, Robert C.;
- Kullmann, Dimitri M.;
- Bostock, Hugh;
- Hanna, Michael G.
Publication type:
journal article
Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.
Published in:
Brain: A Journal of Neurology, 2011, v. 134, n. 10, p. 2982, doi. 10.1093/brain/awr129
By:
- Catarino, Claudia B.;
- Liu, Joan Y.W.;
- Liagkouras, Ioannis;
- Gibbons, Vaneesha S.;
- Labrum, Robyn W.;
- Ellis, Rachael;
- Woodward, Cathy;
- Davis, Mary B.;
- Smith, Shelagh J.;
- Cross, J. Helen;
- Appleton, Richard E.;
- Yendle, Simone C.;
- McMahon, Jacinta M.;
- Bellows, Susannah T.;
- Jacques, Thomas S.;
- Zuberi, Sameer M.;
- Koepp, Matthias J.;
- Martinian, Lillian;
- Scheffer, Ingrid E.;
- Thom, Maria
Publication type:
Article
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
Published in:
Brain: A Journal of Neurology, 2005, v. 128, n. 12, p. 2786, doi. 10.1093/brain/awh667
By:
- Naheed L. Khan;
- Shushant Jain;
- John M. Lynch;
- Nicola Pavese;
- Patrick Abou-Sleiman;
- Janice L. Holton;
- Daniel G. Healy;
- William P. Gilks;
- Mary G. Sweeney;
- Milan Ganguly;
- Vaneesha Gibbons;
- Sonia Gandhi;
- Jenny Vaughan;
- Louise H. Eunson;
- Regina Katzenschlager;
- Juliet Gayton;
- Graham Lennox;
- Tamas Revesz;
- David Nicholl;
- Kailash P. Bhatia
Publication type:
Article
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
Published in:
2012
By:
- Kojovic M;
- Sheerin UM;
- Rubio-Agusti I;
- Saha A;
- Bras J;
- Gibbons V;
- Palmer R;
- Houlden H;
- Hardy J;
- Wood NW;
- Bhatia KP;
- Kojovic, Maja;
- Sheerin, Una-Marie;
- Rubio-Agusti, Ignacio;
- Saha, Anirban;
- Bras, Jose;
- Gibbons, Vaneesha;
- Palmer, Rodger;
- Houlden, Henry;
- Hardy, John
Publication type:
Case Study
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
Published in:
Movement Disorders, 2012, v. 27, n. 14, p. 1829, doi. 10.1002/mds.25199
By:
- Kojovic, Maja;
- Sheerin, Una-Marie;
- Rubio-Agusti, Ignacio;
- Saha, Anirban;
- Bras, Jose;
- Gibbons, Vaneesha;
- Palmer, Rodger;
- Houlden, Henry;
- Hardy, John;
- Wood, Nicholas W.;
- Bhatia, Kailash P.
Publication type:
Article

Found: 5

In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.

Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.

Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.

Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.