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Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes
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Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes

Reid, Emma S ; Papandreou, Apostolos ; Drury, Suzanne ; Boustred, Christopher ; Yue, Wyatt W ; Wedatilake, Yehani ; Beesley, Clare ; Jacques, Thomas S ; Anderson, Glenn ; Abulhoul, Lara ; Broomfield, Alex ; Cleary, Maureen ; Grunewald, Stephanie ; Varadkar, Sophia M ; Lench, Nick ; Rahman, Shamima ; Gissen, Paul ; Clayton, Peter T ; Mills, Philippa B

Brain (London, England : 1878), 2016-11, Vol.139 (11), p.2844-2854 [Periódico revisado por pares]

England: Oxford University Press

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2
The importance of early immunotherapy in patients with faciobrachial dystonic seizures
The importance of early immunotherapy in patients with faciobrachial dystonic seizures
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The importance of early immunotherapy in patients with faciobrachial dystonic seizures

Thompson, Julia ; Bi, Mian ; Murchison, Andrew G ; Makuch, Mateusz ; Bien, Christian G ; Chu, Kon ; Farooque, Pue ; Gelfand, Jeffrey M ; Geschwind, Michael D ; Hirsch, Lawrence J ; Somerville, Ernest ; Lang, Bethan ; Vincent, Angela ; Leite, Maria I ; Waters, Patrick ; Irani, Sarosh R

Brain (London, England : 1878), 2018-02, Vol.141 (2), p.348-356 [Periódico revisado por pares]

England: Oxford University Press

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3
Expected value and prediction error abnormalities in depression and schizophrenia
Expected value and prediction error abnormalities in depression and schizophrenia
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Expected value and prediction error abnormalities in depression and schizophrenia

GRADIN, Victoria B ; KUMAR, Poornima ; WAITER, Gordon ; AHEARN, Trevor ; STICKLE, Catriona ; MILDERS, Marteen ; REID, Ian ; HALL, Jeremy ; STEELE, J. Douglas

Brain (London, England : 1878), 2011-06, Vol.134 (Pt 6), p.1751-1764 [Periódico revisado por pares]

Oxford: Oxford University Press

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4
Abnormal temporal difference reward-learning signals in major depression
Abnormal temporal difference reward-learning signals in major depression
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Abnormal temporal difference reward-learning signals in major depression

Kumar, P. ; Waiter, G. ; Ahearn, T. ; Milders, M. ; Reid, I. ; Steele, J. D.

Brain (London, England : 1878), 2008-08, Vol.131 (8), p.2084-2093 [Periódico revisado por pares]

Oxford: Oxford University Press

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5
Epilepsy syndromes in cerebral palsy: varied, evolving and mostly self-limited
Epilepsy syndromes in cerebral palsy: varied, evolving and mostly self-limited
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Epilepsy syndromes in cerebral palsy: varied, evolving and mostly self-limited

Cooper, Monica S ; Mackay, Mark T ; Dagia, Charuta ; Fahey, Michael C ; Howell, Katherine B ; Reddihough, Dinah ; Reid, Susan ; Harvey, A Simon

Brain (London, England : 1878), 2023-02, Vol.146 (2), p.587-599 [Periódico revisado por pares]

England

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6
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease
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The expression of DJ‐1 (PARK7) in normal human CNS and idiopathic Parkinson’s disease

Bandopadhyay, Rina ; Kingsbury, Ann E. ; Cookson, Mark R. ; Reid, Andrew R. ; Evans, Ian M. ; Hope, Andrew D. ; Pittman, Alan M. ; Lashley, Tammaryn ; Canet‐Aviles, Rosa ; Miller, David W. ; McLendon, Chris ; Strand, Catherine ; Leonard, Andrew J. ; Abou‐Sleiman, Patrick M. ; Healy, Daniel G. ; Ariga, Hiroyashi ; Wood, Nicholas W. ; de Silva, Rohan ; Revesz, Tamas ; Hardy, John A. ; Lees, Andrew J.

Brain (London, England : 1878), 2004-02, Vol.127 (2), p.420-430 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scnlb-based model of Dravet syndrome
Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scnlb-based model of Dravet syndrome
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Reduced dendritic arborization and hyperexcitability of pyramidal neurons in a Scnlb-based model of Dravet syndrome

REID, Christopher A ; LEAW, Bryan ; PETROU, Steven ; RICHARDS, Kay L ; RICHARDSON, Robert ; WIMMER, Verena ; YU, Christiaan ; HILL-YARDIN, Elisa L ; LERCHE, Holger ; SCHEFFER, Ingrid E ; BERKOVIC, Samuel F

Brain (London, England : 1878), 2014, Vol.137, p.1701-1715 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia: A clinical and molecular genetic study of 28 United Kingdom families
Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia: A clinical and molecular genetic study of 28 United Kingdom families
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Locus-phenotype correlations in autosomal dominant pure hereditary spastic paraplegia: A clinical and molecular genetic study of 28 United Kingdom families

REID, E ; GRAYSON, C ; ROGERS, M. T ; RUBINSZTEIN, D. C

Brain (London, England : 1878), 1999-09, Vol.122 (9), p.1741-1755 [Periódico revisado por pares]

Oxford: Oxford University Press

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9
Locusphenotype correlations in autosomal dominant pure hereditary spastic paraplegia: A clinical and molecular genetic study of 28 United Kingdom families
Locusphenotype correlations in autosomal dominant pure hereditary spastic paraplegia: A clinical and molecular genetic study of 28 United Kingdom families
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Locusphenotype correlations in autosomal dominant pure hereditary spastic paraplegia: A clinical and molecular genetic study of 28 United Kingdom families

Reid, E.

Brain (London, England : 1878), 1999-09, Vol.122 (9), p.1741-1755 [Periódico revisado por pares]

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10
Locus–phenotype correlations in autosomal dominant pure hereditary spastic paraplegia
Locus–phenotype correlations in autosomal dominant pure hereditary spastic paraplegia
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Locus–phenotype correlations in autosomal dominant pure hereditary spastic paraplegia

Reid, E. ; Grayson, C. ; Rogers, M. T. ; Rubinsztein, D. C.

Brain (London, England : 1878), 1999-09, Vol.122 (9), p.1741-1755 [Periódico revisado por pares]

Oxford University Press

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