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Genotype‐phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery

Benova, Barbora; Jacques, Thomas S.

Brain pathology. Volume 29:Issue 4 (2019); pp 473-484 -- Wiley-Blackwell

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Genotype‐phenotype correlations in focal malformations of cortical development: a pathway to integrated pathological diagnosis in epilepsy surgery

Benova, Barbora; Jacques, Thomas S.

Brain pathology. Volume 29:Number 4 (2019); pp 473-484 -- Wiley-Blackwell

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Review: Neuropathological features of unexplained sudden unexpected death in infancy: current evidence and controversies

Paine, Simon ML; Jacques, Thomas S; Sebire, Neil J

Neuropathology & applied neurobiology. Volume 40:Issue 4 (2014); pp 364-384 -- Wiley

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A quantitative study of white matter hypomyelination and oligodendroglial maturation in focal cortical dysplasia type II

Shepherd, Caterina et al.

Epilepsia: the journal of the International League Against Epilepsy. Volume 54:Issue 5 (2013, May); pp 898-908 -- Wiley-VCH

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Characterization of a population of neural progenitor cells in the infant hippocampus

Paine, Simon M. L. et al.

Neuropathology & applied neurobiology. Volume 40:Issue 5 (2014); pp 544-550 -- Wiley

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RADI-10. RADIOGENOMIC CORRELATION OF THE NEWLY PROPOSED MOLECULAR CHARACTERISATION OF GLIONEURONAL TUMOURS OF THE BRAIN

Mankad, Kshitij

Neuro-oncology volume 20 issue S2 page i171 -- Oxford University Press

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Diffusion-weighted post-mortem magnetic resonance imaging of the human fetal brain in situ

Papadopoulou, Ioanna et al.

European journal of radiology. Volume 85:Issue 6 (2016); pp 1167-1173 -- Elsevier Science Pub. Co

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Diffusion-weighted post-mortem magnetic resonance imaging of the human fetal brain in situ

Papadopoulou, Ioanna et al.

European journal of radiology. Volume 85:Issue 6 (2016); pp 1167-1173 -- Elsevier Science Pub. Co

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Childhood neoplasms presenting at autopsy: A 20‐year experience

Bryant, Victoria A. et al.

Pediatric blood & cancer. Volume 64:Issue 9 (2017); pp n/a-n/a -- John Wiley

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Janus kinase 1/2 inhibition for the treatment of autoinflammation associated with heterozygous TNFAIP3 mutation

Mulhern, Ciara M. et al.

The journal of allergy and clinical immunology. Volume 144:Issue 3 (2019); pp 863-866.e5 -- Elsevier

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  1. Jacques, Thomas S.
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