Search Results - "RITTEY, Christopher"

Vagus nerve stimulation for drug‐resistant epilepsy: A European long‐term study up to 24 months in 347 children by Orosz, Iren, McCormick, David, Zamponi, Nelia, Varadkar, Sophia, Feucht, Martha, Parain, Dominique, Griens, Roger, Vallée, Louis, Boon, Paul, Rittey, Christopher, Jayewardene, Amara K., Bunker, Mark, Arzimanoglou, Alexis, Lagae, Lieven

“…Summary Objective To gain insight into the long‐term impact of vagus nerve stimulation (with VNS Therapy) in children with drug‐resistant epilepsy, we…”
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Outcome of children with hyperventilation‐induced high‐amplitude rhythmic slow activity with altered awareness by BARKER, ALEXANDER, NG, JOANNE, RITTEY, CHRISTOPHER D C, KANDLER, ROSALIND H, MORDEKAR, SANTOSH R

“…Hyperventilation‐induced high‐amplitude rhythmic slow activity with altered awareness (HIHARS) is increasingly being identified in children and is thought to…”
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Neonatal hypertonia – a diagnostic challenge by Hart, Anthony R, Sharma, Ruchi, Rittey, Christopher D, Mordekar, Santosh R

“…In comparison to hypotonia, hypertonia is less commonly expressed in the neonatal period. The scientific literature on the causes of neonatal hypertonia is…”
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Movement disorders associated with complex regional pain syndrome in children by AGRAWAL, SHAKTI K, RITTEY, CHRISTOPHER D, HARROWER, NEIL A, GODDARD, JOHN M, MORDEKAR, SANTOSH R

“…The aim of the present study was to review the history, clinical course, treatment, and outcome of movement disorders in children and young people with complex…”
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Reversible Parainfectious Bilateral “Striatal Necrosis” by Nandish, Shalini, MBBS, Khan, Rafeh, MBBS, Connolly, Daniel J., MD, Rittey, Christopher D., MD, Mordekar, Santosh R., MD

“…Abstract Bilateral striatal necrosis is usually associated with either endogenous or exogenous toxins, and with poor neurodevelopmental outcomes. We describe…”
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The infant with seizures (excluding neonatal) by Rittey, Christopher D.C

“…Abstract Seizures in infancy are common. Although there are a number of clearly defined epilepsy syndromes which begin or occur in infancy many infants cannot…”
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Skull base osteomyelitis leading to lateral medullary syndrome in a child by Ng, Joanne, Connolly, Daniel J.A, Rittey, Christopher D, Mordekar, Santosh R

“…Abstract Skull base osteomyelitis (SBO) arising from the sphenoidal paranasal air sinus infection without associated external otitis is rare. Initially SBO may…”
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A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations by MUNOT, Pinki, SAUNDERS, Dawn E, JACQUES, Thomas S, COX, Timothy C, GANESAN, Vijeya, MILEWICZ, Dianna M, REGALADO, Ellen S, OSTERGAARD, John R, BRAUN, Kees P, KERR, Timothy, LICHTENBELT, Klaske D, PHILIP, Sunny, RITTEY, Christopher

“…Mutations in the ACTA2 gene lead to diffuse and diverse vascular diseases; the Arg179His mutation is associated with an early onset severe phenotype due to…”
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Juvenile neuronal ceroid-lipofuscinosis: developmental progress after supplementation with polyunsaturated fatty acids by Bennett, M J, Gayton, A R, Rittey, C D, Hosking, G P

“…Six patients with juvenile neuronal ceroid-lipofuscinosis (NCL) who were demonstrated to have abnormally low levels of membrane phospholipids were treated by…”
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Pediatric sciatic neuropathy presenting as painful leg: A case report and review of literature by Prasad, Manish, Babiker, Mohamed, Rao, Ganesh, Rittey, Christopher

“…Introduction: Mononeuropathies, in general, are very uncommon in childhood. Sciatic neuropathy (SN) is probably underappreciated in childhood and likely to…”
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Phenotypic Comparison of Two Scottish Families with Mutations in Different Genes Causing Autosomal Dominant Nocturnal Frontal Lobe Epilepsy by 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.

“…Purpose: Mutations in genes coding for the α4 and β2 subunits of the neuronal nicotinic acetylcholine receptor receptor (CHRN) are known to cause autosomal…”
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Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection by Bonthron, David T, Goizet, Cyril, Déry, Catherine, Woods, C Geoffrey, Ali, Manir, Weschke, Bernhard, Jackson, Andrew P, Voit, Thomas, King, Mary D, Baumann, Clarisse, Till, Marianne, Quarrell, Oliver W, Crow, Yanick J, Cau, Daniel, Lacombe, Didier, Lyall, Hermione, Lanzi, Giovanni, Stephenson, John B P, Griffith, Elen, Garner, Anna, Parmar, Rekha, Lebon, Pierre, McKeown, Carole, Rogers, R Curtis, Hayward, Bruce E, Babul-Hirji, Riyana, Bertini, Enrico, Martínez-Frías, María Luisa, Monier, Anne, Leitch, Andrea, Rittey, Christopher D, Semple, Colin, Aicardi, Jean, Chitayat, David, Tolmie, John L, Ponting, Chris P, Baxter, Peter, Tacke, Uta, Mathieu, Michèle, Sanchis, Amparo, Tomlin, Pam, Oade, Yvette, Klepper, Joerg, Fazzi, Elisa, Chandler, Kate E

“…Aicardi-Goutières syndrome (AGS) is an autosomal recessive neurological disorder, the clinical and immunological features of which parallel those of congenital…”
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Pediatric sciatic neuropathy presenting as painful leg: A case report and review of literature by Prasad, Manish, Babiker, Mohamed, Rao, Ganesh, Rittey, Christopher

“…INTRODUCTIONMononeuropathies, in general, are very uncommon in childhood. Sciatic neuropathy (SN) is probably underappreciated in childhood and likely to…”
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Outcome of children with hyperventilation-induced high-amplitude rhythmic slow activity with altered awareness by BARKER, ALEXANDER, NG, JOANNE, RITTEY, CHRISTOPHER D C, KANDLER, ROSALIND H, MORDEKAR, SANTOSH R

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Neonatal Seizures by Rittey, Christopher D C

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