Browse by UCL Departments and Centres
![[up]](/style/images/multi_up.png)
Up a levelGroup by: Author | Type
Number of items: 38.
A
Assaf, Yaniv;
Alexander, Daniel C;
Jones, Derek K;
Bizzi, Albero;
Behrens, Tim EJ;
Clark, Chris A;
Cohen, Yoram;
... CONNECT consortium; + view all
(2013)
The CONNECT project: Combining macro- and micro-structure.
NeuroImage
, 80
pp. 273-282.
10.1016/j.neuroimage.2013.05.055.
|
 |
B
|
Behr, ER;
Ritchie, MD;
Tanaka, T;
Kääb, S;
Crawford, DC;
Nicoletti, P;
Floratos, A;
... Roden, DM; + view all
(2013)
Genome Wide Analysis of Drug-Induced Torsades de Pointes: Lack of Common Variants with Large Effect Sizes.
PLoS One
, 8
(11)
, Article e78511. 10.1371/journal.pone.0078511.
|
 |
|
Bluebond-Langner, MH;
Beecham, E;
Howard, R;
McCulloch, R;
Candy, B;
Laddie, J;
Rees, H;
... Jones, L; + view all
(2013)
Pharmacological interventions for pain for life-limiting conditions in children and adolescents.
Cochrane Database of Systematic Reviews
, 9
10.1002/14651858.CD010750.
|
|
|
Boldrin, L;
Morgan, JE;
(2013)
Grafting of a single donor myofibre promotes hypertrophy in dystrophic mouse muscle.
PLoS One
, 8
(1)
, Article e54599. 10.1371/journal.pone.0054599.
|
|
|
Botcharova, M;
Farmer, SF;
Berthouze, L;
(2013)
A maximum likelihood based technique for validating detrended fluctuation analysis (ML-DFA).
arXiv.org: Ithaca (NY), USA.
|
|
Briggs, D;
Morgan, JE;
(2013)
Recent progress in satellite cell/myoblast engraftment – relevance for therapy.
FEBS Journal
, 280
(17)
pp. 4281-4293.
10.1111/febs.12273.
|
|
|
Burke, G;
Hiscock, A;
Klein, A;
Niks, EH;
Main, M;
Manzur, AY;
Ng, J;
... Robb, S; + view all
(2013)
Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations.
Neuromuscular Disorders
, 23
(2)
170 - 175.
10.1016/j.nmd.2012.11.004.
|
|
C
|
Caicedo, A;
Papademetriou, MD;
Elwell, CE;
Hoskote, A;
Elliott, MJ;
Van Huffel, S;
Tachtsidis, I;
(2013)
Canonical correlation analysis in the study of cerebral and peripheral haemodynamics interrelations with systemic variables in neonates supported on ECMO.
Adv Exp Med Biol
, 765
23 - 29.
10.1007/978-1-4614-4989-8_4.
|
|
|
Cirak, S;
Foley, AR;
Herrmann, R;
Willer, T;
Yau, S;
Stevens, E;
Torelli, S;
... Muntoni, F; + view all
(2013)
ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.
Brain
, 136
(1)
269 -281.
10.1093/brain/aws312.
|
|
|
Clayden, JD;
Dayan, M;
Clark, CA;
(2013)
Principal networks.
PLoS One
, 8
(4)
, Article e60997. 10.1371/journal.pone.0060997.
|
|
|
Cross, JH;
Arora, R;
Heckemann, RA;
Gunny, R;
Chong, K;
Carr, L;
Baldeweg, T;
... Bockenhauer, D; + view all
(2013)
Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome.
Dev Med Child Neurol
, 55
(9)
846 - 856.
10.1111/dmcn.12171.
|
|
D
|
Dyrby, Tim B;
Søgaard, Lise V;
Hall, Matt G;
Ptito, Maurice;
Alexander, Daniel C;
(2013)
Contrast and stability of the axon diameter index from microstructure imaging with diffusion MRI.
Magnetic Resonance in Medicine
, 70
(3)
711 - 721.
10.1002/mrm.24501.
|
F
|
Foley, AR;
Menezes, MP;
Pandraud, A;
Gonzalez, MA;
Al-Odaib, A;
Abrams, AJ;
Sugano, K;
... Houlden, H; + view all
(2013)
Treatable childhood neuronopathy caused by mutations in riboflavin transporter RFVT2.
Brain
, 137
(1)
, Article awt315. 10.1093/brain/awt315.
|
 |
|
Fosi, T;
Lax-Pericall, MT;
Scott, RC;
Neville, BG;
Aylett, SE;
(2013)
Methylphenidate treatment of attention deficit hyperactivity disorder in young people with learning disability and difficult-to-treat epilepsy: Evidence of clinical benefit.
Epilepsia
, 54
(12)
pp. 2071-2081.
10.1111/epi.12399.
|
|
G
|
Garralda, ME;
McConachie, H;
Le Couteur, A;
Sriranjan, S;
Chakrabarti, I;
Cirak, S;
Guglieri, M;
... Muntoni, F; + view all
(2013)
Emotional impact of genetic trials in progressive paediatric disorders: a dose-ranging exon-skipping trial in Duchenne muscular dystrophy.
Child Care Health Dev
, 39
(3)
449 - 455.
10.1111/j.1365-2214.2012.01387.x.
|
|
|
Gavlak, JC;
Stocks, J;
Laverty, A;
Fettes, E;
Bucks, R;
Sonnappa, S;
Cooper, J;
... Kirkham, FJ; + view all
(2013)
The Young Everest Study: preliminary report of changes in sleep and cerebral blood flow velocity during slow ascent to altitude in unacclimatised children.
Archives of Disease in Childhood
, 98
(5)
356 -362.
10.1136/archdischild-2012-302512.
|
|
|
Gibbard, CR;
Seunarine, KK;
Clayden, JD;
Clark, CA;
Ren, J;
Skuse, DH;
(2013)
White matter microstructure correlates with autism trait severity in a combined clinical-control sample of high-functioning adults.
NeuroImage: Clinical
, 3
106 - 114.
10.1016/j.nicl.2013.07.007.
|
|
|
Grant, LR;
O'Brien, SE;
Burbidge, P;
Haston, M;
Zancolli, M;
Cowell, L;
Johnson, M;
... Goldblatt, D; + view all
(2013)
Comparative immunogenicity of 7 and 13-valent pneumococcal conjugate vaccines and the development of functional antibodies to cross-reactive serotypes.
PLoS One
, 8
(9)
, Article e74906. 10.1371/journal.pone.0074906.
|
|
|
Grech-Sollars, M;
Saunders, DE;
Phipps, KP;
Kaur, R;
Paine, SM;
Jacques, TS;
Clayden, JD;
(2013)
Challenges for the functional diffusion map in pediatric brain tumors.
Neuro Oncol
, 16
(3)
pp. 449-456.
10.1093/neuonc/not197.
|
|
H
|
Hamurtekin, E;
Fitzsimmons, BL;
Shubayev, VI;
Grafe, MR;
Deumens, R;
Yaksh, TL;
Walker, SM;
(2013)
Evaluation of Spinal Toxicity and Long-term Spinal Reflex Function after Intrathecal Levobupivaciane in the Neonatal Rat.
Anesthesiology
, 119
(1)
142 - 155.
10.1097/ALN.0b013e31828fc7e7.
|
|
Hogan, AM;
Telfer, PT;
Kirkham, FJ;
de Haan, M;
(2013)
Precursors of executive function in infants with sickle cell anemia.
Journal of Child Neurology
, 28
(10)
1197 -1202.
10.1177/0883073812453495.
|
|
L
|
Liégeois, F;
Tournier, JD;
Pigdon, L;
Connelly, A;
Morgan, AT;
(2013)
Corticobulbar tract changes as predictors of dysarthria in childhood brain injury.
Neurology
, 80
(10)
926 - 932.
10.1212/WNL.0b013e3182840c6d.
|
|
|
Liégeois, FJ;
Mahony, K;
Connelly, A;
Tournier, J-D;
Pigdon, L;
Morgan, AT;
(2013)
Pediatric traumatic brain injury: Language outcomes and their relationship to the arcuate fasciculus.
Brain and Language
, 127
(3)
388 - 398.
10.1016/j.bandl.2013.05.003.
|
|
M
|
Martinos, MM;
Yoong, M;
Patil, S;
Chong, WK;
Mardari, R;
Chin, RF;
Neville, BG;
... Scott, RC; + view all
(2013)
Early developmental outcomes in children following convulsive status epilepticus: a longitudinal study.
Epilepsia
, 54
(6)
1012 - 1019.
10.1111/epi.12136.
|
|
McCormack, P;
Woods, S;
Aartsma-Rus, A;
Hagger, L;
Herczegfalvi, A;
Heslop, E;
Irwin, J;
... Ferlini, A; + view all
(2013)
Guidance in social and ethical issues related to clinical, diagnostic care and novel therapies for hereditary neuromuscular rare diseases: "translating" the translational.
PLoS Curr
, 5
10.1371/currents.md.f90b49429fa814bd26c5b22b13d773ec.
|
|
|
Mitrpant, C;
Porensky, P;
Zhou, H;
Price, L;
Muntoni, F;
Fletcher, S;
Wilton, SD;
(2013)
Improved Antisense Oligonucleotide Design to Suppress Aberrant SMN2 Gene Transcript Processing: Towards a Treatment for Spinal Muscular Atrophy.
PLoS One
, 8
(4)
, Article e62114. 10.1371/journal.pone.0062114.
|
|
O
|
O'Keeffe, F;
Liégeois, F;
Eve, M;
Ganesan, V;
King, J;
Murphy, T;
(2013)
Neuropsychological and neurobehavioral outcome following childhood arterial ischemic stroke: Attention deficits, emotional dysregulation, and executive dysfunction.
Child Neuropsychol
10.1080/09297049.2013.832740.
|
|
P
|
Pahs, G;
Rankin, P;
Helen Cross, J;
Croft, L;
Northam, GB;
Liegeois, F;
Greenway, S;
... Baldeweg, T; + view all
(2013)
Asymmetry of planum temporale constrains interhemispheric language plasticity in children with focal epilepsy.
Brain
, 136
(10)
pp. 3163-3175.
10.1093/brain/awt225.
|
|
|
Papademetriou, M;
Tachtsidis, I;
Elliott, MJ;
Hoskote, A;
Elwell, CE;
(2013)
Wavelet cross-correlation to investigate regional variations in cerebral oxygenation in infants supported on extracorporeal membrane oxygenation.
Adv Exp Med Biol
, 765
203 - 209.
10.1007/978-1-4614-4989-8_28.
|
|
|
Pressler, Ronit;
Auvin, Stéphane;
(2013)
Comparison of brain maturation among species: an example in translational research suggesting the possible use of bumetanide in newborn.
Frontiers in Neurology
, 4
, Article 36. 10.3389/fneur.2013.00036.
|
|
R
|
Robinson, A;
Partridge, D;
Malhas, A;
De Castro, SC;
Gustavsson, P;
Thompson, DN;
Vaux, DJ;
... Greene, ND; + view all
(2013)
Is LMNB1 a susceptibility gene for neural tube defects in humans?
Birth Defects Research Part A: Clinical and Molecular Teratology
, 97
(6)
pp. 398-402.
10.1002/bdra.23141.
|
|
S
|
Stevens, E;
Torelli, S;
Feng, L;
Phadke, R;
Walter, MC;
Schneiderat, P;
Eddaoudi, A;
... Muntoni, F; + view all
(2013)
Flow cytometry for the analysis of α-dystroglycan glycosylation in fibroblasts from patients with dystroglycanopathies.
PLoS One
, 8
(7)
, Article e68958. 10.1371/journal.pone.0068958.
|
|
W
|
Webb, EA;
O'Reilly, MA;
Clayden, JD;
Seunarine, KK;
Dale, N;
Salt, A;
Clark, CA;
(2013)
Reduced ventral cingulum integrity and increased behavioral problems in children with isolated optic nerve hypoplasia and mild to moderate or no visual impairment.
PLoS One
, 8
(3)
, Article e59048. 10.1371/journal.pone.0059048.
|
|
|
Wong, I;
St John-Green, C;
Walker, SM;
(2013)
Opioid-sparing effects of perioperative paracetamol and nonsteroidal anti-inflammatory drugs (NSAIDs) in children.
Paediatr Anaesth
, 23
(6)
475 - 495.
10.1111/pan.12163.
|
|
Y
|
Yoong, M;
Martinos, MM;
Chin, RF;
Clark, CA;
Scott, RC;
(2013)
Hippocampal volume loss following childhood convulsive status epilepticus is not limited to prolonged febrile seizures.
Epilepsia
, 54
(12)
2108 - 2115.
10.1111/epi.12426.
|
|
Yoong, M;
Seunarine, K;
Martinos, M;
Chin, RF;
Clark, CA;
Scott, RC;
(2013)
Prolonged febrile seizures cause reversible reductions in white matter integrity.
Neuroimage Clin
, 3
515 - 521.
10.1016/j.nicl.2013.10.010.
|
|
Z
|
Zaharieva, IT;
Calissano, M;
Scoto, M;
Preston, M;
Cirak, S;
Feng, L;
Collins, J;
... Muntoni, F; + view all
(2013)
Dystromirs as serum biomarkers for monitoring the disease severity in duchenne muscular dystrophy.
PLoS One
, 8
(11)
, Article e80263. 10.1371/journal.pone.0080263.
|
|
|
Zhou, H;
Rokach, O;
Feng, L;
Munteanu, I;
Mamchaoui, K;
Wilmshurst, JM;
Sewry, C;
... Muntoni, F; + view all
(2013)
RyR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling.
Human Mutation
, 34
(7)
pp. 986-996.
10.1002/humu.22326.
|
|
