Browse by UCL Departments and Centres
Group by: Author | Type
Number of items: 7.
B
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
Carr, D;
(2013)
Evaluation of prenatal adenoviral vascular endothelial growth factor gene therapy in the growth-restricted sheep fetus and neonate.
Doctoral thesis (PhD), UCL (University College London).
|
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.
|
M
Maghsoudlou, P;
Georgiades, F;
Tyraskis, A;
Totonelli, G;
Loukogeorgakis, SP;
Orlando, G;
Shangaris, P;
... Coppi, PD; + view all
(2013)
Preservation of micro-architecture and angiogenic potential in a pulmonary acellular matrix obtained using intermittent intra-tracheal flow of detergent enzymatic treatment.
Biomaterials
, 34
(28)
pp. 6638-6648.
10.1016/j.biomaterials.2013.05.015.
|
Minassian, C;
Thomas, SL;
Campbell, O;
Smeeth, L;
Williams, DJ;
(2013)
Acute Maternal Infection and Risk of Pre-Eclampsia: A Population-Based Case-Control Study.
PLoS ONE
, 8
(9)
10.1371/journal.pone.0073047.
|
O
Osellame, LD;
Rahim, AA;
Hargreaves, IP;
Gegg, ME;
Richard-Londt, A;
Brandner, S;
Waddington, SN;
... Duchen, MR; + view all
(2013)
Mitochondria and quality control defects in a mouse model of Gaucher Disease-links to Parkinson's Disease.
Cell Metabolism
, 17
(6)
pp. 941-953.
10.1016/j.cmet.2013.04.014.
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S
Shaw, SS;
(2013)
The potential of amniotic fluid stem cells in prenatal gene and cell therapy.
Doctoral thesis (PhD), UCL (University College London).
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