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Results 1-10 of 29 (Search time: 0.007 seconds).
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Issue Date
Title
Author(s)
2012
Paternal education status significantly influences infants’ measles vaccination uptake, independent of maternal education status
Rammohan, A.
;
Awofeso, N.
;
Fernandez, R.
2012
BRIDGE Study warrants critique
Allen, D.
;
Parry, P.
;
Purssey, R.
;
Spielmans, G.
;
Jureidini, J.
;
Rosenlicht, N.
;
Healy, D.
;
Feinberg, I.
2012
KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy
Weckhuysen, S.
;
Mandelstam, S.
;
Suls, A.
;
Audenaert, D.
;
Deconinck, T.
;
Claes, L.
;
Deprez, L.
;
Smets, K.
;
Hristova, D.
;
Yordanova, I.
;
Jordanova, A.
;
Ceulemans, B.
;
Jansen, A.
;
Hasaerts, D.
;
Roelens, F.
;
Lagae, L.
;
Yendle, S.
;
Stanley, T.
;
Heron, S.
;
Mulley, J.
;
et al.
2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
Huang, L.
;
Jolly, L.
;
Willis-Owen, S.
;
Gardner, A.
;
Sharma, R.
;
Douglas, E.
;
Shoubridge, C.
;
Wieczorek, D.
;
Tzschach, A.
;
Cohen, M.
;
Hackett, A.
;
Field, M.
;
Froyen, G.
;
Hu, H.
;
Haas, S.
;
Ropers, H.
;
Kalscheuer, V.
;
Corbett, M.
;
Gecz, J.
2012
A possible murine model for investigation of pathogenesis of Sudden Infant Death Syndrome
Bettelheim, K.
;
Luke, R.
;
Johnston, N.
;
Pearce, J.
;
Goldwater, P.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
2012
Broadening the phenotype associated with mutations in UPF3B: two further cases with renal dysplasia and variable developmental delay
Lynch, S.
;
Nguyen, L.
;
Ng, L.
;
Waldron, M.
;
McDonald, D.
;
Gecz, J.
2012
Methotrexate chemotherapy promotes osteoclast formation in the long bone of rats via increased pro-inflammatory cytokines and enhanced NF-κB activation
King, T.
;
Georgiou, K.
;
Cool, J.
;
Scherer, M.
;
Ang, E.
;
Foster, B.
;
Xu, J.
;
Xian, C.
2012
CCDC22: a novel candidate gene for syndromic X-linked intellectual disability
Voineagu, J.
;
Huang, L.
;
Winden, K.
;
Lazaro, M.
;
Haan, E.
;
Nelson, J.
;
McGaughran, J.
;
Nguyen, L.
;
Friend, K.
;
Hackett, A.
;
Field, M.
;
Gecz, J.
;
Geschwind, D.
2012
Neonatal gene therapy with a gamma retroviral vector in mucopolysaccharidosis VI cats
Ponder, K.
;
O'Malley, T.
;
Wang, P.
;
O'Donnell, P.
;
Traas, A.
;
Knox, V.
;
Aguirre, G.
;
Ellinwood, N.
;
Metcalf, J.
;
Wang, B.
;
Parkinson-Lawrence, E.
;
Sleeper, M.
;
Brooks, D.
;
Hopwood, J.
;
Haskins, M.
Discover
Author
5
Gecz, J.
3
Haan, E.
3
Jones, T.
3
Marshall, H.
3
Nissen, M.
3
Richmond, P.
2
Corbett, M.
2
Cowin, A.
2
et al.
2
Field, M.
.
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Subject
26
Humans
22
Female
9
Child
8
Mutation
7
Animals
7
Child, Preschool
6
Adult
5
Adolescent
5
Infant
4
Case-Control Studies
.
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