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Issue Date
Title
Author(s)
2008
Pain characteristics and their association with quality of life and self-concept in children with hemiplegic cerebral palsy identified from a population register
Russo, R.
;
Miller, M.
;
Haan, E.
;
Cameron, I.
;
Crotty, M.
2008
Epilepsy and mental retardation limited to females: an under-recognized disorder
Scheffer, I.
;
Turner, S.
;
Dibbens, L.
;
Bayly, M.
;
Friend, K.
;
Hodgson, B.
;
Burrows, L.
;
Shaw, M.
;
Wei, C.
;
Ullmann, R.
;
Ropers, H.
;
Szepetowski, P.
;
Haan, E.
;
Mazarib, A.
;
Afawi, Z.
;
Neufeld, M.
;
Andrews, P.
;
Wallace, G.
;
Kivity, S.
;
Lev, D.
;
et al.
2011
A new syndrome with craniosynostosis and cleft lip and palate
Anderson, P.
;
Haan, E.
;
David, D.
1997
Renal cystic disease in tuberous sclerosis: role of the polycystic kidney disease 1 gene
Sampson, J.
;
Maheshwar, M.
;
Aspinwall, R.
;
Thompson, P.
;
Cheadle, J.
;
Ravine, D.
;
Roy, S.
;
Haan, E.
;
Bernstein, J.
;
Harris, P.
1995
Localization of craniosynostosis Adelaide type to 4p16
Hollway, G.
;
Phillips, H.
;
Ades, L.
;
Haan, E.
;
Muley, J.
2009
Sporadic in utero generalized edema caused by mutations in the lymphangiogenic genes VEGFR3 and FOXC2
Ghalamkarpour, A.
;
Debauche, C.
;
Haan, E.
;
Van Regemorter, N.
;
Snzajer, Y.
;
Thomas, D.
;
Revencu, N.
;
Gillerot, Y.
;
Boon, L.
;
Vikkula, M.
2008
Self-Esteem, Self-Concept, and Quality of Life in Children with Hemiplegic Cerebral Palsy
Russo, R.
;
Goodwin, E.
;
Miller, M.
;
Haan, E.
;
Connell, T.
;
Crotty, M.
2010
CP or not CP? A review of diagnoses in a cerebral palsy register
Zarrinkalam, R.
;
Russo, R.
;
Gibson, C.
;
van Essen, P.
;
Peek, A.
;
Haan, E.
2012
New mutations and sporadic intellectual disability
Gecz, J.
;
Haan, E.
1995
A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
Laing, N.
;
Wilton, S.
;
Akkari, P.
;
Dorosz, S.
;
Boundy, K.
;
Kneebone, C.
;
Blumbergs, P.
;
White, S.
;
Watkins, H.
;
Love, D.
;
Haan, E.
Discover
Author
13
Gecz, J.
12
Thompson, E.
9
Ades, L.
9
Chan, A.
9
et al.
6
Sutherland, G.
6
Suthers, G.
5
Butow, P.
5
Eyre, H.
5
Friend, K.
.
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Subject
64
Humans
50
Female
41
Male
25
Adult
18
Child
15
Pedigree
15
Syndrome
13
Abnormalities, Multiple
13
Child, Preschool
13
Mutation
.
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Date issued
24
2010 - 2016
35
2000 - 2009
32
1995 - 1999