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Results: 1-25/26
Authors:
Leonard, H
Fyfe, S
Leonard, S
Msall, M
Citation: H. Leonard et al., Functional status, medical impairments, and rehabilitation resources in 84females with Rett syndrome: a snapshot across the world from the parental perspective, DISABIL REH, 23(3-4), 2001, pp. 107-117
Authors:
Leonard, H
Fyfe, S
Leonard, S
Msall, M
Citation: H. Leonard et al., Functional status, medical impairments, and rehabilitation resources in 84females with Rett syndrome: a snapshot across the world from the parental perspective (vol 23, pg 107, 2001), DISABIL REH, 23(15), 2001, pp. 690-690
Authors:
Ellaway, CJ
Badawi, N
Raffaele, L
Christodoulou, J
Leonard, H
Citation: Cj. Ellaway et al., A case of multiple congenital anomalies in association with Rett syndrome confirmed by MECP2 mutation screening, CLIN DYSMOR, 10(3), 2001, pp. 185-188
Authors:
Leonard, H
Silberstein, J
Falk, R
Houwink-Manville, I
Ellaway, C
Raffaele, LS
Engerstrom, IW
Schanen, C
Citation: H. Leonard et al., Occurrence of Rett syndrome in boys, J CHILD NEU, 16(5), 2001, pp. 333-338
Authors:
Kerr, AM
Nomura, Y
Armstrong, D
Anvret, M
Belichenko, PV
Budden, S
Cass, H
Christodoulou, J
Clarke, A
Ellaway, C
d'Esposito, M
Francke, U
Hulten, M
Julu, P
Leonard, H
Naidu, S
Schanen, C
Webb, T
Engerstrom, IW
Yamashita, Y
Segawa, M
Citation: Am. Kerr et al., Guidelines for reporting clinical features in cases with MECP2 mutations, BRAIN DEVEL, 23(4), 2001, pp. 208-211
Authors:
Fyfe, S
Leonard, H
Gelmi, R
Tassell, A
Strack, R
Citation: S. Fyfe et al., Using the Internet to pilot a questionnaire on childhood disability in Rett syndrome, CHILD CAR H, 27(6), 2001, pp. 535-543
Authors:
Leonard, H
Barrett, AM
Scott, JES
Wren, C
Citation: H. Leonard et al., The influence of congenital heart disease on survival of infants with oesophageal atresia, ARCH DIS CH, 85(3), 2001, pp. F204-F206
Authors:
Leonard, H
Forsyth, R
Citation: H. Leonard et R. Forsyth, Friedreich's ataxia presenting after cardiac transplantation, ARCH DIS CH, 84(2), 2001, pp. 167-168
Authors:
Leonard, H
Derrick, G
O'Sullivan, J
Wren, C
Citation: H. Leonard et al., Natural and unnatural history of pulmonary atresia, HEART, 84(5), 2000, pp. 499-503
Authors:
Qiu, L
Burgess, A
Fairlie, DP
Leonard, H
Parsons, PG
Gabrielli, BG
Citation: L. Qiu et al., Histone deacetylase inhibitors trigger a G2 checkpoint in normal cells that is defective in tumor cells, MOL BIOL CE, 11(6), 2000, pp. 2069
Authors:
Leonard, H
Fyfe, S
Dye, D
Hockey, A
Christodoulou, J
Citation: H. Leonard et al., Family data in Rett syndrome: Association with other genetic disorders, J PAEDIAT C, 36(4), 2000, pp. 336-339
Authors:
Bower, C
Leonard, H
Petterson, B
Citation: C. Bower et al., Intellectual disability in Western Australia, J PAEDIAT C, 36(3), 2000, pp. 213-215
Authors:
Cheadle, JP
Gill, H
Fleming, N
Maynard, J
Kerr, A
Leonard, H
Krawczak, M
Cooper, DN
Lynch, S
Thomas, N
Hughes, H
Hulten, M
Ravine, D
Sampson, JR
Clarke, A
Citation: Jp. Cheadle et al., Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location, HUM MOL GEN, 9(7), 2000, pp. 1119-1129
Authors:
Cheadle, JP
Gill, H
Fleming, N
Maynard, J
Kerr, A
Leonard, H
Krawczak, M
Cooper, DN
Lynch, S
Thomas, N
Hughes, H
Hulten, M
Ravine, D
Sampson, JR
Clarke, A
Citation: Jp. Cheadle et al., Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location (vol 9, pg 1119, 2000), HUM MOL GEN, 9(11), 2000, pp. 1717-1717
Authors:
Leonard, H
Eastham, K
Dark, J
Citation: H. Leonard et al., Heart and heart-lung transplantation in Down's syndrome, BR MED J, 320(7238), 2000, pp. 816-817
Authors:
Leonard, S
Bower, C
Petterson, B
Leonard, H
Citation: S. Leonard et al., Survival of infants born with Down's syndrome: 1980-96, PAED PERIN, 14(2), 2000, pp. 163-171
Authors:
Leonard, H
Fyfe, S
Dye, D
Leonard, S
Citation: H. Leonard et al., Using genetic epidemiology to study Rett syndrome: the design of a case-control study, PAED PERIN, 14(1), 2000, pp. 85-95
Authors:
Fyfe, S
Leonard, H
Dye, D
Leonard, S
Citation: S. Fyfe et al., Patterns of pregnancy loss, perinatal mortality, and postneonatal childhood deaths in families of girls with Rett syndrome, J CHILD NEU, 14(7), 1999, pp. 440-445
Authors:
Ellaway, C
Williams, K
Leonard, H
Higgins, G
Wilcken, B
Christodoulou, J
Citation: C. Ellaway et al., Rett Syndrome: Randomized controlled trial of L-carnitine, J CHILD NEU, 14(3), 1999, pp. 162-167
Authors:
Leonard, H
Thomson, M
Glasson, E
Fyfe, S
Leonard, S
Ellaway, C
Christodoulou, J
Bower, C
Citation: H. Leonard et al., Metacarpophalangeal pattern profile and bone age in Rett syndrome: Furtherradiological clues to the diagnosis, AM J MED G, 83(2), 1999, pp. 88-95
Authors:
Leonard, H
Fyfe, S
Dye, D
Leonard, S
Citation: H. Leonard et al., Familial aggregation in Rett syndrome: What is the evidence for clusteringof other disorders in the families of affected girls?, AM J MED G, 82(3), 1999, pp. 228-234
Authors:
Wisner, KL
Gelenberg, AJ
Leonard, H
Zarin, D
Frank, E
Citation: Kl. Wisner et al., Pharmacologic treatment of depression during pregnancy, J AM MED A, 282(13), 1999, pp. 1264-1269
Authors:
Leonard, H
Thomson, MR
Glasson, EJ
Fyfe, S
Leonard, S
Bower, C
Christodoulou, J
Ellaway, C
Citation: H. Leonard et al., A population-based approach to the investigation of osteopenia in Rett syndrome, DEVELOP MED, 41(5), 1999, pp. 323-328
Authors:
Leonard, S
Bower, C
Petterson, B
Leonard, H
Citation: S. Leonard et al., Medical aspects of school-aged children with Down syndrome, DEVELOP MED, 41(10), 1999, pp. 683-688
Authors:
Ellaway, CJ
Sholler, G
Leonard, H
Christodoulou, J
Citation: Cj. Ellaway et al., Prolonged QT interval in Rett syndrome, ARCH DIS CH, 80(5), 1999, pp. 470-472