Leonard H - Search Results

1

Rett syndrome: revised diagnostic criteria and nomenclature.

Neul JL, Kaufmann WE, Glaze DG, Christodoulou J, Clarke AJ, Bahi-Buisson N, Leonard H, Bailey ME, Schanen NC, Zappella M, Renieri A, Huppke P, Percy AK; RettSearch Consortium. Neul JL, et al. Among authors: leonard h. Ann Neurol. 2010 Dec;68(6):944-50. doi: 10.1002/ana.22124. Ann Neurol. 2010. PMID: 21154482 Free PMC article.

2

Rett syndrome: significant clinical overlap with Angelman syndrome but not with methylation status.

Ellaway C, Buchholz T, Smith A, Leonard H, Christodoulou J. Ellaway C, et al. Among authors: leonard h. J Child Neurol. 1998 Sep;13(9):448-51. doi: 10.1177/088307389801300907. J Child Neurol. 1998. PMID: 9733292

3

Diagnosis of Rett syndrome: can a radiograph help?

Glasson EJ, Bower C, Thomson MR, Fyfe S, Leonard S, Rousham E, Christodoulou J, Ellaway C, Leonard H. Glasson EJ, et al. Among authors: leonard s, leonard h. Dev Med Child Neurol. 1998 Nov;40(11):737-42. doi: 10.1111/j.1469-8749.1998.tb12341.x. Dev Med Child Neurol. 1998. PMID: 9881802 Free article.

4

Rett syndrome: randomized controlled trial of L-carnitine.

Ellaway C, Williams K, Leonard H, Higgins G, Wilcken B, Christodoulou J. Ellaway C, et al. Among authors: leonard h. J Child Neurol. 1999 Mar;14(3):162-7. doi: 10.1177/088307389901400306. J Child Neurol. 1999. PMID: 10190267 Clinical Trial.

5

Metacarpophalangeal pattern profile and bone age in Rett syndrome: further radiological clues to the diagnosis.

Leonard H, Thomson M, Glasson E, Fyfe S, Leonard S, Ellaway C, Christodoulou J, Bower C. Leonard H, et al. Among authors: leonard s. Am J Med Genet. 1999 Mar 12;83(2):88-95. doi: 10.1002/(sici)1096-8628(19990312)83:2<88::aid-ajmg3>3.0.co;2-7. Am J Med Genet. 1999. PMID: 10190478

6

Prolonged QT interval in Rett syndrome.

Ellaway CJ, Sholler G, Leonard H, Christodoulou J. Ellaway CJ, et al. Among authors: leonard h. Arch Dis Child. 1999 May;80(5):470-2. doi: 10.1136/adc.80.5.470. Arch Dis Child. 1999. PMID: 10208957 Free PMC article.

7

A population-based approach to the investigation of osteopenia in Rett syndrome.

Leonard H, Thomson MR, Glasson EJ, Fyfe S, Leonard S, Bower C, Christodoulou J, Ellaway C. Leonard H, et al. Among authors: leonard s. Dev Med Child Neurol. 1999 May;41(5):323-8. doi: 10.1017/s0012162299000717. Dev Med Child Neurol. 1999. PMID: 10378758 Free article.

8

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

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. Cheadle JP, et al. Among authors: leonard h. Hum Mol Genet. 2000 Apr 12;9(7):1119-29. doi: 10.1093/hmg/9.7.1119. Hum Mol Genet. 2000. PMID: 10767337

9

Family data in Rett syndrome: association with other genetic disorders.

Leonard H, Fyfe S, Dye D, Hockey A, Christodoulou J. Leonard H, et al. J Paediatr Child Health. 2000 Aug;36(4):336-9. doi: 10.1046/j.1440-1754.2000.00531.x. J Paediatr Child Health. 2000. PMID: 10940166

10

Guidelines for reporting clinical features in cases with MECP2 mutations.

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. Kerr AM, et al. Among authors: leonard h. Brain Dev. 2001 Jul;23(4):208-11. doi: 10.1016/s0387-7604(01)00193-0. Brain Dev. 2001. PMID: 11376997

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