Vellodi A - Search Results

1

Response of 33 UK patients with infantile-onset Pompe disease to enzyme replacement therapy.

Broomfield A, Fletcher J, Davison J, Finnegan N, Fenton M, Chikermane A, Beesley C, Harvey K, Cullen E, Stewart C, Santra S, Vijay S, Champion M, Abulhoul L, Grunewald S, Chakrapani A, Cleary MA, Jones SA, Vellodi A. Broomfield A, et al. Among authors: vellodi a. J Inherit Metab Dis. 2016 Mar;39(2):261-71. doi: 10.1007/s10545-015-9898-5. Epub 2015 Oct 26. J Inherit Metab Dis. 2016. PMID: 26497565

2

Treatment of infantile Pompe disease with alglucosidase alpha: the UK experience.

Chakrapani A, Vellodi A, Robinson P, Jones S, Wraith JE. Chakrapani A, et al. Among authors: vellodi a. J Inherit Metab Dis. 2010 Dec;33(6):747-50. doi: 10.1007/s10545-010-9206-3. Epub 2010 Sep 24. J Inherit Metab Dis. 2010. PMID: 20865334

3

Changes in gait pattern as assessed by the GAITRite™ walkway system in MPS II patients undergoing enzyme replacement therapy.

Wood M, Cleary MA, Alderson L, Vellodi A. Wood M, et al. Among authors: vellodi a. J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S127-35. doi: 10.1007/s10545-009-1103-2. Epub 2009 Mar 25. J Inherit Metab Dis. 2009. PMID: 19319660

4

Pulmonary hemorrhage in type 3 Gaucher disease: a case report.

Vellodi A, Ashworth M, Finnegan N, Wallis C. Vellodi A, et al. J Inherit Metab Dis. 2010 Dec;33 Suppl 3:S329-31. doi: 10.1007/s10545-010-9176-5. Epub 2010 Aug 6. J Inherit Metab Dis. 2010. PMID: 20689991

5

Treatment of mucopolysaccharidosis type II (Hunter syndrome) with idursulfase: the relevance of clinical trial end points.

Glamuzina E, Fettes E, Bainbridge K, Crook V, Finnegan N, Abulhoul L, Vellodi A. Glamuzina E, et al. Among authors: vellodi a. J Inherit Metab Dis. 2011 Jun;34(3):749-54. doi: 10.1007/s10545-011-9280-1. Epub 2011 Feb 16. J Inherit Metab Dis. 2011. PMID: 21327479

6

Urine analysis of glucose tetrasaccharide by HPLC; a useful marker for the investigation of patients with Pompe and other glycogen storage diseases.

Manwaring V, Prunty H, Bainbridge K, Burke D, Finnegan N, Franses R, Lam A, Vellodi A, Heales S. Manwaring V, et al. Among authors: vellodi a. J Inherit Metab Dis. 2012 Mar;35(2):311-6. doi: 10.1007/s10545-011-9360-2. Epub 2011 Jun 18. J Inherit Metab Dis. 2012. PMID: 21687968

7

Successful Desensitisation in a Patient with CRIM-Positive Infantile-Onset Pompe Disease.

Baruteau J, Broomfield A, Crook V, Finnegan N, Harvey K, Burke D, Burch M, Shepherd G, Vellodi A. Baruteau J, et al. Among authors: vellodi a. JIMD Rep. 2014;12:99-102. doi: 10.1007/8904_2013_250. Epub 2013 Sep 4. JIMD Rep. 2014. PMID: 24002816 Free PMC article.

8

Molecular defects in Sanfilippo syndrome type B (mucopolysaccharidosis IIIB).

Beesley CE, Jackson M, Young EP, Vellodi A, Winchester BG. Beesley CE, et al. Among authors: vellodi a. J Inherit Metab Dis. 2005;28(5):759-67. doi: 10.1007/s10545-005-0093-y. J Inherit Metab Dis. 2005. PMID: 16151907

9

A Clinically Severe Variant of β-Mannosidosis, Presenting with Neonatal Onset Epilepsy with Subsequent Evolution of Hydrocephalus.

Broomfield A, Gunny R, Ali I, Vellodi A, Prabhakar P. Broomfield A, et al. Among authors: vellodi a. JIMD Rep. 2013;11:93-7. doi: 10.1007/8904_2013_227. Epub 2013 Apr 16. JIMD Rep. 2013. PMID: 23588843 Free PMC article.

10

Mortality and cause of death in mucopolysaccharidosis type II-a historical review based on data from the Hunter Outcome Survey (HOS).

Jones SA, Almássy Z, Beck M, Burt K, Clarke JT, Giugliani R, Hendriksz C, Kroepfl T, Lavery L, Lin SP, Malm G, Ramaswami U, Tincheva R, Wraith JE; HOS Investigators. Jones SA, et al. J Inherit Metab Dis. 2009 Aug;32(4):534-43. doi: 10.1007/s10545-009-1119-7. Epub 2009 Jul 14. J Inherit Metab Dis. 2009. PMID: 19597960

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