Bailey L - Search Results

1

CNS, lung, and lymph node involvement in Gaucher disease type 3 after 11 years of therapy: clinical, histopathologic, and biochemical findings.

Burrow TA, Sun Y, Prada CE, Bailey L, Zhang W, Brewer A, Wu SW, Setchell KDR, Witte D, Cohen MB, Grabowski GA. Burrow TA, et al. Among authors: bailey l. Mol Genet Metab. 2015 Feb;114(2):233-241. doi: 10.1016/j.ymgme.2014.08.011. Epub 2014 Sep 2. Mol Genet Metab. 2015. PMID: 25219293 Free PMC article.

2

Enzyme therapy of gaucher disease: clinical and biochemical changes during production of and tolerization for neutralizing antibodies.

Zhao H, Bailey LA, Grabowski GA. Zhao H, et al. Blood Cells Mol Dis. 2003 Jan-Feb;30(1):90-6. doi: 10.1016/s1079-9796(03)00012-3. Blood Cells Mol Dis. 2003. PMID: 12667990

3

Gaucher disease: alendronate disodium improves bone mineral density in adults receiving enzyme therapy.

Wenstrup RJ, Bailey L, Grabowski GA, Moskovitz J, Oestreich AE, Wu W, Sun S. Wenstrup RJ, et al. Among authors: bailey l. Blood. 2004 Sep 1;104(5):1253-7. doi: 10.1182/blood-2003-11-3854. Epub 2004 Mar 9. Blood. 2004. PMID: 15010365 Free article. Clinical Trial.

4

Outcomes of screening for gammopathies in children and adults with Gaucher disease type 1 in a cohort from Brazil and the United States.

Abell K, Chadwell SE, Burrow TA, Becker APP, Bailey L, Steele P, Zhang X, Islas-Ohlmayer M, Bittencourt R, Schwartz IVD, Prada CE. Abell K, et al. Among authors: bailey l. Am J Med Genet C Semin Med Genet. 2020 Dec;184(4):1052-1059. doi: 10.1002/ajmg.c.31870. Epub 2020 Dec 5. Am J Med Genet C Semin Med Genet. 2020. PMID: 33277783

5

Gaucher's disease: identification of novel mutant alleles and genotype-phenotype relationships.

Zhao H, Keddache M, Bailey L, Arnold G, Grabowski G. Zhao H, et al. Among authors: bailey l. Clin Genet. 2003 Jul;64(1):57-64. doi: 10.1034/j.1399-0004.2003.00100.x. Clin Genet. 2003. PMID: 12791040

6

Gaucher disease: in vivo evidence for allele dose leading to neuronopathic and nonneuronopathic phenotypes.

Zhao H, Bailey LA, Elsas LJ 2nd, Grinzaid KA, Grabowski GA. Zhao H, et al. Am J Med Genet A. 2003 Jan 1;116A(1):52-6. doi: 10.1002/ajmg.a.10029. Am J Med Genet A. 2003. PMID: 12476451

7

Acute progression of neuromuscular findings in infantile Pompe disease.

Burrow TA, Bailey LA, Kinnett DG, Hopkin RJ. Burrow TA, et al. Pediatr Neurol. 2010 Jun;42(6):455-8. doi: 10.1016/j.pediatrneurol.2010.02.006. Pediatr Neurol. 2010. PMID: 20472203

8

Arrhythmia and Clinical Cardiac Findings in Children With Anderson-Fabry Disease.

Wilson HC, Hopkin RJ, Madueme PC, Czosek RJ, Bailey LA, Taylor MD, Jefferies JL. Wilson HC, et al. Among authors: bailey la. Am J Cardiol. 2017 Jul 15;120(2):251-255. doi: 10.1016/j.amjcard.2017.04.016. Epub 2017 Apr 27. Am J Cardiol. 2017. PMID: 28550929

9

Comparison of health-related quality of life between heterozygous women with Fabry disease, a healthy control population, and patients with other chronic disease.

Street NJ, Yi MS, Bailey LA, Hopkin RJ. Street NJ, et al. Genet Med. 2006 Jun;8(6):346-53. doi: 10.1097/01.gim.0000223545.63012.5a. Genet Med. 2006. PMID: 16778596 Free article.

10

Burden of Valvular Heart Disease in Patients with Fabry Disease.

Yogasundaram H, Nikhanj A, Chatur S, Qi A, Hagen L, Bailey L, Khan A, Hopkin RJ, Fine NM, Jefferies JL, Oudit GY. Yogasundaram H, et al. Among authors: bailey l. J Am Soc Echocardiogr. 2022 Feb;35(2):236-238. doi: 10.1016/j.echo.2021.09.013. Epub 2021 Oct 7. J Am Soc Echocardiogr. 2022. PMID: 34627970 No abstract available.

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