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159 results
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Radiological evidence of early cerebral microvascular disease in young children with Fabry disease.
Cabrera-Salazar MA, O'Rourke E, Charria-Ortiz G, Barranger JA. Cabrera-Salazar MA, et al. Among authors: barranger ja. J Pediatr. 2005 Jul;147(1):102-5. doi: 10.1016/j.jpeds.2005.03.004. J Pediatr. 2005. PMID: 16027705
Fabry disease in genetic counseling practice: recommendations of the National Society of Genetic Counselors.
Bennett RL, Hart KA, O'Rourke E, Barranger JA, Johnson J, MacDermot KD, Pastores GM, Steiner RD, Thadhani R. Bennett RL, et al. Among authors: barranger ja. J Genet Couns. 2002 Apr;11(2):121-46. doi: 10.1023/a:1014545521753. J Genet Couns. 2002. PMID: 12735292
Gene therapy for the lysosomal storage disorders.
Cabrera-Salazar MA, Novelli E, Barranger JA. Cabrera-Salazar MA, et al. Among authors: barranger ja. Curr Opin Mol Ther. 2002 Aug;4(4):349-58. Curr Opin Mol Ther. 2002. PMID: 12222873 Review.
Correlation of surrogate markers of Gaucher disease. Implications for long-term follow up of enzyme replacement therapy.
Cabrera-Salazar MA, O'Rourke E, Henderson N, Wessel H, Barranger JA. Cabrera-Salazar MA, et al. Among authors: barranger ja. Clin Chim Acta. 2004 Jun;344(1-2):101-7. doi: 10.1016/j.cccn.2004.02.018. Clin Chim Acta. 2004. PMID: 15149877
Retrovirus-mediated transfer of human alpha-galactosidase A gene to human CD34+ hematopoietic progenitor cells.
Takiyama N, Dunigan JT, Vallor MJ, Kase R, Sakuraba H, Barranger JA. Takiyama N, et al. Among authors: barranger ja. Hum Gene Ther. 1999 Dec 10;10(18):2881-9. doi: 10.1089/10430349950016302. Hum Gene Ther. 1999. PMID: 10609650
Molecular biology of glucocerebrosidase and the treatment of Gaucher disease.
Barranger JA, Tomich J, Weiler S, Sakallah S, Sansieri C, Mifflin T, Bahnson A, Wei FS, Wei JF, Vallor M, et al. Barranger JA, et al. Cytokines Mol Ther. 1995 Sep;1(3):149-63. Cytokines Mol Ther. 1995. PMID: 9384672 Review.
Gaucher's disease: studies of gene transfer to haematopoietic cells.
Barranger JA, Rice EO, Dunigan J, Sansieri C, Takiyama N, Beeler M, Lancia J, Lucot S, Scheirer-Fochler S, Mohney T, Swaney W, Bahnson A, Ball E. Barranger JA, et al. Baillieres Clin Haematol. 1997 Dec;10(4):765-78. doi: 10.1016/s0950-3536(97)80039-x. Baillieres Clin Haematol. 1997. PMID: 9497863 Review.
Lessons learned from the development of enzyme therapy for Gaucher disease.
Barranger JA, O'Rourke E. Barranger JA, et al. J Inherit Metab Dis. 2001;24 Suppl 2:89-96; discussion 87-8. doi: 10.1023/a:1012440428282. J Inherit Metab Dis. 2001. PMID: 11758684 Review.
Fabry disease, an under-recognized multisystemic disorder: expert recommendations for diagnosis, management, and enzyme replacement therapy.
Desnick RJ, Brady R, Barranger J, Collins AJ, Germain DP, Goldman M, Grabowski G, Packman S, Wilcox WR. Desnick RJ, et al. Ann Intern Med. 2003 Feb 18;138(4):338-46. doi: 10.7326/0003-4819-138-4-200302180-00014. Ann Intern Med. 2003. PMID: 12585833 Review.
Gaucher disease: studies of phenotype, molecular diagnosis and treatment.
Rice EO, Mifflin TE, Sakallah S, Lee RE, Sansieri CA, Barranger JA. Rice EO, et al. Among authors: barranger ja. Clin Genet. 1996 Mar;49(3):111-8. doi: 10.1111/j.1399-0004.1996.tb03268.x. Clin Genet. 1996. PMID: 8737974
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