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Enzyme replacement therapy (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Enzyme replacement therapy" in English language version.

refsWebsite
Global rank English rank
12nih.gov
4th place
4th place
9doi.org
2nd place
2nd place
4semanticscholar.org
11th place
8th place
1rarediseases.org
5,181st place
3,260th place
1medlineplus.gov
1,581st place
1,299th place
1web.archive.org
1st place
1st place

doi.org

  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877.
  • Booth, C; Hershfield, M; Notarangelo, L; Buckley, R; Hoenig, M; Mahlaoui, N; Cavazzana-Calvo, M; Aiuti, A; Gaspar, H. B. (2007). "Management options for adenosine deaminase deficiency; proceedings of the EBMT satellite workshop (Hamburg, March 2006)". Clinical Immunology. 123 (2): 139–47. doi:10.1016/j.clim.2006.12.009. PMID 17300989.
  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877. [verification needed]
  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877. [verification needed]
  • Poznansky, M. J. (1984). "Enzyme-albumin polymers. New approaches to the use of enzymes in medicine". Applied Biochemistry and Biotechnology. 10: 41–56. doi:10.1007/BF02783734. PMID 6395807. S2CID 87349537.
  • Weiss, N (2012). "Cross-talk between TRPML1 channel, lipids and lysosomal storage diseases". Communicative & Integrative Biology. 5 (2): 111–113. doi:10.4161/cib.20373. PMC 3376041. PMID 22808310.
  • Tartibi, H. M.; Hershfield, M. S.; Bahna, S. L. (2016). "A 24-Year Enzyme Replacement Therapy in an Adenosine-deaminase-Deficient Patient". Pediatrics. 137 (1): e20152169. doi:10.1542/peds.2015-2169. PMID 26684479.
  • Coutinho, M. F.; Santos, J. I.; Alves, S (2016). "Less is More: Substrate Reduction Therapy for Lysosomal Storage Disorders". International Journal of Molecular Sciences. 17 (7): 1065. doi:10.3390/ijms17071065. PMC 4964441. PMID 27384562.
  • Biffi, A (2016). "Gene therapy for lysosomal storage disorders: A good start". Human Molecular Genetics. 25 (R1): R65–75. doi:10.1093/hmg/ddv457. PMID 26604151.

medlineplus.gov

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877.
  • Booth, C; Hershfield, M; Notarangelo, L; Buckley, R; Hoenig, M; Mahlaoui, N; Cavazzana-Calvo, M; Aiuti, A; Gaspar, H. B. (2007). "Management options for adenosine deaminase deficiency; proceedings of the EBMT satellite workshop (Hamburg, March 2006)". Clinical Immunology. 123 (2): 139–47. doi:10.1016/j.clim.2006.12.009. PMID 17300989.
  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877. [verification needed]
  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877. [verification needed]
  • Neufeld EF (2006). "Chapter 10: Enzyme replacement therapy – a brief history". In Mehta A, Beck M, Sunder-Plassmann G (eds.). Fabry Disease: Perspectives from 5 Years of FOS. Oxford: Oxford PharmaGenesis. ISBN 978-1-903539-03-3. PMID 21290685.
  • Poznansky, M. J. (1984). "Enzyme-albumin polymers. New approaches to the use of enzymes in medicine". Applied Biochemistry and Biotechnology. 10: 41–56. doi:10.1007/BF02783734. PMID 6395807. S2CID 87349537.
  • Weiss, N (2012). "Cross-talk between TRPML1 channel, lipids and lysosomal storage diseases". Communicative & Integrative Biology. 5 (2): 111–113. doi:10.4161/cib.20373. PMC 3376041. PMID 22808310.
  • Tartibi, H. M.; Hershfield, M. S.; Bahna, S. L. (2016). "A 24-Year Enzyme Replacement Therapy in an Adenosine-deaminase-Deficient Patient". Pediatrics. 137 (1): e20152169. doi:10.1542/peds.2015-2169. PMID 26684479.
  • Coutinho, M. F.; Santos, J. I.; Alves, S (2016). "Less is More: Substrate Reduction Therapy for Lysosomal Storage Disorders". International Journal of Molecular Sciences. 17 (7): 1065. doi:10.3390/ijms17071065. PMC 4964441. PMID 27384562.
  • Biffi, A (2016). "Gene therapy for lysosomal storage disorders: A good start". Human Molecular Genetics. 25 (R1): R65–75. doi:10.1093/hmg/ddv457. PMID 26604151.

ncbi.nlm.nih.gov

rarediseases.org

semanticscholar.org

api.semanticscholar.org

  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877.
  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877. [verification needed]
  • Ries, M (2017). "Enzyme replacement therapy and beyond-in memoriam Roscoe O. Brady, M.D. (1923–2016)". Journal of Inherited Metabolic Disease. 40 (3): 343–356. doi:10.1007/s10545-017-0032-8. PMID 28314976. S2CID 31320877. [verification needed]
  • Poznansky, M. J. (1984). "Enzyme-albumin polymers. New approaches to the use of enzymes in medicine". Applied Biochemistry and Biotechnology. 10: 41–56. doi:10.1007/BF02783734. PMID 6395807. S2CID 87349537.

web.archive.org

  • Domen, J., Wagers, A., & Weissman, I. "Bone Marrow (Hematopoietic) Stem Cells." April 19, 2017, from [1] .