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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 2
1993 7
1994 8
1995 6
1996 4
1997 10
1998 8
1999 7
2000 5
2001 15
2002 3
2003 2
2006 2
2007 3
2008 2
2009 4
2010 4
2011 3
2012 1
2013 2
2020 0
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93 results
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Page 1
Fabry disease (alpha-galactosidase A deficiency): renal involvement and enzyme replacement therapy.
Desnick RJ, Wasserstein MP, Banikazemi M. Desnick RJ, et al. Contrib Nephrol. 2001;(136):174-92. doi: 10.1159/000060184. Contrib Nephrol. 2001. PMID: 11688379 Review. No abstract available.
Fabry disease: clinical features and recent advances in enzyme replacement therapy.
Desnick RJ, Wasserstein MP. Desnick RJ, et al. Adv Nephrol Necker Hosp. 2001;31:317-39. Adv Nephrol Necker Hosp. 2001. PMID: 11692469 Review. No abstract available.
Experiences in molecular-based prenatal screening for Ashkenazi Jewish genetic diseases.
Eng CM, Desnick RJ. Eng CM, et al. Adv Genet. 2001;44:275-96. doi: 10.1016/s0065-2660(01)44086-7. Adv Genet. 2001. PMID: 11596990 Review.
Enzyme replacement therapy for Fabry disease, an inherited nephropathy.
Desnick RJ, Banikazemi M, Wasserstein M. Desnick RJ, et al. Clin Nephrol. 2002 Jan;57(1):1-8. doi: 10.5414/cnp57001. Clin Nephrol. 2002. PMID: 11837797 Review.
SSRIs in the treatment of obsessive-compulsive disorder.
Cartwright C, Hollander E. Cartwright C, et al. Depress Anxiety. 1998;8 Suppl 1:105-13. doi: 10.1002/(sici)1520-6394(1998)8:1+<105::aid-da16>;2-t. Depress Anxiety. 1998. PMID: 9809222 Review.
Molecular genetics of congenital erythropoietic porphyria.
Desnick RJ, Glass IA, Xu W, Solis C, Astrin KH. Desnick RJ, et al. Semin Liver Dis. 1998;18(1):77-84. doi: 10.1055/s-2007-1007143. Semin Liver Dis. 1998. PMID: 9516681 Review.
Neurally mediated syncope: pathogenesis, diagnosis, and treatment.
Kaufmann H. Kaufmann H. Neurology. 1995 Apr;45(4 Suppl 5):S12-8. Neurology. 1995. PMID: 7746368 Review.
Clonal chromosomal abnormalities in Fanconi's anaemia: what do they really mean?
Alter BP, Scalise A, McCombs J, Najfeld V. Alter BP, et al. Br J Haematol. 1993 Nov;85(3):627-30. doi: 10.1111/j.1365-2141.1993.tb03362.x. Br J Haematol. 1993. PMID: 8136289 Review.
Morbidity and mortality in type B Niemann-Pick disease.
McGovern MM, Lippa N, Bagiella E, Schuchman EH, Desnick RJ, Wasserstein MP. McGovern MM, et al. Genet Med. 2013 Aug;15(8):618-23. doi: 10.1038/gim.2013.4. Epub 2013 Feb 14. Genet Med. 2013. PMID: 23412609 Free article.
Molecular basis of Fabry disease: mutations and polymorphisms in the human alpha-galactosidase A gene.
Eng CM, Desnick RJ. Eng CM, et al. Hum Mutat. 1994;3(2):103-11. doi: 10.1002/humu.1380030204. Hum Mutat. 1994. PMID: 7911050 Review.
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