Warren IB - Search Results

1

Homozygous presence of the crossover (fusion gene) mutation identified in a type II Gaucher disease fetus: is this analogous to the Gaucher knock-out mouse model?

Strasberg PM, Skomorowski MA, Warren IB, Hilson WL, Callahan JW, Clarke JT. Strasberg PM, et al. Among authors: warren ib. Biochem Med Metab Biol. 1994 Oct;53(1):16-21. doi: 10.1006/bmmb.1994.1052. Biochem Med Metab Biol. 1994. PMID: 7857677

2

Genotype-phenotype pitfalls in Gaucher disease.

Strasberg PM, Triggs-Raine BL, Warren IB, Skomorowski MA, McInnes B, Becker LE, Callahan JW, Clarke JT. Strasberg PM, et al. Among authors: warren ib. J Clin Lab Anal. 1994;8(4):228-36. doi: 10.1002/jcla.1860080409. J Clin Lab Anal. 1994. PMID: 7931818 Review.

3

Homozygosity for the common Ashkenazi jewish Tay-Sachs +1 IVS-12 splice-junction mutation: first report.

Strasberg P, Warren I, Skomorowski MA, Feigenbaum A. Strasberg P, et al. Hum Mutat. 1997;10(1):82-3. doi: 10.1002/(SICI)1098-1004(1997)10:1<82::AID-HUMU13>3.0.CO;2-W. Hum Mutat. 1997. PMID: 9222766 No abstract available.

4

Decreased incorporation of D-glucosamine into glycosphingolipids of intact Familial Dysautonomia lymphoblasts.

Strasberg PM, Novak A, Warren IB. Strasberg PM, et al. Among authors: warren ib. J Mol Neurosci. 1995;6(2):121-30. doi: 10.1007/BF02736771. J Mol Neurosci. 1995. PMID: 8746450

5

Increased globotriaosylceramide in familial dysautonomia.

Strasberg P, Yeger H, Warren I. Strasberg P, et al. Lipids. 1992 Dec;27(12):978-83. doi: 10.1007/BF02535575. Lipids. 1992. PMID: 1336803

6

Simultaneous fractionation of four placental neutral glycosphingolipids with a continuous gradient.

Strasberg P, Grey A, Warren I, Skomorowski MA. Strasberg P, et al. J Lipid Res. 1989 Jan;30(1):121-7. J Lipid Res. 1989. PMID: 2918246 Free article.

7

A novel mutation in the Norrie disease gene predicted to disrupt the cystine knot growth factor motif.

Strasberg P, Liede HA, Stein T, Warren I, Sutherland J, Ray PN. Strasberg P, et al. Hum Mol Genet. 1995 Nov;4(11):2179-80. doi: 10.1093/hmg/4.11.2179. Hum Mol Genet. 1995. PMID: 8589700 No abstract available.

8

HPLC analysis of neutral glycolipids: an aid in the diagnosis of lysosomal storage disease.

Strasberg PM, Warren I, Skomorowski MA, Lowden JA. Strasberg PM, et al. Clin Chim Acta. 1983 Jul 31;132(1):29-41. doi: 10.1016/0009-8981(83)90230-9. Clin Chim Acta. 1983. PMID: 6616861

9

HPLC analysis of urinary sulfatide: an aid in the diagnosis of metachromatic leukodystrophy.

Strasberg PM, Warren I, Skomorowski MA, Lowden JA. Strasberg PM, et al. Clin Biochem. 1985 Apr;18(2):92-7. doi: 10.1016/s0009-9120(85)80088-6. Clin Biochem. 1985. PMID: 2861921

10

Regulation of renal sulfoglycolipid biosynthesis.

Lingwood CA, Dennis J, Hsu E, Sakac D, Oda K, Strasberg P, Taylor T, Warren I, Yeger H, Baumal R. Lingwood CA, et al. Biochim Biophys Acta. 1986 Jun 27;877(2):246-51. doi: 10.1016/0005-2760(86)90301-2. Biochim Biophys Acta. 1986. PMID: 3459553

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