Percy AK - Search Results

1

Glycolipids and glycosyltransferases in permanent cell lines established from human medulloblastomas.

Gottfries J, Percy AK, Månsson JE, Fredman P, Wikstrand CJ, Friedman HS, Bigner DD, Svennerholm L. Gottfries J, et al. Among authors: percy ak. Biochim Biophys Acta. 1991 Feb 5;1081(3):253-61. doi: 10.1016/0005-2760(91)90279-q. Biochim Biophys Acta. 1991. PMID: 1825612

2

Glycosphingolipid glycosyltransferases in human fetal brain.

Percy AK, Gottfries J, Vilbergsson G, Månsson JE, Svennerholm L. Percy AK, et al. J Neurochem. 1991 May;56(5):1461-5. doi: 10.1111/j.1471-4159.1991.tb02038.x. J Neurochem. 1991. PMID: 1901591

3

Determination of gangliosides in six human primary medulloblastomas.

Gottfries J, Fredman P, Månsson JE, Collins VP, von Holst H, Armstrong DD, Percy AK, Wikstrand CJ, Bigner DD, Svennerholm L. Gottfries J, et al. Among authors: percy ak. J Neurochem. 1990 Oct;55(4):1322-6. doi: 10.1111/j.1471-4159.1990.tb03142.x. J Neurochem. 1990. PMID: 2398361

4

The fatty acid composition of placenta in intrauterine growth retardation.

Percy P, Vilbergsson G, Percy A, Månsson JE, Wennergren M, Svennerholm L. Percy P, et al. Biochim Biophys Acta. 1991 Jul 9;1084(2):173-7. doi: 10.1016/0005-2760(91)90217-6. Biochim Biophys Acta. 1991. PMID: 1854802

5

Gangliosides in human fetal brain.

Svennerholm L, Rynmark BM, Vilbergsson G, Fredman P, Gottfries J, Månsson JE, Percy A. Svennerholm L, et al. J Neurochem. 1991 May;56(5):1763-8. doi: 10.1111/j.1471-4159.1991.tb02078.x. J Neurochem. 1991. PMID: 2013764

6

Essential fatty acid status is altered in pregnancies complicated by intrauterine growth retardation.

Vilbergsson G, Wennergren M, Samsioe G, Percy P, Percy A, Månsson JE, Svennerholm L. Vilbergsson G, et al. World Rev Nutr Diet. 1994;76:105-9. doi: 10.1159/000424003. World Rev Nutr Diet. 1994. PMID: 7856217 No abstract available.

7

Rett syndrome: biogenic amines and metabolites in postmortem brain.

Lekman A, Witt-Engerström I, Gottfries J, Hagberg BA, Percy AK, Svennerholm L. Lekman A, et al. Among authors: percy ak. Pediatr Neurol. 1989 Nov-Dec;5(6):357-62. doi: 10.1016/0887-8994(89)90049-0. Pediatr Neurol. 1989. PMID: 2604799

8

Late-infantile Gaucher disease in a child with myoclonus and bulbar signs: neuropathological and neurochemical findings.

Conradi N, Kyllerman M, Månsson JE, Percy AK, Svennerholm L. Conradi N, et al. Among authors: percy ak. Acta Neuropathol. 1991;82(2):152-7. doi: 10.1007/BF00293959. Acta Neuropathol. 1991. PMID: 1718128

9

Rapidly progressive type III Gaucher disease: deterioration following partial splenectomy.

Kyllerman M, Conradi N, Månsson JE, Percy AK, Svennerholm L. Kyllerman M, et al. Among authors: percy ak. Acta Paediatr Scand. 1990 Apr;79(4):448-53. doi: 10.1111/j.1651-2227.1990.tb11492.x. Acta Paediatr Scand. 1990. PMID: 2349880

10

Distal infantile neuroaxonal dystrophy--a new familial variant with perineuronal argyrophilic bodies.

Kyllerman M, Månsson JE, Lichtenstein M, Percy AK, Nordborg C. Kyllerman M, et al. Among authors: percy ak. Acta Neuropathol. 2001 Jul;102(1):83-8. doi: 10.1007/s004010000358. Acta Neuropathol. 2001. PMID: 11547955

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