Blennow G - Search Results

1

Linkage of a locus for carbohydrate-deficient glycoprotein syndrome type I (CDG1) to chromosome 16p, and linkage disequilibrium to microsatellite marker D16S406.

Martinsson T, Bjursell C, Stibler H, Kristiansson B, Skovby F, Jaeken J, Blennow G, Strömme P, Hanefeld F, Wahlström J. Martinsson T, et al. Among authors: blennow g. Hum Mol Genet. 1994 Nov;3(11):2037-42. Hum Mol Genet. 1994. PMID: 7874123

2

Carbohydrate-deficient glycoprotein syndrome: clinical expression in adults with a new metabolic disease.

Stibler H, Blennow G, Kristiansson B, Lindehammer H, Hagberg B. Stibler H, et al. Among authors: blennow g. J Neurol Neurosurg Psychiatry. 1994 May;57(5):552-6. doi: 10.1136/jnnp.57.5.552. J Neurol Neurosurg Psychiatry. 1994. PMID: 8201322 Free PMC article.

3

Fine mapping of the gene for carbohydrate-deficient glycoprotein syndrome, type I (CDG1): linkage disequilibrium and founder effect in Scandinavian families.

Bjursell C, Stibler H, Wahlström J, Kristiansson B, Skovby F, Strömme P, Blennow G, Martinsson T. Bjursell C, et al. Among authors: blennow g. Genomics. 1997 Feb 1;39(3):247-53. doi: 10.1006/geno.1996.4488. Genomics. 1997. PMID: 9119361

4

Carbohydrate-deficient glycoprotein syndromes: peculiar group of new disorders.

Hagberg BA, Blennow G, Kristiansson B, Stibler H. Hagberg BA, et al. Among authors: blennow g. Pediatr Neurol. 1993 Jul-Aug;9(4):255-62. doi: 10.1016/0887-8994(93)90060-p. Pediatr Neurol. 1993. PMID: 8216537 Review.

5

The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigrees.

Barth PG, Blennow G, Lenard HG, Begeer JH, van der Kley JM, Hanefeld F, Peters AC, Valk J. Barth PG, et al. Among authors: blennow g. Neurology. 1995 Feb;45(2):311-7. doi: 10.1212/wnl.45.2.311. Neurology. 1995. PMID: 7854532

6

Full-field electroretinograms in patients with the carbohydrate-deficient glycoprotein syndrome.

Andréasson S, Blennow G, Ehinger B, Strömland K. Andréasson S, et al. Among authors: blennow g. Am J Ophthalmol. 1991 Jul 15;112(1):83-6. doi: 10.1016/s0002-9394(14)76218-x. Am J Ophthalmol. 1991. PMID: 1715674

7

[Adrenoleukodystrophy. A disease of current interest and many aspects].

Kyllerman M, Blennow G, Månsson JE, Wahlström J, von Döbeln U. Kyllerman M, et al. Among authors: blennow g. Lakartidningen. 1994 Jan 5;91(1-2):54-6. Lakartidningen. 1994. PMID: 8289555 Swedish. No abstract available.

8

Disorders of the cerebral white matter in children. The spectrum of lesions.

Kristjánsdóttir R, Uvebrant P, Hagberg B, Kyllerman M, Wiklund LM, Blennow G, Flodmark O, Gustavsson L, Ekholm S, Månsson JE. Kristjánsdóttir R, et al. Among authors: blennow g. Neuropediatrics. 1996 Dec;27(6):295-8. doi: 10.1055/s-2007-973797. Neuropediatrics. 1996. PMID: 9050046 Clinical Trial.

9

Neurological deviations in newborns at psychiatric high risk.

Blennow G, McNeil TF. Blennow G, et al. Acta Psychiatr Scand. 1991 Aug;84(2):179-84. doi: 10.1111/j.1600-0447.1991.tb03125.x. Acta Psychiatr Scand. 1991. PMID: 1950614

10

Anterior spinal artery syndrome. Report of seven cases in childhood.

Blennow G, Starck L. Blennow G, et al. Pediatr Neurosci. 1987;13(1):32-7. Pediatr Neurosci. 1987. PMID: 3684813

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