Ramsay D - Search Results

1

Case of multiple sulfatase deficiency and ocular albinism: a diagnostic odyssey.

Prasad C, Rupar CA, Campbell C, Napier M, Ramsay D, Tay KY, Sharan S, Prasad AN. Prasad C, et al. Among authors: ramsay d. Can J Neurol Sci. 2014 Sep;41(5):626-31. doi: 10.1017/cjn.2014.12. Can J Neurol Sci. 2014. PMID: 25373814

2

Fatal cerebral edema from late-onset ornithine transcarbamylase deficiency in a juvenile male patient receiving valproic acid.

Thakur V, Rupar CA, Ramsay DA, Singh R, Fraser DD. Thakur V, et al. Among authors: ramsay da. Pediatr Crit Care Med. 2006 May;7(3):273-6. doi: 10.1097/01.PCC.0000216682.56067.23. Pediatr Crit Care Med. 2006. PMID: 16575347

3

Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency.

Farhan SM, Wang J, Robinson JF, Lahiry P, Siu VM, Prasad C, Kronick JB, Ramsay DA, Rupar CA, Hegele RA. Farhan SM, et al. Mol Genet Genomic Med. 2014 Jan;2(1):73-80. doi: 10.1002/mgg3.46. Epub 2013 Nov 18. Mol Genet Genomic Med. 2014. PMID: 24498631 Free PMC article.

4

MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation.

Prasad M, Narayan B, Prasad AN, Rupar CA, Levin S, Kronick J, Ramsay D, Tay KY, Prasad C. Prasad M, et al. Among authors: ramsay d. Can J Neurol Sci. 2014 Mar;41(2):210-9. doi: 10.1017/s0317167100016607. Can J Neurol Sci. 2014. PMID: 24534033

5

Isolated sulfite oxidase deficiency.

Rupar CA, Gillett J, Gordon BA, Ramsay DA, Johnson JL, Garrett RM, Rajagopalan KV, Jung JH, Bacheyie GS, Sellers AR. Rupar CA, et al. Among authors: ramsay da. Neuropediatrics. 1996 Dec;27(6):299-304. doi: 10.1055/s-2007-973798. Neuropediatrics. 1996. PMID: 9050047

6

A multiplex human syndrome implicates a key role for intestinal cell kinase in development of central nervous, skeletal, and endocrine systems.

Lahiry P, Wang J, Robinson JF, Turowec JP, Litchfield DW, Lanktree MB, Gloor GB, Puffenberger EG, Strauss KA, Martens MB, Ramsay DA, Rupar CA, Siu V, Hegele RA. Lahiry P, et al. Am J Hum Genet. 2009 Feb;84(2):134-47. doi: 10.1016/j.ajhg.2008.12.017. Epub 2009 Jan 29. Am J Hum Genet. 2009. PMID: 19185282 Free PMC article.

7

Multiple cerebral infarcts in patient with Moyamoya disease.

Casserly CS, Salmon A, Ramsay DA, Pelz DM, Lownie SP, Strong MJ. Casserly CS, et al. Among authors: ramsay da. Can J Neurol Sci. 2012 May;39(3):378-82. doi: 10.1017/s0317167100013548. Can J Neurol Sci. 2012. PMID: 22547520 No abstract available.

8

Gliomas in families.

Ikizler Y, van Meyel DJ, Ramsay DA, Abdallah GL, Allaster RM, Macdonald DR, Cavenee WK, Cairncross JG. Ikizler Y, et al. Among authors: ramsay da. Can J Neurol Sci. 1992 Nov;19(4):492-7. Can J Neurol Sci. 1992. PMID: 1423046

9

Loss of heterozygosity analysis of chromosomes 9, 10 and 17 in gliomas in families.

Watling CJ, van Meyel DJ, Ramsay DA, Macdonald DR, Cairncross JG. Watling CJ, et al. Among authors: ramsay da. Can J Neurol Sci. 1995 Feb;22(1):17-21. doi: 10.1017/s0317167100040440. Can J Neurol Sci. 1995. PMID: 7750067

10

Fatal streptokinase-induced intracerebral haemorrhage in cerebral amyloid angiopathy.

Ramsay DA, Penswick JL, Robertson DM. Ramsay DA, et al. Can J Neurol Sci. 1990 Aug;17(3):336-41. doi: 10.1017/s0317167100030705. Can J Neurol Sci. 1990. PMID: 2207893

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