Cochius J - Search Results

1

Isolation and characterization of GT335, a novel human gene conserved in Escherichia coli and mapping to 21q22.3.

Lafrenière RG, Rochefort DL, Kibar Z, Fon EA, Han F, Cochius J, Kang X, Baird S, Korneluk RG, Andermann E, Rommens JM, Rouleau GA. Lafrenière RG, et al. Among authors: cochius j. Genomics. 1996 Dec 15;38(3):264-72. doi: 10.1006/geno.1996.0627. Genomics. 1996. PMID: 8975701

2

Unstable insertion in the 5' flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1.

Lafrenière RG, Rochefort DL, Chrétien N, Rommens JM, Cochius JI, Kälviäinen R, Nousiainen U, Patry G, Farrell K, Söderfeldt B, Federico A, Hale BR, Cossio OH, Sørensen T, Pouliot MA, Kmiec T, Uldall P, Janszky J, Pranzatelli MR, Andermann F, Andermann E, Rouleau GA. Lafrenière RG, et al. Among authors: cochius ji. Nat Genet. 1997 Mar;15(3):298-302. doi: 10.1038/ng0397-298. Nat Genet. 1997. PMID: 9054946

3

Sweat gland vacuoles in Unverricht-Lundborg disease: a clue to diagnosis?

Cochius J, Carpenter S, Andermann E, Rouleau G, Nousiainen U, Kalviainen R, Farrell K, Andermann F. Cochius J, et al. Neurology. 1994 Dec;44(12):2372-5. doi: 10.1212/wnl.44.12.2372. Neurology. 1994. PMID: 7991128 Clinical Trial.

4

Progressive myoclonus epilepsies: clinical and genetic aspects.

Berkovic SF, Cochius J, Andermann E, Andermann F. Berkovic SF, et al. Among authors: cochius j. Epilepsia. 1993;34 Suppl 3:S19-30. doi: 10.1111/j.1528-1167.1993.tb06256.x. Epilepsia. 1993. PMID: 8500430 Review.

5

Unverricht-Lundborg disease: absence of nonallelic genetic heterogeneity.

Cochius JI, Figlewicz DA, Kälviäinen R, Nousiainen U, Farrell K, Patry G, Söderfeldt B, Frydman M, Lerman P, Andermann F, et al. Cochius JI, et al. Ann Neurol. 1993 Nov;34(5):739-41. doi: 10.1002/ana.410340519. Ann Neurol. 1993. PMID: 8239570

6

Creutzfeldt-Jakob disease in a recipient of human pituitary-derived gonadotrophin: a second case.

Cochius JI, Hyman N, Esiri MM. Cochius JI, et al. J Neurol Neurosurg Psychiatry. 1992 Nov;55(11):1094-5. doi: 10.1136/jnnp.55.11.1094. J Neurol Neurosurg Psychiatry. 1992. PMID: 1469410 Free PMC article.

7

DCTN1 mutation associated parkinsonism: case series of three new families with perry syndrome.

Stoker TB, Dostal V, Cochius J, Williams-Gray CH, Scherzer CR, Wang J, Liu G, Coyle-Gilchrist I. Stoker TB, et al. Among authors: cochius j. J Neurol. 2022 Dec;269(12):6667-6672. doi: 10.1007/s00415-022-11308-3. Epub 2022 Jul 27. J Neurol. 2022. PMID: 35895135 No abstract available.

8

CNS cryptococcosis: unusual aspects.

Cochius JI, Burns RJ, Willoughby JO. Cochius JI, et al. Clin Exp Neurol. 1989;26:183-91. Clin Exp Neurol. 1989. PMID: 2561997

9

Creutzfeldt-Jakob disease in a recipient of human pituitary-derived gonadotrophin.

Cochius JI, Burns RJ, Blumbergs PC, Mack K, Alderman CP. Cochius JI, et al. Aust N Z J Med. 1990 Aug;20(4):592-3. doi: 10.1111/j.1445-5994.1990.tb01322.x. Aust N Z J Med. 1990. PMID: 2222355

10

Delayed postanoxic encephalopathy and pseudodeficiency of arylsulphatase A.

Barker RA, Dick DJ, Cochius JI. Barker RA, et al. Among authors: cochius ji. J Neurol. 1999 Nov;246(11):1103-4. doi: 10.1007/s004150050523. J Neurol. 1999. PMID: 10631649 No abstract available.

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