Lanser JB - Search Results

1

White matter lesions and cognitive deterioration in presymptomatic carriers of the amyloid precursor protein gene codon 693 mutation.

Bornebroek M, Haan J, van Buchem MA, Lanser JB, de Vries-vd Weerd MA, Zoeteweij M, Roos RA. Bornebroek M, et al. Among authors: lanser jb. Arch Neurol. 1996 Jan;53(1):43-8. doi: 10.1001/archneur.1996.00550010053016. Arch Neurol. 1996. PMID: 8599557

2

[The Mini Mental Status test inadequate as screening test for cognitive deterioration in a neurological department].

Harder H, Lanser JB, de Haan EH, Roos RA. Harder H, et al. Among authors: lanser jb. Ned Tijdschr Geneeskd. 1995 Aug 26;139(34):1742-5. Ned Tijdschr Geneeskd. 1995. PMID: 7566242 Dutch.

3

Hereditary cerebral hemorrhage with amyloidosis-Dutch type: better correlation of cognitive deterioration with advancing age than with number of focal lesions or white matter hyperintensities.

Bornebroek M, Van Buchem MA, Haan J, Brand R, Lanser JB, de Bruïne FT, Roos RA. Bornebroek M, et al. Among authors: lanser jb. Alzheimer Dis Assoc Disord. 1996 Winter;10(4):224-31. doi: 10.1097/00002093-199601040-00008. Alzheimer Dis Assoc Disord. 1996. PMID: 8939282

4

Early cognitive and motor symptoms in identified carriers of the gene for Huntington disease.

de Boo GM, Tibben A, Lanser JB, Jennekens-Schinkel A, Hermans J, Maat-Kievit A, Roos RA. de Boo GM, et al. Among authors: lanser jb. Arch Neurol. 1997 Nov;54(11):1353-7. doi: 10.1001/archneur.1997.00550230030012. Arch Neurol. 1997. PMID: 9362982

5

Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon.

Terwindt GM, Haan J, Ophoff RA, Groenen SM, Storimans CW, Lanser JB, Roos RA, Bleeker-Wagemakers EM, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: lanser jb. Brain. 1998 Feb;121 ( Pt 2):303-16. doi: 10.1093/brain/121.2.303. Brain. 1998. PMID: 9549508

6

Hereditary cerebral haemorrhage with amyloidosis--Dutch type. Magnetic resonance imaging findings in 7 cases.

Haan J, Roos RA, Algra PR, Lanser JB, Bots GT, Vegter-Van der Vlis M. Haan J, et al. Among authors: lanser jb. Brain. 1990 Oct;113 ( Pt 5):1251-67. doi: 10.1093/brain/113.5.1251. Brain. 1990. PMID: 2245295

7

Dementia in hereditary cerebral hemorrhage with amyloidosis-Dutch type.

Haan J, Lanser JB, Zijderveld I, van der Does IG, Roos RA. Haan J, et al. Among authors: lanser jb. Arch Neurol. 1990 Sep;47(9):965-7. doi: 10.1001/archneur.1990.00530090035010. Arch Neurol. 1990. PMID: 2396937

8

Cognitive and motor functioning in gene carriers for Huntington's disease: a baseline study.

Witjes-Ané MN, Vegter-van der Vlis M, van Vugt JP, Lanser JB, Hermans J, Zwinderman AH, van Ommen GJ, Roos RA. Witjes-Ané MN, et al. Among authors: lanser jb. J Neuropsychiatry Clin Neurosci. 2003 Winter;15(1):7-16. doi: 10.1176/jnp.15.1.7. J Neuropsychiatry Clin Neurosci. 2003. PMID: 12556566

9

Tourette's syndrome and right hemisphere dysfunction.

Lanser JB, Van Santen WH, Jennekens-Schinkel A, Roos RA. Lanser JB, et al. Br J Psychiatry. 1993 Jul;163:116-8. doi: 10.1192/bjp.163.1.116. Br J Psychiatry. 1993. PMID: 8353679

10

Intelligence indices in people with a high/low risk for developing Huntington's disease.

de Boo GM, Tibben A, Lanser JB, Jennekens-Schinkel A, Hermans J, Vegter-van der Vlis M, Roos RA. de Boo GM, et al. Among authors: lanser jb. J Med Genet. 1997 Jul;34(7):564-8. doi: 10.1136/jmg.34.7.564. J Med Genet. 1997. PMID: 9222964 Free PMC article.

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