Bolhuis PA - Search Results

1

Concentrations of amyloid-beta protein in cerebrospinal fluid increase with age in patients free from neurodegenerative disease.

van Gool WA, Schenk DB, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. Neurosci Lett. 1994 May 19;172(1-2):122-4. doi: 10.1016/0304-3940(94)90677-7. Neurosci Lett. 1994. PMID: 8084515

2

Concentrations of amyloid beta protein in cerebrospinal fluid of patients with Alzheimer's disease.

van Gool WA, Kuiper MA, Walstra GJ, Wolters EC, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. Ann Neurol. 1995 Feb;37(2):277-9. doi: 10.1002/ana.410370221. Ann Neurol. 1995. PMID: 7847870

3

[Studies of cerebrospinal fluid diagnosis in Alzheimer's disease: a review of the literature and of current developments].

van Gool WA, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. Tijdschr Gerontol Geriatr. 1992 Dec;23(6):212-6. Tijdschr Gerontol Geriatr. 1992. PMID: 1362298 Review. Dutch.

4

Cerebrospinal fluid markers of Alzheimer's disease.

van Gool WA, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. J Am Geriatr Soc. 1991 Oct;39(10):1025-39. doi: 10.1111/j.1532-5415.1991.tb04052.x. J Am Geriatr Soc. 1991. PMID: 1918775 Review.

5

[Abnormal proteins in Alzheimer's disease].

van Gool WA, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. Ned Tijdschr Geneeskd. 1990 Mar 10;134(10):468-9. Ned Tijdschr Geneeskd. 1990. PMID: 1969120 Review. Dutch. No abstract available.

6

[Prion disease: a new class of neurodegenerative disorders].

van Gool WA, Hoogerwaard EM, Kuiper MA, Portegies P, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. Ned Tijdschr Geneeskd. 1995 Mar 25;139(12):606-13. Ned Tijdschr Geneeskd. 1995. PMID: 7700403 Review. Dutch. No abstract available.

7

Hypokinesia and presenile dementia in a Dutch family with a novel insertion in the prion protein gene.

van Gool WA, Hensels GW, Hoogerwaard EM, Wiezer JH, Wesseling P, Bolhuis PA. van Gool WA, et al. Among authors: bolhuis pa. Brain. 1995 Dec;118 ( Pt 6):1565-71. doi: 10.1093/brain/118.6.1565. Brain. 1995. PMID: 8595485

8

Molecular basis of an adult form of Sandhoff disease: substitution of glutamine for arginine at position 505 of the beta-chain of beta-hexosaminidase results in a labile enzyme.

Bolhuis PA, Ponne NJ, Bikker H, Baas F, Vianney de Jong JM. Bolhuis PA, et al. Biochim Biophys Acta. 1993 Sep 8;1182(2):142-6. doi: 10.1016/0925-4439(93)90134-m. Biochim Biophys Acta. 1993. PMID: 8357844

9

Deletion of the 5'-region in one or two alleles of HEXB in 15 out of 30 patients with Sandhoff disease.

Bolhuis PA, Bikker H. Bolhuis PA, et al. Hum Genet. 1992 Nov;90(3):328-9. doi: 10.1007/BF00220096. Hum Genet. 1992. PMID: 1487253 No abstract available.

10

Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1.

Jöbsis GJ, Weber JW, Barth PG, Keizers H, Baas F, van Schooneveld MJ, van Hilten JJ, Troost D, Geesink HH, Bolhuis PA. Jöbsis GJ, et al. Among authors: bolhuis pa. J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):367-71. doi: 10.1136/jnnp.62.4.367. J Neurol Neurosurg Psychiatry. 1997. PMID: 9120450 Free PMC article.

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