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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 2
1979 5
1980 2
1981 2
1982 3
1983 3
1984 3
1985 2
1986 3
1987 6
1988 5
1989 6
1990 8
1991 6
1992 7
1993 11
1994 10
1995 16
1996 16
1997 7
1998 4
2000 3
2001 1
2003 1
2005 1
2012 1
2024 0

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134 results

Results by year

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Page 1
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.
Cultured human muscle cells and respiratory chain deficiencies.
Herzberg NH, Bolhuis PA, van den Bogert C, Barth PG. Herzberg NH, et al. Among authors: bolhuis pa. Neuromuscul Disord. 1994 Jan;4(1):3-11. doi: 10.1016/0960-8966(94)90042-6. Neuromuscul Disord. 1994. PMID: 8173349 Review.
Genetic localization of Bethlem myopathy.
Jobsis GJ, Bolhuis PA, Boers JM, Baas F, Wolterman RA, Hensels GW, de Visser M. Jobsis GJ, et al. Among authors: bolhuis pa. Neurology. 1996 Mar;46(3):779-82. doi: 10.1212/wnl.46.3.779. Neurology. 1996. PMID: 8618682
[Importance of pharmacogenetics].
Bolhuis PA. Bolhuis PA. Ned Tijdschr Geneeskd. 2001 Jan 6;145(1):15-8. Ned Tijdschr Geneeskd. 2001. PMID: 11198959 Review. Dutch.
Two intronic mutations in the adrenoleukodystrophy gene.
Kemp S, Ligtenberg MJ, van Geel BM, Barth PG, Sarde CO, van Oost BA, Bolhuis PA. Kemp S, et al. Among authors: bolhuis pa. Hum Mutat. 1995;6(3):272-3. doi: 10.1002/humu.1380060316. Hum Mutat. 1995. PMID: 8535452 No abstract available.
An unusual variant of Becker muscular dystrophy.
de Visser M, Bakker E, Defesche JC, Bolhuis PA, van Ommen GJ. de Visser M, et al. Among authors: bolhuis pa. Ann Neurol. 1990 May;27(5):578-81. doi: 10.1002/ana.410270521. Ann Neurol. 1990. PMID: 2193611
[Molecular genetics of Duchenne's disease].
Bolhuis PA. Bolhuis PA. Ned Tijdschr Geneeskd. 1989 Jul 8;133(27):1347-8. Ned Tijdschr Geneeskd. 1989. PMID: 2571948 Review. Dutch. No abstract available.
X chromosome inactivation in carriers of Barth syndrome.
Orstavik KH, Orstavik RE, Naumova AK, D'Adamo P, Gedeon A, Bolhuis PA, Barth PG, Toniolo D. Orstavik KH, et al. Among authors: bolhuis pa. Am J Hum Genet. 1998 Nov;63(5):1457-63. doi: 10.1086/302095. Am J Hum Genet. 1998. PMID: 9792874 Free PMC article.
134 results