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The evolution of renal angiomyolipomas in patients with tuberous sclerosis.
van Baal JG, Smits NJ, Keeman JN, Lindhout D, Verhoef S. van Baal JG, et al. Among authors: lindhout d. J Urol. 1994 Jul;152(1):35-8. doi: 10.1016/s0022-5347(17)32809-4. J Urol. 1994. PMID: 8201681
Mutational spectrum of the TSC1 gene in a cohort of 225 tuberous sclerosis complex patients: no evidence for genotype-phenotype correlation.
van Slegtenhorst M, Verhoef S, Tempelaars A, Bakker L, Wang Q, Wessels M, Bakker R, Nellist M, Lindhout D, Halley D, van den Ouweland A. van Slegtenhorst M, et al. Among authors: lindhout d. J Med Genet. 1999 Apr;36(4):285-9. J Med Genet. 1999. PMID: 10227394 Free PMC article.
[From gene to disease; TSC1 and TSC2 genes and tuberous sclerosis complex].
Verhoef S, Lindhout D, Halley DJ, van den Ouweland AM. Verhoef S, et al. Among authors: lindhout d. Ned Tijdschr Geneeskd. 2001 Oct 6;145(40):1928-30. Ned Tijdschr Geneeskd. 2001. PMID: 11675974 Review. Dutch.
Analysis of TSC2 stop codon variants found in tuberous sclerosis patients.
Goedbloed MA, Nellist M, Verhaaf B, Reuser AJ, Lindhout D, Sunde L, Verhoef S, Halley DJ, van den Ouweland AM. Goedbloed MA, et al. Among authors: lindhout d. Eur J Hum Genet. 2001 Nov;9(11):823-8. doi: 10.1038/sj.ejhg.5200728. Eur J Hum Genet. 2001. PMID: 11781698
Large deletion at the TSC1 locus in a family with tuberous sclerosis complex.
Nellist M, Sancak O, Goedbloed MA, van Veghel-Plandsoen M, Maat-Kievit A, Lindhout D, Eussen BH, de Klein A, Halley DJ, van den Ouweland AM. Nellist M, et al. Among authors: lindhout d. Genet Test. 2005 Fall;9(3):226-30. doi: 10.1089/gte.2005.9.226. Genet Test. 2005. PMID: 16225402
Identification of a large insertion and two novel point mutations (3671del8 and S1221X) in tuberous sclerosis complex (TSC) patients. Mutations in brief no. 119. Online.
Wang Q, Verhoef S, Tempelaars AM, Bakker PL, Vrtel R, Hesseling-Janssen AL, Nellist M, Oranje AP, Stroink H, Lindhout D, Halley DJ, van den Ouweland AM. Wang Q, et al. Among authors: lindhout d. Hum Mutat. 1998;11(4):331-2. doi: 10.1002/(SICI)1098-1004(1998)11:4<331::AID-HUMU12>3.0.CO;2-3. Hum Mutat. 1998. PMID: 10215407
Malignant pancreatic tumour within the spectrum of tuberous sclerosis complex in childhood.
Verhoef S, van Diemen-Steenvoorde R, Akkersdijk WL, Bax NM, Ariyurek Y, Hermans CJ, van Nieuwenhuizen O, Nikkels PG, Lindhout D, Halley DJ, Lips K, van den Ouweland AM. Verhoef S, et al. Among authors: lindhout d. Eur J Pediatr. 1999 Apr;158(4):284-7. doi: 10.1007/s004310051073. Eur J Pediatr. 1999. PMID: 10206124
Recurrent mutation 4882delTT in the GAP-related domain of the tuberous sclerosis TSC2 gene.
Verhoef S, Vrtel R, Bakker L, Stolte-Dijkstra I, Nellist M, Begeer JH, Zaremba J, Jozwiak S, Tempelaars AM, Lindhout D, Halley DJ, van den Ouweland AM. Verhoef S, et al. Among authors: lindhout d. Hum Mutat. 1998;Suppl 1:S85-7. doi: 10.1002/humu.1380110129. Hum Mutat. 1998. PMID: 9452050 No abstract available.
Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.
van Slegtenhorst M, de Hoogt R, Hermans C, Nellist M, Janssen B, Verhoef S, Lindhout D, van den Ouweland A, Halley D, Young J, Burley M, Jeremiah S, Woodward K, Nahmias J, Fox M, Ekong R, Osborne J, Wolfe J, Povey S, Snell RG, Cheadle JP, Jones AC, Tachataki M, Ravine D, Sampson JR, Reeve MP, Richardson P, Wilmer F, Munro C, Hawkins TL, Sepp T, Ali JB, Ward S, Green AJ, Yates JR, Kwiatkowska J, Henske EP, Short MP, Haines JH, Jozwiak S, Kwiatkowski DJ. van Slegtenhorst M, et al. Among authors: lindhout d. Science. 1997 Aug 8;277(5327):805-8. doi: 10.1126/science.277.5327.805. Science. 1997. PMID: 9242607
[Tuberous sclerosis].
Stroink H, Oranje AP, Hoff M, Lindhout D, Willems MH, Fleury P. Stroink H, et al. Among authors: lindhout d. Ned Tijdschr Geneeskd. 1990 Aug 11;134(32):1535-40. Ned Tijdschr Geneeskd. 1990. PMID: 2202910 Review. Dutch. No abstract available.
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