Aalfs CM - Search Results

1

Aalfs CM, Vervenne-van Spaendonk R, Pijnenburg YAL, Cohn-Hokke PE, Meijers HJ, Scheltens P. Aalfs CM, et al. Ned Tijdschr Geneeskd. 2017;161:D1774. Ned Tijdschr Geneeskd. 2017. PMID: 28936933 Review. Dutch.

2

[DNA-analysis in hereditary cancer: the importance of a reliable family history].

Kapma S, Leschot NJ, Aalfs CM. Kapma S, et al. Among authors: aalfs cm. Ned Tijdschr Geneeskd. 2005 Jan 8;149(2):57-60. Ned Tijdschr Geneeskd. 2005. PMID: 15688834 Dutch.

3

[A young man with intestinal polyposis and epistaxis].

Menko FH, Jacobs MA, Mager JJ, Nicolaï JJ, Mensenkamp AR, Aalfs CM. Menko FH, et al. Among authors: aalfs cm. Ned Tijdschr Geneeskd. 2014;158:A7398. Ned Tijdschr Geneeskd. 2014. PMID: 25269631 Dutch.

4

[Making better use of the clinical geneticist's expertise; treating physician could request a DNA test for most cancer patients].

Aalfs CM, Westermann AM, van El CG. Aalfs CM, et al. Ned Tijdschr Geneeskd. 2017;161:D1525. Ned Tijdschr Geneeskd. 2017. PMID: 28589870 Dutch.

5

Early life involvement in C9orf72 repeat expansion carriers.

Gossink F, Dols A, Stek ML, Scheltens P, Nijmeijer B, Cohn Hokke P, Dijkstra A, Van Ruissen F, Aalfs C, Pijnenburg YAL. Gossink F, et al. J Neurol Neurosurg Psychiatry. 2022 Jan;93(1):93-100. doi: 10.1136/jnnp-2020-325994. Epub 2021 Apr 27. J Neurol Neurosurg Psychiatry. 2022. PMID: 33906932

6

SORL1 deficiency in human excitatory neurons causes APP-dependent defects in the endolysosome-autophagy network.

Hung C, Tuck E, Stubbs V, van der Lee SJ, Aalfs C, van Spaendonk R, Scheltens P, Hardy J, Holstege H, Livesey FJ. Hung C, et al. Cell Rep. 2021 Jun 15;35(11):109259. doi: 10.1016/j.celrep.2021.109259. Cell Rep. 2021. PMID: 34133918 Free PMC article.

7

[Wilson's disease; diagnosis with the aid of magnetic resonance tomography].

van den Berg JS, Hoogenraad TU, Duyn JA, Verbeeten B Jr, Aalfs CM, de Visser M. van den Berg JS, et al. Among authors: aalfs cm. Ned Tijdschr Geneeskd. 1995 Apr 15;139(15):796-9. Ned Tijdschr Geneeskd. 1995. PMID: 7723883 Dutch.

8

[Smith-Lemli-Opitz syndrome; a special defect in cholesterol metabolism].

Aalfs CM, Hennekam RC, Wanders RJ, Jira PE, Pilon JW, Wijburg FA. Aalfs CM, et al. Ned Tijdschr Geneeskd. 1996 Jul 13;140(28):1463-6. Ned Tijdschr Geneeskd. 1996. PMID: 8766772 Dutch.

9

[Genetic counseling: should side issues become main issues?].

van Langen IM, Aalfs CM, Smets EM, de Haes JC, Jansweijer MC, Leschot NJ. van Langen IM, et al. Among authors: aalfs cm. Ned Tijdschr Geneeskd. 1997 Sep 20;141(38):1801-4. Ned Tijdschr Geneeskd. 1997. PMID: 9545732 Dutch.

10

[Prenatal genetic counseling in pregnancy: the importance of (early) timely referral ].

Aalfs CM, Smets EM, de Haes JC, Leschot NJ. Aalfs CM, et al. Ned Tijdschr Geneeskd. 2001 Aug 18;145(33):1577-81. Ned Tijdschr Geneeskd. 2001. PMID: 11534373 Review. Dutch.

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