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Items: 12

1.

Integrated multidisciplinary care in Parkinson's disease: a non-randomised, controlled trial (IMPACT).

van der Marck MA, Munneke M, Mulleners W, Hoogerwaard EM, Borm GF, Overeem S, Bloem BR; IMPACT study group..

Lancet Neurol. 2013 Oct;12(10):947-56. doi: 10.1016/S1474-4422(13)70196-0. Epub 2013 Aug 27.

PMID:
23988337
2.

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy.

Schade van Westrum SM, Hoogerwaard EM, Dekker L, Standaar TS, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, van Essen AJ, Leschot NJ, Wilde AA, de Haan RJ, de Visser M, van der Kooi AJ.

Neurology. 2011 Jul 5;77(1):62-6. doi: 10.1212/WNL.0b013e318221ad14. Epub 2011 Jun 22.

PMID:
21700587
3.

The ParkinsonNet concept: development, implementation and initial experience.

Nijkrake MJ, Keus SH, Overeem S, Oostendorp RA, Vlieland TP, Mulleners W, Hoogerwaard EM, Bloem BR, Munneke M.

Mov Disord. 2010 May 15;25(7):823-9. doi: 10.1002/mds.22813.

PMID:
20461798
4.

Dystrophin analysis in carriers of Duchenne and Becker muscular dystrophy.

Hoogerwaard EM, Ginjaar IB, Bakker E, de Visser M.

Neurology. 2005 Dec 27;65(12):1984-6.

PMID:
16380627
5.

[Hypocalcemic delirium due to magnesium sulphate therapy in a pregnant woman with pre-eclampsia].

Ganzevoort JW, Hoogerwaard EM, van der Post JA.

Ned Tijdschr Geneeskd. 2002 Aug 3;146(31):1453-6. Dutch.

PMID:
12190013
6.

Troponin T and troponin I in carriers of Duchenne and Becker muscular dystrophy with cardiac involvement.

Hoogerwaard EM, Schouten Y, van der Kooi AJ, Gorgels JP, de Visser M, Sanders GT.

Clin Chem. 2001 May;47(5):962-3. No abstract available.

7.

[The heartache of muscular dystrophy].

Hoogerwaard EM, Ginjaar HB, Wilde AA, Leschot NJ, de Voogt WG, de Visser M.

Ned Tijdschr Geneeskd. 2000 Nov 11;144(46):2181-4. Review. Dutch.

PMID:
11103252
8.

Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy.

Hoogerwaard EM, van der Wouw PA, Wilde AA, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, van Essen AJ, Leschot NJ, de Visser M.

Neuromuscul Disord. 1999 Jul;9(5):347-51.

PMID:
10407858
9.

Signs and symptoms of Duchenne muscular dystrophy and Becker muscular dystrophy among carriers in The Netherlands: a cohort study.

Hoogerwaard EM, Bakker E, Ippel PF, Oosterwijk JC, Majoor-Krakauer DF, Leschot NJ, Van Essen AJ, Brunner HG, van der Wouw PA, Wilde AA, de Visser M.

Lancet. 1999 Jun 19;353(9170):2116-9.

PMID:
10382696
10.

Evolution of cardiac abnormalities in Becker muscular dystrophy over a 13-year period.

Hoogerwaard EM, de Voogt WG, Wilde AA, van der Wouw PA, Bakker E, van Ommen GJ, de Visser M.

J Neurol. 1997 Oct;244(10):657-63.

PMID:
9402544
11.

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.

Brain. 1995 Dec;118 ( Pt 6):1565-71.

PMID:
8595485
12.

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

van Gool WA, Hoogerwaard EM, Kuiper MA, Portegies P, Bolhuis PA.

Ned Tijdschr Geneeskd. 1995 Mar 25;139(12):606-13. Review. Dutch. No abstract available. Erratum in: Ned Tijdschr Geneeskd 1995 Dec 30;139(52):2768. Ned Tijdschr Geneeskd 1995 May 6;139(18):960.

PMID:
7700403

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