Ippel PF - Search Results

1

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. Hoogerwaard EM, et al. Among authors: ippel pf. Lancet. 1999 Jun 19;353(9170):2116-9. doi: 10.1016/s0140-6736(98)10028-4. Lancet. 1999. PMID: 10382696

2

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. Hoogerwaard EM, et al. Among authors: ippel pf. Neuromuscul Disord. 1999 Jul;9(5):347-51. doi: 10.1016/s0960-8966(99)00018-8. Neuromuscul Disord. 1999. PMID: 10407858

3

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. Schade van Westrum SM, et al. Among authors: ippel pf. Neurology. 2011 Jul 5;77(1):62-6. doi: 10.1212/WNL.0b013e318221ad14. Epub 2011 Jun 22. Neurology. 2011. PMID: 21700587

4

Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples.

Straathof CS, Van Heusden D, Ippel PF, Post JG, Voermans NC, De Visser M, Brusse E, Van Den Bergen JC, Van Der Kooi AJ, Verschuuren JJ, Ginjaar HB. Straathof CS, et al. Among authors: ippel pf. Muscle Nerve. 2016 Jan;53(1):44-8. doi: 10.1002/mus.24691. Epub 2015 Jun 3. Muscle Nerve. 2016. PMID: 25900853

5

Diagnostic, predictive, and prenatal testing for facioscapulohumeral muscular dystrophy: diagnostic approach for sporadic and familial cases.

Bakker E, Van der Wielen MJ, Voorhoeve E, Ippel PF, Padberg GW, Frants RR, Wijmenga C. Bakker E, et al. Among authors: ippel pf. J Med Genet. 1996 Jan;33(1):29-35. doi: 10.1136/jmg.33.1.29. J Med Genet. 1996. PMID: 8825045 Free PMC article.

6

Prenatal testing for Huntington's disease in the Netherlands from 1998 to 2008.

van Rij MC, de Koning Gans PA, Aalfs CM, Elting M, Ippel PF, Maat-Kievit JA, Vermeer S, Verschuuren-Bemelmans CC, van Belzen MJ, Belfroid RD, Losekoot M, Geraedts JP, Roos RA, Tibben A, de Die-Smulders CE, Bijlsma EK. van Rij MC, et al. Among authors: ippel pf. Clin Genet. 2014 Jan;85(1):78-86. doi: 10.1111/cge.12090. Epub 2013 Mar 27. Clin Genet. 2014. PMID: 23350614

7

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.

van de Warrenburg BP, Sinke RJ, Verschuuren-Bemelmans CC, Scheffer H, Brunt ER, Ippel PF, Maat-Kievit JA, Dooijes D, Notermans NC, Lindhout D, Knoers NV, Kremer HP. van de Warrenburg BP, et al. Among authors: ippel pf. Neurology. 2002 Mar 12;58(5):702-8. doi: 10.1212/wnl.58.5.702. Neurology. 2002. PMID: 11889231

8

[DNA and dystrophin analysis in Duchenne's and Becker's disease; benefit to the patient].

Jennekens FG, Ippel PF. Jennekens FG, et al. Among authors: ippel pf. Ned Tijdschr Geneeskd. 1993 Jan 9;137(2):61-3. Ned Tijdschr Geneeskd. 1993. PMID: 8421528 Dutch. No abstract available.

9

Differences between hereditary motor and sensory neuropathy type 2 and chronic idiopathic axonal neuropathy. A clinical and electrophysiological study.

Teunissen LL, Notermans NC, Franssen H, van der Graaf Y, Oey PL, Linssen WH, van Engelen BG, Ippel PF, van Dijk GW, Gabreëls-Festen AA, Wokke JH. Teunissen LL, et al. Among authors: ippel pf. Brain. 1997 Jun;120 ( Pt 6):955-62. doi: 10.1093/brain/120.6.955. Brain. 1997. PMID: 9217680

10

A Dutch family with benign hereditary chorea of early onset: differentiation from Huntington's disease.

Hageman G, Ippel PF, van Hout MS, Rozeboom AR. Hageman G, et al. Among authors: ippel pf. Clin Neurol Neurosurg. 1996 May;98(2):165-70. doi: 10.1016/0303-8467(96)00015-7. Clin Neurol Neurosurg. 1996. PMID: 8836592

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