Ippel PF - Search Results

1

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

2

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

3

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

4

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

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

A new variant of sensory ataxic neuropathy with autosomal dominant inheritance.

van Dijk GW, Wokke JH, Oey PL, Franssen H, Ippel PF, Veldman H. van Dijk GW, et al. Among authors: ippel pf. Brain. 1995 Dec;118 ( Pt 6):1557-63. doi: 10.1093/brain/118.6.1557. Brain. 1995. PMID: 8595484

7

Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia.

Schelhaas HJ, Ippel PF, Hageman G, Sinke RJ, van der Laan EN, Beemer FA. Schelhaas HJ, et al. Among authors: ippel pf. J Neurol. 2001 Feb;248(2):113-20. doi: 10.1007/s004150170245. J Neurol. 2001. PMID: 11284128

8

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

9

Familial, alternating Bell's palsy with dominant inheritance.

Hageman G, Ippel PF, Jansen EN, Rozeboom AR. Hageman G, et al. Among authors: ippel pf. Eur Neurol. 1990;30(6):310-3. doi: 10.1159/000117362. Eur Neurol. 1990. PMID: 2289506

10

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

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