E-LIB Suche - Ergebnisse für: Ippel, P. F.

1

G.P.1:

Straathof, C.S.M. ; van Heusden, D. ; Ippel, P.F....
Neuromuscular Disorders. 24 (2014) 9-10 - p. 794 , 2014

Link: https://doi.org/10.1016/..

2

Cardiac abnormalities in a follow-up study on carriers of D..:

van Westrum, S.M. Schade ; Hoogerwaard, E.M. ; Dekker, L....
Neurology. 77 (2011) 1 - p. 62-66 , 2011

Link: https://doi.org/10.1212/..

3

WRN mutations in Werner syndrome patients: genomic rearrang..:

Friedrich, Katrin ; Lee, Lin ; Leistritz, Dru F....
Human Genetics. 128 (2010) 1 - p. 103-111 , 2010

Link: https://doi.org/10.1007/..

4

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goe..:

Gierga, K. ; Schelhaas, H. J. ; Brunt, E. R....
Neuropathology and Applied Neurobiology. 35 (2009) 5 - p. 515-527 , 2009

Link: https://doi.org/10.1111/..

5

D.P.3.03 Inflammatory myopathy in scapulo-ilio-peroneal atr..:

van der Kooi, A.J. ; Kraak, M.M.J. ; Ippel, P.F....
Neuromuscular Disorders. 18 (2008) 9-10 - p. 765-766 , 2008

Link: https://doi.org/10.1016/..

6

Gly118Asp is a SCA14 founder mutation in the Dutch ataxia p..:

Verbeek, Dineke S. ; Warrenburg, Bart P. C. van de ; Hennekam, F. A. M....
Human Genetics. 117 (2005) 1 - p. 88-91 , 2005

Link: https://doi.org/10.1007/..

7

Spinocerebellar ataxias in the Netherlands: Prevalence and ..:

van de Warrenburg, B.P.C. ; Sinke, R.J. ; Verschuuren–Bemelmans, C.C....
Neurology. 58 (2002) 5 - p. 702-708 , 2002

Link: https://doi.org/10.1212/..

8

Clinical and genetic analysis of a four-generation family w..:

Schelhaas, H.J. ; Ippel, P.F. ; Hageman, G....
Journal of Neurology. 248 (2001) 2 - p. 113-120 , 2001

Link: https://doi.org/10.1007/..

9

Similarities and differences in the phenotype, genotype and..:

Schelhaas, H. J. ; Ippel, P. F. ; Beemer, F. A..
European Journal of Neurology. 7 (2000) 3 - p. 309-314 , 2000

Link: https://doi.org/10.1046/..

10

Cardiac involvement in carriers of Duchenne and Becker musc..:

Hoogerwaard, E.M. ; van der Wouw, P.A. ; Wilde, A.A.M....
Neuromuscular Disorders. 9 (1999) 5 - p. 347-351 , 1999

Link: https://doi.org/10.1016/..

11

Atelencephalic microcephaly: a case report and review of th..:

Ippel, P. F. ; Breslau-Siderius, E. J. ; Hack, W. W. M....
European Journal of Pediatrics. 157 (1998) 6 - p. 493-497 , 1998

Link: https://doi.org/10.1007/..

12

A Dutch family with benign hereditary chorea of early onset..:

Hageman, G. ; Ippel, P.F. ; van Hout, M.S.E..
Clinical Neurology and Neurosurgery. 98 (1996) 2 - p. 165-170 , 1996

Link: https://doi.org/10.1016/..

13

A new variant of sensory ataxic neuropathy with autosomal d..:

Dijk, G. W. van ; Wokke, J. H. J. ; Oey, P. L....
Brain. 118 (1995) 6 - p. 1557-1563 , 1995

Link: https://doi.org/10.1093/..

14

Greig cephalopolysyndactyly syndrome in a large family: a c..:

AUSEMS, M. G.E.M. ; IPPEL, P. F. ; A RENARDEL DE LAVALETTE, P. A.W.
Clinical Dysmorphology. 3 (1994) 1 - p. 21???30 , 1994

Link: https://doi.org/10.1097/..

15

DOOR syndrome: additional case and literature review:

BOS, C. J.M. ; IPPEL, P. F. ; BEEMER, F. A.
Clinical Dysmorphology. 3 (1994) 1 - p. 15???20 , 1994

Link: https://doi.org/10.1097/..