Padberg GW - Search Results

1

Population-based incidence and prevalence of facioscapulohumeral dystrophy.

Deenen JC, Arnts H, van der Maarel SM, Padberg GW, Verschuuren JJ, Bakker E, Weinreich SS, Verbeek AL, van Engelen BG. Deenen JC, et al. Among authors: padberg gw. Neurology. 2014 Sep 16;83(12):1056-9. doi: 10.1212/WNL.0000000000000797. Epub 2014 Aug 13. Neurology. 2014. PMID: 25122204 Free PMC article.

2

Adult adrenoleukodystrophy: the clinical spectrum in a large Dutch family.

Zwetsloot CP, Padberg GW, van Seters AP, Maaswinkel-Mooy PD, Onkenhout W. Zwetsloot CP, et al. Among authors: padberg gw. J Neurol. 1992 Feb;239(2):107-11. doi: 10.1007/BF00862985. J Neurol. 1992. PMID: 1313076

3

Why cells die in facioscapulohumeral muscular dystrophy.

Padberg GW. Padberg GW. Clin Neurol Neurosurg. 1992;94 Suppl:S21-4. doi: 10.1016/0303-8467(92)90012-r. Clin Neurol Neurosurg. 1992. PMID: 1320508 Review. No abstract available.

4

The influence of handedness on the distribution of muscular weakness of the arm in facioscapulohumeral muscular dystrophy.

Brouwer OF, Padberg GW, van der Ploeg RJ, Ruys CJ, Brand R. Brouwer OF, et al. Among authors: padberg gw. Brain. 1992 Oct;115 ( Pt 5):1587-98. doi: 10.1093/brain/115.5.1587. Brain. 1992. PMID: 1422805

5

Hearing loss in facioscapulohumeral muscular dystrophy.

Brouwer OF, Padberg GW, Ruys CJ, Brand R, de Laat JA, Grote JJ. Brouwer OF, et al. Among authors: padberg gw. Neurology. 1991 Dec;41(12):1878-81. doi: 10.1212/wnl.41.12.1878. Neurology. 1991. PMID: 1745341

6

Location of facioscapulohumeral muscular dystrophy gene on chromosome 4.

Wijmenga C, Frants RR, Brouwer OF, Moerer P, Weber JL, Padberg GW. Wijmenga C, et al. Among authors: padberg gw. Lancet. 1990 Sep 15;336(8716):651-3. doi: 10.1016/0140-6736(90)92148-b. Lancet. 1990. PMID: 1975852

7

Facioscapulohumeral muscular dystrophy gene in Dutch families is not linked to markers for familial adenomatous polyposis on the long arm of chromosome 5.

Wijmenga C, Frants RR, Brouwer OF, van der Klift HM, Meera Khan P, Padberg GW. Wijmenga C, et al. Among authors: padberg gw. J Neurol Sci. 1990 Feb;95(2):225-9. doi: 10.1016/0022-510x(90)90245-i. J Neurol Sci. 1990. PMID: 2157824

8

The FSHD-linked locus D4F104S1 (p13E-11) on 4q35 has a homologue on 10qter.

Bakker E, Wijmenga C, Vossen RH, Padberg GW, Hewitt J, van der Wielen M, Rasmussen K, Frants RR. Bakker E, et al. Among authors: padberg gw. Muscle Nerve Suppl. 1995;2:S39-44. Muscle Nerve Suppl. 1995. PMID: 7739624 Free article.

9

Early onset facioscapulohumeral muscular dystrophy.

Brouwer OF, Padberg GW, Bakker E, Wijmenga C, Frants RR. Brouwer OF, et al. Among authors: padberg gw. Muscle Nerve Suppl. 1995;2:S67-72. Muscle Nerve Suppl. 1995. PMID: 7739629

10

On the significance of retinal vascular disease and hearing loss in facioscapulohumeral muscular dystrophy.

Padberg GW, Brouwer OF, de Keizer RJ, Dijkman G, Wijmenga C, Grote JJ, Frants RR. Padberg GW, et al. Muscle Nerve Suppl. 1995;2:S73-80. Muscle Nerve Suppl. 1995. PMID: 7739630 Free article.

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