Padberg GW - Search Results

1

No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy.

van der Kooi EL, de Greef JC, Wohlgemuth M, Frants RR, van Asseldonk RJ, Blom HJ, van Engelen BG, van der Maarel SM, Padberg GW. van der Kooi EL, et al. Among authors: padberg gw. Neuromuscul Disord. 2006 Nov;16(11):766-9. doi: 10.1016/j.nmd.2006.08.005. Epub 2006 Sep 26. Neuromuscul Disord. 2006. PMID: 17005397 Free article.

2

Transmission of de-novo mutation associated with facioscapulohumeral muscular dystrophy.

Wijmenga C, Brouwer OF, Padberg GW, Frants RR. Wijmenga C, et al. Among authors: padberg gw. Lancet. 1992 Oct 17;340(8825):985-6. doi: 10.1016/0140-6736(92)92885-j. Lancet. 1992. PMID: 1357400 No abstract available.

3

Diagnostic criteria for facioscapulohumeral muscular dystrophy.

Padberg GW, Lunt PW, Koch M, Fardeau M. Padberg GW, et al. Neuromuscul Disord. 1991;1(4):231-4. doi: 10.1016/0960-8966(91)90094-9. Neuromuscul Disord. 1991. PMID: 1822799 No abstract available.

4

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

5

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

6

Fish mapping of 250 cosmid and 26 YAC clones to chromosome 4 with special emphasis on the FSHD region at 4q35.

Wijmenga C, Dauwerse HG, Padberg GW, Meyer N, Murray JC, Mills K, van Ommen GB, Hofker MH, Frants RR. Wijmenga C, et al. Among authors: padberg gw. Muscle Nerve Suppl. 1995;2:S14-8. Muscle Nerve Suppl. 1995. PMID: 7739620 Free article.

7

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35.

van Deutekom JC, Hofker MH, Romberg S, van Geel M, Rommens J, Wright TJ, Hewitt JE, Padberg GW, Wijmenga C, Frants RR. van Deutekom JC, et al. Among authors: padberg gw. Muscle Nerve Suppl. 1995;2:S19-26. Muscle Nerve Suppl. 1995. PMID: 7739621 Free article.

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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