Padberg GW - Search Results

1

Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy.

Tim RW, Gilbert JR, Stajich JM, Rampersaud E, Viles KD, Tawil R, Padberg GW, Frants R, van der Maarel S, Bossen EH, Friedman AH, Pericak-Vance MA, Speer MC. Tim RW, et al. Among authors: padberg gw. J Clin Neuromuscul Dis. 2001 Sep;3(1):1-7. doi: 10.1097/00131402-200109000-00001. J Clin Neuromuscul Dis. 2001. PMID: 19078645

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

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

4

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.

5

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

6

Mapping of facioscapulohumeral muscular dystrophy gene to chromosome 4q35-qter by multipoint linkage analysis and in situ hybridization.

Wijmenga C, Padberg GW, Moerer P, Wiegant J, Liem L, Brouwer OF, Milner EC, Weber JL, van Ommen GB, Sandkuyl LA, et al. Wijmenga C, et al. Among authors: padberg gw. Genomics. 1991 Apr;9(4):570-5. doi: 10.1016/0888-7543(91)90348-i. Genomics. 1991. PMID: 2037288

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

An exclusion map for facioscapulohumeral (Landouzy-Déjérine) disease.

Sarfarazi M, Upadhyaya M, Padberg G, Pericak-Vance M, Siddique T, Lucotte G, Lunt P. Sarfarazi M, et al. J Med Genet. 1989 Aug;26(8):481-4. doi: 10.1136/jmg.26.8.481. J Med Genet. 1989. PMID: 2769720 Free PMC article.

9

Linkage studies in facioscapulohumeral muscular dystrophy.

Padberg GW, Klasen EC, Volkers WS, De Lange GG, Wintzen AR. Padberg GW, et al. Muscle Nerve. 1988 Aug;11(8):833-5. doi: 10.1002/mus.880110806. Muscle Nerve. 1988. PMID: 3140007

10

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.

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