Brouwer OF - Search Results

1

Partial cosegregation of familial hemiplegic migraine and a benign familial infantile epileptic syndrome.

Terwindt GM, Ophoff RA, Lindhout D, Haan J, Halley DJ, Sandkuijl LA, Brouwer OF, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: brouwer of. Epilepsia. 1997 Aug;38(8):915-21. doi: 10.1111/j.1528-1157.1997.tb01257.x. Epilepsia. 1997. PMID: 9579893 Free article.

2

Refinement of the chromosome 16 locus for benign familial infantile convulsions.

Callenbach PM, van den Boogerd EH, de Coo RF, ten Houten R, Oosterwijk JC, Hageman G, Frants RR, Brouwer OF, van den Maagdenberg AM. Callenbach PM, et al. Among authors: brouwer of. Clin Genet. 2005 Jun;67(6):517-25. doi: 10.1111/j.1399-0004.2005.00445.x. Clin Genet. 2005. PMID: 15857419

3

Acute confusional migraine. Case report and review of literature.

Haan J, Ferrari MD, Brouwer OF. Haan J, et al. Among authors: brouwer of. Clin Neurol Neurosurg. 1988;90(3):275-8. doi: 10.1016/0303-8467(88)90037-6. Clin Neurol Neurosurg. 1988. PMID: 3197358

4

Facioscapulohumeral muscular dystrophy in the Dutch population.

Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Padberg GW, et al. Among authors: brouwer of. Muscle Nerve Suppl. 1995;2:S81-4. Muscle Nerve Suppl. 1995. PMID: 7739631 Free article.

5

Facioscapulohumeral muscular dystrophy: the impact of genetic research.

Brouwer OF, Wijmenga C, Frants RR, Padberg GW. Brouwer OF, et al. Clin Neurol Neurosurg. 1993 Mar;95(1):9-21. doi: 10.1016/0303-8467(93)90086-v. Clin Neurol Neurosurg. 1993. PMID: 8095870 Review.

6

Facioscapulohumeral muscular dystrophy in early childhood.

Brouwer OF, Padberg GW, Wijmenga C, Frants RR. Brouwer OF, et al. Arch Neurol. 1994 Apr;51(4):387-94. doi: 10.1001/archneur.1994.00540160085011. Arch Neurol. 1994. PMID: 8155016 Review.

7

Angelman syndrome without detectable chromosome 15q11-13 anomaly: clinical study of familial and isolated cases.

Laan LA, Halley DJ, den Boer AT, Hennekam RC, Renier WO, Brouwer OF. Laan LA, et al. Among authors: brouwer of. Am J Med Genet. 1998 Mar 19;76(3):262-8. Am J Med Genet. 1998. PMID: 9508247 Review.

8

Facioscapulohumeral muscular dystrophy in the Dutch population.

Padberg GW, Frants RR, Brouwer OF, Wijmenga C, Bakker E, Sandkuijl LA. Padberg GW, et al. Among authors: brouwer of. Muscle Nerve Suppl. 1995;(2):S81-4. Muscle Nerve Suppl. 1995. PMID: 23573591

9

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: brouwer of. Lancet. 1990 Sep 15;336(8716):651-3. doi: 10.1016/0140-6736(90)92148-b. Lancet. 1990. PMID: 1975852

10

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: brouwer of. J Neurol Sci. 1990 Feb;95(2):225-9. doi: 10.1016/0022-510x(90)90245-i. J Neurol Sci. 1990. PMID: 2157824

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