Sandkuijl LA[Author] - Search Results

Year	Number of Results
1991	2
1992	14
1993	4
1994	11
1995	14
1996	5
1997	4
1998	5
1999	7
2000	1
2001	10
2002	8
2003	12
2004	8
2007	1
2008	1
2024	0

1

Migraine, ataxia and epilepsy: a challenging spectrum of genetically determined calcium channelopathies. Dutch Migraine Genetics Research Group.

Terwindt GM, Ophoff RA, Haan J, Sandkuijl LA, Frants RR, Ferrari MD. Terwindt GM, et al. Among authors: sandkuijl la. Eur J Hum Genet. 1998 Jul-Aug;6(4):297-307. doi: 10.1038/sj.ejhg.5200206. Eur J Hum Genet. 1998. PMID: 9781035 Review.

2

X-linked recessive inheritance of radial ray deficiencies in a family with four affected males.

Galjaard RJ, Kostakoglu N, Hoogeboom JJ, Breedveld GJ, van der Linde HC, Hovius SE, Oostra BA, Sandkuijl LA, Akarsu AN, Heutink P. Galjaard RJ, et al. Among authors: sandkuijl la. Eur J Hum Genet. 2001 Sep;9(9):653-8. doi: 10.1038/sj.ejhg.5200692. Eur J Hum Genet. 2001. PMID: 11571552 Review.

3

Genetic heterogeneity of familial hemiplegic migraine.

Ophoff RA, van Eijk R, Sandkuijl LA, Terwindt GM, Grubben CP, Haan J, Lindhout D, Ferrari MD, Frants RR. Ophoff RA, et al. Among authors: sandkuijl la. Genomics. 1994 Jul 1;22(1):21-6. doi: 10.1006/geno.1994.1340. Genomics. 1994. PMID: 7959770

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: sandkuijl la. Muscle Nerve Suppl. 1995;2:S81-4. Muscle Nerve Suppl. 1995. PMID: 7739631 Free article.

5

Genetic heterogeneity of polycystic kidney disease in Europe.

Peters DJ, Sandkuijl LA. Peters DJ, et al. Among authors: sandkuijl la. Contrib Nephrol. 1992;97:128-39. doi: 10.1159/000421651. Contrib Nephrol. 1992. PMID: 1633713 No abstract available.

6

Schizophrenia susceptibility and chromosome 6p24-22.

Mowry BJ, Nancarrow DJ, Lennon DP, Sandkuijl LA, Crowe RR, Silverman JM, Mohs RC, Siever LJ, Endicott J, Sharpe L, et al. Mowry BJ, et al. Among authors: sandkuijl la. Nat Genet. 1995 Nov;11(3):233-4. doi: 10.1038/ng1195-233. Nat Genet. 1995. PMID: 7581441 No abstract available.

7

A recombination event that redefines the Huntington disease region.

Snell RG, Thompson LM, Tagle DA, Holloway TL, Barnes G, Harley HG, Sandkuijl LA, MacDonald ME, Collins FS, Gusella JF, et al. Snell RG, et al. Among authors: sandkuijl la. Am J Hum Genet. 1992 Aug;51(2):357-62. Am J Hum Genet. 1992. PMID: 1386495 Free PMC article.

8

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy.

Wijmenga C, Hewitt JE, Sandkuijl LA, Clark LN, Wright TJ, Dauwerse HG, Gruter AM, Hofker MH, Moerer P, Williamson R, et al. Wijmenga C, et al. Among authors: sandkuijl la. Nat Genet. 1992 Sep;2(1):26-30. doi: 10.1038/ng0992-26. Nat Genet. 1992. PMID: 1363881

9

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa.

Bleeker-Wagemakers LM, Gal A, Kumar-Singh R, van den Born LI, Li Y, Schwinger E, Sandkuijl LA, Bergen AA, Kenna P, Humphries P, et al. Bleeker-Wagemakers LM, et al. Among authors: sandkuijl la. Genomics. 1992 Nov;14(3):811-2. doi: 10.1016/s0888-7543(05)80195-8. Genomics. 1992. PMID: 1427914

10

Molecular genetic reevaluation of the Dutch hyperekplexia family.

Tijssen MA, Shiang R, van Deutekom J, Boerman RH, Wasmuth JJ, Sandkuijl LA, Frants RR, Padberg GW. Tijssen MA, et al. Among authors: sandkuijl la. Arch Neurol. 1995 Jun;52(6):578-82. doi: 10.1001/archneur.1995.00540300052012. Arch Neurol. 1995. PMID: 7763205 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

107 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

107 results

Results by year