Kremer HP - Search Results

1

Aspergillus meningitis: diagnosis by non-culture-based microbiological methods and management.

Verweij PE, Brinkman K, Kremer HP, Kullberg BJ, Meis JF. Verweij PE, et al. Among authors: kremer hp. J Clin Microbiol. 1999 Apr;37(4):1186-9. doi: 10.1128/JCM.37.4.1186-1189.1999. J Clin Microbiol. 1999. PMID: 10074549 Free PMC article.

2

Cervical spinal epidural abscess due to group B streptococcus in a previously healthy elderly male.

Meis JF, Kullberg BJ, Kremer HP, Verweij PE. Meis JF, et al. Among authors: kremer hp. Scand J Infect Dis. 2000;32(5):577. doi: 10.1080/003655400458974. Scand J Infect Dis. 2000. PMID: 11055674 No abstract available.

3

Molecular diagnosis of hereditary hearing impairment.

Kremer H, Hoefsloot LH. Kremer H, et al. Adv Otorhinolaryngol. 2002;61:11-27. doi: 10.1159/000066799. Adv Otorhinolaryngol. 2002. PMID: 12408058 Review. No abstract available.

4

Q10 therapy in patients with idiopathic Parkinson's disease.

Strijks E, Kremer HP, Horstink MW. Strijks E, et al. Among authors: kremer hp. Mol Aspects Med. 1997;18 Suppl:S237-40. doi: 10.1016/s0098-2997(97)00008-3. Mol Aspects Med. 1997. PMID: 9266528 Clinical Trial.

5

Identification of 51 novel exons of the Usher syndrome type 2A (USH2A) gene that encode multiple conserved functional domains and that are mutated in patients with Usher syndrome type II.

van Wijk E, Pennings RJ, te Brinke H, Claassen A, Yntema HG, Hoefsloot LH, Cremers FP, Cremers CW, Kremer H. van Wijk E, et al. Am J Hum Genet. 2004 Apr;74(4):738-44. doi: 10.1086/383096. Epub 2004 Mar 10. Am J Hum Genet. 2004. PMID: 15015129 Free PMC article.

6

Mutations in the calcium-binding motifs of CDH23 and the 35delG mutation in GJB2 cause hearing loss in one family.

de Brouwer AP, Pennings RJ, Roeters M, Van Hauwe P, Astuto LM, Hoefsloot LH, Huygen PL, van den Helm B, Deutman AF, Bork JM, Kimberling WJ, Cremers FP, Cremers CW, Kremer H. de Brouwer AP, et al. Hum Genet. 2003 Feb;112(2):156-63. doi: 10.1007/s00439-002-0833-0. Epub 2002 Oct 29. Hum Genet. 2003. PMID: 12522556

7

Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).

Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW. Pennings RJ, et al. Arch Otolaryngol Head Neck Surg. 2003 Apr;129(4):421-6. doi: 10.1001/archotol.129.4.421. Arch Otolaryngol Head Neck Surg. 2003. PMID: 12707188

8

A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.

Kemperman MH, De Leenheer EM, Huygen PL, van Wijk E, van Duijnhoven G, Cremers FP, Kremer H, Cremers CW. Kemperman MH, et al. Arch Otolaryngol Head Neck Surg. 2004 Mar;130(3):281-8. doi: 10.1001/archotol.130.3.281. Arch Otolaryngol Head Neck Surg. 2004. PMID: 15023833

9

Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).

Luijendijk MW, Van Wijk E, Bischoff AM, Krieger E, Huygen PL, Pennings RJ, Brunner HG, Cremers CW, Cremers FP, Kremer H. Luijendijk MW, et al. Hum Genet. 2004 Jul;115(2):149-56. doi: 10.1007/s00439-004-1137-3. Epub 2004 Jun 2. Hum Genet. 2004. PMID: 15221449

10

USH2A mutation analysis in 70 Dutch families with Usher syndrome type II.

Pennings RJ, Te Brinke H, Weston MD, Claassen A, Orten DJ, Weekamp H, Van Aarem A, Huygen PL, Deutman AF, Hoefsloot LH, Cremers FP, Cremers CW, Kimberling WJ, Kremer H. Pennings RJ, et al. Hum Mutat. 2004 Aug;24(2):185. doi: 10.1002/humu.9259. Hum Mutat. 2004. PMID: 15241801

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