dr. Nathalie Bax

Oogarts
Zorgkaart Nederland Klantwaardering Nathalie Bax
9.0
dr. Nathalie Bax

Werkervaring/Opleiding

  • Opleiding tot oogarts: Radboudumc
  • PhD: “Stargardt disease” olv prof. dr. Carel Hoyng en prof. dr. Frans Cremers

 

Lees meer

Publicaties

  • Foveal Sparing in Central Retinal Dystrophies. Bax NM, Valkenburg D, Lambertus S, Klevering BJ, Boon CJF, Holz FG, Cremers FPM, Fleckenstein M, Hoyng CB, Lindner M; Foveal Sparing Atrophy Study Team (FAST).Bax NM, et al. Invest Ophthalmol Vis Sci. 2019 Aug 1;60(10):3456-3467. doi: 10.1167/iovs.18-26533.Invest Ophthalmol Vis Sci. 2019. PMID: 31398255
  • In Silico Functional Meta-Analysis of 5,962 ABCA4 Variants in 3,928 Retinal Dystrophy Cases.
  • Cornelis SS, Bax NM, Zernant J, Allikmets R, Fritsche LG, den Dunnen JT, Ajmal M, Hoyng CB, Cremers FP.Cornelis SS, et al. Hum Mutat. 2017 Apr;38(4):400-408. doi: 10.1002/humu.23165. Epub 2017 Feb 3.Hum Mutat. 2017. PMID: 28044389
  • Foveal sparing in Stargardt disease. van Huet RA, Bax NM, Westeneng-Van Haaften SC, Muhamad M, Zonneveld-Vrieling MN, Hoefsloot LH, Cremers FP, Boon CJ, Klevering BJ, Hoyng CB.van Huet RA, et al. Invest Ophthalmol Vis Sci. 2014 Oct 16;55(11):7467-78. doi: 10.1167/iovs.13-13825.Invest Ophthalmol Vis Sci. 2014. PMID: 25324290
  • The absence of fundus abnormalities in Stargardt disease. Bax NM, Lambertus S, Cremers FPM, Klevering BJ, Hoyng CB.Bax NM, et al. Graefes Arch Clin Exp Ophthalmol. 2019 Jun;257(6):1147-1157. doi: 10.1007/s00417-019-04280-8. Epub 2019 Mar 22.Graefes Arch Clin Exp Ophthalmol. 2019. PMID: 30903310
  • Highly Variable Disease Courses in Siblings with Stargardt Disease. Valkenburg D, Runhart EH, Bax NM, Liefers B, Lambertus SL, Sánchez CI, Cremers FPM, Hoyng CB.Valkenburg D, et al. Ophthalmology. 2019 Dec;126(12):1712-1721. doi: 10.1016/j.ophtha.2019.07.010. Epub 2019 Jul 16.Ophthalmology. 2019. PMID: 31522899
  • Asymmetric Inter-Eye Progression in Stargardt Disease. Lambertus S, Bax NM, Groenewoud JM, Cremers FP, van der Wilt GJ, Klevering BJ, Theelen T, Hoyng CB.Lambertus S, et al. Invest Ophthalmol Vis Sci. 2016 Dec 1;57(15):6824-6830. doi: 10.1167/iovs.16-20963.Invest Ophthalmol Vis Sci. 2016. PMID: 28002570
  • Photoreceptor Progenitor mRNA Analysis Reveals Exon Skipping Resulting from the ABCA4 c.5461-10T→C Mutation in Stargardt Disease. Sangermano R, Bax NM, Bauwens M, van den Born LI, De Baere E, Garanto A, Collin RW, Goercharn-Ramlal AS, den Engelsman-van Dijk AH, Rohrschneider K, Hoyng CB, Cremers FP, Albert S.Sangermano R, et al. Ophthalmology. 2016 Jun;123(6):1375-85. doi: 10.1016/j.ophtha.2016.01.053. Epub 2016 Mar 12.Ophthalmology. 2016. PMID: 26976702.
  • Antisense Oligonucleotide-Based Splicing Correction in Individuals with Leber Congenital Amaurosis due to Compound Heterozygosity for the c.2991+1655A>G Mutation in CEP290. Duijkers L, van den Born LI, Neidhardt J, Bax NM, Pierrache LHM, Klevering BJ, Collin RWJ, Garanto A.Duijkers L, et al. Int J Mol Sci. 2018 Mar 7;19(3):753. doi: 10.3390/ijms19030753.Int J Mol Sci. 2018. PMID: 29518907.

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