Rabenau J - Search Results

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2011	1
2016	1
2018	1
2025	0

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The German ROP Registry: data from 90 infants treated for retinopathy of prematurity.

Walz JM, Bemme S, Pielen A, Aisenbrey S, Breuß H, Alex AF, Wagenfeld L, Schiedel S, Krohne TU, Stahl A; Retina.net ROP Registry. Walz JM, et al. Acta Ophthalmol. 2016 Dec;94(8):e744-e752. doi: 10.1111/aos.13069. Epub 2016 May 20. Acta Ophthalmol. 2016. PMID: 27197876 Free article.

Characterization of two common 5' polymorphisms in PEX1 and correlation to survival in PEX1 peroxisome biogenesis disorder patients.

Thoms S, Grønborg S, Rabenau J, Ohlenbusch A, Rosewich H, Gärtner J. Thoms S, et al. Among authors: rabenau j. BMC Med Genet. 2011 Aug 16;12:109. doi: 10.1186/1471-2350-12-109. BMC Med Genet. 2011. PMID: 21846392 Free PMC article.

[Treated cases of retinopathy of prematurity in Germany : 5-year data from the Retina.net ROP registry].

Walz JM, Bemme S, Reichl S, Akman S, Breuß H, Süsskind D, Glitz B, Müller VC, Wagenfeld L, Gabel-Pfisterer A, Aisenbrey S, Engelmann K, Koutsonas A, Krohne TU, Stahl A; Retina.net ROP-Register-Studiengruppe. Walz JM, et al. Ophthalmologe. 2018 Jun;115(6):476-488. doi: 10.1007/s00347-018-0701-5. Ophthalmologe. 2018. PMID: 29637302 German.

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