Bernert G - Search Results

1

Long-term MRI observations of childhood-onset relapsing-remitting multiple sclerosis.

Balássy C, Bernert G, Wöber-Bingöl C, Csapó B, Kornek B, Széles J, Fleischmann D, Prayer D. Balássy C, et al. Among authors: bernert g. Neuropediatrics. 2001 Feb;32(1):28-37. doi: 10.1055/s-2001-12219. Neuropediatrics. 2001. PMID: 11315199

2

Occurrence of Andermann syndrome out of French Canada--agenesis of the corpus callosum with neuronopathy.

Hauser E, Bittner R, Liegl C, Bernert G, Zeitlhofer J. Hauser E, et al. Among authors: bernert g. Neuropediatrics. 1993 Apr;24(2):107-10. doi: 10.1055/s-2008-1071524. Neuropediatrics. 1993. PMID: 8292134

3

Effects of oral creatine supplementation in a patient with MELAS phenotype and associated nephropathy.

Barisic N, Bernert G, Ipsiroglu O, Stromberger C, Müller T, Gruber S, Prayer D, Moser E, Bittner RE, Stöckler-Ipsiroglu S. Barisic N, et al. Among authors: bernert g. Neuropediatrics. 2002 Jun;33(3):157-61. doi: 10.1055/s-2002-33679. Neuropediatrics. 2002. PMID: 12200746

4

Auxological, ophthalmological, neurological and MRI findings in 25 Austrian patients with septo-optic dysplasia (SOD). Preliminary data.

Riedl SW, Müllner-Eidenböck A, Prayer D, Bernert G, Frisch H. Riedl SW, et al. Among authors: bernert g. Horm Res. 2002;58 Suppl 3:16-9. doi: 10.1159/000066484. Horm Res. 2002. PMID: 12435890 Clinical Trial.

5

Glatiramer acetate treatment in patients with childhood and juvenile onset multiple sclerosis.

Kornek B, Bernert G, Balassy C, Geldner J, Prayer D, Feucht M. Kornek B, et al. Among authors: bernert g. Neuropediatrics. 2003 Jun;34(3):120-6. doi: 10.1055/s-2003-41274. Neuropediatrics. 2003. PMID: 12910434 Clinical Trial.

6

Degree of hypomyelination and magnetic resonance spectroscopy findings in patients with Pelizaeus Merzbacher phenotype.

Plecko B, Stöckler-Ipsiroglu S, Gruber S, Mlynarik V, Moser E, Simbrunner J, Ebner F, Bernert G, Harrer G, Gal A, Prayer D. Plecko B, et al. Among authors: bernert g. Neuropediatrics. 2003 Jun;34(3):127-36. doi: 10.1055/s-2003-41276. Neuropediatrics. 2003. PMID: 12910435

7

Magnetic resonance imaging in foetuses with bilateral moderate ventriculomegaly and suspected anomaly of the corpus callosum on ultrasound scan.

Blaicher W, Prayer D, Mittermayer C, Pollak A, Bernert G, Deutinger J, Bernaschek G. Blaicher W, et al. Among authors: bernert g. Ultraschall Med. 2003 Aug;24(4):255-60. doi: 10.1055/s-2003-41709. Ultraschall Med. 2003. PMID: 14521152

8

Isolated cytochrome c oxidase deficiency as a cause of MELAS.

Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Thier K, Prayer D, Bernert G, Bittner RE. Rossmanith W, et al. Among authors: bernert g. J Med Genet. 2008 Feb;45(2):117-21. doi: 10.1136/jmg.2007.052076. J Med Genet. 2008. PMID: 18245391

9

Long-term follow-up of pediatric patients treated with mitoxantrone for multiple sclerosis.

Kornek B, Bernert G, Rostasy K, Mlczoch E, Feucht M, Prayer D, Vass K, Seidl R. Kornek B, et al. Among authors: bernert g. Neuropediatrics. 2011 Feb;42(1):7-12. doi: 10.1055/s-0031-1275345. Epub 2011 May 9. Neuropediatrics. 2011. PMID: 21557144

10

Isolated cytochrome c oxidase deficiency as a cause of MELAS.

Rossmanith W, Freilinger M, Roka J, Raffelsberger T, Moser-Their K, Prayer D, Bernert G, Bittner R. Rossmanith W, et al. Among authors: bernert g. BMJ Case Rep. 2009;2009:bcr08.2008.0666. doi: 10.1136/bcr.08.2008.0666. Epub 2009 Jan 23. BMJ Case Rep. 2009. PMID: 21686692 Free PMC article.

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