Neubauer BA - Search Results

1

Progressive biological behavior of a dysembryoplastic neuroepithelial tumor.

Preuss M, Nestler U, Zühlke CJ, Kuchelmeister K, Neubauer BA, Jödicke A. Preuss M, et al. Among authors: neubauer ba. Pediatr Neurosurg. 2010;46(4):294-8. doi: 10.1159/000320729. Epub 2010 Dec 30. Pediatr Neurosurg. 2010. PMID: 21196795

2

About the operative management and post-operative neural development of patients with cloverleaf skull deformity.

Preuss M, Stein M, Neubauer BA, Schaaf H, Howaldt HP, Nestler U, Christophis P. Preuss M, et al. Among authors: neubauer ba. Childs Nerv Syst. 2010 Sep;26(9):1211-8. doi: 10.1007/s00381-010-1114-1. Epub 2010 Mar 26. Childs Nerv Syst. 2010. PMID: 20340027

3

Endoscopic surgical anatomy of the paediatric third ventricle studied using virtual neuroendoscopy based on 3-D ultrasonography.

Jödicke A, Berthold LD, Scharbrodt W, Schroth I, Reiss I, Neubauer BA, Böker DK. Jödicke A, et al. Among authors: neubauer ba. Childs Nerv Syst. 2003 Jun;19(5-6):325-31. doi: 10.1007/s00381-003-0748-7. Epub 2003 May 16. Childs Nerv Syst. 2003. PMID: 12750936

4

Association of homozygous LMNA mutation R471C with new phenotype: mandibuloacral dysplasia, progeria, and rigid spine muscular dystrophy.

Zirn B, Kress W, Grimm T, Berthold LD, Neubauer B, Kuchelmeister K, Müller U, Hahn A. Zirn B, et al. Am J Med Genet A. 2008 Apr 15;146A(8):1049-54. doi: 10.1002/ajmg.a.32259. Am J Med Genet A. 2008. PMID: 18348272

5

Stress-induced upregulation of SLC19A3 is impaired in biotin-thiamine-responsive basal ganglia disease.

Schänzer A, Döring B, Ondrouschek M, Goos S, Garvalov BK, Geyer J, Acker T, Neubauer B, Hahn A. Schänzer A, et al. Brain Pathol. 2014 Apr;24(3):270-9. doi: 10.1111/bpa.12117. Epub 2014 Jan 29. Brain Pathol. 2014. PMID: 24372704 Free PMC article.

6

Normal Head Shape Parameters in the First 2 Years of Life and Effect of Helmet Therapy.

Wilbrand JF, Kaps K, Tabak D, Bierther U, Wilbrand M, Neubauer BA, Pons-Kuehnemann J, Howaldt HP, Hahn A. Wilbrand JF, et al. Among authors: neubauer ba. Neuropediatrics. 2017 Dec;48(6):432-441. doi: 10.1055/s-0037-1604482. Epub 2017 Aug 9. Neuropediatrics. 2017. PMID: 28793359 No abstract available.

7

Polyneuropathy, scoliosis, tall stature, and oligodontia represent novel features of the interstitial 6p deletion phenotype.

Zirn B, Hempel M, Hahn A, Neubauer B, Wagenstaller J, Rivera-Bruguès N, Strom TM, Köhler A. Zirn B, et al. Am J Med Genet A. 2008 Nov 15;146A(22):2960-5. doi: 10.1002/ajmg.a.32536. Am J Med Genet A. 2008. PMID: 18924226 No abstract available.

8

Ring chromosome 22 and neurofibromatosis type II: proof of two-hit model for the loss of the NF2 gene in the development of meningioma.

Zirn B, Arning L, Bartels I, Shoukier M, Hoffjan S, Neubauer B, Hahn A. Zirn B, et al. Clin Genet. 2012 Jan;81(1):82-7. doi: 10.1111/j.1399-0004.2010.01598.x. Epub 2010 Dec 22. Clin Genet. 2012. PMID: 21175598

9

Duchenne muscular dystrophy in a 4-year-old girl due to heterozygous frame shift deletion of the dystrophin gene and skewed X-inactivation.

Schänzer A, Rau I, Kress W, Köhler A, Neubauer B, Hahn A. Schänzer A, et al. Klin Padiatr. 2012 Jul;224(4):256-8. doi: 10.1055/s-0032-1304626. Epub 2012 Apr 27. Klin Padiatr. 2012. PMID: 22549471

10

[Hemiconvulsion-Hemiplegia-Epilepsy-Syndrome (HHE)].

Herbst F, Heckmann M, Reiss I, Hügens-Penzel M, Gortner L, Neubauer B. Herbst F, et al. Klin Padiatr. 2002 May-Jun;214(3):126-7. doi: 10.1055/s-2002-30147. Klin Padiatr. 2002. PMID: 12015645 German.

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