Klein A - Search Results

1

Clinical, neuroradiological and molecular characterization of cerebellar dysplasia with cysts (Poretti-Boltshauser syndrome).

Micalizzi A, Poretti A, Romani M, Ginevrino M, Mazza T, Aiello C, Zanni G, Baumgartner B, Borgatti R, Brockmann K, Camacho A, Cantalupo G, Haeusler M, Hikel C, Klein A, Mandrile G, Mercuri E, Rating D, Romaniello R, Santorelli FM, Schimmel M, Spaccini L, Teber S, von Moers A, Wente S, Ziegler A, Zonta A, Bertini E, Boltshauser E, Valente EM. Micalizzi A, et al. Among authors: klein a. Eur J Hum Genet. 2016 Aug;24(9):1262-7. doi: 10.1038/ejhg.2016.19. Epub 2016 Mar 2. Eur J Hum Genet. 2016. PMID: 26932191 Free PMC article.

2

Cervical myelomeningocele--follow-up of five patients.

Meyer-Heim AD, Klein A, Boltshauser E. Meyer-Heim AD, et al. Among authors: klein a. Eur J Paediatr Neurol. 2003;7(6):407-12. doi: 10.1016/s1090-3798(03)00108-9. Eur J Paediatr Neurol. 2003. PMID: 14623220

3

Episodic ataxia type 1 with distal weakness: a novel manifestation of a potassium channelopathy.

Klein A, Boltshauser E, Jen J, Baloh RW. Klein A, et al. Neuropediatrics. 2004 Apr;35(2):147-9. doi: 10.1055/s-2004-817921. Neuropediatrics. 2004. PMID: 15127317

4

Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy (PEHO) syndrome in a Swiss child.

Klein A, Schmitt B, Boltshauser E. Klein A, et al. Eur J Paediatr Neurol. 2004;8(6):317-21. doi: 10.1016/j.ejpn.2004.08.006. Eur J Paediatr Neurol. 2004. PMID: 15542387

5

Facial nerve palsy-an unusual complication after evacuation of a subdural haematoma or hygroma in children.

Klein A, Balmer B, Brehmer U, Huisman TA, Boltshauser E. Klein A, et al. Childs Nerv Syst. 2006 Jun;22(6):562-6. doi: 10.1007/s00381-006-0060-4. Epub 2006 Mar 14. Childs Nerv Syst. 2006. PMID: 16552565 Free article.

6

Clinical profiles of four patients with Rett syndrome carrying a novel exon 1 mutation or genomic rearrangement in the MECP2 gene.

Bartholdi D, Klein A, Weissert M, Koenig N, Baumer A, Boltshauser E, Schinzel A, Berger W, Mátyás G. Bartholdi D, et al. Among authors: klein a. Clin Genet. 2006 Apr;69(4):319-26. doi: 10.1111/j.1399-0004.2006.00604.x. Clin Genet. 2006. PMID: 16630165

7

Serial MR imaging, diffusion tensor imaging, and MR spectroscopic findings in a child with progressive encephalopathy, edema, hypsarrhythmia, and optic atrophy (PEHO) syndrome.

Huisman TA, Klein A, Werner B, Straube T, Boltshauser E. Huisman TA, et al. Among authors: klein a. AJNR Am J Neuroradiol. 2006 Aug;27(7):1555-8. AJNR Am J Neuroradiol. 2006. PMID: 16908579 Free PMC article.

8

Long-term outcome of ten children with opsoclonus-myoclonus syndrome.

Klein A, Schmitt B, Boltshauser E. Klein A, et al. Eur J Pediatr. 2007 Apr;166(4):359-63. doi: 10.1007/s00431-006-0247-4. Epub 2006 Nov 7. Eur J Pediatr. 2007. PMID: 17089089 Free article.

9

Pontocerebellar hypoplasia type 2: variability in clinical and imaging findings.

Steinlin M, Klein A, Haas-Lude K, Zafeiriou D, Strozzi S, Müller T, Gubser-Mercati D, Schmitt Mechelke T, Krägeloh-Mann I, Boltshauser E. Steinlin M, et al. Among authors: klein a. Eur J Paediatr Neurol. 2007 May;11(3):146-52. doi: 10.1016/j.ejpn.2006.11.012. Epub 2007 Feb 22. Eur J Paediatr Neurol. 2007. PMID: 17320436

10

Siblings with infantile cerebral stroke and delayed multivessel involvement--a new hereditary vasculopathy?

Klein A, Fasnacht M, Huisman TA, Neuhaus TJ, Martin E, Boltshauser E. Klein A, et al. Eur J Paediatr Neurol. 2007 Sep;11(5):292-6. doi: 10.1016/j.ejpn.2007.02.007. Epub 2007 Apr 10. Eur J Paediatr Neurol. 2007. PMID: 17428710

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