Weber P - Search Results

1

Congenital muscular dystrophy with dropped head phenotype and cognitive impairment due to a novel mutation in the LMNA gene.

Bonati U, Bechtel N, Heinimann K, Rutz E, Schneider J, Frank S, Weber P, Fischer D. Bonati U, et al. Among authors: weber p. Neuromuscul Disord. 2014 Jun;24(6):529-32. doi: 10.1016/j.nmd.2014.02.004. Epub 2014 Feb 15. Neuromuscul Disord. 2014. PMID: 24684859

2

Attention problems in children with epilepsy. How is the long-term outcome?

Bechtel N, Weber P. Bechtel N, et al. Among authors: weber p. Eur J Paediatr Neurol. 2015 May;19(3):383-5. doi: 10.1016/j.ejpn.2014.12.020. Epub 2015 Jan 9. Eur J Paediatr Neurol. 2015. PMID: 25604809

3

Chronic headaches: change as challenge.

Weber P, Bächli H, Schneider J. Weber P, et al. Klin Padiatr. 2011 Sep;223(5):290-1. doi: 10.1055/s-0031-1275263. Epub 2011 Apr 20. Klin Padiatr. 2011. PMID: 21509707 No abstract available.

4

Association Between Health-Related Quality of Life and Motor Function in Ambulant and Nonambulant Duchenne Muscular Dystrophy Patients.

Gocheva V, Schmidt S, Orsini AL, Hafner P, Schaedelin S, Rueedi N, Weber P, Fischer D. Gocheva V, et al. Among authors: weber p. J Child Neurol. 2019 Dec;34(14):873-885. doi: 10.1177/0883073819865681. Epub 2019 Aug 6. J Child Neurol. 2019. PMID: 31385745

5

Psychosocial adjustment and parental stress in Duchenne Muscular Dystrophy.

Gocheva V, Schmidt S, Orsini AL, Hafner P, Schaedelin S, Weber P, Fischer D. Gocheva V, et al. Among authors: weber p. Eur J Paediatr Neurol. 2019 Nov;23(6):832-841. doi: 10.1016/j.ejpn.2019.09.008. Epub 2019 Sep 20. Eur J Paediatr Neurol. 2019. PMID: 31585833

6

Are vigabatrin induced T2 hyperintensities in cranial MRI associated with acute encephalopathy and extrapyramidal symptoms?

Dill P, Datta AN, Weber P, Schneider J. Dill P, et al. Among authors: weber p. Eur J Paediatr Neurol. 2013 May;17(3):311-5. doi: 10.1016/j.ejpn.2012.10.009. Epub 2012 Nov 27. Eur J Paediatr Neurol. 2013. PMID: 23199677

7

Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome.

Filges I, Röthlisberger B, Boesch N, Weber P, Wenzel F, Huber AR, Heinimann K, Miny P. Filges I, et al. Among authors: weber p. Am J Med Genet A. 2010 Apr;152A(4):987-93. doi: 10.1002/ajmg.a.33330. Am J Med Genet A. 2010. PMID: 20358614

8

Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM).

Dill P, Schneider J, Weber P, Trachsel D, Tekin M, Jakobs C, Thöny B, Blau N. Dill P, et al. Among authors: weber p. Mol Genet Metab. 2011 Nov;104(3):362-8. doi: 10.1016/j.ymgme.2011.05.019. Epub 2011 Jun 2. Mol Genet Metab. 2011. PMID: 21752681

9

Fast improvement of verbal memory function after left temporal tumour resection.

Jourdan Moser S, Schneider J, Lütschg J, Weber P. Jourdan Moser S, et al. Among authors: weber p. Acta Paediatr. 2006 Oct;95(10):1306-9. doi: 10.1080/08035250600719721. Acta Paediatr. 2006. PMID: 16982508

10

Effects of methylphenidate on working memory functioning in children with attention deficit/hyperactivity disorder.

Kobel M, Bechtel N, Weber P, Specht K, Klarhöfer M, Scheffler K, Opwis K, Penner IK. Kobel M, et al. Among authors: weber p. Eur J Paediatr Neurol. 2009 Nov;13(6):516-23. doi: 10.1016/j.ejpn.2008.10.008. Epub 2008 Dec 3. Eur J Paediatr Neurol. 2009. PMID: 19056305 Clinical Trial.

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