Weber P - Search Results

1

Bruder E, Rougemont AL, Furlano RI, Schneider JF, Mayr J, Haecker FM, Beier K, Schneider J, Weber P, Berberich T, Cathomas G, Meier-Ruge WA. Bruder E, et al. Among authors: weber p. Pathologe. 2013 Mar;34(2):118-32. doi: 10.1007/s00292-012-1727-0. Pathologe. 2013. PMID: 23440290 Review. German.

2

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.

3

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

4

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

5

Dual independent genetic etiologies in a lethal complex malformation phenotype.

Filges I, Genewein A, Weber P, Meier S, Deigendesch N, Bruder E, Prüfer F, Tercanli S. Filges I, et al. Among authors: weber p. Ultraschall Med. 2020 Apr;41(2):112-114. doi: 10.1055/a-1104-3625. Epub 2020 Apr 7. Ultraschall Med. 2020. PMID: 32259861 English. No abstract available.

6

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

7

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

8

[Differential diagnosis of visual hallucinations].

Weber P, Ruof H, Jourdan S. Weber P, et al. Klin Padiatr. 2005 Jan-Feb;217(1):25-30. doi: 10.1055/s-2004-818792. Klin Padiatr. 2005. PMID: 15640968 German.

9

The role of sleep and the hypothalamic-pituitary-adrenal axis for behavioral and emotional problems in very preterm children during middle childhood.

Perkinson-Gloor N, Hagmann-von Arx P, Brand S, Holsboer-Trachsler E, Grob A, Weber P, Lemola S. Perkinson-Gloor N, et al. Among authors: weber p. J Psychiatr Res. 2015 Jan;60:141-7. doi: 10.1016/j.jpsychires.2014.10.005. Epub 2014 Oct 16. J Psychiatr Res. 2015. PMID: 25454023

10

Incidence and diagnosis of unilateral arterial cerebral infarction in newborn infants.

Schulzke S, Weber P, Luetschg J, Fahnenstich H. Schulzke S, et al. Among authors: weber p. J Perinat Med. 2005;33(2):170-5. doi: 10.1515/JPM.2005.032. J Perinat Med. 2005. PMID: 15843270

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