Items where Author is "Weber, P."

2013

Hubacher, M. and Weber, P. and Stoecklin, M. and Specht, K. and Kappos, L. and Opwis, K. and Penner, I.-K.. (2013) Case-based approach to evaluate the efficacy of working memory training in juvenile Multiple Sclerosis. Multiple Sclerosis Journal, 19 (7). pp. 975-976.

2012

Bechtel, N. and Kobel, M. and Penner, I. -K. and Specht, K. and Klarhöfer, M. and Scheffler, K. and Opwis, K. and Schmitt-Mechleke, T. and Capone, A. and Weber, P.. (2012) Attention deficit/ hyperactivity disorder in childhood epilepsy: A neuropsychological and fMRI study. Epilepsia, 53 (2). pp. 325-333.

Penner, I. -K. and Hubacher, M. and Rasenack, M. and Sprenger, T. and Weber, P. and Naegelin, Y.. (2012) Cognitive relapse in the absence of new neurological symptoms : clinical utility of neuropsychological assessment in a case with juvenile multiple sclerosis. Multiple sclerosis journal, Vol. 18, H. 4. p. 303.

Penner, I. K. and Hubacher, M. and Rasenack, M. and Sprenger, T. and Weber, P. and Naegelin, Y.. (2012) Utility of neuropsychological testing for guiding treatment decisions in paediatric multiple sclerosis. Multiple sclerosis journal, Vol. 19, H. 3. pp. 366-368.

2011

Weber, P. and Bächli, H. and Schneider, J.. (2011) Chronic headaches : change as challenge. Klinische Pädiatrie, Vol. 223, H. 5. pp. 290-291.

Filges, I. and Röthlisberger, B. and Blattner, A. and Boesch, N. and Demougin, P. and Wenzel, F. and Huber, A. R. and Heinimann, K. and Weber, P. and Miny, P.. (2011) Deletion in Xp22.11 : PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism. Clinical genetics, Vol. 79, H. 1. pp. 79-85.

Weber, P. and Hamburger, M. and Schafroth, N. and Potterat, O.. (2011) Flash chromatography on cartridges for the separation of plant extracts - Rules for the selection of chromatographic conditions and comparison with medium pressure liquid chromatography. Fitoterapia, Vol. 82. pp. 155-161.

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Specht, M. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Pfister, H. and Zimmermann, P. and Lieb, R. and Pütz, B. and Uhr, M. and Weber, P. and Deussing, J. M. and Gonik, M. and Bunck, M. and Kebler, M. S. and Frank, E. and Hohoff, C. and Domschke, K. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Jacob, C. and Deckert, J. and Schreiber, S. and Strohmaier, J. and Nöthen, M. and Cichon, S. and Rietschel, M. and Bettecken, T. and Keck, M. E. and Landgraf, R. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular Psychiatry, 16 (6). pp. 647-663.

2010

van Kuilenburg, A. B. P. and Meijer, J. and Gökcay, G. and Baykal, T. and Rubio-Gozalbo, M. E. and Mul, A. N. P. M. and de Die-Smulders, C. E. M. and Weber, P. and Mori, A. Capone and Bierau, J. and Fowler, B. and Macke, K. and Sass, J. O. and Meinsma, R. and Hennermann, J. B. and Miny, P. and Zoetekouw, L. and Roelofsen, J. and Vijzelaar, R. and Nicolai, J. and Hennekam, R. C. M.. (2010) Dihydropyrimidine dehydrogenase deficiency caused by a novel genomic deletion c.505_513del of DPYD. Nucleosides, nucleotides & nucleic acids, Vol. 29, H. 4-6. pp. 509-514.

Kobel, M. and Bechtel, N. and Specht, K. and Klarhöfer, M. and Weber, P. and Scheffler, K. and Opwis, K. and Penner, I. -K.. (2010) Structural and functional imaging approaches in attention deficit/hyperactivity disorder : does the temporal lobe play a key role? Psychiatry research. Neuroimaging : the official publication of the International Society for Neuroimaging in Psychiatry, Vol. 183, No. 3. pp. 230-236.

Bechtel, N. and Penner, I. -K. and Klarhöfer, M. and Scheffler, K. and Opwis, K. and Weber, P.. (2010) The effect of methylphenidate on n-back task performance in boys with epilepsy and or ADHD : a behavioral and functional MRI study. Epilepsia : journal of the International League against Epilepsy, Vol. 51, H. Suppl. 4. pp. 16-17.

2009

Bechtel, N. and Kobel, M. and Penner, I. K. and Klarhöfer, M. and Scheffler, K. and Opwis, K. and Weber, P.. (2009) Decreased fractional anisotropy in the middle cerebellar peduncle in children with epilepsy and / or attention deficit/hyperactivity disorder : a preliminary study. Epilepsy & behavior, Vol. 15. pp. 294-298.

Emmert, S. and Ueda, T. and Zumsteg, U. and Weber, P. and Khan, S. G. and Oh, K. S. and Boyle, J. and Laspe, P. and Zachmann, K. and Boeckmann, L. and Kuschal, C. and Bircher, A. and Kraemer, K. H.. (2009) Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2). Experimental dermatology, Vol. 18. pp. 64-68.

Ramelli, G. P. and Weber, P.. (2009) [Non epileptic paroxysmal movements disorders in infant]. Schweizerische Rundschau für Medizin Praxis = Revue suisse de médecine PRAXIS, Vol. 98. pp. 649-654.

2005

Tillmann, B. U. and Tillmann, H. C. and Heininger, U. and Lutschg, J. and Weber, P.. (2005) Acceptance and timeliness of standard vaccination in children with chronic neurological deficits in north-western Switzerland. European journal of pediatrics, Vol. 164, H. 5. pp. 320-325.