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Items where contributor is "Weber, Peter"

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2015

Perkinson-Gloor, Nadine and Hagmann-von Arx, Priska and Brand, Serge and Holsboer-Trachsler, Edith and Grob, Alexander and Weber, Peter and Lemola, Sakari. (2015) The role of sleep and the hypothalamic-pituitary-adrenal axis for behavioral and emotional problems in very preterm children during middle childhood. Journal of psychiatric research, Vol. 60. S. 141-147.

Lemola, Sakari and Perkinson-Gloor, Nadine and Hagmann-von Arx, Priska and Brand, Serge and Holsboer-Trachsler, Edith and Grob, Alexander and Weber, Peter. (2015) Morning cortisol secretion in school-age children is related to the sleep pattern of the preceding night. Psychoneuroendocrinology, Vol. 52 , S. 297–301.

Perkinson-Gloor, Nadine and Hagmann-von Arx, Priska and Brand, Serge and Holsboer-Trachsler, Edith and Grob, Alexander and Weber, Peter and Lemola, Sakari. (2015) Intraindividual long-term stability of sleep electroencephalography in school-aged children. Sleep Medicine, 16 (11). pp. 1348-1351.

2014

Hagmann-von Arx, Priska and Perkinson-Gloor, Nadine and Brand, Serge and Albert, Djana and Holsboer-Trachsler, Edith and Grob, Alexander and Weber, Peter and Lemola, Sakari. (2014) In school-age children who were born very preterm sleep efficiency is associated with cognitive function. Neuropsychobiology, Vol. 70, H. 4 , S. 244–252.

2013

Weber, Peter and Zimmermann, Heinz. (2013) Hedge Fund Activism and Information Disclosure: The Case of Germany. European financial management, Vol. 19. S. 1017-1050.

2012

Weber, Peter and Zimmermann, Heinz and Brändli, Beat. (2012) The Price Effects of the Disclosure of Significant Holdings in Listed Companies: The Case of Groups Acting in Concert. Schweizerische Zeitschrift für Wirtschafts- und Finanzmarktrecht, Jg. 84 , H. 3. S. 198-216.

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. S. 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. S. 366-368.

2011

Willi, Bettina and Fahnenstich, Hubert and Weber, Peter. (2011) Encephalitis after vaccination against H1N1 influenza virus. European journal of paediatric neurology, Vol. 15, H. 3. S. 276-277.

Filges, Isabel and Shimojima, Keiko and Okamoto, Nobuhiko and Röthlisberger, Benno and Weber, Peter and Huber, Andreas R. and Nishizawa, Tsutomu and Datta, Alexandre N. and Miny, Peter and Yamamoto, Toshiyuki. (2011) Reduced expression by SETBP1 haploinsufficiency causes developmental and expressive language delay indicating a phenotype distinct from Schinzel-Giedion syndrome. Journal of medical genetics, Vol. 48, H. 2. S. 117-122.

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. S. 79-85.

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

Dill, Patricia and Schneider, Jacques and Weber, Peter and Trachsel, Daniel and Tekin, Mustafa and Jakobs, Cornelis and Thöny, Beat and Blau, Nenad. (2011) Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM). Molecular genetics and metabolism, Vol. 104, no. 3. S. 362-368.

Bigi, Sandra and Fischer, Urs and Wehrli, Edith and Mattle, Heinrich P. and Boltshauser, Eugen and Bürki, Sarah and Jeannet, Pierre-Yves and Fluss, Joel and Weber, Peter and Nedeltchev, Krassen and El-Koussy, Marwan and Steinlin, Maja and Arnold, Marcel. (2011) Acute ischemic stroke in children versus young adults. Annals of neurology, Vol. 70, H. 2. S. 245-254.

2010

Frey, Sarabel G. and Chelo, David and Kinkela, Mina N. and Djoukoue, Florence and Tietche, Felix and Hatz, Christoph and Weber, Peter. (2010) Artesunate-mefloquine combination therapy in acute Plasmodium falciparum malaria in young children: a field study regarding neurological and neuropsychiatric safety. Malaria Journal, Vol. 9 , 291.

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. S. 230-236.

Weber, Peter. (2010) Levetiracetam in nonconvulsive status epilepticus in a child with Angelman syndrome. Journal of child neurology, Vol. 25, no. 3. S. 393-396.

Filges, Isabel and Röthlisberger, Benno and Boesch, Nemya and Weber, Peter and Wenzel, Friedel and Huber, Andreas R. and Heinimann, Karl and Miny, Peter. (2010) Interstitial deletion 1q42 in a patient with agenesis of corpus callosum : Phenotype-genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome. American journal of medical genetics. Part A, Vol. 152, H. 4. S. 987-993.

Zimmer, Klaus-Peter and Fischer, Ina and Mothes, Thomas and Weissen-Plenz, Gabriele and Schmitz, Martina and Wieser, Herbert and Büning, Jürgen and Lerch, Markus M. and Ciclitira, Paul C. and Weber, Peter and Naim, Hassan Y.. (2010) Endocytotic segregation of gliadin peptide 31-49 in enterocytes. Gut, Vol. 59, H. 2. S. 300-310.

Grunt, Sebastian and Wingeier, Kevin and Wehrli, Edith and Boltshauser, Eugen and Capone, Andrea and Fluss, Joel and Gubser-Mercati, Danielle and Jeannet, Pierre-Yves and Keller, Elmar and Marcoz, Jean-Pierre and Schmitt-Mechelke, Thomas and Weber, Peter and Weissert, Markus and Steinlin, Maja and Swiss Neuropaediatric Stroke Registry, . (2010) Cerebral sinus venous thrombosis in Swiss children. Developmental medicine and child neurology, Vol. 52, H. 12. S. 1145-1150.

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. S. 509-514.

2009

van Kuilenburg, André B. P. and Meijer, Judith and Mul, Adri N. P. M. and Hennekam, Raoul C. M. and Hoovers, Jan M. N. and de Die-Smulders, Christine E. M. and Weber, Peter and Mori, Andrea Capone and Bierau, Jörgen and Fowler, Brian and Macke, Klaus and Sass, Jörn Oliver and Meinsma, Rutger and Hennermann, Julia B. and Miny, Peter and Zoetekouw, Lida and Vijzelaar, Raymon and Nicolai, Joost and Ylstra, Bauke and Rubio-Gozalbo, M. Estela. (2009) Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3). Human genetics, Vol. 125, H. 5-6. S. 581-590.

Kobel, Maja and Bechtel, Nina and Weber, Peter and Specht, Karsten and Klarhöfer, Markus and Scheffler, Klaus and Opwis, Klaus and Penner, Iris-Katharina. (2009) Effects of methylphenidate on working memory functioning in children with attention deficit/hyperactivity disorder. European journal of paediatric neurology, Vol. 13. S. 516-523.

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. S. 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. S. 64-8.

Denora, Paola S. and Schlesinger, David and Casali, Carlo and Kok, Fernando and Tessa, Alessandra and Boukhris, Amir and Azzedine, Hamid and Dotti, Maria Teresa and Bruno, Claudio and Truchetto, Jeremy and Biancheri, Roberta and Fedirko, Estelle and Di Rocco, Maja and Bueno, Clarissa and Malandrini, Alessandro and Battini, Roberta and Sickl, Elisabeth and de Leva, Maria Fulvia and Boespflug-Tanguy, Odile and Silvestri, Gabriella and Simonati, Alessandro and Said, Edith and Ferbert, Andreas and Criscuolo, Chiara and Heinimann, Karl and Modoni, Anna and Weber, Peter and Palmeri, Silvia and Plasilova, Martina and Pauri, Flavia and Cassandrini, Denise and Battisti, Carla and Pini, Antonella and Tosetti, Michela and Hauser, Erwin and Masciullo, Marcella and Di Fabio, Roberto and Piccolo, Francesca and Denis, Elodie and Cioni, Giovanni and Massa, Roberto and Della Giustina, Elvio and Calabrese, Olga and Melone, Marina A. B. and De Michele, Giuseppe and Federico, Antonio and Bertini, Enrico and Durr, Alexandra and Brockmann, Knut and van der Knaap, Marjo S. and Zatz, Mayana and Filla, Alessandro and Brice, Alexis and Stevanin, Giovanni and Santorelli, Filippo M.. (2009) Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion. Human mutation : variations, databases, and diseases, Vol. 30 , E500-519.

Jourdan Moser, Sonya and Cutini, Simone and Weber, Peter and Schroeter, Matthias L.. (2009) Right prefrontal brain activation due to Stroop interference is altered in attention-deficit hyperactivity disorder : a functional near-infrared spectroscopy study. Psychiatry research : an international journal for rapid communication, Vol. 173. S. 190-195.

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. S. 649-654.

Weber, Peter and Rost, Barbara. (2009) Anorexia nervosa und Nervus peronaeus-Läsion. Zeitschrift für Kinder- und Jugendpsychiatrie und Psychotherapie, Vol. 37. S. 469-472.