Uni Basel Research Database

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Publications

Showing records 1 - 20 (of 28)

Publication: JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)

ID	Author	Year	Title	Publisher
1196724	Ramelli, G P; Weber, P	2009	[Non epileptic paroxysmal movements disorders in infant]	Schweizerische Rundschau für Medizin Praxis = Revue suisse de médecine PRAXIS
1473775	Penner, Iris-Katharina; Hubacher, Martina; Rasenack, Maria; Sprenger, Till; Weber, Peter; Naegelin, Yvonne	2012	Utility of neuropsychological testing for guiding treatment decisions in paediatric multiple sclerosis	Multiple sclerosis journal
2724991	Perkinson-Gloor, Nadine; Hagmann-von Arx, Priska; Brand, Serge; Holsboer-Trachsler, Edith; Grob, Alexander; Weber, Peter; 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
1194083	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
1192528	Emmert,S; Ueda,T; Zumsteg,U; Weber,P; Khan,SG; Oh,KS; Boyle,J; Laspe,P; Zachmann,K; Boeckmann,L; Kuschal,C; Bircher,A; Kraemer,KH	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
1193605	Denora, Paola S; Schlesinger, David; Casali, Carlo; Kok, Fernando; Tessa, Alessandra; Boukhris, Amir; Azzedine, Hamid; Dotti, Maria Teresa; Bruno, Claudio; Truchetto, Jeremy; Biancheri, Roberta; Fedirko, Estelle; Di Rocco, Maja; Bueno, Clarissa; Malandrini, Alessandro; Battini, Roberta; Sickl, Elisabeth; de Leva, Maria Fulvia; Boespflug-Tanguy, Odile; Silvestri, Gabriella; Simonati, Alessandro; Said, Edith; Ferbert, Andreas; Criscuolo, Chiara; Heinimann, Karl; Modoni, Anna; Weber, Peter; Palmeri, Silvia; Plasilova, Martina; Pauri, Flavia; Cassandrini, Denise; Battisti, Carla; Pini, Antonella; Tosetti, Michela; Hauser, Erwin; Masciullo, Marcella; Di Fabio, Roberto; Piccolo, Francesca; Denis, Elodie; Cioni, Giovanni; Massa, Roberto; Della Giustina, Elvio; Calabrese, Olga; Melone, Marina A B; De Michele, Giuseppe; Federico, Antonio; Bertini, Enrico; Durr, Alexandra; Brockmann, Knut; van der Knaap, Marjo S; Zatz, Mayana; Filla, Alessandro; Brice, Alexis; Stevanin, Giovanni; 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
1194308	Jourdan Moser, Sonya; Cutini, Simone; Weber, Peter; 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
1196148	Filges, Isabel; Shimojima, Keiko; Okamoto, Nobuhiko; Röthlisberger, Benno; Weber, Peter; Huber, Andreas R; Nishizawa, Tsutomu; Datta, Alexandre N; Miny, Peter; 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
1194199	Dill, Patricia; Schneider, Jacques; Weber, Peter; Trachsel, Daniel; Tekin, Mustafa; Jakobs, Cornelis; Thöny, Beat; 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
2783195	Lemola, Sakari; Perkinson-Gloor, Nadine; Hagmann-von Arx, Priska; Brand, Serge; Holsboer-Trachsler, Edith; Grob, Alexander; Weber, Peter	2015	Morning cortisol secretion in school-age children is related to the sleep pattern of the preceding night	Psychoneuroendocrinology
1195117	Weber, Peter	2010	Levetiracetam in nonconvulsive status epilepticus in a child with Angelman syndrome	Journal of child neurology
3169871	Perkinson-Gloor, Nadine; Hagmann-von Arx, Priska; Brand, Serge; Holsboer-Trachsler, Edith; Grob, Alexander; Weber, Peter; Lemola, Sakari	2015	Intraindividual long-term stability of sleep electroencephalography in school-aged children	Sleep Medicine
1192680	Filges, Isabel; Röthlisberger, Benno; Boesch, Nemya; Weber, Peter; Wenzel, Friedel; Huber, Andreas R; Heinimann, Karl; 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
2729495	Hagmann-von Arx, Priska; Perkinson-Gloor, Nadine; Brand, Serge; Albert, Djana; Holsboer-Trachsler, Edith; Grob, Alexander; Weber, Peter; Lemola, Sakari	2014	In school-age children who were born very preterm sleep efficiency is associated with cognitive function	Neuropsychobiology
3304162	Hagmann-von Arx, Priska; Manicolo, Olivia; Perkinson-Gloor, Nadine; Weber, Peter; Grob, Alexander; Lemola, Sakari	2015	Gait in very preterm school-aged children in dual-task paradigms	PLoS ONE
1196691	Zimmer, Klaus-Peter; Fischer, Ina; Mothes, Thomas; Weissen-Plenz, Gabriele; Schmitz, Martina; Wieser, Herbert; Büning, Jürgen; Lerch, Markus M; Ciclitira, Paul C; Weber, Peter; Naim, Hassan Y	2010	Endocytotic segregation of gliadin peptide 31-49 in enterocytes	Gut
104745	Penner, Iris-Katharina	2009	Effects of methylphenidate on working memory functioning in children with attention deficit/hyperactivity disorder	European journal of paediatric neurology
1196521	van Kuilenburg, A. B. P.; Meijer, J.; Gokcay, G.; Baykal, T.; Rubio-Gozalbo, M. E.; Mul, A. N. P. M.; de Die-Smulders, C. E. M.; Weber, P.; Mori, A. Capone; Bierau, J.; Fowler, B.; Macke, K.; Sass, J. O.; Meinsma, R.; Hennermann, J. B.; Miny, P.; Zoetekouw, L.; Roelofsen, J.; Vijzelaar, R.; Nicolai, J.; Hennekam, R. C. M.	2010	Dihydropyrimidine dehydrogenase deficiency caused by a novel genomic deletion c.505_513del of DPYD	Nucleosides, nucleotides & nucleic acids
1192682	Filges, I.; Roethlisberger, B.; Blattner, A.; Boesch, N.; Demougin, P.; Wenzel, F.; Huber, A. R.; Heinimann, K.; Weber, P.; Miny, P.	2011	Deletion in Xp22.11 : PTCHD1 is a candidate gene for X-linked intellectual disability with or without autism	Clinical genetics
1194886	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

Showing records 1 - 20 (of 28)

29/04/2024

Research Database / FORSCHUNGSDATENBANK