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The Journal of Pediatrics|August 31, 2006
Quality of life and psychological adjustment in children and adolescents with neurofibromatosis type 1Anna Graf, Markus A Landolt, Andrea Capone Mori, et al.
American Journal of Medical Genetics. Part A|April 27, 2004
Natural history of twin disruption sequenceAndreas Zankl, Daniela Brooks, Eugen Boltshauser, et al.
Neuropediatrics|August 23, 2012
Bannayan-Riley-Ruvalcaba syndrome with progressive spinal epidural lipomatosisSandra Toelle, Andrea Poretti, Ianina Scheer, et al.
Handbook of Clinical Neurology|February 27, 2018
Von Hippel-Lindau disease and Sturge-Weber syndromeSusan Perlman
Brain & Development|May 28, 2015
Differential diagnosis of ventriculomegaly and brainstem kinking on fetal MRITali Amir, Andrea Poretti, Eugen Boltshauser, et al.
European Journal of Pediatrics|February 27, 2004
Severe neurological impairment in hereditary methaemoglobinaemia type 2Sandra P Toelle, Eugen Boltshauser, Ekkehard Mössner, et al.
European Journal of Medical Genetics|March 18, 2008
Gomez-Lopez-Hernandez syndrome: an easily missed diagnosisAndrea Poretti, Deborah Bartholdi, Sonja Gobara, et al.
Developmental Medicine and Child Neurology|April 14, 2004
Outcome of craniopharyngioma in children: long-term complications and quality of lifeAndrea Poretti, Michael A Grotzer, Karin Ribi, et al.
AJNR. American Journal of Neuroradiology|September 13, 2005
Diffusion tensor imaging in progressive multifocal leukoencephalopathy: early predictor for demyelination?Thierry A G M Huisman, Eugen Boltshauser, Ernst Martin, et al.
American Journal of Medical Genetics. Part A|November 4, 2004
Novel mutation in the tyrosine kinase domain of FGFR2 in a patient with Pfeiffer syndromeAndreas Zankl, Gudrun Jaeger, Luisa Bonafé, et al.
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