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Schweizerische Medizinische Wochenschrift|October 5, 1991
[Neurofibromatosis Type 1: genetic studies with DNA markers in 38 families]R Spiegel, M Mächler, H P Stocker, et al.Journal of Computer Assisted Tomography|March 2, 1999
Unusual presentations of neuroborreliosis (Lyme disease) in childhoodT A Huisman, G Wohlrab, D Nadal, et al.Journal of Child Neurology|September 17, 1999
Clinical features and revised diagnostic criteria in Joubert syndromeB L Maria, E Boltshauser, S C Palmer, et al.European Journal of Pediatrics|October 1, 1992
Cortical visual impairment following bacterial meningitis: magnetic resonance imaging and visual evoked potentials findings in two casesL Thun-Hohenstein, B Schmitt, H Steinlin, et al.Journal of Neuroradiology = Journal De Neuroradiologie|August 12, 2008
Commissural malformations: beyond the corpus callosumT Smith, A Tekes, E Boltshauser, et al.Neuroradiology|April 1, 1994
Transient bifrontal solitary periventricular cysts in term neonatesL Thun-Hohenstein, I Forster, C Künzle, et al.Neuropediatrics|June 21, 2002
"Vanishing white matter" and ovarian dysgenesis in an infant with cerebro-oculo-facio-skeletal phenotypeE Boltshauser, P G Barth, D Troost, et al.AJNR. American Journal of Neuroradiology|June 18, 2011
Joubert syndrome and related disorders: spectrum of neuroimaging findings in 75 patientsA Poretti, T A G M Huisman, I Scheer, et al.Neuroradiology|May 1, 1996
Cerebellomedullary compression in recessive craniometaphyseal dysplasiaE Boltshauser, B Schmitt, W Wichmann, et al.Archiv Fur Gynakologie|January 1, 1975
[Triploidy as a cause of midtrimester gestosis(author's transl)]A Schinzel, K Hayashi, W Schmid, et al.Pageof 758