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Helvetica Paediatrica Acta|May 1, 1979
Myoclonic encephalopathy of infants or "dancing eyes syndrome". Report of 7 cases with long-term follow-up and review of the literature (cases with and without neuroblastoma)E Boltshauser, T Deonna, H R HirtKlinische Monatsblatter Fur Augenheilkunde|May 1, 1992
[Congenital oculomotor apraxia. Presentation--developmental problems--differential diagnosis]M Steinlin, L Thun-Hohenstein, E BoltshauserEuropean Journal of Pediatrics|January 25, 2002
Trichothiodystrophy with severe cardiac and neurological involvement in two sistersS P Toelle, E Valsangiacomo, E BoltshauserNeuropediatrics|January 4, 2005
Cerebellar agenesis and diabetes insipidusD I Zafeiriou, E Vargiami, E BoltshauserNeuropediatrics|May 1, 1981
Joubert syndrome: clinical and polygraphic observations in a further caseE Boltshauser, M Herdan, G Dumermuth, et al.European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|August 1, 1991
Traumatic spinal cord injury: unusual recovery in 3 childrenM Meuli, P Sacher, U Lässer, et al.Neuropediatrics|December 1, 1995
Joubert syndrome: are kidneys involved?E Boltshauser, I Forster, T Deonna, et al.Neuropediatrics|August 1, 1997
Follow-up in children with Joubert syndromeM Steinlin, M Schmid, K Landau, et al.Neuroradiology|January 1, 1981
Computed tomography in Pelizaeus-Merzbacher diseaseA Statz, E Boltshauser, A Schinzel, et al.Biological Chemistry Hoppe-Seyler|December 1, 1990
A point mutation at the X-chromosomal proteolipid protein locus in Pelizaeus-Merzbacher disease leads to disruption of myelinogenesisT Weimbs, T Dick, W Stoffel, et al.Pageof 758