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Brain & Development|July 1, 1992
Myelination of the optic radiation in Leber congenital amaurosisM Steinlin, E Martin, K Schenker, et al.Neuropediatrics|August 26, 2004
Cerebral actinomycosis before adolescenceE Olah, C Berger, E Boltshauser, et al.Schweizerische Medizinische Wochenschrift|August 6, 1996
[Back pain in children: symptoms which should be taken seriously]M Steinlin, G Eich, T Huisman, et al.Archives of Disease in Childhood|January 1, 1988
Acrodermatitis chronica atrophicansD Nadal, R Gundelfinger, U Flueler, et al.European Journal of Pediatrics|November 1, 1985
Craniosynostosis in hyper-IgE-syndromeP H Höger, E Boltshauser, W H HitzigNeuropediatrics|August 1, 1981
Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two casesA Probst, J Ulrich, A Bischoff, et al.Schweizerische Medizinische Wochenschrift|May 25, 1996
[Molecular genetic diagnosis and deletion analysis in Type I-III spinal muscular atrophy]R Spiegel, A Hagmann, E Boltshauser, et al.Schweizerische Medizinische Wochenschrift|January 9, 1988
[Childbirth in 2 patients with congenital analgesia]R Zimmermann, J Benz, J Gysel, et al.Journal of Medical Genetics|February 1, 1989
Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?E Boltshauser, W Lang, T Spillmann, et al.Neurofibromatosis|January 1, 1989
Intracranial abnormalities associated with facial plexiform neurofibromas in neurofibromatosis type 1E Boltshauser, H Stocker, H Sailer, et al.Pageof 758