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Journal of Neurogenetics|January 1, 1987
Myotonic dystrophy and chromosome translocation segregating in the same familyG Neri, E Bertini, A Serra, et al.Neurology|August 26, 1998
Giant dystrophin deletion associated with congenital cataract and mild muscular dystrophyM Mirabella, G Galluzzi, G Manfredi, et al.Neuroscience|April 22, 2006
Modulation of laser-evoked potentials by experimental cutaneous tonic painM Valeriani, P Tonali, D Le Pera, et al.Journal of the Neurological Sciences|March 1, 1993
Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a familyG Manfredi, G Silvestri, S Servidei, et al.American Journal of Medical Genetics|May 8, 2000
X-linked congenital ataxia: a clinical and genetic studyE Bertini, V des Portes, G Zanni, et al.Neurology|April 1, 1997
The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsyA Battaglia, F Gurrieri, E Bertini, et al.Journal of Neurology|August 1, 1986
The spectrum of the so-called rigid spine syndrome: nosological considerations and report of three female casesE Bertini, R Marini, G Sabetta, et al.Acta Neuropathologica|January 1, 1994
Autosomal recessive hypermyelinating neuropathyM Sabatelli, T Mignogna, G Lippi, et al.Neuropediatrics|August 26, 2004
Severe abnormalities of the pons in two infants with goldenhar syndromeM Pane, G Baranello, D Battaglia, et al.Journal of Molecular Biology|November 17, 2007
Complex of a protective antibody with its Ebola virus GP peptide epitope: unusual features of a V lambda x light chainJeffrey E Lee, Ana Kuehne, Dafna M Abelson, et al.Pageof 29