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M Gennarelli

Showing results (51-60 of 71) with videos related to

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Journal of Neurology|July 16, 2010
The new Alzheimer's criteria in a naturalistic series of patients with mild cognitive impairmentS Galluzzi, C Geroldi, R Ghidoni, et al.
Biochemical and Biophysical Research Communications|January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5A Pizzuti, A Colosimo, A Ratti, et al.
Neurology|November 9, 2000
Natural history of cardiac involvement in myotonic dystrophy: correlation with CTG repeatsG Antonini, F Giubilei, A Mammarella, et al.
Biological Psychiatry|August 31, 2001
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in ratsF Tascedda, J M Blom, N Brunello, et al.
Journal of Medical Genetics|November 1, 1992
Expansion of the myotonic dystrophy gene in Italian and Spanish patientsS Melchionda, A Cobo, M Gennarelli, et al.
Biochemical and Molecular Medicine|June 1, 1997
Expression study of survival motor neuron gene in human fetal tissuesG Novelli, L Calzà, P Amicucci, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patientsG Novelli, M Gennarelli, E Menegazzo, et al.
Acta Psychiatrica Scandinavica|August 21, 2013
Association between baseline serum vascular endothelial growth factor levels and response to electroconvulsive therapyA Minelli, E Maffioletti, M Bortolomasi, et al.
Human Mutation|August 6, 2009
Mutation within TARDBP leads to frontotemporal dementia without motor neuron diseaseB Borroni, C Bonvicini, A Alberici, et al.
Gastroenterology|May 1, 1996
Linkage analysis identifies gene carriers among members of families with hereditary nonpolyposis colorectal cancerA Piepoli, R Santoro, G Cristofaro, et al.
Pageof 8

Showing results (51-60 of 71) with videos related to

Sort By:
Pageof 8
Journal of Neurology|July 16, 2010
The new Alzheimer's criteria in a naturalistic series of patients with mild cognitive impairmentS Galluzzi, C Geroldi, R Ghidoni, et al.
Biochemical and Biophysical Research Communications|January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5A Pizzuti, A Colosimo, A Ratti, et al.
Neurology|November 9, 2000
Natural history of cardiac involvement in myotonic dystrophy: correlation with CTG repeatsG Antonini, F Giubilei, A Mammarella, et al.
Biological Psychiatry|August 31, 2001
Modulation of glutamate receptors in response to the novel antipsychotic olanzapine in ratsF Tascedda, J M Blom, N Brunello, et al.
Journal of Medical Genetics|November 1, 1992
Expansion of the myotonic dystrophy gene in Italian and Spanish patientsS Melchionda, A Cobo, M Gennarelli, et al.
Biochemical and Molecular Medicine|June 1, 1997
Expression study of survival motor neuron gene in human fetal tissuesG Novelli, L Calzà, P Amicucci, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
(CTG)n triplet mutation and phenotype manifestations in myotonic dystrophy patientsG Novelli, M Gennarelli, E Menegazzo, et al.
Acta Psychiatrica Scandinavica|August 21, 2013
Association between baseline serum vascular endothelial growth factor levels and response to electroconvulsive therapyA Minelli, E Maffioletti, M Bortolomasi, et al.
Human Mutation|August 6, 2009
Mutation within TARDBP leads to frontotemporal dementia without motor neuron diseaseB Borroni, C Bonvicini, A Alberici, et al.
Gastroenterology|May 1, 1996
Linkage analysis identifies gene carriers among members of families with hereditary nonpolyposis colorectal cancerA Piepoli, R Santoro, G Cristofaro, et al.
Pageof 8