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M Mirabella

Showing results (11-20 of 49) with videos related to

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Neurology|June 25, 2003
Cervical cord dysfunction during neck flexion in Hirayama's diseaseD Restuccia, M Rubino, M Valeriani, et al.
Molecular and Cellular Neurosciences|April 21, 2001
Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathiesS Di Giovanni, M Mirabella, M Papacci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1M Mirabella, K Christodoulou, S Di Giovanni, et al.
Annals of Neurology|December 1, 1996
Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body myositis and myopathiesM Mirabella, R B Alvarez, W K Engel, et al.
Neurology|July 21, 2010
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathyA Broccolini, T Gidaro, G Tasca, et al.
Journal of Endocrinological Investigation|April 7, 2019
Transition memories: experiences of trans adult women with hormone therapy and their beliefs on the usage of hormone blockers to suppress pubertyG Giovanardi, P Morales, M Mirabella, et al.
Experimental and Molecular Pathology|July 20, 1999
Molecular characterization of a novel endonuclease (Xib) and possible involvement in lysosomal glycogen storage disordersG Malferrari, U Mazza, C Tresoldi, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Premature termination mutations in exon 3 of the SMN1 gene are associated with exon skipping and a relatively mild SMA phenotypeV Sossi, A Giuli, T Vitali, et al.
Neurogenetics|February 7, 2001
The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcriptionM Mirabella, S Servidei, A Broccolini, et al.
Neurology|November 1, 1993
Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophyM Mirabella, S Servidei, G Manfredi, et al.
Pageof 5

Showing results (11-20 of 49) with videos related to

Sort By:
Pageof 5
Neurology|June 25, 2003
Cervical cord dysfunction during neck flexion in Hirayama's diseaseD Restuccia, M Rubino, M Valeriani, et al.
Molecular and Cellular Neurosciences|April 21, 2001
Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathiesS Di Giovanni, M Mirabella, M Papacci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 11, 2000
An Italian family with autosomal recessive quadriceps-sparing inclusion-body myopathy (ARQS-IBM) linked to chromosome 9p1M Mirabella, K Christodoulou, S Di Giovanni, et al.
Annals of Neurology|December 1, 1996
Apolipoprotein E and apolipoprotein E messenger RNA in muscle of inclusion body myositis and myopathiesM Mirabella, R B Alvarez, W K Engel, et al.
Neurology|July 21, 2010
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathyA Broccolini, T Gidaro, G Tasca, et al.
Journal of Endocrinological Investigation|April 7, 2019
Transition memories: experiences of trans adult women with hormone therapy and their beliefs on the usage of hormone blockers to suppress pubertyG Giovanardi, P Morales, M Mirabella, et al.
Experimental and Molecular Pathology|July 20, 1999
Molecular characterization of a novel endonuclease (Xib) and possible involvement in lysosomal glycogen storage disordersG Malferrari, U Mazza, C Tresoldi, et al.
European Journal of Human Genetics : EJHG|April 21, 2001
Premature termination mutations in exon 3 of the SMN1 gene are associated with exon skipping and a relatively mild SMA phenotypeV Sossi, A Giuli, T Vitali, et al.
Neurogenetics|February 7, 2001
The drastic reduction of SMN protein in SMA I spinal cord motor neurons is not due to inefficient transcriptionM Mirabella, S Servidei, A Broccolini, et al.
Neurology|November 1, 1993
Cardiomyopathy may be the only clinical manifestation in female carriers of Duchenne muscular dystrophyM Mirabella, S Servidei, G Manfredi, et al.
Pageof 5