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Journal of Cellular Physiology
|
April 29, 2006
Human fibroblasts undergo oxidative stress-induced apoptosis without internucleosomal DNA fragmentation
P Formichi, E Radi, C Battisti, et al.
Journal of the Neurological Sciences
|
August 1, 1997
Palpebral ptosis and muscle fatiguability associated with perineurial cell ensheathment of muscle fibers: a new disease of the neuromuscular junction?
A Federico, K Plewnia, C Battisti, et al.
European Neurology
|
January 1, 1991
Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case report
A Federico, C Battisti, M P Eusebi, et al.
Journal of Neurology
|
November 27, 2013
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations
L Di Toro Mammarella, A Mignarri, C Battisti, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
October 11, 1992
Sensitivity, resolution and image quality with a multi-head SPECT camera
F H Fahey, B A Harkness, J W Keyes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 5, 2000
McLeod syndrome and neuroacanthocytosis with a novel mutation in the XK gene
M T Dotti, C Battisti, A Malandrini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 5, 2008
A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies
C Battisti, F Forte, M Molinelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 19, 2004
Cell response to oxidative stress induced apoptosis in patients with Leber's hereditary optic neuropathy
C Battisti, P Formichi, E Cardaioli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 3, 2004
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence?
C Battisti, M T Dotti, G Loudianos, et al.
Brain & Development
|
July 14, 1998
Clinical and stabilometric monitoring in a case of cerebellar atrophy with vitamin E deficiency
C Battisti, E D Toffola, A P Verri, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 66) with videos related to
Sort By:
Page
of 7
Journal of Cellular Physiology
|
April 29, 2006
Human fibroblasts undergo oxidative stress-induced apoptosis without internucleosomal DNA fragmentation
P Formichi, E Radi, C Battisti, et al.
Journal of the Neurological Sciences
|
August 1, 1997
Palpebral ptosis and muscle fatiguability associated with perineurial cell ensheathment of muscle fibers: a new disease of the neuromuscular junction?
A Federico, K Plewnia, C Battisti, et al.
European Neurology
|
January 1, 1991
Vitamin E deficiency secondary to chronic intestinal malabsorption and effect of vitamin supplement: a case report
A Federico, C Battisti, M P Eusebi, et al.
Journal of Neurology
|
November 27, 2013
Two-year follow-up after chelating therapy in a patient with adult-onset parkinsonism and hypermanganesaemia due to SLC30A10 mutations
L Di Toro Mammarella, A Mignarri, C Battisti, et al.
Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine
|
October 11, 1992
Sensitivity, resolution and image quality with a multi-head SPECT camera
F H Fahey, B A Harkness, J W Keyes, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
December 5, 2000
McLeod syndrome and neuroacanthocytosis with a novel mutation in the XK gene
M T Dotti, C Battisti, A Malandrini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
January 5, 2008
A new case of short-chain acyl-CoA dehydrogenase deficiency: clinical, biochemical, genetic and (1)H-NMR spectroscopic studies
C Battisti, F Forte, M Molinelli, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 19, 2004
Cell response to oxidative stress induced apoptosis in patients with Leber's hereditary optic neuropathy
C Battisti, P Formichi, E Cardaioli, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
April 3, 2004
Wilson's disease with Leu492Ser mutation and arylsulfatase A pseudodeficiency: just a coincidence?
C Battisti, M T Dotti, G Loudianos, et al.
Brain & Development
|
July 14, 1998
Clinical and stabilometric monitoring in a case of cerebellar atrophy with vitamin E deficiency
C Battisti, E D Toffola, A P Verri, et al.
Page
of 7