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Journal of the Neurological Sciences
|
August 20, 2016
Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome
M T Bonati, C Vanelli, D Sangalli, et al.
Experimental Neurology
|
May 5, 2005
Neuro-glial differentiation of human bone marrow stem cells in vitro
P Bossolasco, L Cova, C Calzarossa, et al.
Journal of Neurology
|
June 1, 1995
Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm
A Massari, M Gennarelli, E Menegazzo, et al.
Functional Neurology
|
July 1, 1991
Maintained cellular function of adrenal medullary cells in parkinsonian dysautonomia
A Falini, V Silani, A Pizzuti, et al.
Progress in Brain Research
|
January 1, 1988
Characterization of purified populations of human fetal chromaffin cells: considerations for grafting in parkinsonian patients
V Silani, G Pezzoli, E Motti, et al.
Vascular and Endovascular Surgery
|
October 11, 2011
Endovascular management of symptomatic cerebral malperfusion due to carotid dissection after type A aortic dissection repair
R Casana, V Tolva, A Robecchi Majnardi, et al.
Progress in Brain Research
|
January 1, 1990
Adrenal medulla autograft in 3 parkinsonian patients: results using two different approaches
G Pezzoli, E Motti, A Zecchinelli, et al.
Neuroreport
|
May 28, 1998
Immunomagnetic isolation of human developing motor neurons
V Silani, A Brioschi, M Braga, et al.
Cell Death & Disease
|
March 3, 2011
Mutant Huntingtin induces activation of the Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3)
J Sassone, C Colciago, P Marchi, et al.
Biochemical and Biophysical Research Communications
|
January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5
A Pizzuti, A Colosimo, A Ratti, et al.
Page
of 10
Search research articles
Search
Showing results (51-60 of 96) with videos related to
Sort By:
Page
of 10
Journal of the Neurological Sciences
|
August 20, 2016
Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome
M T Bonati, C Vanelli, D Sangalli, et al.
Experimental Neurology
|
May 5, 2005
Neuro-glial differentiation of human bone marrow stem cells in vitro
P Bossolasco, L Cova, C Calzarossa, et al.
Journal of Neurology
|
June 1, 1995
Postzygotic instability of the myotonic dystrophy p[AGC] in repeat supported by larger expansions in muscle and reduced amplifications in sperm
A Massari, M Gennarelli, E Menegazzo, et al.
Functional Neurology
|
July 1, 1991
Maintained cellular function of adrenal medullary cells in parkinsonian dysautonomia
A Falini, V Silani, A Pizzuti, et al.
Progress in Brain Research
|
January 1, 1988
Characterization of purified populations of human fetal chromaffin cells: considerations for grafting in parkinsonian patients
V Silani, G Pezzoli, E Motti, et al.
Vascular and Endovascular Surgery
|
October 11, 2011
Endovascular management of symptomatic cerebral malperfusion due to carotid dissection after type A aortic dissection repair
R Casana, V Tolva, A Robecchi Majnardi, et al.
Progress in Brain Research
|
January 1, 1990
Adrenal medulla autograft in 3 parkinsonian patients: results using two different approaches
G Pezzoli, E Motti, A Zecchinelli, et al.
Neuroreport
|
May 28, 1998
Immunomagnetic isolation of human developing motor neurons
V Silani, A Brioschi, M Braga, et al.
Cell Death & Disease
|
March 3, 2011
Mutant Huntingtin induces activation of the Bcl-2/adenovirus E1B 19-kDa interacting protein (BNip3)
J Sassone, C Colciago, P Marchi, et al.
Biochemical and Biophysical Research Communications
|
January 5, 1995
Identification of multiple transcribed sequences from the spinal muscular atrophy region of human chromosome 5
A Pizzuti, A Colosimo, A Ratti, et al.
Page
of 10