Search research articles
Contact Us
Filters
Showing results (41-50 of 53) with videos related to
Page
of 6
Sort By:
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL families
M T Dotti, A Federico, R Mazzei, et al.
Neurology
|
October 13, 2004
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)
F L Conforti, M Muglia, R Mazzei, et al.
Neurology
|
December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL
M Liguori, R Mazzei, C Ungaro, et al.
Membranes
|
September 11, 2020
Poly[3-ethyl-1-vinyl-imidazolium] diethyl phosphate/Pebax<sup>®</sup> 1657 Composite Membranes and Their Gas Separation Performance
Irene R Mazzei, Daria Nikolaeva, Alessio Fuoco, et al.
Epilepsia
|
October 3, 2001
Silent celiac disease in patients with childhood localization-related epilepsies
A Labate, A Gambardella, D Messina, et al.
Archives of Neurology
|
September 18, 2001
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings
R L Oliveri, M Muglia, N De Stefano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2007
First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL
R Mazzei, D Guidetti, C Ungaro, et al.
The American Journal of Cardiology
|
December 8, 2009
Usefulness of the Duke Sudden Cardiac Death risk score for predicting sudden cardiac death in patients with angiographic (>75% narrowing) coronary artery disease
Brett D Atwater, Vivian P Thompson, Richard N Vest, et al.
Neurology
|
January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy
M Muglia, M Zappia, V Timmerman, et al.
Neurology
|
August 12, 2004
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL
R Mazzei, F L Conforti, P L Lanza, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 53) with videos related to
Sort By:
Page
of 6
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 19, 2005
The spectrum of Notch3 mutations in 28 Italian CADASIL families
M T Dotti, A Federico, R Mazzei, et al.
Neurology
|
October 13, 2004
A new SBF2 mutation in a family with recessive demyelinating Charcot-Marie-Tooth (CMT4B2)
F L Conforti, M Muglia, R Mazzei, et al.
Neurology
|
December 6, 2008
Conventional MRI and NOTCH3 gene screening in sporadic CADASIL
M Liguori, R Mazzei, C Ungaro, et al.
Membranes
|
September 11, 2020
Poly[3-ethyl-1-vinyl-imidazolium] diethyl phosphate/Pebax<sup>®</sup> 1657 Composite Membranes and Their Gas Separation Performance
Irene R Mazzei, Daria Nikolaeva, Alessio Fuoco, et al.
Epilepsia
|
October 3, 2001
Silent celiac disease in patients with childhood localization-related epilepsies
A Labate, A Gambardella, D Messina, et al.
Archives of Neurology
|
September 18, 2001
A novel mutation in the Notch3 gene in an Italian family with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: genetic and magnetic resonance spectroscopic findings
R L Oliveri, M Muglia, N De Stefano, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2007
First evidence of a pathogenic insertion in the NOTCH3 gene causing CADASIL
R Mazzei, D Guidetti, C Ungaro, et al.
The American Journal of Cardiology
|
December 8, 2009
Usefulness of the Duke Sudden Cardiac Death risk score for predicting sudden cardiac death in patients with angiographic (>75% narrowing) coronary artery disease
Brett D Atwater, Vivian P Thompson, Richard N Vest, et al.
Neurology
|
January 10, 2001
Clinical and genetic study of a large Charcot-Marie-Tooth type 2A family from southern Italy
M Muglia, M Zappia, V Timmerman, et al.
Neurology
|
August 12, 2004
A novel Notch3 gene mutation not involving a cysteine residue in an Italian family with CADASIL
R Mazzei, F L Conforti, P L Lanza, et al.
Page
of 6