Search research articles
Contact Us
Filters
Showing results (281-290 of 420) with videos related to
Page
of 42
Sort By:
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.
Cardiologia (Rome, Italy)
|
June 1, 1992
[Aortic stenosis and coronary pathology. Their implications for the transvalvular gradient]
G Di Tano, A Mazzù, R Cogode, et al.
Epilepsia
|
May 5, 2026
Can we predict surgical outcomes: A systematic review and critical appraisal of clinical prediction models in epilepsy surgery
Alyssa A Federico, Mandavi Kashyap, Chantelle Q Y Lin, et al.
Neurology
|
December 30, 2009
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients
L Pantoni, F Pescini, S Nannucci, et al.
Acta Neurologica
|
May 1, 1974
[Sanfilippo's disease: clinico-genetic and biological study of 2 families]
S Carlomagno, A Federico, F Vitiello, et al.
European Journal of Neurology
|
April 21, 2010
Four novel CYP27A1 mutations in seven Italian patients with CTX
G N Gallus, M T Dotti, A Mignarri, 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.
Acta Neurologica
|
June 1, 1994
Primary antiphospholipid syndrome: two case reports, one with histological examination of skin, peripheral nerve and muscle
M Macucci, M T Dotti, S Battistini, et al.
Environmental Monitoring and Assessment
|
May 13, 2014
Hidden sources of mercury in clinical laboratories
C R Alvarez-Chavez, R A Federico-Perez, A Gomez-Alvarez, et al.
Acta Neurologica
|
May 1, 1974
[Familial sulfatidosis associated with systemic ponto-cerebellar atrophy: clinical, biochemical, genetic and anatomo-pathological study]
A Federico, G Turchiaro, S Carlomagno, et al.
Page
of 42
Search research articles
Search
Showing results (281-290 of 420) with videos related to
Sort By:
Page
of 42
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.
Cardiologia (Rome, Italy)
|
June 1, 1992
[Aortic stenosis and coronary pathology. Their implications for the transvalvular gradient]
G Di Tano, A Mazzù, R Cogode, et al.
Epilepsia
|
May 5, 2026
Can we predict surgical outcomes: A systematic review and critical appraisal of clinical prediction models in epilepsy surgery
Alyssa A Federico, Mandavi Kashyap, Chantelle Q Y Lin, et al.
Neurology
|
December 30, 2009
Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients
L Pantoni, F Pescini, S Nannucci, et al.
Acta Neurologica
|
May 1, 1974
[Sanfilippo's disease: clinico-genetic and biological study of 2 families]
S Carlomagno, A Federico, F Vitiello, et al.
European Journal of Neurology
|
April 21, 2010
Four novel CYP27A1 mutations in seven Italian patients with CTX
G N Gallus, M T Dotti, A Mignarri, 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.
Acta Neurologica
|
June 1, 1994
Primary antiphospholipid syndrome: two case reports, one with histological examination of skin, peripheral nerve and muscle
M Macucci, M T Dotti, S Battistini, et al.
Environmental Monitoring and Assessment
|
May 13, 2014
Hidden sources of mercury in clinical laboratories
C R Alvarez-Chavez, R A Federico-Perez, A Gomez-Alvarez, et al.
Acta Neurologica
|
May 1, 1974
[Familial sulfatidosis associated with systemic ponto-cerebellar atrophy: clinical, biochemical, genetic and anatomo-pathological study]
A Federico, G Turchiaro, S Carlomagno, et al.
Page
of 42