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Minerva Medica
|
April 30, 1987
[Syncope]
G Beccari, P Cicognani, G Piscaglia
Minerva Cardioangiologica
|
October 1, 1986
[Precordial pain and cardiac amyloidosis]
G Beccari, M G Piscaglia, B Cavallini, et al.
American Journal of Human Genetics
|
June 12, 1999
A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia
J Kaukonen, M Zeviani, G P Comi, et al.
European Neurology
|
January 1, 1989
Lacunar infarcts: a personal series of 92 consecutive cases
G Ciucci, A Stracciari, G Bissi, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
New therapeutic perspectives for demyelinating retrobulbar optic neuritis
B Currò Dossi, A Amadori, C Cirafisi, et al.
American Journal of Human Genetics
|
April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p
J A Kaukonen, P Amati, A Suomalainen, et al.
Journal of Inherited Metabolic Disease
|
September 3, 1999
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa
G M Hadjigeorgiou, G P Comi, A Bordoni, et al.
Neurology and Therapy
|
August 2, 2024
Predicted Expenditure for Prescription Drugs for Multiple Sclerosis in the Italian Market Between 2023 and 2028: Results of the Oracle Project
Damiano Paolicelli, Giovanna Borriello, Raffaella Clerici, et al.
Multiple Sclerosis and Related Disorders
|
December 1, 2024
Hypogammaglobulinemia and severe infections in Multiple Sclerosis patients on anti-CD20 agents: A multicentre study
K Smolik, F Camilli, I Panzera, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Minerva Medica
|
April 30, 1987
[Syncope]
G Beccari, P Cicognani, G Piscaglia
Minerva Cardioangiologica
|
October 1, 1986
[Precordial pain and cardiac amyloidosis]
G Beccari, M G Piscaglia, B Cavallini, et al.
American Journal of Human Genetics
|
June 12, 1999
A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia
J Kaukonen, M Zeviani, G P Comi, et al.
European Neurology
|
January 1, 1989
Lacunar infarcts: a personal series of 92 consecutive cases
G Ciucci, A Stracciari, G Bissi, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
New therapeutic perspectives for demyelinating retrobulbar optic neuritis
B Currò Dossi, A Amadori, C Cirafisi, et al.
American Journal of Human Genetics
|
April 1, 1996
An autosomal locus predisposing to multiple deletions of mtDNA on chromosome 3p
J A Kaukonen, P Amati, A Suomalainen, et al.
Journal of Inherited Metabolic Disease
|
September 3, 1999
Novel donor splice site mutations of AGL gene in glycogen storage disease type IIIa
G M Hadjigeorgiou, G P Comi, A Bordoni, et al.
Neurology and Therapy
|
August 2, 2024
Predicted Expenditure for Prescription Drugs for Multiple Sclerosis in the Italian Market Between 2023 and 2028: Results of the Oracle Project
Damiano Paolicelli, Giovanna Borriello, Raffaella Clerici, et al.
Multiple Sclerosis and Related Disorders
|
December 1, 2024
Hypogammaglobulinemia and severe infections in Multiple Sclerosis patients on anti-CD20 agents: A multicentre study
K Smolik, F Camilli, I Panzera, et al.
Page
of 1