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Neuromuscular Disorders : NMD
|
June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study
S Messina, M Mora, E Pegoraro, et al.
Neurology
|
September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population study
S Messina, C Bruno, I Moroni, et al.
International Journal of Cardiology
|
February 11, 2023
Corrigendum to "Impact of hemoglobin levels at admission on outcomes among elderly patients with acute coronary syndrome treated with low-dose Prasugrel or clopidogrel: A sub-study of the ELDERLY ACS 2 trial" [Int J Cardiol. 2022 Dec 15;369:5-11]
G De Luca, M Verdoia, N Morici, et al.
Neurology
|
March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study
E Mercuri, S Messina, C Bruno, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathies
Lorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 35) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 35 results.
Neuromuscular Disorders : NMD
|
June 3, 2008
POMT1 and POMT2 mutations in CMD patients: a multicentric Italian study
S Messina, M Mora, E Pegoraro, et al.
Neurology
|
September 8, 2010
Congenital muscular dystrophies with cognitive impairment. A population study
S Messina, C Bruno, I Moroni, et al.
International Journal of Cardiology
|
February 11, 2023
Corrigendum to "Impact of hemoglobin levels at admission on outcomes among elderly patients with acute coronary syndrome treated with low-dose Prasugrel or clopidogrel: A sub-study of the ELDERLY ACS 2 trial" [Int J Cardiol. 2022 Dec 15;369:5-11]
G De Luca, M Verdoia, N Morici, et al.
Neurology
|
March 21, 2009
Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study
E Mercuri, S Messina, C Bruno, et al.
American Journal of Medical Genetics. Part A
|
September 19, 2009
Expanding CEP290 mutational spectrum in ciliopathies
Lorena Travaglini, Francesco Brancati, Tania Attie-Bitach, et al.
Page
of 4