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The International Journal of Developmental Biology
|
February 11, 2000
Initiation, establishment and maintenance of Hox gene expression patterns in the mouse
J Deschamps, E van den Akker, S Forlani, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology
|
October 5, 2001
[Aortocoronary bypass in severe left ventricular dysfunction: 9 years of clinical experience and mid-term results]
P Nardi, R De Paulis, A Penta de Peppo, et al.
The Journal of Cardiovascular Surgery
|
March 12, 2002
Troponin I release after CABG surgery using two different strategies of myocardial protection and systemic perfusion
R De Paulis, A Penta De Peppo, L Colagrande, et al.
Neurology
|
January 13, 2006
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
M Namekawa, P Ribai, I Nelson, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology
|
February 24, 2001
[Bentall-DeBono intervention: 8 years of clinical experience]
A Scafuri, P Nardi, S Forlani, et al.
The Journal of Cardiovascular Surgery
|
June 5, 2004
Preoperative shift from glibenclamide to insulin is cardioprotective in diabetic patients undergoing coronary artery bypass surgery
S Forlani, F Tomai, R De Paulis, et al.
Giornale Italiano Di Cardiologia
|
August 12, 1999
Mid-term results of conventional bypass surgery for complex proximal left anterior descending coronary artery stenoses
S Forlani, C Bassano, F Tomai, et al.
Giornale Italiano Di Cardiologia
|
October 9, 1999
Beneficial impact of isoflurane during coronary bypass surgery on troponin I release
F Tomai, R De Paulis, A Penta de Peppo, et al.
Neurology
|
April 10, 2009
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24
R Schüle, M Bonin, A Dürr, et al.
Neurology
|
October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
C Goizet, A Boukhris, D Maltete, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
The International Journal of Developmental Biology
|
February 11, 2000
Initiation, establishment and maintenance of Hox gene expression patterns in the mouse
J Deschamps, E van den Akker, S Forlani, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology
|
October 5, 2001
[Aortocoronary bypass in severe left ventricular dysfunction: 9 years of clinical experience and mid-term results]
P Nardi, R De Paulis, A Penta de Peppo, et al.
The Journal of Cardiovascular Surgery
|
March 12, 2002
Troponin I release after CABG surgery using two different strategies of myocardial protection and systemic perfusion
R De Paulis, A Penta De Peppo, L Colagrande, et al.
Neurology
|
January 13, 2006
SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years
M Namekawa, P Ribai, I Nelson, et al.
Italian Heart Journal. Supplement : Official Journal of the Italian Federation of Cardiology
|
February 24, 2001
[Bentall-DeBono intervention: 8 years of clinical experience]
A Scafuri, P Nardi, S Forlani, et al.
The Journal of Cardiovascular Surgery
|
June 5, 2004
Preoperative shift from glibenclamide to insulin is cardioprotective in diabetic patients undergoing coronary artery bypass surgery
S Forlani, F Tomai, R De Paulis, et al.
Giornale Italiano Di Cardiologia
|
August 12, 1999
Mid-term results of conventional bypass surgery for complex proximal left anterior descending coronary artery stenoses
S Forlani, C Bassano, F Tomai, et al.
Giornale Italiano Di Cardiologia
|
October 9, 1999
Beneficial impact of isoflurane during coronary bypass surgery on troponin I release
F Tomai, R De Paulis, A Penta de Peppo, et al.
Neurology
|
April 10, 2009
Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24
R Schüle, M Bonin, A Dürr, et al.
Neurology
|
October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
C Goizet, A Boukhris, D Maltete, et al.
Page
of 2