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G Airoldi

Showing results (31-40 of 38) with videos related to

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Minerva Nefrologica|January 1, 1979
[Plasma catecholamines and chronic hypotension in hemodialysis]G Verzetti, G B Picotti, C Ravazzani, et al.
Clinical Genetics|September 20, 2007
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraineA Tonelli, A Gallanti, A Bersano, et al.
European Journal of Clinical Pharmacology|January 1, 1985
Multicentre comparison of the antihypertensive effect of acebutolol and hydrochlorothiazide in uncomplicated mild-moderate hypertension in the elderlyA Salvetti, M Lucchini, G Airoldi, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|July 1, 1991
[Variability of the response to recombinant human erythropoietin in patients undergoing hemodialysis treatment]A Baroni, G Airoldi, S Agliata, et al.
Lipids in Health and Disease|May 26, 2018
LDL-cholesterol lowering effect of a new dietary supplement: an open label, controlled, randomized, cross-over clinical trial in patients with mild-to-moderate hypercholesterolemiaS Magno, G Ceccarini, C Pelosini, et al.
Journal of Medical Genetics|August 6, 2010
The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2KC Crimella, A Tonelli, G Airoldi, et al.
Clinical Genetics|June 1, 2011
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2C Crimella, C Baschirotto, A Arnoldi, et al.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Minerva Nefrologica|January 1, 1979
[Plasma catecholamines and chronic hypotension in hemodialysis]G Verzetti, G B Picotti, C Ravazzani, et al.
Clinical Genetics|September 20, 2007
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraineA Tonelli, A Gallanti, A Bersano, et al.
European Journal of Clinical Pharmacology|January 1, 1985
Multicentre comparison of the antihypertensive effect of acebutolol and hydrochlorothiazide in uncomplicated mild-moderate hypertension in the elderlyA Salvetti, M Lucchini, G Airoldi, et al.
Minerva Urologica E Nefrologica = the Italian Journal of Urology and Nephrology|July 1, 1991
[Variability of the response to recombinant human erythropoietin in patients undergoing hemodialysis treatment]A Baroni, G Airoldi, S Agliata, et al.
Lipids in Health and Disease|May 26, 2018
LDL-cholesterol lowering effect of a new dietary supplement: an open label, controlled, randomized, cross-over clinical trial in patients with mild-to-moderate hypercholesterolemiaS Magno, G Ceccarini, C Pelosini, et al.
Journal of Medical Genetics|August 6, 2010
The GST domain of GDAP1 is a frequent target of mutations in the dominant form of axonal Charcot Marie Tooth type 2KC Crimella, A Tonelli, G Airoldi, et al.
Clinical Genetics|June 1, 2011
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2C Crimella, C Baschirotto, A Arnoldi, et al.
Neurology|October 24, 2008
Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunctionR Del Bo, M Moggio, M Rango, et al.
Pageof 4