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Restagno

Showing results (81-90 of 166) with videos related to

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Neuromuscular Disorders : NMD|May 1, 1996
Prenatal diagnosis of limb-girdle muscular dystrophy type 2AG Restagno, N Romero, I Richard, et al.
Nature Communications|July 7, 2025
Mrc1 (MMR, CD206) controls the blood proteome in reducing inflammation, age-associated organ dysfunction and mortality in sepsisDamien Restagno, Mayank Saraswat, Peter V Aziz, et al.
The Journal of Biological Chemistry|August 10, 2004
Effect of ryanodine receptor mutations on interleukin-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia-susceptible individuals and patients affected by central core diseaseSylvie Ducreux, Francesco Zorzato, Clemens Müller, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 15, 2008
The rare G93D mutation causes a slowly progressing lower motor neuron diseaseGabriella Restagno, Federica Lombardo, Luca Sbaiz, et al.
Clinical Chemistry and Laboratory Medicine|September 5, 2009
Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator geneCaterina Mari, Francesca Bruno, Silvia Galbiati, et al.
Soft Matter|September 21, 2017
Interplay between bulk self-assembly, interfacial and foaming properties in a catanionic surfactant mixture of varying compositionJosé Ferreira, Alesya Mikhailovskaya, Alexis Chenneviere, et al.
American Journal of Medical Genetics|April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney DiseaseP Mandich, G Restagno, G Novelli, et al.
Clinical Chemistry|August 19, 2007
Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosisStefania Stenirri, Gabriella Restagno, Giovanni Battista Ferrero, et al.
Neurobiology of Aging|September 17, 2011
Mutational analysis of the VCP gene in Parkinson's diseaseElisa Majounie, Bryan J Traynor, Adriano Chiò, et al.
American Journal of Medical Genetics|October 16, 1996
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 GeneS Rossetti, E Bresin, G Restagno, et al.
Pageof 17

Showing results (81-90 of 166) with videos related to

Sort By:
Pageof 17
Neuromuscular Disorders : NMD|May 1, 1996
Prenatal diagnosis of limb-girdle muscular dystrophy type 2AG Restagno, N Romero, I Richard, et al.
Nature Communications|July 7, 2025
Mrc1 (MMR, CD206) controls the blood proteome in reducing inflammation, age-associated organ dysfunction and mortality in sepsisDamien Restagno, Mayank Saraswat, Peter V Aziz, et al.
The Journal of Biological Chemistry|August 10, 2004
Effect of ryanodine receptor mutations on interleukin-6 release and intracellular calcium homeostasis in human myotubes from malignant hyperthermia-susceptible individuals and patients affected by central core diseaseSylvie Ducreux, Francesco Zorzato, Clemens Müller, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|February 15, 2008
The rare G93D mutation causes a slowly progressing lower motor neuron diseaseGabriella Restagno, Federica Lombardo, Luca Sbaiz, et al.
Clinical Chemistry and Laboratory Medicine|September 5, 2009
Application of pyrosequencing to the identification of sequence variations in the cystic fibrosis transmembrane conductance regulator geneCaterina Mari, Francesca Bruno, Silvia Galbiati, et al.
Soft Matter|September 21, 2017
Interplay between bulk self-assembly, interfacial and foaming properties in a catanionic surfactant mixture of varying compositionJosé Ferreira, Alesya Mikhailovskaya, Alexis Chenneviere, et al.
American Journal of Medical Genetics|April 1, 1990
Autosomal dominant polycystic kidney disease: a linkage evaluation of heterogeneity in Italy. Italian Collaborative Group on Polycystic Kidney DiseaseP Mandich, G Restagno, G Novelli, et al.
Clinical Chemistry|August 19, 2007
Integrated strategy for fast and automated molecular characterization of genes involved in craniosynostosisStefania Stenirri, Gabriella Restagno, Giovanni Battista Ferrero, et al.
Neurobiology of Aging|September 17, 2011
Mutational analysis of the VCP gene in Parkinson's diseaseElisa Majounie, Bryan J Traynor, Adriano Chiò, et al.
American Journal of Medical Genetics|October 16, 1996
Autosomal dominant polycystic kidney disease (ADPKD) in an Italian family carrying a novel nonsense mutation and two missense changes in exons 44 and 45 of the PKD1 GeneS Rossetti, E Bresin, G Restagno, et al.
Pageof 17