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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 17, 2015
Paternal germline mosaicism in collagen VI related myopathies
Annarita Armaroli, Cecilia Trabanelli, Chiara Scotton, et al.
The Journal of Headache and Pain
|
June 9, 2017
De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Stella Gagliardi, Gaetano Salvatore Grieco, Francesca Gualandi, et al.
Journal of the American College of Cardiology
|
June 4, 2021
Type 1 Brugada Pattern Is Associated With Echocardiography-Detected Delayed Right Ventricular Outflow Tract Contraction
Filippo Trevisan, Matteo Bertini, Cristina Balla, et al.
Circulation. Genomic and Precision Medicine
|
November 9, 2021
Novel <i>SCN5A</i> Variant Shows Multiple Phenotypic Expression in the Same Family
Cristina Balla, Daniela Mele, Francesco Vitali, et al.
Chemotherapy
|
March 7, 2019
Ivabradine in Cancer Treatment-Related Left Ventricular Dysfunction
Matteo Sarocchi, Eleonora Arboscello, Giorgio Ghigliotti, et al.
Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology
|
April 14, 2021
Different Susceptibility of T and B Cells to Cladribine Depends On Their Levels of Deoxycytidine Kinase Activity Linked to Activation Status
Federico Carlini, Federico Ivaldi, Francesca Gualandi, et al.
The Journal of Headache and Pain
|
July 14, 2017
Erratum to: De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Stella Gagliardi, Gaetano Salvatore Grieco, Francesca Gualandi, et al.
Annals of Neurology
|
November 8, 2014
A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield
Arunkanth Ankala, Cristina da Silva, Francesca Gualandi, et al.
Plos One
|
September 18, 2020
Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study
Borut Peterlin, Francesca Gualandi, Ales Maver, et al.
Prenatal Diagnosis
|
October 10, 2006
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories
Alessandra Ferlini, Anna Ravani, Anna Venturoli, et al.
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of 17
Search research articles
Search
Showing results (31-40 of 169) with videos related to
Sort By:
Page
of 17
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
May 17, 2015
Paternal germline mosaicism in collagen VI related myopathies
Annarita Armaroli, Cecilia Trabanelli, Chiara Scotton, et al.
The Journal of Headache and Pain
|
June 9, 2017
De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Stella Gagliardi, Gaetano Salvatore Grieco, Francesca Gualandi, et al.
Journal of the American College of Cardiology
|
June 4, 2021
Type 1 Brugada Pattern Is Associated With Echocardiography-Detected Delayed Right Ventricular Outflow Tract Contraction
Filippo Trevisan, Matteo Bertini, Cristina Balla, et al.
Circulation. Genomic and Precision Medicine
|
November 9, 2021
Novel <i>SCN5A</i> Variant Shows Multiple Phenotypic Expression in the Same Family
Cristina Balla, Daniela Mele, Francesco Vitali, et al.
Chemotherapy
|
March 7, 2019
Ivabradine in Cancer Treatment-Related Left Ventricular Dysfunction
Matteo Sarocchi, Eleonora Arboscello, Giorgio Ghigliotti, et al.
Journal of Neuroimmune Pharmacology : the Official Journal of the Society on Neuroimmune Pharmacology
|
April 14, 2021
Different Susceptibility of T and B Cells to Cladribine Depends On Their Levels of Deoxycytidine Kinase Activity Linked to Activation Status
Federico Carlini, Federico Ivaldi, Francesca Gualandi, et al.
The Journal of Headache and Pain
|
July 14, 2017
Erratum to: De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report
Stella Gagliardi, Gaetano Salvatore Grieco, Francesca Gualandi, et al.
Annals of Neurology
|
November 8, 2014
A comprehensive genomic approach for neuromuscular diseases gives a high diagnostic yield
Arunkanth Ankala, Cristina da Silva, Francesca Gualandi, et al.
Plos One
|
September 18, 2020
Genetic testing offer for inherited neuromuscular diseases within the EURO-NMD reference network: A European survey study
Borut Peterlin, Francesca Gualandi, Ales Maver, et al.
Prenatal Diagnosis
|
October 10, 2006
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories
Alessandra Ferlini, Anna Ravani, Anna Venturoli, et al.
Page
of 17