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European Journal of Neurology
|
November 7, 2025
Joint Modelling of Growth and Motor Function Centiles in Corticosteroids Treated Boys With Duchenne Muscular Dystrophy
Georgia Stimpson, Deborah Ridout, Amy Wolfe, et al.
International Journal of Cardiology
|
August 15, 2006
Diffuse coronary dilation in a young patient with LEOPARD syndrome
Giuseppe Pacileo, Paolo Calabrò, Giuseppe Limongelli, et al.
Nature Reviews. Neurology
|
February 3, 2018
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction
Heinz Jungbluth, Susan Treves, Francesco Zorzato, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2008
Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome)
M Cristina Digilio, Flaminia Calzolari, Rossella Capolino, et al.
International Journal of Cardiology
|
March 20, 2009
Exclusion of Cx43 gene mutation as a major cause of criss-cross heart anomaly in man
Alessandro De Luca, Anna Sarkozy, Federica Consoli, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2003
Nonsyndromic pulmonary valve stenosis and the PTPN11 gene
Anna Sarkozy, Emanuela Conti, Giorgia Esposito, et al.
European Journal of Human Genetics : EJHG
|
April 18, 2003
DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 gene
Emanuela Conti, Nicoletta Grifone, Anna Sarkozy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 5, 2024
Understanding North Star Ambulatory Assessment total scores and their implications for standards of care using observational data
Georgia Stimpson, Meredith K James, Michela Guglieri, et al.
Plos Currents
|
June 22, 2013
Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis
Elizabeth Harris, Steve Laval, Judith Hudson, et al.
American Journal of Medical Genetics. Part A
|
January 12, 2005
ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia
Anna Sarkozy, Emanuela Conti, Rita D'Agostino, et al.
Page
of 14
Search research articles
Search
Showing results (31-40 of 137) with videos related to
Sort By:
Page
of 14
European Journal of Neurology
|
November 7, 2025
Joint Modelling of Growth and Motor Function Centiles in Corticosteroids Treated Boys With Duchenne Muscular Dystrophy
Georgia Stimpson, Deborah Ridout, Amy Wolfe, et al.
International Journal of Cardiology
|
August 15, 2006
Diffuse coronary dilation in a young patient with LEOPARD syndrome
Giuseppe Pacileo, Paolo Calabrò, Giuseppe Limongelli, et al.
Nature Reviews. Neurology
|
February 3, 2018
Congenital myopathies: disorders of excitation-contraction coupling and muscle contraction
Heinz Jungbluth, Susan Treves, Francesco Zorzato, et al.
American Journal of Medical Genetics. Part A
|
June 17, 2008
Congenital heart defects in patients with oculo-auriculo-vertebral spectrum (Goldenhar syndrome)
M Cristina Digilio, Flaminia Calzolari, Rossella Capolino, et al.
International Journal of Cardiology
|
March 20, 2009
Exclusion of Cx43 gene mutation as a major cause of criss-cross heart anomaly in man
Alessandro De Luca, Anna Sarkozy, Federica Consoli, et al.
American Journal of Medical Genetics. Part A
|
January 11, 2003
Nonsyndromic pulmonary valve stenosis and the PTPN11 gene
Anna Sarkozy, Emanuela Conti, Giorgia Esposito, et al.
European Journal of Human Genetics : EJHG
|
April 18, 2003
DiGeorge subtypes of nonsyndromic conotruncal defects: evidence against a major role of TBX1 gene
Emanuela Conti, Nicoletta Grifone, Anna Sarkozy, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 5, 2024
Understanding North Star Ambulatory Assessment total scores and their implications for standards of care using observational data
Georgia Stimpson, Meredith K James, Michela Guglieri, et al.
Plos Currents
|
June 22, 2013
Undiagnosed genetic muscle disease in the north of England: an in depth phenotype analysis
Elizabeth Harris, Steve Laval, Judith Hudson, et al.
American Journal of Medical Genetics. Part A
|
January 12, 2005
ZFPM2/FOG2 and HEY2 genes analysis in nonsyndromic tricuspid atresia
Anna Sarkozy, Emanuela Conti, Rita D'Agostino, et al.
Page
of 14