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E Mercuri

Showing results (121-130 of 150) with videos related to

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Neuromuscular Disorders : NMD|January 7, 2018
Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functionsR Battini, D Chieffo, S Bulgheroni, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
Neuropediatrics|November 7, 2007
Antenatal post-hemorrhagic ventriculomegaly: a prospective follow-up studyR Luciano, G Baranello, L Masini, et al.
Neuropediatrics|July 2, 2009
Visual function in Noonan and LEOPARD syndromeP Alfieri, L Cesarini, G Zampino, et al.
Neuropediatrics|August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxityE Mercuri, A Lampe, V Straub, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 24, 2008
Muscular dystrophies due to defective glycosylation of dystroglycanF Muntoni, M Brockington, C Godfrey, et al.
American Journal of Human Genetics|October 10, 2001
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycanM Brockington, D J Blake, P Prandini, et al.
Neuromuscular Disorders : NMD|March 8, 2013
Duchenne muscular dystrophy and epilepsyM Pane, S Messina, C Bruno, et al.
Human Mutation|October 15, 2008
Transcriptional behavior of DMD gene duplications in DMD/BMD malesF Gualandi, M Neri, M Bovolenta, et al.
Brain & Development|February 17, 2006
Auditory attention at the onset of West syndrome: correlation with EEG patterns and visual functionG Baranello, T Randò, A Bancale, et al.
Pageof 15

Showing results (121-130 of 150) with videos related to

Sort By:
Pageof 15
Neuromuscular Disorders : NMD|January 7, 2018
Cognitive profile in Duchenne muscular dystrophy boys without intellectual disability: The role of executive functionsR Battini, D Chieffo, S Bulgheroni, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndromeM Villanova, E Mercuri, E Bertini, et al.
Neuropediatrics|November 7, 2007
Antenatal post-hemorrhagic ventriculomegaly: a prospective follow-up studyR Luciano, G Baranello, L Masini, et al.
Neuropediatrics|July 2, 2009
Visual function in Noonan and LEOPARD syndromeP Alfieri, L Cesarini, G Zampino, et al.
Neuropediatrics|August 26, 2004
Congenital muscular dystrophy with short stature, proximal contractures and distal laxityE Mercuri, A Lampe, V Straub, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 24, 2008
Muscular dystrophies due to defective glycosylation of dystroglycanF Muntoni, M Brockington, C Godfrey, et al.
American Journal of Human Genetics|October 10, 2001
Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy with secondary laminin alpha2 deficiency and abnormal glycosylation of alpha-dystroglycanM Brockington, D J Blake, P Prandini, et al.
Neuromuscular Disorders : NMD|March 8, 2013
Duchenne muscular dystrophy and epilepsyM Pane, S Messina, C Bruno, et al.
Human Mutation|October 15, 2008
Transcriptional behavior of DMD gene duplications in DMD/BMD malesF Gualandi, M Neri, M Bovolenta, et al.
Brain & Development|February 17, 2006
Auditory attention at the onset of West syndrome: correlation with EEG patterns and visual functionG Baranello, T Randò, A Bancale, et al.
Pageof 15