Silvia Morlino

Management of pain and fatigue in the joint hypermobility syndrome (a.k.a. Ehlers–Danlos syndrome, hypermobility type): Principles and proposal for a multidisciplinary approach

Marco Castori, Silvia Morlino, Claudia Celletti et al. · American Journal of Medical Genetics Part A · 2012 · 150 citations

Nosology and inheritance pattern(s) of joint hypermobility syndrome and Ehlers‐Danlos syndrome, hypermobility type: A study of intrafamilial and interfamilial variability in 23 Italian pedigrees

Marco Castori, Chiara Dordoni, Michele Valiante et al. · American Journal of Medical Genetics Part A · 2014 · 79 citations

<i>COL1</i> ‐related overlap disorder: A novel connective tissue disorder incorporating the osteogenesis imperfecta/Ehlers‐Danlos syndrome overlap

Silvia Morlino, Lucia Micale, Marco Ritelli et al. · Clinical Genetics · 2019 · 55 citations

Missense mutations of CACNA1A are a frequent cause of autosomal dominant nonprogressive congenital ataxia

Lorena Travaglini, Marta Nardella, Emanuele Bellacchio et al. · European Journal of Paediatric Neurology · 2016 · 54 citations

Missense Mutations, Developmental Biology, Mendelian Disorder +6

Severity classes in adults with hypermobile Ehlers–Danlos syndrome/hypermobility spectrum disorders: a pilot study of 105 Italian patients

Massimiliano Copetti, Silvia Morlino, Marina Colombi et al. · Lara D. Veeken · 2019 · 53 citations · Full text