Author

Martina Petrollini

Institution: Istituto Neurologico Mediterraneo

Observed institutions: Hospital de Sant Pau, Istituto Neurologico Mediterraneo, Complejo Hospitalario de Navarra, Hospital Universitario de Burgos, Hospital Universitario Fundación Jiménez Díaz

OpenAlex ID: A5074558071

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

2017 · Davina J Hensman Moss, Antonio F Pardiñas, et al. · The Lancet Neurology · 310

Clinical manifestations of intermediate allele carriers in Huntington disease

2016 · Esther Cubo, María A. Ramos-Arroyo, et al. · Neurology · 53

The role of iron in gray matter degeneration in Huntington's disease: A magnetic resonance imaging study

2014 · Cristina Sánchez-Castañeda, Ferdinando Squitieri, et al. · Human Brain Mapping · 46

Reduced Cancer Incidence in Huntington’s Disease: Analysis in the Registry Study

2018 · Paul McNulty, Richard Pilcher, et al. · Journal of Huntington s Disease · 35

The personal experience of parenting a child with Juvenile Huntington’s Disease: perceptions across Europe

2013 · Virginia Eatough, Helen Santini, et al. · European Journal of Human Genetics · 20

Works count: 5

Citation count: 464

H-index: 5

I10-index: 5