Patrizia Suppressa

Worldwide experience of homozygous familial hypercholesterolaemia: retrospective cohort study

Tycho R. Tromp, Merel L. Hartgers, G. Kees Hovingh et al. · The Lancet · 2022 · 189 citations · Full text

Metabolic Syndrome, Lipid Disorder, Cardiovascular Disease +7

Hereditary hemorrhagic telangiectasia: clinical features in ENG and ALK1 mutation carriers

Carlo Sabbà, Giuseppe Pasculli, Gennaro Mariano Lenato et al. · Journal of Thrombosis and Haemostasis · 2007 · 180 citations · Full text

Alk1 Mutation Carriers, Hereditary Hemorrhagic Telangiectasia, Genetic Disorder +7

A long diagnostic delay in patients with Hereditary Haemorrhagic Telangiectasia: a questionnaire-based retrospective study

Paola Pierucci, Gennaro Mariano Lenato, Patrizia Suppressa et al. · Orphanet Journal of Rare Diseases · 2012 · 109 citations · Full text

Health-related quality of life in a rare disease: Hereditary hemorrhagic telangiectasia (HHT) or Rendu?Osler?Weber Disease

Giovanna Pasculli, Francesco Resta, Edoardo Guastamacchia et al. · Quality of Life Research · 2004 · 107 citations

Quality Of Life, Rare Disease, Health-related Quality +8

Liver involvement in a large cohort of patients with hereditary hemorrhagic telangiectasia: Echo-color-Doppler vs multislice computed tomography study

Paolo Buonamico, Patrizia Suppressa, Gennaro Mariano Lenato et al. · Journal of Hepatology · 2008 · 83 citations

Hepatology, Liver Involvement, Pathology +5