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23 results for Fortunato,+Giuliana

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Rare variants in PKHD1 associated with Caroli syndrome: Two case reports
Author / Creator:Giacobbe, Carola ; Di Dato, Fabiola ; Palma, Daniela ; Amitrano, Michele ; Iorio, Raffaele ; Fortunato, Giuliana
Publisher:Bognor Regis: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2022-08, Vol.10 (8), p.e1998-n/a
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Age-related changes of cholestanol and lathosterol plasma concentrations: an explorative study
Author / Creator:Gelzo, Monica ; Di Taranto, Maria Donata ; Sica, Concetta ; Boscia, Antonio ; Papagni, Francesco ; Fortunato, Giuliana ; Corso, Gaetano ; Dello Russo, Antonio
Publisher:England: BioMed Central Ltd
Journal title:Lipids in health and disease, 2019-12, Vol.18 (1), p.235-6, Article 235
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Assessment of Platelet Aggregation and Thrombin Generation in Patients with Familial Chylomicronemia Syndrome Treated with Volanesorsen: A Cross-Sectional Study
Author / Creator:Calcaterra, Ilenia Lorenza ; Santoro, Renata ; Vitelli, Nicoletta ; Cirillo, Ferdinando ; D’Errico, Guido ; Guerrino, Cornelia ; Cardiero, Giovanna ; Di Taranto, Maria Donata ; Fortunato, Giuliana ; Iannuzzo, Gabriella ; Di Minno, Matteo Nicola Dario
Publisher:Switzerland: MDPI AG
Journal title:Biomedicines, 2024-09, Vol.12 (9), p.2017
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Calprotectin Levels and Neutrophil Count Are Prognostic Markers of Mortality in COVID-19 Patients
Author / Creator:Cardiero, Giovanna ; Palma, Daniela ; Vano, Martina ; Anastasio, Claudia ; Pinchera, Biagio ; Ferrandino, Martina ; Gianfico, Carlo ; Gentile, Luca ; Savoia, Marcella ; Gentile, Ivan ; Di Taranto, Maria Donata ; Fortunato, Giuliana
Publisher:Basel: MDPI AG
Journal title:Diagnostics (Basel), 2022-10, Vol.12 (10), p.2554
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Corrigendum to “Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy”
Author / Creator:Sacchetti, Lucia ; Contaldo, Franco ; Finelli, Carmine ; Nardelli, Carmela ; Fortunato, Giuliana ; Pasanisi, Fabrizio ; Labruna, Giuseppe ; Farinaro, Eduardo
Publisher:Cairo, Egypt: Hindawi Publishing Corporation
Journal title:Journal of obesity, 2018, Vol.2018 (2018), p.1-1
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Paraoxonase and Superoxide Dismutase Gene Polymorphisms and Noise-Induced Hearing Loss
Author / Creator:Fortunato, Giuliana ; Marciano, Elio ; Zarrilli, Federica ; Mazzaccara, Cristina ; Intrieri, Mariano ; Calcagno, Giuseppe ; Vitale, Dino F ; La Manna, Paolo ; Saulino, Claudio ; Marcelli, Vincenzo ; Sacchetti, Lucia
Publisher:Washington, DC: Am Assoc Clin Chem
Journal title:Clinical chemistry (Baltimore, Md.), 2004-11, Vol.50 (11), p.2012-2018
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The percentage of CD133+ cells in human colorectal cancer cell lines is influenced by Mycoplasma hyorhinis infection
Author / Creator:Mariotti, Elisabetta ; Gemei, Marica ; Mirabelli, Peppino ; D'Alessio, Francesca ; Di Noto, Rosa ; Fortunato, Giuliana ; Del Vecchio, Luigi
Publisher:England: BioMed Central Ltd
Journal title:BMC cancer, 2010-03, Vol.10 (1), p.120-120, Article 120
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Comparative Characteristics of Mesenchymal Stem Cells from Human Bone Marrow and Placenta: CD10, CD49d, and CD56 Make a Difference
Author / Creator:Mariotti, Elisabetta ; Mirabelli, Peppino ; Abate, Giovanna ; Schiattarella, Maria ; Martinelli, Pasquale ; Fortunato, Giuliana ; Noto, Rosa Di ; Vecchio, Luigi Del
Publisher:United States: Mary Ann Liebert, Inc. publishers
Journal title:Stem cells and development, 2008-12, Vol.17 (6), p.139-1042
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Galectin-3 in Cardiovascular Diseases
Author / Creator:Blanda, Valeria ; Bracale, Umberto Marcello ; Di Taranto, Maria Donata ; Fortunato, Giuliana
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2020-12, Vol.21 (23), p.9232
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Genetic Heterogeneity of Familial Hypercholesterolemia: Repercussions for Molecular Diagnosis
Author / Creator:Di Taranto, Maria Donata ; Fortunato, Giuliana
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2023-02, Vol.24 (4), p.3224
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Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries
Author / Creator:Futema, Marta ; Shah, Sonia ; Cooper, Jackie A ; Li, KaWah ; Whittall, Ros A ; Sharifi, Mahtab ; Goldberg, Olivia ; Drogari, Euridiki ; Mollaki, Vasiliki ; Wiegman, Albert ; Defesche, Joep ; D'Agostino, Maria N ; D'Angelo, Antonietta ; Rubba, Paolo ; Fortunato, Giuliana ; Waluś-Miarka, Małgorzata ; Hegele, Robert A ; Aderayo Bamimore, Mary ; Durst, Ronen ; Leitersdorf, Eran ; Mulder, Monique T ; Roeters van Lennep, Jeanine E ; Sijbrands, Eric J G ; Whittaker, John C ; Talmud, Philippa J ; Humphries, Steve E
Publisher:England: Oxford University Press
Journal title:Clinical chemistry (Baltimore, Md.), 2015-01, Vol.61 (1), p.231-238
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Identification and in vitro characterization of two new PCSK9 Gain of Function variants found in patients with Familial Hypercholesterolemia
Author / Creator:Di Taranto, Maria Donata ; Benito-Vicente, Asier ; Giacobbe, Carola ; Uribe, Kepa Belloso ; Rubba, Paolo ; Etxebarria, Aitor ; Guardamagna, Ornella ; Gentile, Marco ; Martín, Cesar ; Fortunato, Giuliana
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2017-11, Vol.7 (1), p.15282-9, Article 15282
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Identification of a novel mutation in the ryanodine receptor gene (RYR1) in a malignant hyperthermia Italian family
Author / Creator:Fortunato, Giuliana ; Berruti, Renata ; Brancadoro, Virginia ; Fattore, Morena ; Salvatore, Francesco ; Carsana, Antonella
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2000-02, Vol.8 (2), p.149-152
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Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia
Author / Creator:Cardiero, Giovanna ; Ferrandino, Martina ; Calcaterra, Ilenia Lorenza ; Iannuzzo, Gabriella ; Di Minno, Matteo Nicola Dario ; Buganza, Raffaele ; Guardamagna, Ornella ; Auricchio, Renata ; Di Taranto, Maria Donata ; Fortunato, Giuliana
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-04, Vol.15 (4), p.462
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Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome
Author / Creator:Ferrandino, Martina ; Cardiero, Giovanna ; Di Dato, Fabiola ; Cerrato, Ylenia ; Vitagliano, Luigi ; Mandato, Claudia ; Morisco, Filomena ; Spagnuolo, Maria Immacolata ; Iorio, Raffaele ; Di Taranto, Maria Donata ; Fortunato, Giuliana
Publisher:Switzerland: MDPI AG
Journal title:Genes, 2024-08, Vol.15 (8), p.1034
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Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey
Author / Creator:D’Erasmo, Laura ; Gallo, Antonio ; Cefalù, Angelo Baldassare ; Di Costanzo, Alessia ; Saheb, Samir ; Giammanco, Antonina ; Averna, Maurizio ; Buonaiuto, Alessio ; Iannuzzo, Gabriella ; Fortunato, Giuliana ; Puja, Arturo ; Montalcini, Tiziana ; Pavanello, Chiara ; Calabresi, Laura ; Vigna, Giovanni Battista ; Bucci, Marco ; Bonomo, Katia ; Nota, Fabio ; Sampietro, Tiziana ; Sbrana, Francesco ; Suppressa, Patrizia ; Sabbà, Carlo ; Fimiani, Fabio ; Cesaro, Arturo ; Calabrò, Paolo ; Palmisano, Silvia ; D’Addato, Sergio ; Pisciotta, Livia ; Bertolini, Stefano ; Bittar, Randa ; Kalmykova, Olga ; Béliard, Sophie ; Carrié, Alain ; Arca, Marcello ; Bruckert, Eric
Publisher:London: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2021-09, Vol.16 (1), p.1-381, Article 381
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B-Type Natriuretic Peptides and High-Sensitive Troponin I as COVID-19 Survival Factors: Which One Is the Best Performer?
Author / Creator:de Falco, Renato ; Vargas, Maria ; Palma, Daniela ; Savoia, Marcella ; Miscioscia, Anna ; Pinchera, Biagio ; Vano, Martina ; Servillo, Giuseppe ; Gentile, Ivan ; Fortunato, Giuliana
Publisher:Basel: MDPI AG
Journal title:Journal of clinical medicine, 2021-06, Vol.10 (12), p.2726
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Impact of biomarker type on periprocedural myocardial infarction in patients undergoing elective PCI
Author / Creator:Piccolo, Raffaele ; Leone, Attilio ; Avvedimento, Marisa ; Simonetti, Fiorenzo ; Ippolito, Domenico ; Angellotti, Domenico ; Verde, Nicola ; Manzi, Lina ; Cirillo, Plinio ; Serafino, Luigi Di ; Fortunato, Giuliana ; Franzone, Anna ; Esposito, Giovanni
Publisher:Oxford: Oxford University Press
Journal title:European heart journal. Quality of care & clinical outcomes, 2023-11, Vol.9 (7), p.680-690
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Cerebrotendinous xanthomatosis, a metabolic disease with different neurological signs: two case reports
Author / Creator:Di Taranto, Maria Donata ; Gelzo, Monica ; Giacobbe, Carola ; Gentile, Marco ; Marotta, Gennaro ; Savastano, Silvia ; Dello Russo, Antonio ; Fortunato, Giuliana ; Corso, Gaetano
Publisher:New York: Springer US
Journal title:Metabolic brain disease, 2016-10, Vol.31 (5), p.1185-1188
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A Real-World Experience of Clinical, Biochemical and Genetic Assessment of Patients with Homozygous Familial Hypercholesterolemia
Author / Creator:Di Taranto, Maria Donata ; Giacobbe, Carola ; Buonaiuto, Alessio ; Calcaterra, Ilenia ; Palma, Daniela ; Maione, Giovanna ; Iannuzzo, Gabriella ; Di Minno, Matteo Nicola Dario ; Rubba, Paolo ; Fortunato, Giuliana
Publisher:Switzerland: MDPI AG
Journal title:Journal of clinical medicine, 2020-01, Vol.9 (1), p.219
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Showing 1 to 20 of 23 results

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Rare variants in PKHD1 associated with Caroli syndrome: Two case reports

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Age-related changes of cholestanol and lathosterol plasma concentrations: an explorative study

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Assessment of Platelet Aggregation and Thrombin Generation in Patients with Familial Chylomicronemia Syndrome Treated with Volanesorsen: A Cross-Sectional Study

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Calprotectin Levels and Neutrophil Count Are Prognostic Markers of Mortality in COVID-19 Patients

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Corrigendum to “Sequence Analysis of the UCP1 Gene in a Severe Obese Population from Southern Italy”

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Paraoxonase and Superoxide Dismutase Gene Polymorphisms and Noise-Induced Hearing Loss

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The percentage of CD133+ cells in human colorectal cancer cell lines is influenced by Mycoplasma hyorhinis infection

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Comparative Characteristics of Mesenchymal Stem Cells from Human Bone Marrow and Placenta: CD10, CD49d, and CD56 Make a Difference

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Galectin-3 in Cardiovascular Diseases

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Genetic Heterogeneity of Familial Hypercholesterolemia: Repercussions for Molecular Diagnosis

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Refinement of Variant Selection for the LDL Cholesterol Genetic Risk Score in the Diagnosis of the Polygenic Form of Clinical Familial Hypercholesterolemia and Replication in Samples from 6 Countries

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Identification and in vitro characterization of two new PCSK9 Gain of Function variants found in patients with Familial Hypercholesterolemia

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Identification of a novel mutation in the ryanodine receptor gene (RYR1) in a malignant hyperthermia Italian family

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Impact of 12-SNP and 6-SNP Polygenic Scores on Predisposition to High LDL-Cholesterol Levels in Patients with Familial Hypercholesterolemia

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Association of Very Rare NOTCH2 Variants with Clinical Features of Alagille Syndrome

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Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey

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B-Type Natriuretic Peptides and High-Sensitive Troponin I as COVID-19 Survival Factors: Which One Is the Best Performer?

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Impact of biomarker type on periprocedural myocardial infarction in patients undergoing elective PCI

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Cerebrotendinous xanthomatosis, a metabolic disease with different neurological signs: two case reports

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A Real-World Experience of Clinical, Biochemical and Genetic Assessment of Patients with Homozygous Familial Hypercholesterolemia

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