Samuela Landini - Department of Clinical and Experimental Biomedical Sciences "Mario Serio", University of Florence

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论文共 31 篇作者统计合作学者相似作者

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#369 Anti-nephrin Antibodies Identify Patients with Steroid-Resistant Nephrotic Syndrome Responsive to Immunosuppressants

Valentina Raglianti,Maria Lucia Angelotti,Luigi Cirillo,Samuela Landini,Viviana Palazzo,Gian Marco Ghiggeri,Andrea Angeletti,Benedetta Mazzinghi,Becherucci Francesca,Paola Romagnani

NEPHROLOGY DIALYSIS TRANSPLANTATION (2024): I43-I43

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Broadening the Ocular Phenotypic Spectrum of Ultra-Rare BRPF1 Variants: Report of Two Cases

Elisa Marziali,Samuela Landini, Erika Fiorentini,Camilla Rocca,Lucia Tiberi,Rosangela Artuso, Laila Zaroili,Elia Dirupo,Pina Fortunato,Sara Bargiacchi,Roberto Caputo,Giacomo Maria Bacci

OPHTHALMIC GENETICS（2024）

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Multimodal Phenotyping of Foveal Hypoplasia in Albinism and Albino-Like Conditions: a Pediatric Case Series with Adaptive Optics Insights

Giacomo M Bacci,Elisa Marziali,Sara Bargiacchi, Michel Paques,Gianni Virgili,Pina Fortunato,Marine Durand,Camilla Rocca,Angelica Pagliazzi,Viviana Palazzo,Lucia Tiberi,Debora Vergani,Samuela Landini,Angela Peron,Rosangela Artuso,Bianca Pacini, Monica Stabile,Andrea Sodi, Roberto Caputo

Scientific reportsno. 1 (2024): 15454-15454

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#2814 Characterization of Cardiological Manifestations in Patients with Sodium-Wasting Tubulopathies

Luigi Cirillo, Carlotta Cocchini,Valentina Raglianti,Samantha Innocenti,Samuela Landini,Carmela Errichiello,Elisa Buti,Benedetta Mazzinghi,Becherucci Francesca

NEPHROLOGY DIALYSIS TRANSPLANTATION (2024): I437-I437

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Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria (vol 29, pg 1186, 2021)

EUROPEAN JOURNAL OF HUMAN GENETICSno. 1 (2024): 132-132

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Multimodal phenotyping of foveal hypoplasia in albinism and albino-like conditions: a pediatric case series with adaptive optics insights

Giacomo M Bacci,Elisa Marziali,Sara Bargiacchi,Michel Paques,Gianni Virgili,Pina Fortunato,Marine Durand,Camilla Rocca,Angelica Pagliazzi,Viviana Palazzo,Lucia Tiberi,Debora Vergani,Samuela Landini,Angela Peron,Rosangela Artuso,Bianca Pacini, Monica Stabile,Andrea Sodi,Roberto Caputo

Scientific reportsno. 1 (2024): 15454-15454

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Novel Mutations in BLOC-1 and BLOC-2 HPS Genes in Patients with Non-Syndromic Ocular Albinism: Using NGS to Improve Diagnosis and Follow-Up

Rosangela Artuso,Lucia Tiberi,Camilla Rocca,Sara Bargiacchi,Giacomo Bacci,Elisa Marziali,Pina Fortunato,Samuela Landini,Debora Vergani,Elia Dirupo, Laila Zaroili,Elena Sieni, Marialuisa Coniglio, Lisa Pieri,Roberto Caputo,Angela Peron

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 381-382

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#6307 EARLY IDENTIFICATION OF PODOCYTHOPATHIES AND COLLAGENOPATHIES REDUCE UNNECESSARY MEDICATION FOR PATIENTS AND ECONOMIC BURDEN ON HEALTHCARE SYSTEM

Luigi Cirillo,Becherucci Francesca,Tommaso Mazzierli,Jacopo Lomi, Eleonora Superchi,Valentina Raglianti,Gianmarco Lugli,Samuela Landini,Viviana Palazzo,Benedetta Mazzinghi,Paola Romagnani

NEPHROLOGY DIALYSIS TRANSPLANTATION（2023）

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Financial Implications of Genetic Testing in Nephrology: A Real-Life Evaluation of the Costs Related to Podocytopathy and Collagenopathy Diagnosis

Luigi Cirillo,Tommaso Mazzierli,Jacopo Lomi, Eleonora Superchi,Valentina Raglianti,Gianmarco Lugli,Samuela Landini,Viviana Palazzo,Benedetta Mazzinghi,Paola Romagnani,Francesca Becherucci

Journal of the American Society of Nephrologyno. 11S (2023): 214-214

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Correction: Consensus Statement on Standards and Guidelines for the Molecular Diagnostics of Alport Syndrome: Refining the ACMG Criteria

European Journal of Human Genetics（2023）

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