Leila B. Salehi - Dept Biopathol & Diagnost Imaging, Tor Vergata Univ

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论文共 10 篇作者统计合作学者相似作者

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Implementing the Risk Stratification and Clinical Management of Breast Cancer Families Using Polygenic Risk Score Evaluation: A Pilot Study

Barbara Rizzacasa, Vanessa Nicolì, Chantal Tancredi,Chiara Conte,Leila B Salehi,Miriam Lucia Carriero,Giuliana Longo,Vincenzo Cirigliano, Luis Izquierdo Lopez, Bibiana Palao,Ilaria Portarena,Oreste Claudio Buonomo,Giuseppe Novelli,Michela Biancolella

Journal of personalized medicineno. 10 (2024)

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Identification of a Novel RUNX2 Gene Mutation and Early Diagnosis of CCD in a Cleidocranial Dysplasia Suspected Iranian Family

Omid Daneshjoo, Parvin Ebrahimi,Leila Salehi, Antonio Pizzuti,Masoud Garshasbi

Clinical case reports (2020)

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An Enormous Italian Pedigree of Marfan Syndrome with a Novel Mutation in the FBN1 Gene

Omid Daneshjoo,Leila B. Salehi,Antonio Pizzuti,Giuseppe Novelli,Federica Sangiuolo

Clinical case reportsno. 8 (2020): 1445-1451

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Neurovascular Manifestations in Connective Tissue Diseases: the Case of Marfan Syndrome

Giovanni Parlapiano,Francesca Di Lorenzo,Leila B. Salehi,Giovanni Ruvolo,Giuseppe Novelli,Federica Sangiuolo

Mechanisms of Ageing and Development (2020)

引用3浏览0WOS引用

RETRACTED: Identification of a novel RUNX2 gene mutation and early diagnosis of CCD in a cleidocranial dysplasia suspected Iranian family (Retracted Article)

Omid Daneshjoo,Pirooz Ebrahimi,Leila B. Salehi,Antonio Pizzuti,Masoud Garshasbi

CLINICAL CASE REPORTS（2020）

引用3浏览0WOS引用

Retraction: Identification Of A Novel Runx2 Gene Mutation And Early Diagnosis Of Ccd In A Cleidocranial Dysplasia Suspected Iranian Family (Apr, 10.1002/Ccr3.2825, 2020) (Retraction Of Vol 2020, Pg 1, 2020)

Omid Daneshjoo,Pirooz Ebrahimi,Leila B. Salehi,Antonio Pizzuti,Masoud Garshasbi

CLINICAL CASE REPORTS（2020）

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Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience

Liliana Mannucci, Serena Luciano,Leila B. Salehi,Laura Gigante,Chiara Conte,Giuliana Longo,Valentina Ferradini, Nunzia Piumelli,Francesco Brancati,Giovanni Ruvolo,Giuseppe Novelli,Federica Sangiuolo

CLINICA CHIMICA ACTA（2020）

引用14浏览0WOS引用

Focal Dystonia Caused by Mohr–Tranebjaerg Syndrome with Complete Deletion of the DDP1 Gene

Antonio Pizzuti,Giovanni Fabbrini,Leila Salehi,Laura Vacca,Maurizio Inghilleri,Bruno Dallapiccola,Alfredo Berardelli

Neurology（2004）

引用16浏览0引用

Assignment of a Locus for Autosomal Dominant Idiopathic Scoliosis (IS) to Human Chromosome 17P11

Leila Salehi,Massimo Mangino, Salvatore De Serio, Domenico De Cicco,Francesca Capon,Sabrina Semprini,Antonio Pizzuti,Giuseppe Novelli,Bruno Dallapiccola

Human Geneticsno. 4 (2002): 401-404

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