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British Journal of Haematology
|
November 6, 2023
From clinical findings to the pathomechanism of poikiloderma with neutropenia
Lidia Larizza
International Journal of Molecular Sciences
|
May 27, 2023
Rare Diseases: Implementation of Molecular Diagnosis, Pathogenesis Insights and Precision Medicine Treatment
Lidia Larizza, Maria Vittoria Cubellis
International Journal of Molecular Sciences
|
September 14, 2024
Interdependence between Nuclear Pore Gatekeepers and Genome Caretakers: Cues from Genome Instability Syndromes
Lidia Larizza, Elisa Adele Colombo
Leukemia & Lymphoma
|
December 29, 2004
The Kasumi-1 cell line: a t(8;21)-kit mutant model for acute myeloid leukemia
Lidia Larizza, Ivana Magnani, Alessandro Beghini
Hereditary Cancer in Clinical Practice
|
March 13, 2010
Update on the cytogenetics and molecular genetics of chordoma
Lidia Larizza, Pietro Mortini, Paola Riva
Orphanet Journal of Rare Diseases
|
February 2, 2010
Rothmund-Thomson syndrome
Lidia Larizza, Gaia Roversi, Ludovica Volpi
Cancer Letters
|
November 8, 2005
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping
Lidia Larizza, Ivana Magnani, Gaia Roversi
International Journal of Molecular Sciences
|
June 12, 2026
Special Issue "Human Traits and Genomics: An Integrative Perspective"
Salvatore Saccone, Lidia Larizza, Giovanni Malerba
Current Molecular Medicine
|
July 16, 2009
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1
Lidia Larizza, Cristina Gervasini, Federica Natacci, et al.
Neural Regeneration Research
|
June 8, 2021
Genes for RNA-binding proteins involved in neural-specific functions and diseases are downregulated in Rubinstein-Taybi iNeurons
Lidia Larizza, Luciano Calzari, Valentina Alari, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 150) with videos related to
Sort By:
Page
of 15
British Journal of Haematology
|
November 6, 2023
From clinical findings to the pathomechanism of poikiloderma with neutropenia
Lidia Larizza
International Journal of Molecular Sciences
|
May 27, 2023
Rare Diseases: Implementation of Molecular Diagnosis, Pathogenesis Insights and Precision Medicine Treatment
Lidia Larizza, Maria Vittoria Cubellis
International Journal of Molecular Sciences
|
September 14, 2024
Interdependence between Nuclear Pore Gatekeepers and Genome Caretakers: Cues from Genome Instability Syndromes
Lidia Larizza, Elisa Adele Colombo
Leukemia & Lymphoma
|
December 29, 2004
The Kasumi-1 cell line: a t(8;21)-kit mutant model for acute myeloid leukemia
Lidia Larizza, Ivana Magnani, Alessandro Beghini
Hereditary Cancer in Clinical Practice
|
March 13, 2010
Update on the cytogenetics and molecular genetics of chordoma
Lidia Larizza, Pietro Mortini, Paola Riva
Orphanet Journal of Rare Diseases
|
February 2, 2010
Rothmund-Thomson syndrome
Lidia Larizza, Gaia Roversi, Ludovica Volpi
Cancer Letters
|
November 8, 2005
Rothmund-Thomson syndrome and RECQL4 defect: splitting and lumping
Lidia Larizza, Ivana Magnani, Gaia Roversi
International Journal of Molecular Sciences
|
June 12, 2026
Special Issue "Human Traits and Genomics: An Integrative Perspective"
Salvatore Saccone, Lidia Larizza, Giovanni Malerba
Current Molecular Medicine
|
July 16, 2009
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1
Lidia Larizza, Cristina Gervasini, Federica Natacci, et al.
Neural Regeneration Research
|
June 8, 2021
Genes for RNA-binding proteins involved in neural-specific functions and diseases are downregulated in Rubinstein-Taybi iNeurons
Lidia Larizza, Luciano Calzari, Valentina Alari, et al.
Page
of 15