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Virchows Archiv : an International Journal of Pathology
|
May 14, 2025
Endometrial stromal tumor with whorling and GREB1::CTNNB1 fusion: expanding the knowledge on a recently described entity
Antonio Travaglino, Damiano Arciuolo, Susanna Ronchi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 16, 2013
Description of a novel TUBA1A mutation in Arg-390 associated with asymmetrical polymicrogyria and mid-hindbrain dysgenesis
Ginevra Zanni, Giovanna S Colafati, Sabina Barresi, et al.
Genes, Chromosomes & Cancer
|
April 3, 2025
EGFR-KDD Myofibroblastic Neoplasm or Congenital Peribronchial Myofibroblastic Tumor (CPMT)? Report of a Congenital Myofibroblastic Neoplasm With Unusual Histologic Features
Emma Rullo, Sabina Barresi, Sabrina Rossi, et al.
Virchows Archiv : an International Journal of Pathology
|
February 20, 2026
Novel EWSR1::HOXB8 fusion identified in a rare spindle cell sarcoma of a young woman
Alessandro Cioce, Sabina Barresi, Sara Patrizi, et al.
Frontiers in Neurology
|
February 24, 2023
Case report: Novel compound heterozygosity for pathogenic variants in <i>MED23</i> in a syndromic patient with postnatal microcephaly
Emanuela Salzano, Marcello Niceta, Simone Pizzi, et al.
Virchows Archiv : an International Journal of Pathology
|
March 22, 2025
DEK::AFF2 rearranged neoplasm with undifferentiated morphology and neuroendocrine phenotype in a pediatric patient
Emma Rullo, Sabina Barresi, Evelina Miele, et al.
European Journal of Medical Genetics
|
September 7, 2018
TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations
Marcello Niceta, Sabina Barresi, Francesca Pantaleoni, et al.
International Journal of Environmental Research and Public Health
|
February 15, 2022
Cerebellar Agenesis and Bilateral Polimicrogyria Associated with Rare Variants of CUB and Sushi Multiple Domains 1 Gene (CSMD1): A Longitudinal Neuropsychological and Neuroradiological Case Study
Floriana Costanzo, Ginevra Zanni, Elisa Fucà, et al.
Pathologica
|
December 27, 2025
Expanding the spectrum of <i>AFF2</i> undifferentiated sarcoma associated to endometriosis: a novel <i>ZDHHC9::AFF2</i> fusion sarcoma with high-grade features and poor prognosis
Damiano Arciuolo, Rita Alaggio, Antonio Travaglino, et al.
Journal of Cellular and Molecular Medicine
|
October 14, 2025
Unique Genetic and Epigenetic Alterations in Glioblastoma Long-Term Survivors: Insights From Two Clinical Cases
Elena Anghileri, Evelina Miele, Sara Patrizi, et al.
Page
of 9
Search research articles
Search
Showing results (21-30 of 90) with videos related to
Sort By:
Page
of 9
Virchows Archiv : an International Journal of Pathology
|
May 14, 2025
Endometrial stromal tumor with whorling and GREB1::CTNNB1 fusion: expanding the knowledge on a recently described entity
Antonio Travaglino, Damiano Arciuolo, Susanna Ronchi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 16, 2013
Description of a novel TUBA1A mutation in Arg-390 associated with asymmetrical polymicrogyria and mid-hindbrain dysgenesis
Ginevra Zanni, Giovanna S Colafati, Sabina Barresi, et al.
Genes, Chromosomes & Cancer
|
April 3, 2025
EGFR-KDD Myofibroblastic Neoplasm or Congenital Peribronchial Myofibroblastic Tumor (CPMT)? Report of a Congenital Myofibroblastic Neoplasm With Unusual Histologic Features
Emma Rullo, Sabina Barresi, Sabrina Rossi, et al.
Virchows Archiv : an International Journal of Pathology
|
February 20, 2026
Novel EWSR1::HOXB8 fusion identified in a rare spindle cell sarcoma of a young woman
Alessandro Cioce, Sabina Barresi, Sara Patrizi, et al.
Frontiers in Neurology
|
February 24, 2023
Case report: Novel compound heterozygosity for pathogenic variants in <i>MED23</i> in a syndromic patient with postnatal microcephaly
Emanuela Salzano, Marcello Niceta, Simone Pizzi, et al.
Virchows Archiv : an International Journal of Pathology
|
March 22, 2025
DEK::AFF2 rearranged neoplasm with undifferentiated morphology and neuroendocrine phenotype in a pediatric patient
Emma Rullo, Sabina Barresi, Evelina Miele, et al.
European Journal of Medical Genetics
|
September 7, 2018
TARP syndrome: Long-term survival, anatomic patterns of congenital heart defects, differential diagnosis and pathogenetic considerations
Marcello Niceta, Sabina Barresi, Francesca Pantaleoni, et al.
International Journal of Environmental Research and Public Health
|
February 15, 2022
Cerebellar Agenesis and Bilateral Polimicrogyria Associated with Rare Variants of CUB and Sushi Multiple Domains 1 Gene (CSMD1): A Longitudinal Neuropsychological and Neuroradiological Case Study
Floriana Costanzo, Ginevra Zanni, Elisa Fucà, et al.
Pathologica
|
December 27, 2025
Expanding the spectrum of <i>AFF2</i> undifferentiated sarcoma associated to endometriosis: a novel <i>ZDHHC9::AFF2</i> fusion sarcoma with high-grade features and poor prognosis
Damiano Arciuolo, Rita Alaggio, Antonio Travaglino, et al.
Journal of Cellular and Molecular Medicine
|
October 14, 2025
Unique Genetic and Epigenetic Alterations in Glioblastoma Long-Term Survivors: Insights From Two Clinical Cases
Elena Anghileri, Evelina Miele, Sara Patrizi, et al.
Page
of 9