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The Lancet. Oncology
|
July 28, 2022
Response assessment in paediatric intracranial ependymoma: recommendations from the Response Assessment in Pediatric Neuro-Oncology (RAPNO) working group
Holly B Lindsay, Maura Massimino, Shivaram Avula, et al.
Pediatric Blood & Cancer
|
January 18, 2021
Medulloblastoma and familial adenomatous polyposis: Good prognosis and good quality of life in the long-term?
Maura Massimino, Stefano Signoroni, Luna Boschetti, et al.
The Journal of Pediatrics
|
September 21, 2021
Evidence of Treatment Benefits in Patients with Mucopolysaccharidosis Type I-Hurler in Long-term Follow-up Using a New Magnetic Resonance Imaging Scoring System
Silvia Pontesilli, Cristina Baldoli, Pasquale Anthony Della Rosa, et al.
Journal of Neuro-Oncology
|
June 16, 2023
Optimizing reirradiation for relapsed medulloblastoma: identifying the ideal patient and tumor profiles
Maura Massimino, Sabina Vennarini, Francesca Romana Buttarelli, et al.
Journal of Neuro-Oncology
|
April 24, 2026
Surgery and radiotherapy strategies at first relapse of pediatric intracranial ependymoma: an Italian retrospective study integrating molecular subgrouping
Maura Massimino, Giorgio Carrabba, Sabina Vennarini, et al.
Audiology Research
|
May 28, 2024
Multi-Magnet Cochlear Implant Technology and Magnetic Resonance Imaging: The Safety Issue
Pietro Canzi, Elena Carlotto, Elisabetta Zanoletti, et al.
Brain : a Journal of Neurology
|
May 8, 2021
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness
Antonella Sferra, Paola Fortugno, Marialetizia Motta, et al.
Neurology. Genetics
|
March 27, 2020
<i>MYORG</i>-related disease is associated with central pontine calcifications and atypical parkinsonism
Viorica Chelban, Miryam Carecchio, Gillian Rea, et al.
American Journal of Human Genetics
|
December 24, 2013
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation
Sabrina Dusi, Lorella Valletta, Tobias B Haack, et al.
Journal of Clinical Immunology
|
February 7, 2024
Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease
Clémence David, Mihaly Badonyi, Robin Kechiche, et al.
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of 20
Search research articles
Search
Showing results (171-180 of 194) with videos related to
Sort By:
Page
of 20
The Lancet. Oncology
|
July 28, 2022
Response assessment in paediatric intracranial ependymoma: recommendations from the Response Assessment in Pediatric Neuro-Oncology (RAPNO) working group
Holly B Lindsay, Maura Massimino, Shivaram Avula, et al.
Pediatric Blood & Cancer
|
January 18, 2021
Medulloblastoma and familial adenomatous polyposis: Good prognosis and good quality of life in the long-term?
Maura Massimino, Stefano Signoroni, Luna Boschetti, et al.
The Journal of Pediatrics
|
September 21, 2021
Evidence of Treatment Benefits in Patients with Mucopolysaccharidosis Type I-Hurler in Long-term Follow-up Using a New Magnetic Resonance Imaging Scoring System
Silvia Pontesilli, Cristina Baldoli, Pasquale Anthony Della Rosa, et al.
Journal of Neuro-Oncology
|
June 16, 2023
Optimizing reirradiation for relapsed medulloblastoma: identifying the ideal patient and tumor profiles
Maura Massimino, Sabina Vennarini, Francesca Romana Buttarelli, et al.
Journal of Neuro-Oncology
|
April 24, 2026
Surgery and radiotherapy strategies at first relapse of pediatric intracranial ependymoma: an Italian retrospective study integrating molecular subgrouping
Maura Massimino, Giorgio Carrabba, Sabina Vennarini, et al.
Audiology Research
|
May 28, 2024
Multi-Magnet Cochlear Implant Technology and Magnetic Resonance Imaging: The Safety Issue
Pietro Canzi, Elena Carlotto, Elisabetta Zanoletti, et al.
Brain : a Journal of Neurology
|
May 8, 2021
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness
Antonella Sferra, Paola Fortugno, Marialetizia Motta, et al.
Neurology. Genetics
|
March 27, 2020
<i>MYORG</i>-related disease is associated with central pontine calcifications and atypical parkinsonism
Viorica Chelban, Miryam Carecchio, Gillian Rea, et al.
American Journal of Human Genetics
|
December 24, 2013
Exome sequence reveals mutations in CoA synthase as a cause of neurodegeneration with brain iron accumulation
Sabrina Dusi, Lorella Valletta, Tobias B Haack, et al.
Journal of Clinical Immunology
|
February 7, 2024
Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease
Clémence David, Mihaly Badonyi, Robin Kechiche, et al.
Page
of 20