Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group
2020 · Familial Cancer · 28 citations
https://doi.org/10.1007/s10689-020-00204-2
O
Orli Michaeli
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
42
Papers
519
Citations
14
h-index
15
i10-index
Orli Michaeli is an academic researcher from Tel Aviv University. The author has contributed to research in topics: Glioma Diagnosis and Treatment & Neurofibromatosis and Schwannoma Cases & Neuroblastoma Research and Treatments. The author has an h-index of 14, co-authored 36 publications.
ORCID: 0000-0002-6097-6457Papers by this author
worksUpdate on Pediatric Cancer Surveillance Recommendations for Patients with Neurofibromatosis Type 1, Noonan Syndrome, CBL Syndrome, Costello Syndrome, and Related RASopathies
2024 · Clinical Cancer Research · 22 citations
https://doi.org/10.1158/1078-0432.ccr-24-1611
Update on Cancer Screening in Children with Syndromes of Bone Lesions, Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome, and Other Rare Syndromes
2024 · Clinical Cancer Research · 4 citations
https://doi.org/10.1158/1078-0432.ccr-24-2171
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat