Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lauren M Vasta"'
Autor:
Kris Ann P. Schultz, Murali Chintagumpala, Jin Piao, Kenneth S. Chen, Rachana Shah, Robyn D. Gartrell, Emily Christison-Lagay, Farzana Pashnakar, Jesse L. Berry, Allison F. O’Neill, Lauren M. Vasta, Ashley Flynn, Sarah G. Mitchell, Brittani KN. Seynnaeve, Jeremy Rosenblum, Samara L. Potter, Junne Kamihara, Carlos Rodriguez-Galindo, Douglas S. Hawkins, Theodore W. Laetsch
Publikováno v:
EJC Paediatric Oncology, Vol 2, Iss , Pp 100024- (2023)
While all childhood cancers are rare, tumors that are particularly infrequent or underrepresented within pediatrics are studied under the umbrella of the Children’s Oncology Group Rare Tumor committee, divided into the Retinoblastoma and Infrequent
Externí odkaz:
https://doaj.org/article/1d78ae7efc7f48d693fb7d9771fddd5b
Autor:
Lauren M. Vasta, Alison Nichols, Laura A. Harney, Ana F. Best, Ann G. Carr, Anne K. Harris, Markku Miettinen, Kris Ann P. Schultz, Hung Jeffrey Kim, Douglas R. Stewart
Publikováno v:
Rhinology Online, Vol 3, Pp 15-24 (2020)
Background: Nasal chondromesenchymal hamartomas are benign, rare nasal tumors associated with DICER1 pathogenic germ-line variation. They can be locally destructive and recurrent if not completely resected. Methodology: In this single-center, case-co
Externí odkaz:
https://doaj.org/article/b172e575cdc8420aa3eaf0ef7dc0e837
Autor:
Mary L. McMaster, Laura A. Harney, Nicolas Sirvent, Carole Corsini, Dominique Stoppa-Lyonnet, Nicholas G. Cost, Lauren M. Vasta, Stéphanie Haouy, Catherine Dubois d'Enghien, Frédérique Dijoud, Arnaud Gauthier, Marion Gauthier-Villars, Kris Ann P. Schultz, Sabine Irtan, Valérie Duflos, Douglas R. Stewart, Lisa Golmard, Alexander Ling, Daniel Orbach, Ann G. Carr, Markku Miettinen, Isabelle Coupier
Publikováno v:
Journal of Medical Genetics. 59:346-350
DICER1 syndrome is a rare paediatric autosomal dominant inherited disorder predisposing to various benign and malignant tumours. It is caused by a germline pathogenic variant in DICER1, and the second hit for tumour development is usually a missense
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6eb4b98fee53d5caae68e2c6c160df7c
https://doi.org/10.1136/jmedgenet-2020-107434
https://doi.org/10.1136/jmedgenet-2020-107434
Autor:
Karen S. Vogt, Sarah M Reynolds, Dina S. Parekh, Seppideh Sami, Jill E Emerick, Lauren M Vasta, John P Schacht
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e496-e499
We describe a 21-month-old male with relapsed clear cell sarcoma of the kidney receiving enteral nutrition who experienced recurrent, ketotic hypoglycemia. During relapse therapy, he had recurrent hypoglycemia episodes, in the setting of hematochezia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d3ad0c3b303562ea1d717186635a8a8
https://doi.org/10.1097/mph.0000000000002128
https://doi.org/10.1097/mph.0000000000002128
Autor:
Lauren M Vasta, Katherine L. Nathanson, Alexander Ling, Kris Ann P. Schultz, Mark H. Greene, Scott M. Damrauer, Rachel L. Kember, Laura A. Harney, Douglas R. Stewart, Peter A. Kanetsky, Anne K. Harris, Louise C. Pyle, Daniel J. Rader, Jung Kim, Mary L McMaster, Ann G Carr
Publikováno v:
Cancer Genet
Background Several studies have reported conflicting evidence on the inclusion of testicular germ cell tumors (TGCT) in the DICER1 tumor-predisposition phenotype. We evaluated the relationship between DICER1 and TGCT by reviewing scrotal ultrasounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b432ea48ec818de930367bbcbfe92f7
https://doi.org/10.1016/j.cancergen.2020.10.002
https://doi.org/10.1016/j.cancergen.2020.10.002
Autor:
Hung Jeffrey Kim, Kris Ann P. Schultz, Laura A. Harney, Ana F. Best, Markku M. Miettinen, Anne K. Harris, Alison Nichols, Ann G. Carr, Lauren M Vasta, Douglas R. Stewart
Publikováno v:
Rhinology Online, Vol 3, Pp 15-24 (2020)
Background: Nasal chondromesenchymal hamartomas are benign, rare nasal tumors associated with DICER1 pathogenic germ-line variation. They can be locally destructive and recurrent if not completely resected. Methodology: In this single-center, case-co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58f2318be9d6ea3969652d9cb745ca43
https://www.rhinologyonline.org/Rhinology_online_issues/manuscript_64.pdf
https://www.rhinologyonline.org/Rhinology_online_issues/manuscript_64.pdf
Publikováno v:
Journal of Pediatric Hematology/Oncology. 43:e1145-e1147
Hyperhemolysis is a life-threatening condition of exaggerated hemolysis of red blood cells which occurs in patients receiving chronic transfusion therapy. We present a 19-year-old male with the β-thalassemia major with an episode of hyperhemolysis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3482ebcf71cb90ed381bcb3dad6e3959
https://doi.org/10.1097/mph.0000000000002059
https://doi.org/10.1097/mph.0000000000002059
Autor:
Lauren M, Vasta, Alison, Nichols, Laura A, Harney, Ana F, Best, Ann G, Carr, Anne K, Harris, Markku, Miettinen, Kris Ann P, Schultz, Hung Jeffrey, Kim, Douglas R, Stewart
Publikováno v:
Rhinol
BACKGROUND: Nasal chondromesenchymal hamartomas are benign, rare nasal tumors associated with DICER1 pathogenic germline variation. They can be locally destructive and recurrent if not completely resected. METHODOLOGY: In this single-center, case-con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d5e984ab9c568d11df329a97f80f8397
https://pubmed.ncbi.nlm.nih.gov/34164613
https://pubmed.ncbi.nlm.nih.gov/34164613
Introduction: Hyperhemolysis is a life-threatening condition of exaggerated hemolysis of red blood cells which occurs in patients receiving chronic transfusion therapy. Results: We present a 19-year-old male with β-thalassemia major with an episode
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::778db24de69982523f20795886b55603
https://doi.org/10.22541/au.160262393.32375827/v1
https://doi.org/10.22541/au.160262393.32375827/v1
Autor:
Lisa, Golmard, Lauren M, Vasta, Valérie, Duflos, Carole, Corsini, Catherine, Dubois d'Enghien, Mary L, McMaster, Laura A, Harney, Ann G, Carr, Alexander, Ling, Frédérique, Dijoud, Arnaud, Gauthier, Markku, Miettinen, Nicholas G, Cost, Marion, Gauthier-Villars, Daniel, Orbach, Sabine, Irtan, Stéphanie, Haouy, Kris Ann, Schultz, Dominique, Stoppa-Lyonnet, Isabelle, Coupier, Douglas R, Stewart, Nicolas, Sirvent
Publikováno v:
J Med Genet
DICER1 syndrome is a rare pediatric autosomal dominant inherited disorder predisposing to various benign and malignant tumors. It is caused by a germline pathogenic variant in DICER1 and the second hit for tumor development is usually a missense hots
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c973cb9be16b178a2690abf71eacd43d
https://pubmed.ncbi.nlm.nih.gov/33782093
https://pubmed.ncbi.nlm.nih.gov/33782093