Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Robert E. Ruiz"'
Autor:
Emilia Modolo Pinto, Carlos Rodriguez-Galindo, Catherine G. Lam, Robert E. Ruiz, Gerard P. Zambetti, Raul C. Ribeiro
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Pediatric adrenocortical tumors (ACTs) are rare and heterogeneous. Approximately 50% of children with ACT carry a germline TP53 variant; however, the genetic underpinning of remaining cases has not been elucidated. In patients having germline TP53 va
Externí odkaz:
https://doaj.org/article/b185a85e41364ff1b358316a95e9282a
Autor:
Lama Elbahlawan, Jenny McArthur, Cara E. Morin, Hafeez Abdelhafeez, M. Beth McCarville, Robert E. Ruiz, Saumini Srinivasan, Amr Qudeimat
Publikováno v:
Frontiers in Oncology, Vol 11 (2021)
Pulmonary complications are common in children following hematopoietic cell transplantation (HCT) and contribute to their morbidity and mortality. Early diagnosis is essential for management and prevention of progression of lung injury and damage. In
Externí odkaz:
https://doaj.org/article/6d60a2c6aa1d41c2937c7e20d081886e
Autor:
Andrew M Fleming, Caitlyn Duffy, Jessica Gartrell, M Beth McCarville, Max R Langham, Robert E Ruiz, Teresa Santiago, Andrew J Murphy
Publikováno v:
Journal of Surgical Case Reports. 2022
Giant focal nodular hyperplasia (GFNH) is rarely seen in children, presenting complex diagnostic and management considerations. Pathognomonic radiographic findings can be absent in this population, and the nuances of pathologic examination are critic
Autor:
Cara E. Morin, Saumini Srinivasan, Hafeez Abdelhafeez, Jenny McArthur, M. Beth McCarville, Amr Qudeimat, Robert E. Ruiz, Lama Elbahlawan
Publikováno v:
Frontiers in Oncology
Frontiers in Oncology, Vol 11 (2021)
Frontiers in Oncology, Vol 11 (2021)
Pulmonary complications are common in children following hematopoietic cell transplantation (HCT) and contribute to their morbidity and mortality. Early diagnosis is essential for management and prevention of progression of lung injury and damage. In
Autor:
Robert E. Ruiz, Bertram Schnitzer, Riccardo Valdez, Khaldoun Koujok, Nasir A. Bakshi, William G. Finn, Charles W. Ross
Publikováno v:
American Journal of Clinical Pathology. 125:57-63
We describe the clinical, radiologic, and pathologic features of primary bone anaplastic large cell lymphoma (ALCL) in 3 boys. Radiologic imaging showed lytic lesions involving sacrum, femur, or rib. Bone was the only site of disease in 2 cases; an a
Publikováno v:
Modern Pathology. 19:641-647
Synovial sarcomas are highly malignant tumors of soft tissue which are characterized by the t(X;18) resulting in SYT-SSX fusion transcript production. Diagnosis of these tumors based on histology can be challenging, particularly when minimal biopsy s
Publikováno v:
Pediatric Hematology and Oncology. 22:17-24
Angiomyolipoma is a tumor of the kidney and, more rarely, the liver, which histologically consists of smooth muscle cells, adipose cells, and abnormal blood vessels in varying proportions. This tumor is generally benign and resection is curative, but
Publikováno v:
Human Immunology. 39:188-194
Nonhuman primates represent phylogenetic intermediates for studying the divergence of human and murine β 2 Ms. We report the nucleotide sequences of B 2 m cDNA clones from a baboon cell line, 26CB-1 ( Papio hamadryas ); primates: Cercopithecoida), a
Publikováno v:
American journal of perinatology. 25(2)
Birth depression unresponsive to conventional resuscitative measures merits careful consideration. The case of a term infant with primary respiratory failure at birth despite extensive intervention is presented. Postmortem examination revealed bilate
Publikováno v:
Pediatric surgery international. 24(5)
Congenital infantile fibrosarcoma is a rare soft tissue malignancy that occurs in both axial and extremity locations. We report a case of this tumor arising from the left colon in a newborn presenting with an intrauterine perforation and meconium per