Results 61 to 70 of about 4,767,425 (261)

Standard pediatric oncology data and information technology: necessities for cancer care management [PDF]

Cancer is the second leading cause of death in children and survivors require life time follow-up. There is a growing recognition of the need to base cancer control policies on accurate, detailed and timely information on cancer management and outcomes ...
میرزا رحیمی, مهرداد, مسرت, الناز, زالی, محمدرضا, مسرت, الهام   +3 more
core   +1 more source

Covid-19 infection in children with cancer after the first wave in Turkey: A Study of the Turkish Pediatric Oncology (TPOG) and Hematology (TPHD) Societies

, 2021
Covid-19 infection in children with cancer after the first wave in Turkey: A Study of the Turkish Pediatric Oncology (TPOG) and Hematology (TPHD ...
Tuğcu, D., Kebudi, R., Eker, N., İnce, D., Tokuç, G., Uzel, H., Kurucu, N.   +6 more
core  

Classical Complement Pathway Inhibition in a Pediatric Patient With Refractory Immune Thrombocytopenia

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Pediatric refractory immune thrombocytopenia (rITP) is generally characterized by persistent thrombocytopenia and failure to achieve a sustained response to multiple standard therapies. We report a 4‐year‐old female with congenital tufting enteropathy, post‐intestinal transplant patient on immunosuppressants, who developed severe rITP ...
Sarah Hsieh, Susmita Sarangi, Caileigh Pudela, Catherine M. Broome, Tara K. Suntum   +4 more
wiley   +1 more source

Histone H3.3K27M Mobilizes Multiple Cancer/Testis (CT) Antigens in Pediatric Glioma.

, 2018
Lysine to methionine mutations at position 27 (K27M) in the histone H3 (H3.3 and H3.1) are highly prevalent in pediatric high-grade gliomas (HGG) that arise in the midline of the central nervous system.
Zhang, T, Deng, H, Zeng, J, Gong, L, Li, G, Jones, C, Zhang, H, Cheung, E   +7 more
core  

Pediatric cancer screening in hereditary gastrointestinal cancer risk syndromes: an update from the AACR childhood cancer predisposition working group

Gastrointestinal (GI) polyposis and cancer in pediatric patients is frequently due to an underlying hereditary cancer risk syndrome requiring ongoing cancer screening.
Schneider, K.W., Bauer, A., States, L., Plon, Sharon E, Lesmana, H., Becktell, K., Durno, Carol, Tabori, Uri, Savage, S.A., Tabori, U., Becktell, Kerri, States, Lisa, Plon, S.E., Nichols, K.E., Bauer, Andrew, Schultz, K.A., Scott, H., Zelley, Kristin, Meade, Julia, Porter, C.C., Schultz, Kris Ann, Tomlinson, G., Durno, C., Schneider, Kami Wolfe, MacFarland, Suzanne P, Porter, Christopher C., Tamura, Chieko, Tomlinson, Gail, Kuiper, R.P., Savage, Sharon A., Meade, J., Tamura, C., Nichols, Kim E., Kuiper, Roland P, MacFarland, S.P., Lesmana, Harry, Zelley, K., Scott, Hamish   +37 more
core   +1 more source

Cell death pathways as therapeutic targets in rhabdomyosarcoma [PDF]

, 2012
Resistance of rhabdomyosarcoma to current therapies remains one of the key issues in pediatric oncology. Since the success of most cytotoxic therapies in the treatment of cancer, for example, chemotherapy, depends on intact signaling pathways that ...
Fulda, Simone
core   +1 more source

Evidence‐Based Clinical Practice Guidelines for the Management of Pediatric Febrile Neutropenia: Resource‐Sensitive Recommendations for the Asian Continent

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Febrile neutropenia (FN) is a frequent and serious complication in children receiving cancer therapy. Standardizing FN management across Asia is challenging due to variable healthcare infrastructure, diagnostic capacity, and infection patterns; however, it could improve resource use and patient outcomes.
Joliza Patricia Cañeba, Shweta Bansal, Tea Reljic, Allyne Montecillo‐Aguelo, Hamidah Alias, Farrah Amaranto, Maria Stella Aquino‐Calingasan, Bambang Ardianto, Eggi Arguni, Sally Blair, Thi Tam Dang, Maria Beatriz Gepte, Samanmalee Gunasekara, Andini Handayani, Miriam Kimpo, Catherine G. Lam, Nawachai Lertvivatpong, Sergio Licona, Ana Loseo, Ratha Mlis, Vivian Moreno Berrio, Nguyen Hoai Anh, Anna Lisa Ong‐Lim, Ha Thu Pham, Krishna Sagar Sharma, Bun Sereyleak, Sally Jane G. Velasco‐Aro, Su Yadana, Ambuj Kumar, Sheena Mukkada   +29 more
wiley   +1 more source

Adrenocortical carcinoma masquerading as pheochromocytoma: a histopathologic dilemma

Endocrinology, Diabetes & Metabolism Case Reports, 2020
Adrenocortical carcinoma (ACC) is an aggressive cancer that originates in the cortex of the adrenal gland and generally has a poor prognosis. ACC is rare but can be more commonly seen in those with cancer predisposition syndromes (e.g.
Impana Shetty, Sarah Fuller, Margarita Raygada, Maria J Merino, B J Thomas, Brigitte C Widemann, Karlyne M Reilly, Karel Pacak, Jaydira Del Rivero   +8 more
doaj   +1 more source

Bone and Soft Tissue Neoplasms in Infants Versus Older Children: A Report From the Cancer in Young People in Canada Program

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background and Aims Infant bone and soft tissue neoplasms present distinct clinical challenges and lack large‐scale data to inform treatment decisions. This study aims to characterize bone and soft tissue neoplasms in infants in Canada and to compare their outcomes with those of older pediatric patients.
Samuel Sassine, Hallie Coltin, Maria Kondyli, Monia Marzouki, Nicolas Prud'homme, Nida Usmani, Rebecca J. Deyell, Lesleigh Abbott, Tony H. Truong, Sapna Oberoi, Ketan Kulkarni, Josée Brossard, Lynette Bowes, Paul Gibson, Sarah McKillop, Roona Sinha, Lillian Sung, Catherine Vezina, Laura Wheaton, Alexandra P. Zorzi, Marie‐Claude Pelland‐Marcotte, Thai Hoa Tran   +21 more
wiley   +1 more source

Pediatric Cancer Recognition Training in Botswana

Global Pediatric Health, 2016
Delayed presentation of children with cancer is a significant barrier to improving the survival from children’s cancer in low- and middle-income countries (LMICs).
Jeremy S. Slone MD, MPH, Elise Ishigami MPH, Parth S. Mehta MD, MPH   +2 more
doaj   +1 more source