Results 91 to 100 of about 21,170 (204)

Adaptive dosing of anticancer drugs in neonates: facilitating evidence-based dosing regimens [PDF]

open access: yes, 2016
PURPOSE: Selection of the most appropriate chemotherapy dosing regimens for neonates treated within the first weeks of life represents a significant clinical dilemma.
Brock, P   +7 more
core   +1 more source

A Population‐Based Assessment of Cancer Risk in Children With VACTERL

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 5, Page 1004-1011, May 2026.
ABSTRACT Cancer risk in children with VACTERL, a nonrandom co‐occurrence of ≥ 3 defects (vertebral, anal, cardiac, tracheoesophogeal fistula, renal, and limb), remains unclear. We evaluated this association in a population‐based study. We analyzed data from the Genetic Overlap Between Anomalies and Cancer in Kids (GOBACK) Study, a US registry linkage ...
Ji Yun Tark   +15 more
wiley   +1 more source

Cystic hepatoblastoma in an adolescent: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Hepatoblastoma accounts for approximately 1 % of pediatric tumors. It occurs mainly between 6 months and 3 years of age and is extremely rare in adolescents and adults.
Aliou Zabeirou   +7 more
doaj   +1 more source

Little girl who conquered the 'ALPPS' [PDF]

open access: yes, 2014
© 2014 Baishideng Publishing Group Inc. All rights reserved. An insufficient future liver remnant (FLR) is associated with post-hepatectomy liver failure.
Chan, ACY, Chung, HY, Poon, RTP
core   +1 more source

Spontaneous hepatic tumor regression in an infant with trisomy 18

open access: yes
Pediatric Investigation, EarlyView.
Masashi Hotta   +5 more
wiley   +1 more source

Familial Adenomatous Polyposis—Risk of Cancer, Cancer Prevention, and Long‐Term Consequences: Learnings from Five Decades with the Danish Polyposis Register

open access: yesAPMIS, Volume 134, Issue 5, May 2026.
ABSTRACT Familial adenomatous polyposis (FAP) is a hereditary condition marked by the growth of hundreds to thousands of adenomatous polyps in the colon and rectum, significantly elevating the risk of colorectal cancer (CRC) if left untreated. Caused by pathogenic variants in the APC gene, FAP is typically identified in adolescence, often leading to ...
John Gásdal Karstensen
wiley   +1 more source

Congenital tumors: imaging when life just begins [PDF]

open access: yes, 2011
Background The technical developments of imaging methods over the last 2 decades are changing our knowledge of perinatal oncology. Fetal ultrasound is usually the first imaging method used and thus constitutes the reference prenatal study ...
François Gudinchet   +3 more
core   +3 more sources

Plasma microRNA levels following resection of metastatic melanoma [PDF]

open access: yes, 2017
Melanoma remains the leading cause of skin cancer–related deaths. Surgical resection and adjuvant therapies can result in disease-free intervals for stage III and stage IV disease; however, recurrence is common.
Abrams, Zachary B   +10 more
core   +3 more sources

Multiple Haemangiomas, Diaphragmatic Eventration and Beckwith-Wiedemann Syndrome: An Unusual Association [PDF]

open access: yes, 2013
A 6-month-old girl with Beckwith-Wiedemann syndrome, multiple haemangiomas (axillary, laryngeal, pulmonary and hepatic) and diaphragmatic eventration was reported. All tumours responded to treatment with propranolol.
Borges, C   +3 more
core   +1 more source

Mesenchymal Hamartoma Mimicking Hepatoblastoma

open access: yesInternational Journal of Organ Transplantation Medicine, 2014
Mesenchymal hamartoma and hepatoblastoma are common causes of hepatic masses in pediatric population; they have similar radiologic and pathologic features.
A Bahador   +3 more
doaj  

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