Impaired growth outcomes in children with congenital colorectal diseases-Reference-Cited by-同舟云学术

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Impaired growth outcomes in children with congenital colorectal diseases

Published:2018-09 Issue: Volume:229 Page:102-107
ISSN:0022-4804
Container-title:Journal of Surgical Research
language:en
Short-container-title:Journal of Surgical Research

Author:

Veras Laura V.,Chotai Pranit N.,Tumen Andrew Z.,Gosain Ankush^ORCID

Publisher

Elsevier BV

Subject

Surgery

Reference22 articles.

1. Growth and developmental outcomes of infants with hirschsprung disease presenting in the neonatal period: a retrospective study;More;J Pediatr,2014

2. Prospective long-term follow up of children with anorectal malformation: growth and development until 5 years of age;van den Hondel;J Pediatr Surg,2013

3. Cloacal exstrophy: a 25-year experience with 50 cases;Lund;J Pediatr Surg,2001

4. Primary payer status is significantly associated with postoperative mortality, morbidity, and hospital resource utilization in pediatric surgical patients within the United States;Stone;J Pediatr Surg,2013

5. The effect of race and gender on pediatric surgical outcomes within the United States;Stone;J Pediatr Surg,2013

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The impact of social determinants of health on the overall wellbeing of children: A review for the pediatric surgeon;Journal of Pediatric Surgery;2021-10

2. Development of Clinical Referral Score Model for Early Diagnosis of Hirschsprung’s Disease in Suspected Pediatric Patients;Healthcare;2021-06-04

3. Long-term impact of fistula status on growth and anemia in infants with congenital anorectal malformations;ASIA PAC J CLIN NUTR;2020

4. Comparison of Hirschsprung Disease Characteristics between Those with a History of Postoperative Enterocolitis and Those without: Results from the Pediatric Colorectal and Pelvic Learning Consortium;European Journal of Pediatric Surgery;2020-09-18

5. ERNICA guidelines for the management of rectosigmoid Hirschsprung’s disease;Orphanet Journal of Rare Diseases;2020-06-25

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