USC.edu
Are You a Patient?

Manu Raam

Clinical Associate Professor of Pediatrics (Practitioner) (Part-Time)

Image of Manu Raam
Is this your profile? Click to edit
Email [email protected]
CTSI Profile

Publications

  • Self-management for youth and young adults with childhood-onset chronic conditions: A scoping review of parent and caregiver perspectives. Health Care Transit. 2026; 4:100148.. View in PubMed
  • Self-management for youth and young adults with childhood-onset chronic conditions: A scoping review of health care transition planning literature. Health Care Transit. 2026; 4:100147.. View in PubMed
  • Psychosocial needs and outcomes of adults with spina bifida: A scoping review, 1974-2023. Health Care Transit. 2024; 2:100041.. View in PubMed
  • Pre-Emptive Opioid-Sparing Medication Protocol Decreases Pain and Length of Hospital Stay in Children Undergoing Posterior Spinal Instrumented Fusion for Scoliosis. Iowa Orthop J. 2023; 43(1):111-115.. View in PubMed
  • Cytogenetics and holoprosencephaly: A chromosomal microarray study of 222 individuals with holoprosencephaly. Am J Med Genet C Semin Med Genet. 2018 06; 178(2):175-186.. View in PubMed
  • Point-of-Care Thoracic Ultrasonography in the Diagnosis and Management of Kaposiform Lymphangiomatosis. Pediatr Emerg Care. 2016 Dec; 32(12):888-891.. View in PubMed
  • C/EBP transcription factors in human squamous cell carcinoma: selective changes in expression of isoforms correlate with the neoplastic state. PLoS One. 2014; 9(11):e112073.. View in PubMed
  • Analysis of genitourinary anomalies in patients with VACTERL (Vertebral anomalies, Anal atresia, Cardiac malformations, Tracheo-Esophageal fistula, Renal anomalies, Limb abnormalities) association. Congenit Anom (Kyoto). 2011 Jun; 51(2):87-91.. View in PubMed
  • Holoprosencephaly: a guide to diagnosis and clinical management. Indian Pediatr. 2011 Jun; 48(6):457-66.. View in PubMed
  • De novo deletion of chromosome 20q13.33 in a patient with tracheo-esophageal fistula, cardiac defects and genitourinary anomalies implicates GTPBP5 as a candidate gene. Birth Defects Res A Clin Mol Teratol. 2011 Sep; 91(9):862-5.. View in PubMed

Similar People