Manu Raam

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

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Publications

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
Analysis of FOXF1 and the FOX gene cluster in patients with VACTERL association. Eur J Med Genet. 2011 May-Jun; 54(3):323-8.. View in PubMed
Long-term outcomes of adults with features of VACTERL association. Eur J Med Genet. 2011 Jan-Feb; 54(1):34-41.. View in PubMed
Analysis of component findings in 79 patients diagnosed with VACTERL association. Am J Med Genet A. 2010 Sep; 152.. View in PubMed
Evidence for inheritance in patients with VACTERL association. Hum Genet. 2010 Jun; 127(6):731-3.. View in PubMed
Holoprosencephaly and craniosynostosis: A report of two siblings and review of the literature. Am J Med Genet C Semin Med Genet. 2010 Feb 15; 154.. View in PubMed
Holoprosencephaly flashcards: A summary for the clinician. Am J Med Genet C Semin Med Genet. 2010 Feb 15; 154.. View in PubMed
Enzyme-responsive PARACEST MRI contrast agents: a new biomedical imaging approach for studies of the proteasome. Contrast Media Mol Imaging. 2007 Jul; 2(4):189-98.. View in PubMed