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AJNR. American Journal of Neuroradiology|January 16, 2010
Bilateral complete labyrinthine aplasia with bilateral internal carotid artery aplasia, developmental delay, and gaze abnormalities: a presumptive case of a rare HOXA1 mutation syndromeM J Higley, T W Walkiewicz, J H Miller, et al.The Journal of Thoracic and Cardiovascular Surgery|October 10, 1998
Adenovirus infection in the lung results in graft failure after lung transplantationN D Bridges, T L Spray, M H Collins, et al.American Journal of Medical Genetics|January 23, 1999
Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIBR Kosaki, M Gebbia, K Kosaki, et al.Archives of General Psychiatry|December 1, 1986
Gilles de la Tourette's syndrome and obsessive-compulsive disorder. Evidence supporting a genetic relationshipD L Pauls, K E Towbin, J F Leckman, et al.Pediatric Radiology|August 2, 2025
Incidence and factors associated with serosal and soft tissue enhancement after cardiac catheterization in infantsAkhil Dhamija, Joshua D Wermers, Sarosh P Batlivala, et al.Texas Heart Institute Journal|January 1, 1997
The rare association of tetralogy of Fallot with hypertrophic cardiomyopathy. Report of 2 neonatal patientsM B Lewin, J A Towbin, M K Thapar, et al.Journal of Cardiology Cases|December 15, 2018
Left ventricular noncompaction cardiomyopathy in Duchenne muscular dystrophy carriersJohn J Parent, Ryan A Moore, Michael D Taylor, et al.Analytical Biochemistry|May 15, 1985
Chromogenic labeling of monosaccharides using 4'-N,N-dimethylamino-4-aminoazobenzeneG Rosenfelder, M Mörgelin, J Y Chang, et al.Radiology|January 25, 2005
Transgluteal approach for draining pelvic fluid collections in pediatric patientsAnne Marie Cahill, Kevin M Baskin, Robin D Kaye, et al.Pediatric Radiology|January 1, 1987
Dural ectasia as a cause of widening of the internal auditory canals in neurofibromatosisJ C Egelhoff, W S Ball, R B Towbin, et al.Pageof 98