Neonatal Lung Disease Associated with TBX4 Mutations.
Suhrie, K; Pajor, NM; Ahlfeld, SK; Dawson, DB; Dufendach, KR; Kitzmiller, JA; Leino, D; Lombardo, RC; Smolarek, TA; Rathbun, PA; et al.
The Journal of Pediatrics.
2019;
206:286-292.e1.
Collagen COL22A1 maintains vascular stability and mutations in COL22A1 are potentially associated with intracranial aneurysms.
Ton, QV; Leino, D; Mowery, SA; Bredemeier, NO; Lafontant, PJ; Lubert, A; Gurung, S; Farlow, JL; Foroud, TM; Broderick, J; et al.
DMM Disease Models and Mechanisms.
2018;
11:dmm033654-dmm033654.
Zebrafish abcb11b mutant reveals strategies to restore bile excretion impaired by bile salt export pump deficiency.
Ellis, JL; Bove, KE; Schuetz, EG; Leino, D; Valencia, CA; Schuetz, JD; Miethke, A; Yin, C.
Hepatology.
2018;
67:1531-1545.
Refractory respiratory failure and pneumothorax in a full-term newborn.
Reed, BD; Arya, S; Dufendach, KR; Leino, D.
NeoReviews.org.
2018;
19:e109-e111.
Severe cytokine release syndrome in a patient receiving PD-1-directed therapy.
Rotz, SJ; Leino, D; Szabo, S; Mangino, JL; Turpin, BK; Pressey, JG.
Pediatric Blood and Cancer.
2017;
64:e26642-e26642.
Pediatric laryngeal carcinoma in a heterozygous carrier of Fanconi anemia.
D'Souza, AM; Mark, J; Demarcantonio, M; Leino, D; Sisson, R; Geller, JI.
Pediatric Blood and Cancer.
2017;
64:e26463-e26463.
Isolated Upper Extremity Posttransplant Lymphoproliferative Disorder in a Child.
Halula, SE; Leino, DG; Patel, MN; Racadio, JM; Lungren, MP.
Case Reports in Radiology.
2015;
2015:813989-5.