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Autosomal dominant mannose-binding lectin deficiency is associated with worse neurodevelopmental outcomes after cardiac surgery in infants.
Kim DS, Li YK, Kim JH, Bergquist CS, Gerdes M, Bernbaum JC, Burnham N, McDonald-McGinn DM, Zackai EH, Nicolson SC, Spray TL, Nickerson DA, Hakonarson H, Jarvik GP, Gaynor JW. Kim DS, et al. Among authors: gerdes m. J Thorac Cardiovasc Surg. 2018 Mar;155(3):1139-1147.e2. doi: 10.1016/j.jtcvs.2017.08.035. Epub 2017 Dec 7. J Thorac Cardiovasc Surg. 2018. PMID: 29452463 Free PMC article.
MRI, MRA, and neurodevelopmental outcome following neonatal ECMO.
Lago P, Rebsamen S, Clancy RR, Pinto-Martin J, Kessler A, Zimmerman R, Schmelling D, Bernbaum J, Gerdes M, D'Agostino JA, et al. Lago P, et al. Among authors: gerdes m. Pediatr Neurol. 1995 May;12(4):294-304. doi: 10.1016/0887-8994(95)00047-j. Pediatr Neurol. 1995. PMID: 7546003 Free article.
The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
McDonald-McGinn DM, Kirschner R, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Solot C, Wang P, Jacobs I, Handler S, Knightly C, Heher K, Wilson M, Ming JE, Grace K, Driscoll D, Pasquariello P, Randall P, Larossa D, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Among authors: gerdes m. Genet Couns. 1999;10(1):11-24. Genet Couns. 1999. PMID: 10191425
The 22q11.2 deletion: screening, diagnostic workup, and outcome of results; report on 181 patients.
McDonald-McGinn DM, LaRossa D, Goldmuntz E, Sullivan K, Eicher P, Gerdes M, Moss E, Wang P, Solot C, Schultz P, Lynch D, Bingham P, Keenan G, Weinzimer S, Ming JE, Driscoll D, Clark BJ 3rd, Markowitz R, Cohen A, Moshang T, Pasquariello P, Randall P, Emanuel BS, Zackai EH. McDonald-McGinn DM, et al. Among authors: gerdes m. Genet Test. 1997;1(2):99-108. doi: 10.1089/gte.1997.1.99. Genet Test. 1997. PMID: 10464633
256 results