Gerdes M - Search Results

1

Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy.

Kim DS, Stanaway IB, Rajagopalan R, Bernbaum JC, Solot CB, Burnham N, Zackai EH, Clancy RR, Nicolson SC, Gerdes M, Nickerson DA, Hakonarson H, Gaynor JW, Jarvik GP. Kim DS, et al. Among authors: gerdes m. PLoS One. 2012;7(9):e45936. doi: 10.1371/journal.pone.0045936. Epub 2012 Sep 25. PLoS One. 2012. PMID: 23049896 Free PMC article.

2

Survivors of extracorporeal membrane oxygenation at 1 year of age: the relationship of primary diagnosis with health and neurodevelopmental sequelae.

Bernbaum J, Schwartz IP, Gerdes M, D'Agostino JA, Coburn CE, Polin RA. Bernbaum J, et al. Among authors: gerdes m. Pediatrics. 1995 Nov;96(5 Pt 1):907-13. Pediatrics. 1995. PMID: 7478834

3

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.

4

Developmental presentation of 22q11.2 deletion (DiGeorge/velocardiofacial syndrome).

Wang PP, Solot C, Moss EM, Gerdes M, McDonald-McGinn DM, Driscoll DA, Emanuel BS, Zackai EH. Wang PP, et al. Among authors: gerdes m. J Dev Behav Pediatr. 1998 Oct;19(5):342-5. doi: 10.1097/00004703-199810000-00004. J Dev Behav Pediatr. 1998. PMID: 9809264 No abstract available.

5

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

Moss EM, Batshaw ML, Solot CB, Gerdes M, McDonald-McGinn DM, Driscoll DA, Emanuel BS, Zackai EH, Wang PP. Moss EM, et al. Among authors: gerdes m. J Pediatr. 1999 Feb;134(2):193-8. doi: 10.1016/s0022-3476(99)70415-4. J Pediatr. 1999. PMID: 9931529

6

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

7

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

Gerdes M, Solot C, Wang PP, Moss E, LaRossa D, Randall P, Goldmuntz E, Clark BJ 3rd, Driscoll DA, Jawad A, Emanuel BS, McDonald-McGinn DM, Batshaw ML, Zackai EH. Gerdes M, et al. Am J Med Genet. 1999 Jul 16;85(2):127-33. Am J Med Genet. 1999. PMID: 10406665

8

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

9

Follow-up care of the low birth weight infant.

Gerdes M, Bernbaum J. Gerdes M, et al. Indian J Pediatr. 1998 Nov-Dec;65(6):829-39. doi: 10.1007/BF02831342. Indian J Pediatr. 1998. PMID: 10773947

10

Neurodevelopmental outcome and lifestyle assessment in school-aged and adolescent children with hypoplastic left heart syndrome.

Mahle WT, Clancy RR, Moss EM, Gerdes M, Jobes DR, Wernovsky G. Mahle WT, et al. Among authors: gerdes m. Pediatrics. 2000 May;105(5):1082-9. doi: 10.1542/peds.105.5.1082. Pediatrics. 2000. PMID: 10790466

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