Lynch D - Search Results

1

Polymicrogyria in chromosome 22 delection syndrome.

Bingham PM, Lynch D, McDonald-McGinn D, Zackai E. Bingham PM, et al. Among authors: lynch d. Neurology. 1998 Nov;51(5):1500-2. doi: 10.1212/wnl.51.5.1500. Neurology. 1998. PMID: 9818897

2

Cerebellar atrophy in a patient with velocardiofacial syndrome.

Lynch DR, McDonald-McGinn DM, Zackai EH, Emanuel BS, Driscoll DA, Whitaker LA, Fischbeck KH. Lynch DR, et al. J Med Genet. 1995 Jul;32(7):561-3. doi: 10.1136/jmg.32.7.561. J Med Genet. 1995. PMID: 7562973 Free PMC article.

3

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

McDonald-McGinn DM, Driscoll DA, Bason L, Christensen K, Lynch D, Sullivan K, Canning D, Zavod W, Quinn N, Rome J. McDonald-McGinn DM, et al. Among authors: lynch d. Am J Med Genet. 1995 Oct 23;59(1):103-13. doi: 10.1002/ajmg.1320590122. Am J Med Genet. 1995. PMID: 8849001

4

Autosomal dominant transmission of Dejerine-Sottas disease (HMSN III).

Lynch DR, Hara H, Yum SW, Chance PF, Scherer SS, Bird SJ, Fischbeck KH. Lynch DR, et al. Neurology. 1997 Aug;49(2):601-3. doi: 10.1212/wnl.49.2.601. Neurology. 1997. PMID: 9270606

5

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: lynch d. Genet Test. 1997;1(2):99-108. doi: 10.1089/gte.1997.1.99. Genet Test. 1997. PMID: 10464633

6

Juvenile dentatorubral-pallidoluysian atrophy: new clinical features.

Licht DJ, Lynch DR. Licht DJ, et al. Pediatr Neurol. 2002 Jan;26(1):51-4. doi: 10.1016/s0887-8994(01)00346-0. Pediatr Neurol. 2002. PMID: 11814736

7

Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletion.

Kao A, Mariani J, McDonald-McGinn DM, Maisenbacher MK, Brooks-Kayal AR, Zackai EH, Lynch DR. Kao A, et al. Am J Med Genet A. 2004 Aug 15;129A(1):29-34. doi: 10.1002/ajmg.a.30133. Am J Med Genet A. 2004. PMID: 15266612

8

Effects of a functional COMT polymorphism on prefrontal cognitive function in patients with 22q11.2 deletion syndrome.

Bearden CE, Jawad AF, Lynch DR, Sokol S, Kanes SJ, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Am J Psychiatry. 2004 Sep;161(9):1700-2. doi: 10.1176/appi.ajp.161.9.1700. Am J Psychiatry. 2004. PMID: 15337663

9

Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.

Bearden CE, Jawad AF, Lynch DR, Monterossso JR, Sokol S, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Child Neuropsychol. 2005 Feb;11(1):109-17. doi: 10.1080/09297040590911239. Child Neuropsychol. 2005. PMID: 15846854 Free PMC article.

10

Measuring Friedreich ataxia: complementary features of examination and performance measures.

Lynch DR, Farmer JM, Tsou AY, Perlman S, Subramony SH, Gomez CM, Ashizawa T, Wilmot GR, Wilson RB, Balcer LJ. Lynch DR, et al. Neurology. 2006 Jun 13;66(11):1711-6. doi: 10.1212/01.wnl.0000218155.46739.90. Neurology. 2006. PMID: 16769945 Clinical Trial.

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