Meagher-Villemure K - Search Results

1

Aminopterin-like syndrome sine aminopterin associated with translocation involving chromosomes 5 and 10.

Chen MF, Vekemans M, Meagher-Villemure K, Outerbridge E, Fraser FC, Der Kaloustian VM. Chen MF, et al. Am J Med Genet. 1990 Dec;37(4):478-81. doi: 10.1002/ajmg.1320370411. Am J Med Genet. 1990. PMID: 2260592

2

Schinzel-Giedion syndrome: further delineation of the phenotype.

Elliott AM, Meagher-Villemure K, Oudjhane K, der Kaloustian VM. Elliott AM, et al. Clin Dysmorphol. 1996 Apr;5(2):135-42. doi: 10.1097/00019605-199604000-00005. Clin Dysmorphol. 1996. PMID: 8723563 Review.

3

Fetus with two identical reciprocal translocations: description of a rare complication of consanguinity.

Martinet D, Vial Y, Thonney F, Beckmann JS, Meagher-Villemure K, Unger S. Martinet D, et al. Am J Med Genet A. 2006 Apr 1;140(7):769-74. doi: 10.1002/ajmg.a.31150. Am J Med Genet A. 2006. PMID: 16523519

4

Developmental bilateral perisylvian dysplasia.

Shevell MI, Carmant L, Meagher-Villemure K. Shevell MI, et al. Pediatr Neurol. 1992 Jul-Aug;8(4):299-302. doi: 10.1016/0887-8994(92)90370-e. Pediatr Neurol. 1992. PMID: 1388421

5

Familial alternating epilepsia partialis continua with chronic encephalitis: another variant of Rasmussen syndrome?

Silver K, Andermann F, Meagher-Villemure K. Silver K, et al. Arch Neurol. 1998 May;55(5):733-6. doi: 10.1001/archneur.55.5.733. Arch Neurol. 1998. PMID: 9605733

6

Brain dysgenesis and congenital intracerebral calcification associated with 3-hydroxyisobutyric aciduria.

Chitayat D, Meagher-Villemure K, Mamer OA, O'Gorman A, Hoar DI, Silver K, Scriver CR. Chitayat D, et al. J Pediatr. 1992 Jul;121(1):86-9. doi: 10.1016/s0022-3476(05)82549-1. J Pediatr. 1992. PMID: 1625099

7

Masson's vegetant haemangio-endothelioma.

Lam CH, Farmer JP, Meagher-Villemure K, Montes JL. Lam CH, et al. Pediatr Neurosurg. 1995;23(2):93-6. doi: 10.1159/000120943. Pediatr Neurosurg. 1995. PMID: 8555102

8

Infantile epileptic encephalopathy (Ohtahara syndrome) and migrational disorder.

Miller SP, Dilenge ME, Meagher-Villemure K, O'Gorman AM, Shevell MI. Miller SP, et al. Pediatr Neurol. 1998 Jul;19(1):50-4. doi: 10.1016/s0887-8994(98)00009-5. Pediatr Neurol. 1998. PMID: 9682886

9

Ganglioglioma presenting as a vascular lesion in a 10-year-old boy. Case report.

Baltuch GH, Farmer JP, Meagher-Villemure K, O'Gorman AM, Montes JL. Baltuch GH, et al. J Neurosurg. 1993 Dec;79(6):920-3. doi: 10.3171/jns.1993.79.6.0920. J Neurosurg. 1993. PMID: 8246060

10

Fulminant hepatic failure associated with status epilepticus in children: three cases and a review of potential mechanisms.

Decell MK, Gordon JB, Silver K, Meagher-Villemure K. Decell MK, et al. Intensive Care Med. 1994 May;20(5):375-8. doi: 10.1007/BF01720913. Intensive Care Med. 1994. PMID: 7930035 Review.

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