Elias ER - Search Results

1

An interesting case of infant sudden death: severe hypertrophic cardiomyopathy in Pompe's disease.

Metzl JD, Elias ER, Berul CI. Metzl JD, et al. Among authors: elias er. Pacing Clin Electrophysiol. 1999 May;22(5):821-2. doi: 10.1111/j.1540-8159.1999.tb00551.x. Pacing Clin Electrophysiol. 1999. PMID: 10353146

2

Renal findings on radiological followup of patients with Beckwith-Wiedemann syndrome.

Borer JG, Kaefer M, Barnewolt CE, Elias ER, Hobbs N, Retik AB, Peters CA. Borer JG, et al. Among authors: elias er. J Urol. 1999 Jan;161(1):235-9. J Urol. 1999. PMID: 10037413

3

Abnormal cholesterol metabolism in Smith-Lemli-Opitz syndrome.

Elias ER, Irons M. Elias ER, et al. Curr Opin Pediatr. 1995 Dec;7(6):710-4. doi: 10.1097/00008480-199512000-00015. Curr Opin Pediatr. 1995. PMID: 8776024 Review.

4

Trisomy 15 mosaicism and uniparental disomy (UPD) in a liveborn infant.

Milunsky JM, Wyandt HE, Huang XL, Kang XZ, Elias ER, Milunsky A. Milunsky JM, et al. Among authors: elias er. Am J Med Genet. 1996 Jan 22;61(3):269-73. doi: 10.1002/(SICI)1096-8628(19960122)61:3<269::AID-AJMG12>3.0.CO;2-R. Am J Med Genet. 1996. PMID: 8741873

5

Developmental delay and growth failure caused by a peroxisomal disorder, dihydroxyacetonephosphate acyltransferase (DHAP-AT) deficiency.

Elias ER, Mobassaleh M, Hajra AK, Moser AB. Elias ER, et al. Am J Med Genet. 1998 Nov 16;80(3):223-6. Am J Med Genet. 1998. PMID: 9843043

6

MRI and 1H MRS findings in Smith-Lemli-Opitz syndrome.

Caruso PA, Poussaint TY, Tzika AA, Zurakowski D, Astrakas LG, Elias ER, Bay C, Irons MB. Caruso PA, et al. Among authors: elias er. Neuroradiology. 2004 Jan;46(1):3-14. doi: 10.1007/s00234-003-1110-1. Epub 2003 Nov 5. Neuroradiology. 2004. PMID: 14605787

7

Clinical effects of cholesterol supplementation in six patients with the Smith-Lemli-Opitz syndrome (SLOS).

Elias ER, Irons MB, Hurley AD, Tint GS, Salen G. Elias ER, et al. Am J Med Genet. 1997 Jan 31;68(3):305-10. doi: 10.1002/(sici)1096-8628(19970131)68:3<305::aid-ajmg11>3.0.co;2-x. Am J Med Genet. 1997. PMID: 9024564 Clinical Trial.

8

The 3C syndrome: evolution of the phenotype and growth hormone deficiency.

Wheeler PG, Sadeghi-Nejad A, Elias ER. Wheeler PG, et al. Among authors: elias er. Am J Med Genet. 1999 Nov 5;87(1):61-4. doi: 10.1002/(sici)1096-8628(19991105)87:1<61::aid-ajmg12>3.0.co;2-k. Am J Med Genet. 1999. PMID: 10528249

9

Benign hemorrhagic adrenocortical macrocysts in Beckwith-Wiedemann syndrome.

McCauley RG, Beckwith JB, Elias ER, Faerber EN, Prewitt LH Jr, Berdon WE. McCauley RG, et al. Among authors: elias er. AJR Am J Roentgenol. 1991 Sep;157(3):549-52. doi: 10.2214/ajr.157.3.1872243. AJR Am J Roentgenol. 1991. PMID: 1872243

10

Rod photoreceptor responses in children with Smith-Lemli-Opitz syndrome.

Elias ER, Hansen RM, Irons M, Quinn NB, Fulton AB. Elias ER, et al. Arch Ophthalmol. 2003 Dec;121(12):1738-43. doi: 10.1001/archopht.121.12.1738. Arch Ophthalmol. 2003. PMID: 14662594

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