Prasad C - Search Results

1

The floppy infant: retrospective analysis of clinical experience (1990-2000) in a tertiary care facility.

Birdi K, Prasad AN, Prasad C, Chodirker B, Chudley AE. Birdi K, et al. Among authors: prasad an, prasad c. J Child Neurol. 2005 Oct;20(10):803-8. doi: 10.1177/08830738050200100401. J Child Neurol. 2005. PMID: 16417874

2

The floppy infant: contribution of genetic and metabolic disorders.

Prasad AN, Prasad C. Prasad AN, et al. Among authors: prasad c. Brain Dev. 2003 Oct;25(7):457-76. doi: 10.1016/s0387-7604(03)00066-4. Brain Dev. 2003. PMID: 13129589 Review.

3

Genetic evaluation of the floppy infant.

Prasad AN, Prasad C. Prasad AN, et al. Among authors: prasad c. Semin Fetal Neonatal Med. 2011 Apr;16(2):99-108. doi: 10.1016/j.siny.2010.11.002. Epub 2010 Dec 4. Semin Fetal Neonatal Med. 2011. PMID: 21131247 Review.

4

Agenesis of the corpus callosum and cerebral anomalies in inborn errors of metabolism.

Prasad AN, Bunzeluk K, Prasad C, Chodirker BN, Magnus KG, Greenberg CR. Prasad AN, et al. Among authors: prasad c. Congenit Anom (Kyoto). 2007 Dec;47(4):125-35. doi: 10.1111/j.1741-4520.2007.00160.x. Congenit Anom (Kyoto). 2007. PMID: 17988254

5

Genetics and cardiac anomalies: the heart of the matter.

Prasad C, Chudley AE. Prasad C, et al. Indian J Pediatr. 2002 Apr;69(4):321-32. doi: 10.1007/BF02723219. Indian J Pediatr. 2002. PMID: 12019554 Review.

6

Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype.

Prasad C, Prasad AN, Chodirker BN, Lee C, Dawson AK, Jocelyn LJ, Chudley AE. Prasad C, et al. Among authors: prasad an. Clin Genet. 2000 Feb;57(2):103-9. doi: 10.1034/j.1399-0004.2000.570203.x. Clin Genet. 2000. PMID: 10735630

7

Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features.

Dawson AJ, Putnam S, Schultz J, Riordan D, Prasad C, Greenberg CR, Chodirker BN, Mhanni AA, Chudley AE. Dawson AJ, et al. Among authors: prasad c. Clin Genet. 2002 Dec;62(6):488-94. doi: 10.1111/j.1399-0004.2002.tb02255.x. Clin Genet. 2002. PMID: 12515261

8

History of genetics through philately: Sir William Osler (1849-1919) and the Osler-Weber-Rendu syndrome.

Prasad C, Chudley AE. Prasad C, et al. Clin Genet. 2002 Jun;61(6):404-7. doi: 10.1034/j.1399-0004.2002.610602.x. Clin Genet. 2002. PMID: 12121346 No abstract available.

9

Association Between Lysine Reduction Therapies and Cognitive Outcomes in Patients With Pyridoxine-Dependent Epilepsy.

Coughlin CR, Tseng LA, Bok LA, Hartmann H, Footitt E, Striano P, Tabarki BM, Lunsing RJ, Stockler-Ipsiroglu S, Gordon S, Van Hove JLK, Abdenur JE, Boyer M, Longo N, Andrews A, Janssen MCH, van Wegberg A, Prasad C, Prasad AN, Lamb MM, Wijburg FA, Gospe SM Jr, van Karnebeek C; International PDE Consortium. Coughlin CR, et al. Among authors: prasad an, prasad c. Neurology. 2022 Dec 5;99(23):e2627-e2636. doi: 10.1212/WNL.0000000000201222. Neurology. 2022. PMID: 36008148 Free PMC article.

10

Telemedicine diagnosis for fetal alcohol syndrome - The Manitoba experience.

Benoit T, Bowes C, Bowman N, Cantin D, Chudley A, Crolly D, Livingston A, Longstaffe S, Marles S, Miller C, Millar M, Penko M, Prasad C, Riguidel J, Wincott L. Benoit T, et al. Among authors: prasad c. Paediatr Child Health. 2002 Mar;7(3):147-51. doi: 10.1093/pch/7.3.147. Paediatr Child Health. 2002. PMID: 20046287 Free PMC article.

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