Prasad AN - Search Results

1

Debunking Occam's razor: Diagnosing multiple genetic diseases in families by whole-exome sequencing.

Balci TB, Hartley T, Xi Y, Dyment DA, Beaulieu CL, Bernier FP, Dupuis L, Horvath GA, Mendoza-Londono R, Prasad C, Richer J, Yang XR, Armour CM, Bareke E, Fernandez BA, McMillan HJ, Lamont RE, Majewski J, Parboosingh JS, Prasad AN, Rupar CA, Schwartzentruber J, Smith AC, Tétreault M; FORGE Canada Consortium; Care4Rare Canada Consortium; Innes AM, Boycott KM. Balci TB, et al. Among authors: prasad an, prasad c. Clin Genet. 2017 Sep;92(3):281-289. doi: 10.1111/cge.12987. Epub 2017 Mar 13. Clin Genet. 2017. PMID: 28170084

2

Iron deficiency; non-hematological manifestations.

Prasad AN, Prasad C. Prasad AN, et al. Among authors: prasad c. Prog Food Nutr Sci. 1991;15(4):255-83. Prog Food Nutr Sci. 1991. PMID: 1784738 Review.

3

A relationship between increased voluntary alcohol preference and basal hypercorticosteronemia associated with an attenuated rise in corticosterone output during stress.

Prasad C, Prasad A. Prasad C, et al. Alcohol. 1995 Jan-Feb;12(1):59-63. doi: 10.1016/0741-8329(94)00070-t. Alcohol. 1995. PMID: 7748515

4

Short-term consumption of a diet rich in fat decreases anxiety response in adult male rats.

Prasad A, Prasad C. Prasad A, et al. Physiol Behav. 1996 Sep;60(3):1039-42. doi: 10.1016/0031-9384(96)00135-7. Physiol Behav. 1996. PMID: 8873290

5

Agmatine enhances caloric intake and dietary carbohydrate preference in satiated rats.

Prasad A, Prasad C. Prasad A, et al. Physiol Behav. 1996 Oct;60(4):1187-9. doi: 10.1016/0031-9384(96)00151-5. Physiol Behav. 1996. PMID: 8884952

6

Recent advances in the genetics of epilepsy: insights from human and animal studies.

Prasad AN, Prasad C, Stafstrom CE. Prasad AN, et al. Among authors: prasad c. Epilepsia. 1999 Oct;40(10):1329-52. doi: 10.1111/j.1528-1157.1999.tb02004.x. Epilepsia. 1999. PMID: 10528928 Free article. Review.

7

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

8

Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): evidence for a founder effect and results of a pilot study on a DNA-based newborn screening program.

Prasad C, Johnson JP, Bonnefont JP, Dilling LA, Innes AM, Haworth JC, Beischel L, Thuillier L, Prip-Buus C, Singal R, Thompson JR, Prasad AN, Buist N, Greenberg CR. Prasad C, et al. Among authors: prasad an. Mol Genet Metab. 2001 May;73(1):55-63. doi: 10.1006/mgme.2001.3149. Mol Genet Metab. 2001. PMID: 11350183

9

De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus.

Sudha T, Dawson AJ, Prasad AN, Konkin D, de Groot GW, Prasad C. Sudha T, et al. Among authors: prasad an, prasad c. Clin Dysmorphol. 2001 Jul;10(3):193-6. doi: 10.1097/00019605-200107000-00008. Clin Dysmorphol. 2001. PMID: 11446413

10

Outcome of the first 3-years of a DNA-based neonatal screening program for glutaric acidemia type 1 in Manitoba and northwestern Ontario, Canada.

Greenberg CR, Prasad AN, Dilling LA, Thompson JR, Haworth JC, Martin B, Wood-Steiman P, Seargeant LE, Seifert B, Booth FA, Prasad C. Greenberg CR, et al. Among authors: prasad an, prasad c. Mol Genet Metab. 2002 Jan;75(1):70-8. doi: 10.1006/mgme.2001.3270. Mol Genet Metab. 2002. PMID: 11825066

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