AAAAAA

   
Results: 1-10 |
Results: 10
Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): Evidence for a founder effect andresults of a pilot study on a DNA-based newborn screening program
Authors: Prasad, C Johnson, JP Bonnefont, JP Dilling, LA Innes, AM Haworth, JC Beischel, L Thuillier, L Prip-Buus, C Singal, R Thompson, JRG Prasad, AN Buist, N Greenberg, CR
Citation: C. Prasad et al., Hepatic carnitine palmitoyl transferase 1 (CPT1 A) deficiency in North American Hutterites (Canadian and American): Evidence for a founder effect andresults of a pilot study on a DNA-based newborn screening program, MOL GEN MET, 73(1), 2001, pp. 55-63
De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus
Authors: Sudha, T Dawson, AJ Prasad, AN Konkin, D de Groot, GW Prasad, C
Citation: T. Sudha et al., De novo interstitial long arm deletion of chromosome 3 with facial dysmorphism, Dandy-Walker variant malformation and hydrocephalus, CLIN DYSMOR, 10(3), 2001, pp. 193-196
Effects of fertilization rate and crop rotation on diazotrophic cyanobacteria in paddy field
Authors: Jha, MN Prasad, AN Sharma, SG Bharati, RC
Citation: Mn. Jha et al., Effects of fertilization rate and crop rotation on diazotrophic cyanobacteria in paddy field, WORLD J MIC, 17(5), 2001, pp. 463-468
The role of vigabatrin in childhood seizure disorders: Results from a clinical audit
Authors: Prasad, AN Penney, S Buckley, DJ
Citation: An. Prasad et al., The role of vigabatrin in childhood seizure disorders: Results from a clinical audit, EPILEPSIA, 42(1), 2001, pp. 54-61
Clinical correlations of occipital epileptiform discharges in children - Reply
Authors: Libenson, MH Caravale, B Prasad, AN
Citation: Mh. Libenson et al., Clinical correlations of occipital epileptiform discharges in children - Reply, NEUROLOGY, 54(7), 2000, pp. 1545-1545
Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype
Authors: Prasad, C Prasad, AN Chodirker, BN Lee, C Dawson, AK Jocelyn, LJ Chudley, AE
Citation: C. Prasad et al., Genetic evaluation of pervasive developmental disorders: the terminal 22q13 deletion syndrome may represent a recognizable phenotype, CLIN GENET, 57(2), 2000, pp. 103-109
A new approach to the design of robust load-frequency controller for largescale power systems
Authors: Ray, G Prasad, AN Prasad, GD
Citation: G. Ray et al., A new approach to the design of robust load-frequency controller for largescale power systems, ELEC POW SY, 51(1), 1999, pp. 13-22
Design of decentralized robust load-frequency controller based on SVD method
Authors: Ray, G Prasad, AN Bhattacharyya, TK
Citation: G. Ray et al., Design of decentralized robust load-frequency controller based on SVD method, COMPUT ELEC, 25(6), 1999, pp. 477-492
Clinical correlations of occipital epileptiform discharges in children
Authors: Libenson, MH Caravale, B Prasad, AN
Citation: Mh. Libenson et al., Clinical correlations of occipital epileptiform discharges in children, NEUROLOGY, 53(2), 1999, pp. 265-269
Recent advances in the genetics of epilepsy: Insights from human and animal studies
Authors: Prasad, AN Prasad, C Stafstrom, CE
Citation: An. Prasad et al., Recent advances in the genetics of epilepsy: Insights from human and animal studies, EPILEPSIA, 40(10), 1999, pp. 1329-1352
Risultati: 1-10 |