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Results: 1-11 |
Results: 11
Gaucher disease and parkinsonism: A phenotypic and genotypic characterization
Authors: Tayebi, N Callahan, M Madike, V Stubblefield, BK Orvisky, E Krasnewich, D Fillano, JJ Sidransky, E
Citation: N. Tayebi et al., Gaucher disease and parkinsonism: A phenotypic and genotypic characterization, MOL GEN MET, 73(4), 2001, pp. 313-321
Glucocerebrosidase mutations among African-American patients with type 1 Gaucher disease
Authors: Park, JK Koprivica, V Andrews, DQ Madike, V Tayebi, N Stone, DL Sidransky, E
Citation: Jk. Park et al., Glucocerebrosidase mutations among African-American patients with type 1 Gaucher disease, AM J MED G, 99(2), 2001, pp. 147-151
Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease
Authors: Stone, DL Tayebi, N Orvisky, E Stubblefield, B Madike, V Sidransky, E
Citation: Dl. Stone et al., Glucocerebrosidase gene mutations in patients with type 2 Gaucher disease, HUM MUTAT, 15(2), 2000, pp. 181-188
Fracture toughness of polysilicon MEMS devices
Authors: Kahn, H Tayebi, N Ballarini, R Mullen, RL Heuer, AH
Citation: H. Kahn et al., Fracture toughness of polysilicon MEMS devices, SENS ACTU-A, 82(1-3), 2000, pp. 274-280
Gene rearrangement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion gene
Authors: Tayebi, N Park, J Madike, V Sidransky, E
Citation: N. Tayebi et al., Gene rearrangement on 1q21 introducing a duplication of the glucocerebrosidase pseudogene and a metaxin fusion gene, HUM GENET, 107(4), 2000, pp. 400-403
Type 2 Gaucher disease: the collodion baby phenotype revisited
Authors: Stone, DL Carey, WF Christodoulou, J Sillence, D Nelson, P Callahan, M Tayebi, N Sidransky, E
Citation: Dl. Stone et al., Type 2 Gaucher disease: the collodion baby phenotype revisited, ARCH DIS CH, 82(2), 2000, pp. F163-F166
Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher disease
Authors: Koprivica, V Stone, DL Park, JK Callahan, M Frisch, A Cohen, IJ Tayebi, N Sidransky, E
Citation: V. Koprivica et al., Analysis and classification of 304 mutant alleles in patients with type 1 and type 3 Gaucher disease, AM J HU GEN, 66(6), 2000, pp. 1777-1786
Sampling and analytic considerations in molecular genetics studies of ADHD. The advantages of predicting phenotype from genotype in ADHD research - Castellanos replies
Authors: Castellanos, FX Lau, E Tayebi, N Lee, P Long, RE Giedd, JN Sharp, WS Marsh, WL Walter, JM Hamburger, SD Ginns, EI Rapoport, JL Sidransky, E
Citation: Fx. Castellanos et al., Sampling and analytic considerations in molecular genetics studies of ADHD. The advantages of predicting phenotype from genotype in ADHD research - Castellanos replies, MOL PSYCHI, 4(5), 1999, pp. 414-414
Type 2 Gaucher disease: An expanding phenotype
Authors: Tayebi, N Stone, DL Sidransky, E
Citation: N. Tayebi et al., Type 2 Gaucher disease: An expanding phenotype, MOL GEN MET, 68(2), 1999, pp. 209-219
Is the perinatal lethal form of Gaucher disease more common than classic type 2 Gaucher disease?
Authors: Stone, DL van Diggelen, OP de Klerk, JBC Gaillard, JLJ Niermeijer, MF Willemsen, R Tayebi, N Sidransky, E
Citation: Dl. Stone et al., Is the perinatal lethal form of Gaucher disease more common than classic type 2 Gaucher disease?, EUR J HUM G, 7(4), 1999, pp. 505-509
Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease
Authors: Lau, EK Tayebi, N Ingraham, LJ Winfield, SL Koprivica, V Stone, DL Zimran, A Ginns, EI Sidransky, E
Citation: Ek. Lau et al., Two novel polymorphic sequences in the glucocerebrosidase gene region enhance mutational screening and founder effect studies of patients with Gaucher disease, HUM GENET, 104(4), 1999, pp. 293-300
Risultati: 1-11 |