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Results: 1-6 |
Results: 6

Authors: Pena, JA Cardozo, JJ Montiel, CM Molina, OM Boustany, RM
Citation: Ja. Pena et al., Serial MRI findings in the Costa Rican variant of neuronal ceroid-lipofuscinosis, PED NEUROL, 25(1), 2001, pp. 78-80

Authors: Hentati, A Deng, HX Zhai, H Chen, W Yang, Y Hung, WY Azim, AC Bohlega, S Tandan, R Warner, C Laing, NG Cambi, F Mitsumoto, H Roos, RP Boustany, RM Ben Hamida, M Hentati, F Siddique, T
Citation: A. Hentati et al., Novel mutations in spastin gene and absence of correlation with age at onset of symptoms, NEUROLOGY, 55(9), 2000, pp. 1388-1390

Authors: Puranam, KL Guo, WX Qian, WH Nikbakht, K Boustany, RM
Citation: Kl. Puranam et al., CLN3 defines a novel antiapoptotic pathway operative in neurodegeneration and mediated by ceramide, MOL GEN MET, 66(4), 1999, pp. 294-308

Authors: Guo, WX Mao, CG Obeid, LM Boustany, RM
Citation: Wx. Guo et al., A disrupted homologue of the human CLN3 or juvenile neuronal ceroid lipofuscinosis gene in Saccharomyces cerevisiae: A model to study Batten disease, CELL MOL N, 19(5), 1999, pp. 671-680

Authors: Pane, MA Puranam, KL Boustany, RM
Citation: Ma. Pane et al., Expression of cln3 in human NT2 neuronal precursor cells and neonatal rat brain, PEDIAT RES, 46(4), 1999, pp. 367-374

Authors: Sleat, DE Gin, RM Sohar, I Wisniewski, K Sklower-Brooks, S Pullarkat, RK Palmer, DN Lerner, TJ Boustany, RM Uldall, P Siakotos, AN Donnelly, RJ Lobel, P
Citation: De. Sleat et al., Mutational analysis of the defective protease in classic late-infantile neuronal ceroid lipofuscinosis, a neurodegenerative lysosomal storage disorder, AM J HU GEN, 64(6), 1999, pp. 1511-1523
Risultati: 1-6 |