Computer simulation of energy use, greenhouse gas emissions, and costs for alternative methods of processing fluid milk von Tomasula, P. M, Datta, N, Yee, W. C. F, McAloon, A. J, Nutter, D. W, Sampedro, F, Bonnaillie, L. M

Volltext

Correction of dystrophia myotonica type 1 pre-mRNA transcripts by artificial trans-splicing von Chen, H Y, Kathirvel, P, Yee, W C, Lai, P S

Volltext

Computer simulation of energy use, greenhouse gas emissions, and process economics of the fluid milk process von Tomasula, P.M, Yee, W.C.F, McAloon, A.J, Nutter, D.W, Bonnaillie, L.M

Volltext

Phlebosclerotic colitis: imaging findings of a rare entity von Markos, V, Kelly, S, Yee, W C, Davis, J E, Cheifetz, R E, Alsheikh, A

Volltext

Recurrent and founder mutations in the Netherlands: the cardiac phenotype of DES founder mutations p.S13F and p.N342D von van Spaendonck-Zwarts, K. Y., van der Kooi, A. J., van den Berg, M. P., Ippel, E. F., Boven, L. G., Yee, W.-C., van den Wijngaard, A., Brusse, E., Hoogendijk, J. E., Doevendans, P. A., de Visser, M., Jongbloed, J. D. H., van Tintelen, J. P.

Volltext

Improved neuronal transgene expression from an AAV-2 vector with a hybrid CMV enhancer/PDGF-β promoter von Wang, C. Y., Guo, H. Y., Lim, T. M., Ng, Y. K., Neo, H. P., Hwang, P. Y. K., Yee, W.-C., Wang, S.

Volltext

Characterization of the Gene Encoding Human Sarcolipin (SLN), a Proteolipid Associated with SERCA1: Absence of Structural Mutations in Five Patients with Brody Disease von Odermatt, Alex, Taschner, Peter E.M., Scherer, Stephen W., Beatty, Barbara, Khanna, Vijay K., Cornblath, David R., Chaudhry, Vinay, Yee, Won-Chee, Schrank, Bertold, Karpati, George, Breuning, Martijn H., Knoers, Nine, Maclennan, David H.

Volltext

Peripheral nerve regeneration with sustained release of poly(phosphoester) microencapsulated nerve growth factor within nerve guide conduits von Xu, Xiaoyun, Yee, Woon-Chee, Hwang, Peter Y.K, Yu, Hanry, Wan, Andrew C.A, Gao, Shujun, Boon, Kum-Loong, Mao, Hai-Quan, Leong, Kam W, Wang, Shu

Volltext

Rapidly evolving myopathy with myosin-deficient muscle fibers von Al-Lozi, M. T., Pestronk, A., Yee, W. C., Flaris, N., Cooper, J.

Volltext

Childhood chronic inflammatory demyelinating neuropathies : Clinical course and long-term follow-up von NEVO, Y, PESTRONK, A, KORNBERG, A. J, CONNOLLY, A. M, YEE, W.-C, IQBAL, I, SHIELD, L. K

Volltext

Polyneuropathies associated with high titre antisulphatide antibodies: characteristics of patients with and without serum monoclonal proteins von Lopate, G, Parks, B J, Goldstein, J M, Yee, W C, Friesenhahn, G M, Pestronk, A

Volltext

Block of gap junctions eliminates aberrant activity and restores light responses during retinal degeneration von Toychiev, Abduqodir H, Ivanova, Elena, Yee, Christopher W, Sagdullaev, Botir T

Volltext

Hereditary motor and sensory neuropathy IIB : Clinical and electrodiagnostic characteristics von ELLIOTT, J. L, KWON, J. M, GOODFELLOW, P. J, YEE, W.-C

Volltext

Serum IgM monoclonal autoantibody binding to the 301 to 314 amino acid epitope of β-tubulin : Clinical association with slowly progressive demyelinating polyneuropathy von CONNOLLY, A. M, PESTRONK, A, MEHTA, S, YEE, W. C, GREEN, B. J, FELLIN, C, OLNEY, R. K, MILLER, R. G, DEVOR, W. N

Volltext

N lines in a myopathy with myosin loss von Lopate, Glenn, Pestronk, Alan, Yee, Woon-Chee

Volltext

Serum antibodies to heparan sulfate glycosaminoglycans in Guillain–Barré syndrome and other demyelinating polyneuropathies von Pestronk, A, Choksi, R, Yee, W.C, Kornberg, A.J, Lopate, G, Trotter, J

Volltext

A process model to estimate biodiesel production costs von Haas, Michael J., McAloon, Andrew J., Yee, Winnie C., Foglia, Thomas A.

Volltext

Meiotic stability and genotype - phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy von La Spada, Albert R, Roling, Daniel B, Harding, Anita E, Warner, Carolyn L, Spiegel, Roland, Hausmanowa-Petrusewicz, Irena, Yee, Woon-Chee, Fischbeck, Kenneth H

Volltext

Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q von KWON, J. M, ELLIOTT, J. L, WOON-CHEE YEE, IVANOVICH, J, SCAVARDA, N. J, MOOLSINTONG, P. J, GOODFELLOW, P. J

Volltext

Lower motor neuron syndromes defined by patterns of weakness, nerve conduction abnormalities, and high titers of antiglycolipid antibodies von Pestronk, A., Chaudhry, V., Feldman, E. L., Griffin, J. W., Cornblath, D. R., Denys, E. H., Glasberg, M., Kuncl, R. W., Olney, R. K., Yee, W. C.

Volltext