Improving the efficiency of the OSI checksum calculation von Sklower, K.

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The Eifel retransmission timer von Ludwig, R., Sklower, K.

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ESMDIS: Earth System Model Data Information System von Yuechen Chi, Mechoso, C.R., Stonebraker, M., Sklower, K., Troy, R., Muntz, R.R., Mesrobian, E.

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A Data Broker for Distributed computing environments von DRUMMOND, L. A, DEMMEL, J, MECHOSO, C. R, ROBINSON, H, SKLOWER, K, SPAHR, J. A

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A Data Broker for Distributed Computing Environments von Drummond, L. A., Demmel, J., Mechoso, C. R., Robinson, H., Sklower, K., Spahr, J. A.

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Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor von Junaid, Mohammed A., Kowal, Dagmar, Barua, Madhabi, Pullarkat, Premila S., Sklower Brooks, Susan, Pullarkat, Raju K.

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Features of Feingold syndrome 1 dominate in subjects with 2p deletions including MYCN von Burnside, Rachel D., Molinari, Sharon, Botti, Christina, Brooks, Susan Sklower, Chung, Wendy K., Mehta, Lakshmi, Schwartz, Stuart, Papenhausen, Peter

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Mutational Analysis of the Defective Protease in Classic Late-Infantile Neuronal Ceroid Lipofuscinosis, a Neurodegenerative Lysosomal Storage Disorder von Sleat, David E., Gin, Rosalie M., Sohar, Istvan, Wisniewski, Krystyna, Sklower-Brooks, Susan, Pullarkat, Raju K., Palmer, David N., Lerner, Terry J., Boustany, Rose-Mary, Uldall, Peter, Siakotos, Aristotle N., Donnelly, Robert J., Lobel, Peter

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Two common mutations in the CLN2 gene underlie late infantile neuronal ceroid lipofuscinosis von NAN ZHONG, WISNIEWSKI, K. E, HARTIKAINEN, J, WEINA JU, MOROZIEWICZ, D. N, MCLENDON, L, BROOKS, S. S, BROWN, W. T

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Molecular screening of Batten disease : identification of a missense mutation (E295K) in the CLN3 gene von ZHONG, N, WISNIEWSKI, K. E, BROWN, W. T, KACZMARSKI, A. L, JU, W, WEI MIN XU, XU, W. W, MCLENDON, L, LIU, B, KACZMARSKI, W, BROOKS, S. S

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The African Origin of the Common Mutation in African American Patients with Glycogen-Storage Disease Type II von Becker, Jeffrey A., Vlach, John, Raben, Nina, Nagaraju, Kanneboyina, Adams, Elizabeth M., Hermans, Monique M., Reuser, Arnold J.J., Brooks, Susan Sklower, Tifft, Cynthia J., Hirschhorn, Rochelle, Huie, Maryann L., Nicolino, Marc, Plotz, Paul H.

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Specific substrate for CLN2 proteaseltripeptidylpeptidaseI assay von Junaid, Mohammed A., Sklower Brooks, Susan, Pullarkat, Raju K.

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Studies of atypical JNCL suggest overlapping with other NCL forms von Wisniewski, Krystyna E., Zhong, Nan, Kaczmarski, Wojciech, Kaczmarski, Aleksandra, Sklower-Brooks, Susan, Brown, William T.

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A novel assay for lysosomal pepstatin-insensitive proteinase and its application for the diagnosis of late-infantile neuronal ceroid lipofuscinosis von Junaid, Mohammed A., Sklower Brooks, Susan, Wisniewski, Krystyna E., Pullarkat, Raju K.

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Spino-Cerebellar Degeneration With Polyneuropathy Associated With Ceroid Lipofuscinosis in One Family von Wisniewski, K.E., Madrid, R.E., Dambska, M., Rapin, I., Pullarkat, R., Sklower, S.

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Distal duplication 14q: report of three cases and further delineation of the syndrome von SKLOWER, S. L, JENKINS, E. C, TED BROWN, W, NOLIN, S. L, DUNCAN, C. J, WARBURTON, D, ANYANE YEBOA, K, MERKREBS, A, SCHWARTZ, R, WISNIEWSKI, K, STIMSON, C

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Farber lipogranulomatosis: An unusual presentation in a black child von Eviatar, Lydia, Sklower, Susan L., Wisniewski, Krystyna, Feldman, Robert S., Gochoco, Aurora

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On the association of fragile X with autism von Wolf-Schein, E G, Jenkins, E C, Sklower, S, Cohen, I L, Wisniewski, K E, Brown, W T

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81 NEONATAL FORM OF ADRENOLEUKODYSTROPHY von Laure-Kamionowska, M, Wisniewski, K, Pullarkat, R, Sklower, S, Lazarevlc, B, Peterson, H

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Sanfilippo Disease, Type A with some Features of Ceroid Lipofuscinosis von Wisniewski, K., Rudelli, R., Laure-Kamionowska, M., Sklower, S., Houck, G. E., Kieras Jr, F., Ramos, P., Wisniewski, H. M., Braak, H.

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