Mucolipidosis Type IV: The Effect of Increased Lysosomal pH on the Abnormal Lysosomal Storage von Kogot-Levin, Aviram, Zeigler, Marsha, Ornoy, Asher, Bach, Gideon

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The clinical spectrum of fetal Niemann–Pick type C von Spiegel, Ronen, Raas‐Rothschild, Annick, Reish, Orit, Regev, Miriam, Meiner, Vardiella, Bargal, Ruth, Sury, Vivi, Meir, Karen, Nadjari, Michel, Hermann, Gratiana, Iancu, Theodor C., Shalev, Stavit A., Zeigler, Marsha

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A mutation in the saposin A coding region of the prosaposin gene in an infant presenting as Krabbe disease: first report of saposin A deficiency in humans von Spiegel, Ronen, Bach, Gideon, Sury, Vivi, Mengistu, Getu, Meidan, Bela, Shalev, Stavit, Yona Shneor, Mandel, Hanna, Zeigler, Marsha

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Molecular basis of variant pseudo-hurler polydystrophy (mucolipidosis IIIC) von Raas-Rothschild, A, Cormier-Daire, V, Bao, M, Genin, E, Salomon, R, Brewer, K, Zeigler, M, Mandel, H, Toth, S, Roe, B, Munnich, A, Canfield, W M

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Angiokeratoma corporis diffusum in human β-mannosidosis: Report of a new case and a novel mutation von Molho-Pessach, Vered, MD, Bargal, Ruth, MSc, Abramowitz, Yigal, MD, Doviner, Victoria, MD, Ingber, Arieh, MD, Raas-Rothschild, Annick, MD, Ne'eman, Zvi, PhD, Zeigler, Marsha, PhD, Zlotogorski, Abraham, MD

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The metabolism of glycosaminoglycans is impaired in prion diseases von Mayer-Sonnenfeld, Tehila, Zeigler, Marsha, Halimi, Michele, Dayan, Yael, Herzog, Christian, Lasmezas, Corinne I., Gabizon, Ruth

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Characterization of lysosomal acid lipase mutations in the signal peptide and mature polypeptide region causing Wolman disease von Zschenker, O, Jung, N, Rethmeier, J, Trautwein, S, Hertel, S, Zeigler, M, Ameis, D

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Successful treatment of Wolman disease by unrelated umbilical cord blood transplantation von STEIN, Jerry, ZION GARTY, Ben, DROR, Yael, FENIG, Eyal, ZEIGLER, Marsha, YANIV, Isaac

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Niemann-Pick C1 Disease Gene: Homology to Mediators of Cholesterol Homeostasis von Carstea, Eugene D., Morris, Jill A., Coleman, Katherine G., Loftus, Stacie K., Zhang, Dana, Cummings, Christiano, Gu, Jessie, Rosenfeld, Melissa A., Pavan, William J., Krizman, David B., Nagle, James, Polymeropoulos, Mihail H., Sturley, Stephen L., Ioannou, Yiannis A., Higgins, Maureen E., Comly, Marcella, Cooney, Adele, Brown, Anthony, Kaneski, Christine R., Blanchette-Mackie, E. Joan, Dwyer, Nancy K., Neufeld, Edward B., Chang, Ta-Yuan, Liscum, Laura, Strauss, Jerome F., Ohno, Kousaku, Zeigler, Marsha, Carmi, Rivka, Sokol, Jacob, Markie, David, O'Neill, Raymond R., van Diggelen, O. P., Elleder, Milan, Patterson, Marc C., Brady, Roscoe O., Vanier, Marie T., Pentchev, Peter G., Tagle, Danilo A.

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When Mucolipidosis III meets Mucolipidosis II: GNPTA gene mutations in 24 patients von Bargal, Ruth, Zeigler, Marsha, Abu-Libdeh, Bassam, Zuri, Vivi, Mandel, Hanna, Ben Neriah, Ziva, Stewart, Fiona, Elcioglu, Nursel, Hindi, Tareq, Merrer, Martine Le, Bach, Gideon, Raas-Rothschild, Annick

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Genetic screening for Krabbe disease: Learning from the past and looking to the future von Macarov, Michal, Zlotogora, Joel, Meiner, Vardiella, Khatib, Zinab, Sury, Vivi, Mengistu, Getu, Bargal, Ruth, Shmueli, Esther, Meidan, Bela, Zeigler, Marsha

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Treatment Outcome of Pompe Disease Infants with Negative Cross-Reactive Immunologic Material From Israel and Gaza von Mandel, Hanna, Bali, Deeksha, Kishnani, Priya S, Bar-Joseph, Gad, Lorber, Avraham, Khoury, Asaad, Natan, Dalia, Eldad, Dan J, Zeigler, Marsha, Bercovich, Dan, Plotkin, Horachio, Herskovitz, Eli

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Prenatal diagnosis for arginase deficiency by second-trimester fetal erythrocyte arginase assay and first-trimester ARG1 mutation analysis von Korman, Stanley H., Gutman, Alisa, Stemmer, Edia, Kay, Barrie S., Ben-Neriah, Ziva, Zeigler, Marsha

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Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C von Meiner, Vardiella, Shpitzen, Shoshi, Mandel, Hanna, Klar, Aharon, Ben-Neriah, Ziva, Zlotogora, Joël, Sagi, Michal, Lossos, Alex, Bargal, Ruth, Sury, Vivy, Carmi, Rivka, Leitersdorf, Eran, Zeigler, Marsha

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Niemann Pick disease type A in Israeli Arabs: 677delT, a common novel single mutation von Gluck, Iris, Zeigler, Marsha, Bargal, Ruth, Schiff, Elena, Bach, Gideon

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Phenotypic heterogeneity in patients with Gaucher disease and the N370S/V394L genotype von Elstein, Deborah, Scott, C Ronald, Zeigler, Marsha, Abrahamov, Aya, Zimran, Ari

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Effective strategies to reduce high risk drinking among college students and residents in an urban environment von Brinkley, Marsha, Smart, G.T, Zeigler, Donald W

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