Multidimensional analysis and therapeutic development using patient iPSC-derived disease models of Wolfram syndrome von Kitamura, Rie Asada, Maxwell, Kristina G, Ye, Wenjuan, Kries, Kelly, Brown, Cris M, Augsornworawat, Punn, Hirsch, Yoel, Johansson, Martin M, Weiden, Tzvi, Ekstein, Joseph, Cohen, Joshua, Klee, Justin, Leslie, Kent, Simeonov, Anton, Henderson, Mark J, Millman, Jeffrey R, Urano, Fumihiko

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Severe epileptic encephalopathy associated with compound heterozygosity of THG1L variants in the Ashkenazi Jewish population von Rabin, Rachel, Hirsch, Yoel, Johansson, Martin M., Ekstein, Joseph, Ekstein, Ahron, Pappas, John

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Study of carrier frequency of Warsaw breakage syndrome in the Ashkenazi Jewish population and presentation of two cases von Rabin, Rachel, Hirsch, Yoel, Johansson, Martin M., Ekstein, Joseph, Zeevi, David A., Keena, Beth, Zackai, Elaine H., Pappas, John

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Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss von Richard, Elodie M., Bakhtiari, Somayeh, Marsh, Ashley P.L., Kaiyrzhanov, Rauan, Wagner, Matias, Shetty, Sheetal, Pagnozzi, Alex, Nordlie, Sandra M., Cornejo, Patricia, Magee, Helen, Liu, James, Norton, Bethany Y., Webster, Richard I., Hakonarson, Hakon, Li, Jiankang, Guo, Yiran, Jain, Mahim, Blesson, Alyssa, Rodan, Lance H., Abbott, Mary-Alice, Comi, Anne, Cohen, Julie S., Alhaddad, Bader, Meitinger, Thomas, Lenz, Dominic, Ziegler, Andreas, Kotzaeridou, Urania, Brunet, Theresa, Chassevent, Anna, Smith-Hicks, Constance, Ekstein, Joseph, Weiden, Tzvi, Hahn, Andreas, Zharkinbekova, Nazira, Turnpenny, Peter, Tucci, Arianna, Yelton, Melissa, Horvath, Rita, Gungor, Serdal, Hiz, Semra, Oktay, Yavuz, Lochmuller, Hanns, Zollino, Marcella, Morleo, Manuela, Marangi, Giuseppe, Nigro, Vincenzo, Torella, Annalaura, Pinelli, Michele, Amenta, Simona, Husain, Ralf A., Grossmann, Benita, Rapp, Marion, Steen, Claudia, Marquardt, Iris, Grimmel, Mona, Grasshoff, Ute, Korenke, G. Christoph, Owczarek-Lipska, Marta, Neidhardt, John, Radio, Francesca Clementina, Mancini, Cecilia, Claps Sepulveda, Dianela Judith, McWalter, Kirsty, Begtrup, Amber, Crunk, Amy, Guillen Sacoto, Maria J., Schnur, Rhonda E., Mancardi, Maria Margherita, Kreuder, Florian, Striano, Pasquale, Zara, Federico, Chung, Wendy K., Marks, Warren A., van Eyk, Clare L., Webber, Dani L., Corbett, Mark A., Harper, Kelly, Berry, Jesia G., MacLennan, Alastair H., Gecz, Jozef, Tartaglia, Marco, Salpietro, Vincenzo, Christodoulou, John, Kaslin, Jan, Padilla-Lopez, Sergio, Bilguvar, Kaya, Munchau, Alexander, Ahmed, Zubair M., Hufnagel, Robert B., Fahey, Michael C., Maroofian, Reza, Houlden, Henry, Mane, Shrikant M., Rad, Aboulfazl, Jin, Sheng Chih, Haack, Tobias B., Makowski, Christine, Hirsch, Yoel, Riazuddin, Saima, Kruer, Michael C.

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Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation von Edvardson, Simon, Shaag, Avraham, Zenvirt, Shamir, Erlich, Yaniv, Hannon, Gregory J., Shanske, Alan L., Gomori, John Moshe, Ekstein, Joseph, Elpeleg, Orly

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Responsibility of genetic testing von Ekstein, Rabbi Joseph

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A newly identified mutation in the PEX26 gene is associated with a milder form of Zellweger spectrum disorder von Tanaka, Akemi J, Okumoto, Kanji, Tamura, Shigehiko, Abe, Yuichi, Hirsch, Yoel, Deng, Liyong, Ekstein, Joseph, Chung, Wendy K, Fujiki, Yukio

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VAC14 syndrome in two siblings with retinitis pigmentosa and neurodegeneration with brain iron accumulation von Lyon, Gholson J, Marchi, Elaine, Ekstein, Joseph, Meiner, Vardiella, Hirsch, Yoel, Scher, Sholem, Yang, Edward, De Vivo, Darryl C, Madrid, Ricardo, Li, Quan, Wang, Kai, Haworth, Andrea, Chilton, Ilana, Chung, Wendy K, Velinov, Milen

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Breath Sound Distribution Images of Patients With Pneumonia and Pleural Effusion von MOR, Ram, KUSHNIR, Igal, MEYER, Jean-Jacques, EKSTEIN, Joseph, BEN-DOV, Issahar

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The frequency of mucolipidosis type IV in the Ashkenazi Jewish population and the identification of 3 novel MCOLN1 mutations von Bach, Gideon, Webb, Michael B.T., Bargal, Ruth, Zeigler, Marcia, Ekstein, Joseph

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Joubert Syndrome 2 (JBTS2) in Ashkenazi Jews Is Associated with a TMEM216 Mutation von Edvardson, Simon, Shaag, Avraham, Zenvirt, Shamir, Erlich, Yaniv, Hannon, Gregory J., Shanske, Alan L., Gomori, John Moshe, Ekstein, Joseph, Elpeleg, Orly

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Severe epileptic encephalopathy associated with compound heterozygosity of THG1L variants in the Ashkenazi Jewish population von Rabin, Rachel, Hirsch, Yoel, Johansson, Martin M, Ekstein, Joseph, Ekstein, Ahron, Pappas, John

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Cystic fibrosis heterozygote screening in the Orthodox Community of Ashkenazi Jews: the Dor Yesharim approach and heterozygote frequency von Abeliovich, D, Quint, A, Weinberg, N, Verchezon, G, Lerer, I, Ekstein, J, Rubinstein, E

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Game von EKSTEIN JOSEPH

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Game von EKSTEIN JOSEPH

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Laparoscopic surgery may be associated with severe pain and high analgesia requirements in the immediate postoperative period von EKSTEIN, Perla, SZOLD, Amir, SAGIE, Boaz, WERBIN, Nachum, KLAUSNER, Joseph M, WEINBROUM, Avi A

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Holmium Laser Ureteroscopic Treatment of Various Pathologic Features in Pediatrics von Sofer, Mario, Binyamini, Joseph, Ekstein, Perla M, Bar-Yosef, Yuval, Chen, Juza, Matzkin, Haim, Ben-Chaim, Jacob

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The cytochrome oxidase II gene in mitochondria of the sugar-beet Beta vulgaris L von Mann, V. (Hebrew Univ. of Jerusalem (Israel). Dept. of Genetics), Ekstein, I, Nissen, H, Hiser, C, McIntosh, L, Hirschberg, J

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The cytochrome oxidase II gene in mitochondria of the sugar-beetBeta vulgaris L von Mann, Varda, Ekstein, Ilana, Nissen, Hilde, Hiser, Carrie, Mclntosh, Lee, Hirschberg, Joseph

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Corneille's irony von Ekstein, Nina, Harris, Joseph

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