SLC25A19 mutation as a cause of neuropathy and bilateral striatal necrosis von Spiegel, Ronen, Shaag, Avraham, Edvardson, Simon, Mandel, Hanna, Stepensky, Polina, Shalev, Stavit A., Horovitz, Yoseph, Pines, Ophry, Elpeleg, Orly

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TMEM70 deficiency: long-term outcome of 48 patients von Magner, Martin, Dvorakova, Veronika, Tesarova, Marketa, Mazurova, Stella, Hansikova, Hana, Zahorec, Martin, Brennerova, Katarina, Bzduch, Vladimir, Spiegel, Ronen, Horovitz, Yoseph, Mandel, Hanna, Eminoğlu, Fatma Tuba, Mayr, Johannes Adalbert, Koch, Johannes, Martinelli, Diego, Bertini, Enrico, Konstantopoulou, Vassiliki, Smet, Joél, Rahman, Shamima, Broomfield, Alexander, Stojanović, Vesna, Dionisi-Vici, Carlo, van Coster, Rudy, Morava-Kozicz, Eva, Sperl, Wolfgang, Zeman, Jiri, Honzik, Tomas

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Myopathic form of phosphoglycerate kinase (PGK) deficiency: A new case and pathogenic considerations von Spiegel, Ronen, Gomez, Estela Area, Akman, Hasan O, Krishna, Sindu, Horovitz, Yoseph, DiMauro, Salvatore

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Expanding the clinical spectrum of SLC29A3 gene defects von Spiegel, Ronen, Cliffe, Simon T, Buckley, Michael F, Crow, Yanick J, Urquhart, Jill, Horovitz, Yoseph, Tenenbaum-Rakover, Yardena, Newman, William G, Donnai, Dian, Shalev, Stavit A

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Late Relapse of Herpes Simplex Virus Encephalitis in a Child Due to Reactivation of Latent Virus: Clinicopathological Report and Review von Spiegel, Ronen, Miron, Dan, Yodko, Helena, Lumelsky, Dmitry, Habib, Adib, Horovitz, Yoseph

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Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy von Spiegel, Ronen, Saada, Ann, Halvardson, Jonatan, Soiferman, Devorah, Shaag, Avraham, Edvardson, Simon, Horovitz, Yoseph, Khayat, Morad, Shalev, Stavit A, Feuk, Lars, Elpeleg, Orly

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Establishing hospital admission criteria of pediatric Henoch–Schonlein purpura von Masarweh, Kamal, Horovitz, Yoseph, Avital, Avi, Spiegel, Ronen

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Diagnosis of familial Mediterranean fever following the initial presentation of monoarthritis von Horovitz, Yoseph, Tanous, Osama, Khayat, Morad, Shaker, Munir, Shalev, Stavit, Spiegel, Ronen

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TMEM70 mutations are a common cause of nuclear encoded ATP synthase assembly defect: further delineation of a new syndrome von Spiegel, Ronen, Khayat, Morad, Shalev, Stavit A, Horovitz, Yoseph, Mandel, Hanna, Hershkovitz, Eli, Barghuti, Flora, Shaag, Avraham, Saada, Ann, Korman, Stanley H, Elpeleg, Orly, Yatsiv, Ido

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Severe Meningoencephalitis Due to Late Reactivation of Varicella-Zoster Virus in an Immunocompetent Child von Spiegel, Ronen, Miron, Dan, Lumelsky, Dmitry, Horovitz, Yoseph

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Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1: insights into the natural history of a rare disorder von Shalev, Stavit A, Tenenbaum‐Rakover, Yardena, Horovitz, Yoseph, Paz, Veronica P, Ye, Honggang, Carmody, David, Highland, Heather M, Boerwinkle, Eric, Hanis, Craig L, Muzny, Donna M, Gibbs, Richard A, Bell, Graeme I, Philipson, Louis H, Greeley, Siri Atma W

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Acute neonatal suppurative parotitis: case reports and review von Spiegel, Ronen, Miron, Dan, Sakran, Waheeb, Horovitz, Yoseph

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Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene von Mandel, Hanna, Katsanelson, Ksenya Cohen, Khayat, Morad, Chervinsky, Ilana, Vladovski, Eugene, Iancu, Theodor C, Indelman, Margarita, Horovitz, Yoseph, Sprecher, Eli, Shalev, Stavit A, Spiegel, Ronen

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Extreme Clinical Variability of Dilated Cardiomyopathy in Two Siblings With Alström Syndrome von Mahamid, Jamal, Lorber, Avraham, Horovitz, Yoseph, Shalev, Stavit A., Collin, Gayle B., Naggert, Jürgen K., Marshall, Jan D., Spiegel, Ronen

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Pylephlebitis due to perforated appendicitis in a teenager von Levin, Carina, Koren, Ariel, Miron, Dan, Lumelsky, Dimitry, Nussinson, Elchanan, Siplovich, Leonardo, Horovitz, Yoseph

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Erratum to: TMEM70 deficiency: long-term outcome of 48 patients von Magner, Martin, Dvorakova, Veronika, Tesarova, Marketa, Mazurova, Stella, Hansikova, Hana, Zahorec, Martin, Brennerova, Katarina, Bzduch, Vladimir, Spiegel, Ronen, Horovitz, Yoseph, Mandel, Hanna, Eminoğlu, Fatma Tuba, Mayr, Johannes Adalbert, Koch, Johannes, Martinelli, Diego, Bertini, Enrico, Konstantopoulou, Vassiliki, Smet, Joél, Rahman, Shamima, Broomfield, Alexander, Stojanović, Vesna, Dionisi-Vici, Carlo, van Coster, Rudy, Morava, Eva, Sperl, Wolfgang, Zeman, Jiri, Honzik, Tomas

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Is omitting post urinary-tract-infection renal ultrasound safe after normal antenatal ultrasound? An observational study von Miron, Dan, Daas, Ahmed, Sakran, Waheeb, Lumelsky, Dimitry, Koren, Ariel, Horovitz, Yoseph

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Microcephaly, epilepsy, and neonatal diabetes due to compound heterozygous mutations in IER3IP1 : insights into the natural history of a rare disorder: IER3IP1 mutations causing ne... von Shalev, Stavit A, Tenenbaum-Rakover, Yardena, Horovitz, Yoseph, Paz, Veronica P, Ye, Honggang, Carmody, David, Highland, Heather M, Boerwinkle, Eric, Hanis, Craig L, Muzny, Donna M, Gibbs, Richard A, Bell, Graeme I, Philipson, Louis H, Greeley, Siri Atma W

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Acute Human Parvovirus B-19 Infection in Hospitalized Children: A Serologic and Molecular Survey von Miron, Dan, Luder, Anthony, Horovitz, Yoseph, Izkovitz, Andrey, Shizgreen, Irena, David, Eliel Ben, Ohnona, Frederic S, Schlesinger, Yechiel

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Age-related immunoglobulin G seroprevalence of human parvovirus B-19 in Israeli children von Miron, Dan, Horovitz, Yoseph, Luder, Anthony, Ohnona, Frederic S, Schlesinger, Yechiel, Schelisinger, Yechiel

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