EPT1 (selenoprotein I) is critical for the neural development and maintenance of plasmalogen in humans[S]
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Published in Journal of lipid research (2018)
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Missed initial appointments at Israeli child development centres: Rate, reasons, and associated characteristics
Hirsh‐Yechezkel, Galit, Glasser, Saralee, Gabis, Lidia V., Eden, Avi, Savitzki, David, Farhi, Adel, Luxenburg, Osnat, Levitan, Gila, Lerner‐Geva, Liat
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Published in The International journal of health planning and management (01.09.2022)
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Walker-Warburg syndrome and tectocerebellar dysraphia: A novel association caused by a homozygous DAG1 mutation
Leibovitz, Zvi, Mandel, Hanna, Falik-Zaccai, Tzipora C., Ben Harouch, Shani, Savitzki, David, Krajden-Haratz, Karina, Gindes, Liat, Tamarkin, Mordechai, Lev, Dorit, Dobyns, William B., Lerman-Sagie, Tally
Published in European journal of paediatric neurology (01.05.2018)
Published in European journal of paediatric neurology (01.05.2018)
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Phospholipase A2-activating protein is associated with a novel form of leukoencephalopathy
Falik Zaccai, Tzipora C, Savitzki, David, Zivony-Elboum, Yifat, Vilboux, Thierry, Fitts, Eric C, Shoval, Yishay, Kalfon, Limor, Samra, Nadra, Keren, Zohar, Gross, Bella, Chasnyk, Natalia, Straussberg, Rachel, Mullikin, James C, Teer, Jamie K, Geiger, Dan, Kornitzer, Daniel, Bitterman-Deutsch, Ora, Samson, Abraham O, Wakamiya, Maki, Peterson, Johnny W, Kirtley, Michelle L, Pinchuk, Iryna V, Baze, Wallace B, Gahl, William A, Kleta, Robert, Anikster, Yair, Chopra, Ashok K
Published in Brain (London, England : 1878) (01.02.2017)
Published in Brain (London, England : 1878) (01.02.2017)
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Phospholipase A 2 -activating protein is associated with a novel form of leukoencephalopathy
Falik Zaccai, Tzipora C., Savitzki, David, Zivony-Elboum, Yifat, Vilboux, Thierry, Fitts, Eric C., Shoval, Yishay, Kalfon, Limor, Samra, Nadra, Keren, Zohar, Gross, Bella, Chasnyk, Natalia, Straussberg, Rachel, Mullikin, James C., Teer, Jamie K., Geiger, Dan, Kornitzer, Daniel, Bitterman-Deutsch, Ora, Samson, Abraham O., Wakamiya, Maki, Peterson, Johnny W., Kirtley, Michelle L., Pinchuk, Iryna V., Baze, Wallace B., Gahl, William A., Kleta, Robert, Anikster, Yair, Chopra, Ashok K.
Published in Brain (London, England : 1878) (01.02.2017)
Published in Brain (London, England : 1878) (01.02.2017)
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A founder mutation in Vps37A causes autosomal recessive complex hereditary spastic paraparesis
Zivony-Elboum, Yifat, Westbroek, Wendy, Kfir, Nehama, Savitzki, David, Shoval, Yishay, Bloom, Assnat, Rod, Raya, Khayat, Morad, Gross, Bella, Samri, Walid, Cohen, Hector, Sonkin, Vadim, Freidman, Tatiana, Geiger, Dan, Fattal-Valevski, Aviva, Anikster, Yair, Waters, Aoife M, Kleta, Robert, Falik-Zaccai, Tzipora C
Published in Journal of medical genetics (01.07.2012)
Published in Journal of medical genetics (01.07.2012)
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Epilepsia partialis continua associated with widespread gliomatosis cerebri
Shahar, Eli, Kramer, Uri, Nass, Dvora, Savitzki, David
Published in Pediatric neurology (01.11.2002)
Published in Pediatric neurology (01.11.2002)
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Valproic acid therapy inducing absence status evolving into generalized seizures
Shahar, Eli, Andraus, Jameel, Sagie-Lerman, Tally, Savitzki, David
Published in Pediatric neurology (01.05.2002)
Published in Pediatric neurology (01.05.2002)
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