Kidney and urinary tract findings among patients with Kabuki (make-up) syndrome
Merdler-Rabinowicz, Rona, Pode-Shakked, Ben, Vivante, Asaf, Lahav, Einat, Kagan, Maayan, Chorin, Odelia, Somech, Raz, Raas-Rothschild, Annick
Published in Pediatric nephrology (Berlin, West) (01.12.2021)
Published in Pediatric nephrology (Berlin, West) (01.12.2021)
Get full text
Journal Article
Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism
Gilboa, Yinon, Perlman, Sharon, Pode-Shakked, Naomi, Pode-Shakked, Ben, Shrim, Alon, Azaria-Lahav, Einat, Dekel, Benjamin, Yonath, Hagith, Berkenstadt, Michal, Achiron, Reuven
Published in Prenatal diagnosis (01.11.2016)
Published in Prenatal diagnosis (01.11.2016)
Get full text
Journal Article
Whole exome sequencing in childhood-onset lupus frequently detects single gene etiologies
Tirosh, Irit, Spielman, Shiri, Barel, Ortal, Ram, Reut, Stauber, Tali, Paret, Gideon, Rubinsthein, Marina, Pessach, Itai M, Gerstein, Maya, Anikster, Yair, Shukrun, Rachel, Dagan, Adi, Adler, Katerina, Pode-Shakked, Ben, Volkov, Alexander, Perelman, Marina, Greenberger, Shoshana, Somech, Raz, Lahav, Einat, Majmundar, Amar J, Padeh, Shai, Hildebrandt, Friedhelm, Vivante, Asaf
Published in Pediatric rheumatology online journal (30.07.2019)
Published in Pediatric rheumatology online journal (30.07.2019)
Get full text
Journal Article
Kidney and urinary tract findings among patients with Kabuki
Merdler-Rabinowicz, Rona, Lahav, Einat, Somech, Raz, Pode-Shakked, Ben, Vivante, Asaf, Chorin, Odelia, Kagan, Maayan
Published in Pediatric nephrology (Berlin, West) (01.12.2021)
Get full text
Published in Pediatric nephrology (Berlin, West) (01.12.2021)
Journal Article
Incidence of rash after amoxicillin treatment in children with infectious mononucleosis
Chovel-Sella, Aluma, Ben Tov, Amir, Lahav, Einat, Mor, Orna, Rudich, Hagit, Paret, Gideon, Reif, Shimon
Published in Pediatrics (Evanston) (01.05.2013)
Published in Pediatrics (Evanston) (01.05.2013)
Get more information
Journal Article
White epidermal nevus as an early sign of tuberous sclerosis complex—A case series
Ollech, Ayelet, Hilewitz, Daniel, Tzadok, Michal, Lahav, Einat, Debby, Assaf, Eliyahu, Aviva, Barzilai, Aviv, Greenberger, Shoshana
Published in Pediatric dermatology (01.07.2023)
Published in Pediatric dermatology (01.07.2023)
Get full text
Journal Article
Mitochondrial augmentation of hematopoietic stem cells in children with single large-scale mitochondrial DNA deletion syndromes
Jacoby, Elad, Bar-Yosef, Omer, Gruber, Noah, Lahav, Einat, Varda-Bloom, Nira, Bolkier, Yoav, Bar, Diana, Blumkin, Moriya Ben-Yakir, Barak, Sharon, Eisenstein, Etzyona, Ahonniska-Assa, Jaana, Silberg, Tamar, Krasovsky, Tal, Bar, Orly, Erez, Neta, Bielorai, Bella, Golan, Hana, Dekel, Benjamin, Besser, Michal J, Pozner, Gat, Khoury, Hanan, Jacobs, Alan, Campbell, John, Herskovitz, Eli, Sher, Noa, Yivgi-Ohana, Natalie, Anikster, Yair, Toren, Amos
Published in Science translational medicine (21.12.2022)
Published in Science translational medicine (21.12.2022)
Get more information
Journal Article
Long-term hematopoietic dysfunction in patients with large-scale mitochondrial DNA deletion syndromes
Greenberg-Kushnir, Noa, Grossmann, Liron D, Barg, Assaf Arie, Schiby, Ginnete, Mardoukh, Corine, Varda-Bloom, Nira, Marcu-Malina, Victoria, Anikster, Yair, Gruber, Noah, Lahav, Einat, Bolkier, Yoav, Bar, Diana, Bielorai, Bella, Toren, Amos, Jacoby, Elad
Published in Pediatric blood & cancer (13.10.2024)
Published in Pediatric blood & cancer (13.10.2024)
Get full text
Journal Article
A rare variant in the FHL1 gene associated with X-linked recessive hypoparathyroidism
Pillar, Nir, Pleniceanu, Oren, Fang, Mingyan, Ziv, Limor, Lahav, Einat, Botchan, Shay, Cheng, Le, Dekel, Benjamin, Shomron, Noam
Published in Human genetics (01.07.2017)
Published in Human genetics (01.07.2017)
Get full text
Journal Article
A multidisciplinary nephrogenetic referral clinic for children and adults—diagnostic achievements and insights
Pode-Shakked, Ben, Ben-Moshe, Yishay, Barel, Ortal, Regev, Lilach C., Kagan, Maayan, Eliyahu, Aviva, Marek-Yagel, Dina, Atias-Varon, Danit, Lahav, Einat, Issler, Naomi, Shlomovitz, Omer, Semo Oz, Rotem, Kol, Nitzan, Mor, Nofar, Bar-Joseph, Ifat, Khavkin, Yulia, Javasky, Elisheva, Beckerman, Pazit, Greenberg, Meidad, Volovelsky, Oded, Borovitz, Yael, Davidovits, Miriam, Haskin, Orly, Alfandary, Hadas, Levi, Shely, Kaidar, Maital, Katzir, Ze’ev, Angel-Korman, Avital, Becker-Cohen, Rachel, Ben-Shalom, Efrat, Leiba, Adi, Mor, Eytan, Dagan, Amit, Pessach, Itai M., Lotan, Danny, Shashar, Moshe, Anikster, Yair, Raas-Rothschild, Annick, Rechavi, Gideon, Dekel, Benjamin, Vivante, Asaf
Published in Pediatric nephrology (Berlin, West) (01.07.2022)
Published in Pediatric nephrology (Berlin, West) (01.07.2022)
Get full text
Journal Article
Crossed ectopic kidney: prenatal diagnosis and postnatal follow‐up
Zajicek, Michal, Perlman, Sharon, Dekel, Benjamin, Lahav, Einat, Lotan, Danny, Lotan, Dor, Achiron, Reuven, Gilboa, Yinon
Published in Prenatal diagnosis (01.07.2017)
Published in Prenatal diagnosis (01.07.2017)
Get full text
Journal Article
First-in-Human Mitochondrial Augmentation of Hematopoietic Stem Cells in Pearson Syndrome
Jacoby, Elad, Blumkin, Moriya, Anikster, Yair, Varda-Bloom, Nira, Pansheen, Julia, Bar Yoseph, Omer, Gruber, Noah, Lahav, Einat, Besser, Michal J, Schachter, Jacob, Sher, Noa, Yivgi Ohana, Natalie, Toren, Amos
Published in Blood (29.11.2018)
Published in Blood (29.11.2018)
Get full text
Journal Article
Prenatal diagnosis of 17q12 deletion syndrome: from fetal hyperechogenic kidneys to high risk for autism: Prenatal echogenic kidneys and autism in 17q12 deletions
Gilboa, Yinon, Perlman, Sharon, Pode-Shakked, Naomi, Pode-Shakked, Ben, Shrim, Alon, Azaria-Lahav, Einat, Dekel, Benjamin, Yonath, Hagith, Berkenstadt, Michal, Achiron, Reuven
Published in Prenatal diagnosis (01.11.2016)
Published in Prenatal diagnosis (01.11.2016)
Get full text
Journal Article