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A Novel Homozygous Missense Variant in the LRRC32 Gene Is Associated With a New Syndrome of Cleft Palate, Progressive Vitreoretinopathy, Growth Retardation, and Developmental Delay.
Front Pediatr. 2022 May 17;10:859034. doi: 10.3389/fped.2022.859034. eCollection 2022.
Front Pediatr. 2022.
PMID: 35656379
Free PMC article.
Campylobacter gastroenteritis in children in north-eastern Israel comparison with other common pathogens.
Sakran W, Hexner-Erlichman Z, Spiegel R, Batheesh H, Halevy R, Koren A.
Sakran W, et al. Among authors: hexner erlichman z.
Sci Rep. 2020 Apr 2;10(1):5823. doi: 10.1038/s41598-020-62744-y.
Sci Rep. 2020.
PMID: 32242070
Free PMC article.
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Primary autoimmune myelofibrosis: A case report in a child.
Hexner-Erlichman Z, Yacobovich J, Trougouboff P, Avraham-Kelbert M, Eitam H, Spiegel R, Yeganeh S, Levin C.
Hexner-Erlichman Z, et al.
EJHaem. 2020 Jun 28;1(1):304-308. doi: 10.1002/jha2.38. eCollection 2020 Jul.
EJHaem. 2020.
PMID: 35847714
Free PMC article.
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Favorable outcome of empagliflozin treatment in two pediatric glycogen storage disease type 1b patients.
Hexner-Erlichman Z, Veiga-da-Cunha M, Zehavi Y, Vadasz Z, Sabag AD, Tatour S, Spiegel R.
Hexner-Erlichman Z, et al.
Front Pediatr. 2022 Nov 23;10:1071464. doi: 10.3389/fped.2022.1071464. eCollection 2022.
Front Pediatr. 2022.
PMID: 36507137
Free PMC article.
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