Ling G - Search Results

1

Urinary tract infection in young infants discharged from the emergency room with normal urinalysis.

Rivanowitch E, Nassar R, Kristal E, Shalev R, Fruchtman Y, Hazan G, Ling G, Melamed R, Leibovitz E. Rivanowitch E, et al. Among authors: ling g. Acta Paediatr. 2019 Apr;108(4):745-750. doi: 10.1111/apa.14532. Epub 2018 Aug 22. Acta Paediatr. 2019. PMID: 30074636

2

Seasonality of birth affects paediatric coeliac disease.

Daniel S, Kalansky A, Tsur A, Pinsk V, Ling G, Rannan R, Yerushalmi B. Daniel S, et al. Among authors: ling g. Acta Paediatr. 2019 Mar;108(3):529-534. doi: 10.1111/apa.14441. Epub 2018 Jun 29. Acta Paediatr. 2019. PMID: 29885263

3

Central venous catheter-associated bloodstream infections in children diagnosed with intestinal failure in Southern Israel.

Nassar R, Hazan G, Leibovitz E, Ling G, Lazar I, Khalaila A, Fruchtman Y, Yerushalmi B. Nassar R, et al. Among authors: ling g. Eur J Clin Microbiol Infect Dis. 2020 Mar;39(3):517-525. doi: 10.1007/s10096-019-03753-2. Epub 2019 Nov 25. Eur J Clin Microbiol Infect Dis. 2020. PMID: 31768705

4

Pituitary stalk interruption syndrome broadens the clinical spectrum of the TTC26 ciliopathy.

David O, Eskin-Schwartz M, Ling G, Dolgin V, Kristal E, Benkowitz E, Osyntsov L, Gradstein L, Birk OS, Loewenthal N, Yerushalmi B. David O, et al. Among authors: ling g. Clin Genet. 2020 Sep;98(3):303-307. doi: 10.1111/cge.13805. Epub 2020 Aug 3. Clin Genet. 2020. PMID: 32617964

5

Glomerular involvement in children with H syndrome.

David O, Geylis M, Kristal E, Ling G, Schreiber R. David O, et al. Among authors: ling g. Pediatr Nephrol. 2021 Mar;36(3):721-724. doi: 10.1007/s00467-020-04860-5. Epub 2021 Jan 2. Pediatr Nephrol. 2021. PMID: 33387019

6

The effects of the COVID-19 pandemic on patients with lysosomal storage disorders in Israel.

Kristal E, Pode-Shakked B, Hazan G, Banne E, Ling G, David O, Shany E, Raas-Rothschild A, Anikster Y, Kneller K, Hershkovitz E, Landau YE, Spiegel R, Zehavi Y, Staretz-Chacham O. Kristal E, et al. Among authors: ling g. Orphanet J Rare Dis. 2021 Sep 8;16(1):379. doi: 10.1186/s13023-021-02007-9. Orphanet J Rare Dis. 2021. PMID: 34496908 Free PMC article.

7

Hyper IgM in tricho-hepato-enteric syndrome due to TTC37 mutation.

Kristal E, Nahum A, Ling G, Broides A, Shubinsky G, Eskin-Schwartz M, Hadar N, Progador O, Birk O. Kristal E, et al. Among authors: ling g. Immunol Res. 2022 Dec;70(6):775-780. doi: 10.1007/s12026-022-09305-9. Epub 2022 Jul 1. Immunol Res. 2022. PMID: 35776314

8

Early-life liver cirrhosis and variable clinical presentation in telomere disease.

Faingelernt Y, Nassar R, Ling G, Kodman Y, Feuerstein T, Yerushalmi B. Faingelernt Y, et al. Among authors: ling g. Acta Paediatr. 2022 Dec;111(12):2416-2421. doi: 10.1111/apa.16539. Epub 2022 Sep 13. Acta Paediatr. 2022. PMID: 36070080

9

Hypoparathyroidism-Retardation-Dysmorphism Syndrome due to a Variant in the Tubulin-Specific Chaperone E Gene as a Cause of Combined Immune Deficiency.

David O, Kristal E, Ling G, Broides A, Hadad N, Shubinsky G, Nahum A. David O, et al. Among authors: ling g. J Clin Immunol. 2023 Feb;43(2):350-357. doi: 10.1007/s10875-022-01380-9. Epub 2022 Oct 18. J Clin Immunol. 2023. PMID: 36258138 Free PMC article.

10

X-linked C1GALT1C1 mutation causes atypical hemolytic uremic syndrome.

Hadar N, Schreiber R, Eskin-Schwartz M, Kristal E, Shubinsky G, Ling G, Cohen I, Geylis M, Nahum A, Yogev Y, Birk OS. Hadar N, et al. Among authors: ling g. Eur J Hum Genet. 2023 Oct;31(10):1101-1107. doi: 10.1038/s41431-022-01278-5. Epub 2023 Jan 4. Eur J Hum Genet. 2023. PMID: 36599939

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