Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Filters
Results by year
Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2010 | 1 |
2013 | 1 |
2016 | 1 |
2019 | 1 |
2020 | 1 |
2021 | 1 |
2024 | 0 |
Search Results
5 results
Results by year
Filters applied: . Clear all
It looks like you are searching for an author.
Results are currently sorted by Best Match. To see the newest results first,
change the sort order to Most Recent.
Page 1
Pelizaeus-Merzbacher-like disease caused by AIMP1/p43 homozygous mutation.
Am J Hum Genet. 2010 Dec 10;87(6):820-8. doi: 10.1016/j.ajhg.2010.10.016. Epub 2010 Nov 18.
Am J Hum Genet. 2010.
PMID: 21092922
Free PMC article.
Accentuated hyperparathyroidism in type II Bartter syndrome.
Landau D, Gurevich E, Sinai-Treiman L, Shalev H.
Landau D, et al. Among authors: shalev h.
Pediatr Nephrol. 2016 Jul;31(7):1085-90. doi: 10.1007/s00467-016-3337-1. Epub 2016 Feb 8.
Pediatr Nephrol. 2016.
PMID: 26857709
Item in Clipboard
Pediatric chronic kidney disease rates in Southern Israel are higher than reported.
Landau D, Schreiber R, Kleinman A, Vodonos A, Shalev H.
Landau D, et al. Among authors: shalev h.
F1000Res. 2013 Sep 13;2:186. doi: 10.12688/f1000research.2-186.v1. eCollection 2013.
F1000Res. 2013.
PMID: 24555088
Free PMC article.
Item in Clipboard
Classical Xanthinuria in Nine Israeli Families and Two Isolated Cases from Germany: Molecular, Biochemical and Population Genetics Aspects.
Peretz H, Lagziel A, Bittner F, Kabha M, Shtauber-Naamati M, Zhuravel V, Usher S, Rump S, Wollers S, Bork B, Mandel H, Falik-Zaccai T, Kalfon L, Graessler J, Zeharia A, Heib N, Shalev H, Landau D, Levartovsky D.
Peretz H, et al. Among authors: shalev h.
Biomedicines. 2021 Jul 7;9(7):788. doi: 10.3390/biomedicines9070788.
Biomedicines. 2021.
PMID: 34356852
Free PMC article.
Item in Clipboard
An ancestral variant causing type I xanthinuria in Turkmen and Arab families is predicted to prevail in the Afro-Asian stone-forming belt.
Peretz H, Korostishevsky M, Steinberg DM, Kabha M, Usher S, Krause I, Shalev H, Landau D, Levartovsky D.
Peretz H, et al. Among authors: shalev h.
JIMD Rep. 2019 Dec 5;51(1):45-52. doi: 10.1002/jmd2.12077. eCollection 2020 Jan.
JIMD Rep. 2019.
PMID: 32071838
Free PMC article.
Item in Clipboard
Cite
Cite