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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1985 1
1986 1
1987 1
1988 1
1989 1
1990 1
1992 1
1994 2
1995 2
1996 1
1997 2
1998 2
1999 7
2000 2
2001 1
2002 4
2003 2
2004 4
2005 3
2006 2
2007 5
2008 4
2009 4
2010 3
2011 4
2012 7
2013 7
2014 10
2015 5
2016 6
2017 4
2018 5
2019 3
2020 1
2021 2
2022 1
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Search Results

94 results
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Page 1
Benign plexus neuropathy in children.
Zeharia A, Mukamel M, Frishberg Y, Weitz R, Mimouni M. Zeharia A, et al. J Pediatr. 1990 Feb;116(2):276-8. doi: 10.1016/s0022-3476(05)82890-2. J Pediatr. 1990. PMID: 2153791 Review. No abstract available.
The role of orotic acid measurement in routine newborn screening for urea cycle disorders.
Staretz-Chacham O, Daas S, Ulanovsky I, Blau A, Rostami N, Saraf-Levy T, Abu Salah N, Anikster Y, Banne E, Dar D, Dumin E, Fattal-Valevski A, Falik-Zaccai T, Hershkovitz E, Josefsberg S, Khammash H, Keidar R, Korman SH, Landau Y, Lerman-Sagie T, Mandel D, Mandel H, Marom R, Morag I, Nadir E, Yosha-Orpaz N, Pode-Shakked B, Pras E, Reznik-Wolf H, Saada A, Segel R, Shaag A, Shaul Lotan N, Spiegel R, Tal G, Vaisid T, Zeharia A, Almashanu S. Staretz-Chacham O, et al. Among authors: zeharia a. J Inherit Metab Dis. 2021 May;44(3):606-617. doi: 10.1002/jimd.12331. Epub 2020 Nov 30. J Inherit Metab Dis. 2021. PMID: 33190319
Conversion reaction: management by the paediatrician.
Zeharia A, Mukamel M, Carel C, Weitz R, Danziger Y, Mimouni M. Zeharia A, et al. Eur J Pediatr. 1999 Feb;158(2):160-4. doi: 10.1007/s004310051039. Eur J Pediatr. 1999. PMID: 10048616 Review.
Clinical presentations of mitochondrial cardiomyopathies.
Lev D, Nissenkorn A, Leshinsky-Silver E, Sadeh M, Zeharia A, Garty BZ, Blieden L, Barash V, Lerman-Sagie T. Lev D, et al. Among authors: zeharia a. Pediatr Cardiol. 2004 Sep-Oct;25(5):443-50. doi: 10.1007/s00246-003-0490-7. Epub 2004 Jun 8. Pediatr Cardiol. 2004. PMID: 15185043
Mutations in GMPPA cause a glycosylation disorder characterized by intellectual disability and autonomic dysfunction.
Koehler K, Malik M, Mahmood S, Gießelmann S, Beetz C, Hennings JC, Huebner AK, Grahn A, Reunert J, Nürnberg G, Thiele H, Altmüller J, Nürnberg P, Mumtaz R, Babovic-Vuksanovic D, Basel-Vanagaite L, Borck G, Brämswig J, Mühlenberg R, Sarda P, Sikiric A, Anyane-Yeboa K, Zeharia A, Ahmad A, Coubes C, Wada Y, Marquardt T, Vanderschaeghe D, Van Schaftingen E, Kurth I, Huebner A, Hübner CA. Koehler K, et al. Among authors: zeharia a. Am J Hum Genet. 2013 Oct 3;93(4):727-34. doi: 10.1016/j.ajhg.2013.08.002. Epub 2013 Sep 12. Am J Hum Genet. 2013. PMID: 24035193 Free PMC article.
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: zeharia a. Biomedicines. 2021 Jul 7;9(7):788. doi: 10.3390/biomedicines9070788. Biomedicines. 2021. PMID: 34356852 Free PMC article.
94 results