Hershkovitz E - Search Results

1

Cerebral X-linked adrenoleukodystrophy in a girl with Xq27-Ter deletion.

Hershkovitz E, Narkis G, Shorer Z, Moser AB, Watkins PA, Moser HW, Manor E. Hershkovitz E, et al. Ann Neurol. 2002 Aug;52(2):234-7. doi: 10.1002/ana.10248. Ann Neurol. 2002. PMID: 12210797

2

Trends in the incidence of type 1 diabetes among Jews and Arabs in Israel.

Blumenfeld O, Dichtiar R, Shohat T; Israel IDDM Registry Study Group (IIRSG). Blumenfeld O, et al. Pediatr Diabetes. 2014 Sep;15(6):422-7. doi: 10.1111/pedi.12101. Epub 2013 Nov 27. Pediatr Diabetes. 2014. PMID: 24283719

3

Status epilepticus following intravenous N-acetylcysteine therapy.

Hershkovitz E, Shorer Z, Levitas A, Tal A. Hershkovitz E, et al. Isr J Med Sci. 1996 Nov;32(11):1102-4. Isr J Med Sci. 1996. PMID: 8960081

4

Congenital insensitivity to pain with anhidrosis (CIPA) in Israeli-Bedouins: genetic heterogeneity, novel mutations in the TRKA/NGF receptor gene, clinical findings, and results of nerve conduction studies.

Shatzky S, Moses S, Levy J, Pinsk V, Hershkovitz E, Herzog L, Shorer Z, Luder A, Parvari R. Shatzky S, et al. Among authors: hershkovitz e. Am J Med Genet. 2000 Jun 19;92(5):353-60. doi: 10.1002/1096-8628(20000619)92:5<353::aid-ajmg12>3.0.co;2-c. Am J Med Genet. 2000. PMID: 10861667

5

Neurophysiologic studies in congenital insensitivity to pain with anhidrosis.

Shorer Z, Moses SW, Hershkovitz E, Pinsk V, Levy J. Shorer Z, et al. Among authors: hershkovitz e. Pediatr Neurol. 2001 Nov;25(5):397-400. doi: 10.1016/s0887-8994(01)00347-2. Pediatr Neurol. 2001. PMID: 11744315

6

Nerve growth factor-tyrosine kinase A pathway is involved in thermoregulation and adaptation to stress: studies on patients with hereditary sensory and autonomic neuropathy type IV.

Loewenthal N, Levy J, Schreiber R, Pinsk V, Perry Z, Shorer Z, Hershkovitz E. Loewenthal N, et al. Among authors: hershkovitz e. Pediatr Res. 2005 Apr;57(4):587-90. doi: 10.1203/01.PDR.0000155941.37155.41. Epub 2005 Feb 4. Pediatr Res. 2005. PMID: 15695606

7

Infant botulism: be aware of this rare disease.

Baron J, Greenberg D, Shorer Z, Hershkovitz E, Melamed R, Lifshitz M. Baron J, et al. Among authors: hershkovitz e. Isr Med Assoc J. 2007 Sep;9(9):682-3. Isr Med Assoc J. 2007. PMID: 17939636 Free article. No abstract available.

8

Autosomal-recessive hypophosphatemic rickets is associated with an inactivation mutation in the ENPP1 gene.

Levy-Litan V, Hershkovitz E, Avizov L, Leventhal N, Bercovich D, Chalifa-Caspi V, Manor E, Buriakovsky S, Hadad Y, Goding J, Parvari R. Levy-Litan V, et al. Among authors: hershkovitz e. Am J Hum Genet. 2010 Feb 12;86(2):273-8. doi: 10.1016/j.ajhg.2010.01.010. Epub 2010 Feb 4. Am J Hum Genet. 2010. PMID: 20137772 Free PMC article.

9

Autosomal recessive hyponatremia due to isolated salt wasting in sweat associated with a mutation in the active site of Carbonic Anhydrase 12.

Muhammad E, Leventhal N, Parvari G, Hanukoglu A, Hanukoglu I, Chalifa-Caspi V, Feinstein Y, Weinbrand J, Jacoby H, Manor E, Nagar T, Beck JC, Sheffield VC, Hershkovitz E, Parvari R. Muhammad E, et al. Among authors: hershkovitz e. Hum Genet. 2011 Apr;129(4):397-405. doi: 10.1007/s00439-010-0930-4. Epub 2010 Dec 24. Hum Genet. 2011. PMID: 21184099

10

Treatment of X-linked childhood cerebral adrenoleukodystrophy by the use of an allogeneic stem cell transplantation with reduced intensity conditioning regimen.

Resnick IB, Abdul Hai A, Shapira MY, Bitan M, Hershkovitz E, Schwartz A, Ben-Harush M, Or R, Slavin S, Kapelushnik J. Resnick IB, et al. Among authors: hershkovitz e. Clin Transplant. 2005 Dec;19(6):840-7. doi: 10.1111/j.1399-0012.2005.00411.x. Clin Transplant. 2005. PMID: 16313334

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