Inbar D - Search Results

1

X-linked mental retardation with alacrima and achalasia-Triple A syndrome or a new syndrome?

Marom D, Albin A, Schwartz C, Har-Zahav A, Straussberg R, Bartel F, Birk E, Inbar D, Basel-Vanagaite L. Marom D, et al. Among authors: inbar d. Am J Med Genet A. 2011 Aug;155A(8):1959-63. doi: 10.1002/ajmg.a.34121. Epub 2011 Jul 8. Am J Med Genet A. 2011. PMID: 21744492

2

Autosomal recessive mental retardation syndrome with anterior maxillary protrusion and strabismus: MRAMS syndrome.

Basel-Vanagaite L, Rainshtein L, Inbar D, Gothelf D, Hennekam R, Straussberg R. Basel-Vanagaite L, et al. Among authors: inbar d. Am J Med Genet A. 2007 Aug 1;143A(15):1687-91. doi: 10.1002/ajmg.a.31810. Am J Med Genet A. 2007. PMID: 17618476

3

Three sibs with microcephaly, clubfeet and agenesis of corpus callosum: a new genetic syndrome?

Shkalim V, Ben-Sira L, Inbar D, Kaadan W, Basel-Vanagaite L, Straussberg R. Shkalim V, et al. Among authors: inbar d. Am J Med Genet A. 2011 May;155A(5):1060-5. doi: 10.1002/ajmg.a.33978. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465661

4

Mapping of a new locus for autosomal recessive non-syndromic mental retardation in the chromosomal region 19p13.12-p13.2: further genetic heterogeneity.

Basel-Vanagaite L, Alkelai A, Straussberg R, Magal N, Inbar D, Mahajna M, Shohat M. Basel-Vanagaite L, et al. Among authors: inbar d. J Med Genet. 2003 Oct;40(10):729-32. doi: 10.1136/jmg.40.10.729. J Med Genet. 2003. PMID: 14569116 Free PMC article.

5

Familial cognitive impairment with ataxia with oculomotor apraxia.

Mahajnah M, Basel-Vanagaite L, Inbar D, Kornreich L, Weitz R, Straussberg R. Mahajnah M, et al. Among authors: inbar d. J Child Neurol. 2005 Jun;20(6):523-5. doi: 10.1177/088307380502000610. J Child Neurol. 2005. PMID: 15996403

6

Microcephaly-thin corpus callosum syndrome maps to 8q23.2-q24.12.

Halevy A, Basel-Vanagaite L, Shuper A, Helman S, Har-Zahav A, Birk E, Maya I, Kornreich L, Inbar D, Nürnberg G, Nürnberg P, Steinberg T, Straussberg R. Halevy A, et al. Among authors: inbar d. Pediatr Neurol. 2012 Jun;46(6):363-8. doi: 10.1016/j.pediatrneurol.2012.03.014. Pediatr Neurol. 2012. PMID: 22633631

7

Expanding the phenotypic spectrum of L1CAM-associated disease.

Basel-Vanagaite L, Straussberg R, Friez MJ, Inbar D, Korenreich L, Shohat M, Schwartz CE. Basel-Vanagaite L, et al. Among authors: inbar d. Clin Genet. 2006 May;69(5):414-9. doi: 10.1111/j.1399-0004.2006.00607.x. Clin Genet. 2006. PMID: 16650080

8

Benign hereditary chorea: clinical, neuroimaging, and genetic findings.

Mahajnah M, Inbar D, Steinmetz A, Heutink P, Breedveld GJ, Straussberg R. Mahajnah M, et al. Among authors: inbar d. J Child Neurol. 2007 Oct;22(10):1231-4. doi: 10.1177/0883073807306261. J Child Neurol. 2007. PMID: 17940252

9

Fetal alcohol spectrum disorder in Israel.

Senecky Y, Inbar D, Diamond G, Basel-Vanagaite L, Rigler S, Chodick G. Senecky Y, et al. Among authors: inbar d. Isr Med Assoc J. 2009 Oct;11(10):619-22. Isr Med Assoc J. 2009. PMID: 20077950 Free article.

10

An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures.

Straussberg R, Basel-Vanagaite L, Kivity S, Dabby R, Cirak S, Nurnberg P, Voit T, Mahajnah M, Inbar D, Saifi GM, Lupski JR, Delague V, Megarbane A, Richter A, Leshinsky E, Berkovic SF. Straussberg R, et al. Among authors: inbar d. Neurology. 2005 Jan 11;64(1):142-4. doi: 10.1212/01.WNL.0000148600.60470.E6. Neurology. 2005. PMID: 15642921

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