Sadeghin T - Search Results

1

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

Keller MD, Sadeghin T, Samango-Sprouse C, Orange JS. Keller MD, et al. Among authors: sadeghin t. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):50-4. doi: 10.1002/ajmg.c.31348. Epub 2013 Jan 23. Am J Med Genet C Semin Med Genet. 2013. PMID: 23345259 Free PMC article.

2

Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome.

Gropman AL, Rogol A, Fennoy I, Sadeghin T, Sinn S, Jameson R, Mitchell F, Clabaugh J, Lutz-Armstrong M, Samango-Sprouse CA. Gropman AL, et al. Among authors: sadeghin t. Am J Med Genet A. 2010 Jun;152A(6):1523-30. doi: 10.1002/ajmg.a.33307. Am J Med Genet A. 2010. PMID: 20503329

3

Effects of short-course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndrome.

Samango-Sprouse CA, Gropman AL, Sadeghin T, Kingery M, Lutz-Armstrong M, Rogol AD. Samango-Sprouse CA, et al. Among authors: sadeghin t. Acta Paediatr. 2011 Jun;100(6):861-5. doi: 10.1111/j.1651-2227.2011.02252.x. Epub 2011 Apr 20. Acta Paediatr. 2011. PMID: 21362043

4

Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47,XXY syndrome at 36 and 72 months of age.

Samango-Sprouse CA, Sadeghin T, Mitchell FL, Dixon T, Stapleton E, Kingery M, Gropman AL. Samango-Sprouse CA, et al. Among authors: sadeghin t. Am J Med Genet A. 2013 Mar;161A(3):501-8. doi: 10.1002/ajmg.a.35769. Epub 2013 Jan 23. Am J Med Genet A. 2013. PMID: 23345253

5

Is it all the X: familial learning dysfunction and the impact of behavioral aspects of the phenotypic presentation of XXY?

Samango-Sprouse CA, Stapleton E, Sadeghin T, Gropman AL. Samango-Sprouse CA, et al. Among authors: sadeghin t. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):27-34. doi: 10.1002/ajmg.c.31353. Am J Med Genet C Semin Med Genet. 2013. PMID: 23359595

6

Musculoskeletal anomalies in a large cohort of boys with 49, XXXXY.

Sprouse C, Tosi L, Stapleton E, Gropman AL, Mitchell FL, Peret R, Sadeghin T, Haskell K, Samango-Sprouse CA. Sprouse C, et al. Among authors: sadeghin t. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):44-9. doi: 10.1002/ajmg.c.31354. Am J Med Genet C Semin Med Genet. 2013. PMID: 23359596

7

Identification of infants at risk for autism spectrum disorder and developmental language delay prior to 12 months.

Samango-Sprouse CA, Stapleton EJ, Aliabadi F, Graw R, Vickers R, Haskell K, Sadeghin T, Jameson R, Parmele CL, Gropman AL. Samango-Sprouse CA, et al. Among authors: sadeghin t. Autism. 2015 Apr;19(3):327-37. doi: 10.1177/1362361314521329. Epub 2014 Feb 18. Autism. 2015. PMID: 24550549

8

Expanding the phenotypic profile of boys with 47, XXY: the impact of familial learning disabilities.

Samango-Sprouse CA, Stapleton EJ, Mitchell FL, Sadeghin T, Donahue TP, Gropman AL. Samango-Sprouse CA, et al. Among authors: sadeghin t. Am J Med Genet A. 2014 Jun;164A(6):1464-9. doi: 10.1002/ajmg.a.36483. Epub 2014 Apr 8. Am J Med Genet A. 2014. PMID: 24715716

9

Positive effects of early androgen therapy on the behavioral phenotype of boys with 47,XXY.

Samango-Sprouse C, Stapleton EJ, Lawson P, Mitchell F, Sadeghin T, Powell S, Gropman AL. Samango-Sprouse C, et al. Among authors: sadeghin t. Am J Med Genet C Semin Med Genet. 2015 Jun;169(2):150-7. doi: 10.1002/ajmg.c.31437. Epub 2015 May 1. Am J Med Genet C Semin Med Genet. 2015. PMID: 25939399

10

Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX.

Samango-Sprouse C, Keen C, Mitchell F, Sadeghin T, Gropman A. Samango-Sprouse C, et al. Among authors: sadeghin t. Am J Med Genet A. 2015 Oct;167A(10):2251-9. doi: 10.1002/ajmg.a.37198. Epub 2015 Jun 18. Am J Med Genet A. 2015. PMID: 26086740

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