Samango-Sprouse CA - Search Results

1

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. 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

2

Neurodevelopmental profile of infants and toddlers with oculo-auriculo-vertebral spectrum and the correlation of prognosis with physical findings.

Cohen MS, Samango-Sprouse CA, Stern HJ, Custer DA, Vaught DR, Saal HM, Tifft CJ, Rosenbaum KN. Cohen MS, et al. Am J Med Genet. 1995 Dec 18;60(6):535-40. doi: 10.1002/ajmg.1320600610. Am J Med Genet. 1995. PMID: 8825891

3

Mental development in polysomy X Klinefelter syndrome (47,XXY; 48,XXXY): effects of incomplete X inactivation.

Samango-Sprouse C. Samango-Sprouse C. Semin Reprod Med. 2001 Jun;19(2):193-202. doi: 10.1055/s-2001-15400. Semin Reprod Med. 2001. PMID: 11480917 Review.

4

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. 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

5

Expansion of the phenotypic profile of the young child with XXY.

Samango-Sprouse C. Samango-Sprouse C. Pediatr Endocrinol Rev. 2010 Dec;8 Suppl 1:160-8. Pediatr Endocrinol Rev. 2010. PMID: 21217608 Review.

6

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. 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

7

Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations.

Gropman A, Samango-Sprouse CA. Gropman A, et al. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):35-43. doi: 10.1002/ajmg.c.31352. Epub 2013 Jan 18. Am J Med Genet C Semin Med Genet. 2013. PMID: 23335129 Review.

8

Immunodeficiency in patients with 49,XXXXY chromosomal variation.

Keller MD, Sadeghin T, Samango-Sprouse C, Orange JS. Keller MD, et al. 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.

9

Introduction: past, present, and future care of individuals with XXY.

Samango-Sprouse CA, Gropman AL. Samango-Sprouse CA, et al. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):1-2. doi: 10.1002/ajmg.c.31355. Am J Med Genet C Semin Med Genet. 2013. PMID: 23359594 No abstract available.

10

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. 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

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