Samango-Sprouse CA - Search Results

1

Puberty-related influences on brain development.

Giedd JN, Clasen LS, Lenroot R, Greenstein D, Wallace GL, Ordaz S, Molloy EA, Blumenthal JD, Tossell JW, Stayer C, Samango-Sprouse CA, Shen D, Davatzikos C, Merke D, Chrousos GP. Giedd JN, et al. Mol Cell Endocrinol. 2006 Jul 25;254-255:154-62. doi: 10.1016/j.mce.2006.04.016. Epub 2006 Jun 9. Mol Cell Endocrinol. 2006. PMID: 16765510 Review.

2

XXY (Klinefelter syndrome): a pediatric quantitative brain magnetic resonance imaging case-control study.

Giedd JN, Clasen LS, Wallace GL, Lenroot RK, Lerch JP, Wells EM, Blumenthal JD, Nelson JE, Tossell JW, Stayer C, Evans AC, Samango-Sprouse CA. Giedd JN, et al. Pediatrics. 2007 Jan;119(1):e232-40. doi: 10.1542/peds.2005-2969. Pediatrics. 2007. PMID: 17200249

3

Klinefelter syndrome: expanding the phenotype and identifying new research directions.

Simpson JL, de la Cruz F, Swerdloff RS, Samango-Sprouse C, Skakkebaek NE, Graham JM Jr, Hassold T, Aylstock M, Meyer-Bahlburg HF, Willard HF, Hall JG, Salameh W, Boone K, Staessen C, Geschwind D, Giedd J, Dobs AS, Rogol A, Brinton B, Paulsen CA. Simpson JL, et al. Genet Med. 2003 Nov-Dec;5(6):460-8. doi: 10.1097/01.gim.0000095626.54201.d0. Genet Med. 2003. PMID: 14614399

4

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.

5

Effect of ascertainment and genetic features on the phenotype of Klinefelter syndrome.

Zeger MP, Zinn AR, Lahlou N, Ramos P, Kowal K, Samango-Sprouse C, Ross JL. Zeger MP, et al. J Pediatr. 2008 May;152(5):716-22. doi: 10.1016/j.jpeds.2007.10.019. Epub 2007 Dec 21. J Pediatr. 2008. PMID: 18410780 Free PMC article.

6

Androgen receptor CAGn repeat length influences phenotype of 47,XXY (Klinefelter) syndrome.

Zinn AR, Ramos P, Elder FF, Kowal K, Samango-Sprouse C, Ross JL. Zinn AR, et al. J Clin Endocrinol Metab. 2005 Sep;90(9):5041-6. doi: 10.1210/jc.2005-0432. Epub 2005 Jun 14. J Clin Endocrinol Metab. 2005. PMID: 15956082

7

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

8

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

9

Prenatal diagnosis and 47,XXY.

Simpson JL, Samango-Sprouse C. Simpson JL, et al. Am J Med Genet C Semin Med Genet. 2013 Feb 15;163C(1):64-70. doi: 10.1002/ajmg.c.31356. Am J Med Genet C Semin Med Genet. 2013. PMID: 23359597 Review.

10

Klinefelter Syndrome and Turner Syndrome.

Samango-Sprouse C, Song SQ, Lin AE, Powell CM, Gropman AL. Samango-Sprouse C, et al. Pediatr Rev. 2021 May;42(5):272-274. doi: 10.1542/pir.2020-004028. Pediatr Rev. 2021. PMID: 33931514 No abstract available.

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