Samango-Sprouse C - Search Results

1

Outcome measures for clinical drug trials in autism.

Aman MG, Novotny S, Samango-Sprouse C, Lecavalier L, Leonard E, Gadow KD, King BH, Pearson DA, Gernsbacher MA, Chez M. Aman MG, et al. CNS Spectr. 2004 Jan;9(1):36-47. doi: 10.1017/s1092852900008348. CNS Spectr. 2004. PMID: 14999174 Free PMC article. Review.

2

Changing the landscape of autism research: the autism genetic resource exchange.

Lajonchere CM; AGRE Consortium. Lajonchere CM, et al. Neuron. 2010 Oct 21;68(2):187-91. doi: 10.1016/j.neuron.2010.10.009. Neuron. 2010. PMID: 20955925 Free PMC article.

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

Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients.

Iitsuka Y, Bock A, Nguyen DD, Samango-Sprouse CA, Simpson JL, Bischoff FZ. Iitsuka Y, et al. Am J Med Genet. 2001 Jan 1;98(1):25-31. Am J Med Genet. 2001. PMID: 11426451

5

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.

6

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

7

The effect of early hormonal treatment (EHT) on expressive and receptive language capabilities in boys with 47,XXY (Klinefelter syndrome) during infancy and early childhood.

Samango-Sprouse C, Brooks MR, Lasutchinkow P, Sadeghin T, Powell S, Hamzik MP, Song S, Gropman AL. Samango-Sprouse C, et al. Genet Med. 2021 Jun;23(6):1017-1022. doi: 10.1038/s41436-021-01098-w. Epub 2021 Feb 24. Genet Med. 2021. PMID: 33627828 Free article.

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

A longitudinal perspective of hormone replacement therapies (HRTs) on neuromotor capabilities in males with 47,XXY (Klinefelter syndrome).

Samango-Sprouse C, Brooks MR, Counts D, Hamzik MP, Song S, Powell S, Sadeghin T, Gropman AL. Samango-Sprouse C, et al. Genet Med. 2022 Jun;24(6):1274-1282. doi: 10.1016/j.gim.2022.03.004. Epub 2022 Mar 24. Genet Med. 2022. PMID: 35341653 Free article.

10

International investigation of neurocognitive and behavioral phenotype in 47,XXY (Klinefelter syndrome): Predicting individual differences.

Samango-Sprouse C, Stapleton E, Chea S, Lawson P, Sadeghin T, Cappello C, de Sonneville L, van Rijn S. Samango-Sprouse C, et al. Am J Med Genet A. 2018 Apr;176(4):877-885. doi: 10.1002/ajmg.a.38621. Epub 2018 Feb 9. Am J Med Genet A. 2018. PMID: 29423966

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