Samango-Sprouse C - Search Results

1

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.

2

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

3

Early androgen deficiency in infants and young boys with 47,XXY Klinefelter syndrome.

Ross JL, Samango-Sprouse C, Lahlou N, Kowal K, Elder FF, Zinn A. Ross JL, et al. Horm Res. 2005;64(1):39-45. doi: 10.1159/000087313. Epub 2005 Aug 3. Horm Res. 2005. PMID: 16088206

4

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

5

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.

6

The incidence of anxiety symptoms in boys with 47,XXY (Klinefelter syndrome) and the possible impact of timing of diagnosis and hormonal replacement therapy.

Samango-Sprouse C, Lasutschinkow P, Powell S, Sadeghin T, Gropman A. Samango-Sprouse C, et al. Am J Med Genet A. 2019 Mar;179(3):423-428. doi: 10.1002/ajmg.a.61038. Epub 2019 Jan 13. Am J Med Genet A. 2019. PMID: 30637954

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

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.

9

The Effect of Hormonal Therapy on the Behavioral Outcomes in 47,XXY (Klinefelter Syndrome) between 7 and 12 Years of Age.

Hamzik MP, Gropman AL, Brooks MR, Powell S, Sadeghin T, Samango-Sprouse CA. Hamzik MP, et al. Among authors: samango sprouse ca. Genes (Basel). 2023 Jul 6;14(7):1402. doi: 10.3390/genes14071402. Genes (Basel). 2023. PMID: 37510306 Free PMC 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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