Howell S - Search Results

1

48,XXYY, 48,XXXY and 49,XXXXY syndromes: not just variants of Klinefelter syndrome.

Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P. Tartaglia N, et al. Among authors: howell s. Acta Paediatr. 2011 Jun;100(6):851-60. doi: 10.1111/j.1651-2227.2011.02235.x. Epub 2011 Apr 8. Acta Paediatr. 2011. PMID: 21342258 Free PMC article. Review.

2

A review of trisomy X (47,XXX).

Tartaglia NR, Howell S, Sutherland A, Wilson R, Wilson L. Tartaglia NR, et al. Among authors: howell s. Orphanet J Rare Dis. 2010 May 11;5:8. doi: 10.1186/1750-1172-5-8. Orphanet J Rare Dis. 2010. PMID: 20459843 Free PMC article. Review.

3

The spectrum of the behavioral phenotype in boys and adolescents 47,XXY (Klinefelter syndrome).

Tartaglia N, Cordeiro L, Howell S, Wilson R, Janusz J. Tartaglia N, et al. Among authors: howell s. Pediatr Endocrinol Rev. 2010 Dec;8 Suppl 1(0 1):151-9. Pediatr Endocrinol Rev. 2010. PMID: 21217607 Free PMC article. Review.

4

Molecular diagnostic testing for Klinefelter syndrome and other male sex chromosome aneuploidies.

Hager K, Jennings K, Hosono S, Howell S, Gruen JR, Rivkees SA, Tartaglia NR, Rinder HM. Hager K, et al. Among authors: howell s. Int J Pediatr Endocrinol. 2012 Apr 23;2012(1):8. doi: 10.1186/1687-9856-2012-8. Int J Pediatr Endocrinol. 2012. PMID: 22524164 Free PMC article.

5

Timing of diagnosis of 47,XXY and 48,XXYY: a survey of parent experiences.

Visootsak J, Ayari N, Howell S, Lazarus J, Tartaglia N. Visootsak J, et al. Among authors: howell s. Am J Med Genet A. 2013 Feb;161A(2):268-72. doi: 10.1002/ajmg.a.35709. Epub 2013 Jan 15. Am J Med Genet A. 2013. PMID: 23322622 Free PMC article.

6

"How should I tell my child?" Disclosing the diagnosis of sex chromosome aneuploidies.

Dennis A, Howell S, Cordeiro L, Tartaglia N. Dennis A, et al. Among authors: howell s. J Genet Couns. 2015 Feb;24(1):88-103. doi: 10.1007/s10897-014-9741-4. Epub 2014 Sep 3. J Genet Couns. 2015. PMID: 25179748 Free PMC article.

7

The eXtraordinarY Kids Clinic: an interdisciplinary model of care for children and adolescents with sex chromosome aneuploidy.

Tartaglia N, Howell S, Wilson R, Janusz J, Boada R, Martin S, Frazier JB, Pfeiffer M, Regan K, McSwegin S, Zeitler P. Tartaglia N, et al. Among authors: howell s. J Multidiscip Healthc. 2015 Jul 17;8:323-34. doi: 10.2147/JMDH.S80242. eCollection 2015. J Multidiscip Healthc. 2015. PMID: 26229481 Free PMC article.

8

Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.

Davis S, Howell S, Wilson R, Tanda T, Ross J, Zeitler P, Tartaglia N. Davis S, et al. Among authors: howell s. Adv Pediatr. 2016 Aug;63(1):15-46. doi: 10.1016/j.yapd.2016.04.020. Adv Pediatr. 2016. PMID: 27426894 Free PMC article. Review. No abstract available.

9

Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.

Wigby K, D'Epagnier C, Howell S, Reicks A, Wilson R, Cordeiro L, Tartaglia N. Wigby K, et al. Among authors: howell s. Am J Med Genet A. 2016 Nov;170(11):2870-2881. doi: 10.1002/ajmg.a.37688. Epub 2016 Sep 19. Am J Med Genet A. 2016. PMID: 27644018 Free PMC article.

10

Clinical developmental, neuropsychological, and social-emotional features of Turner syndrome.

Hutaff-Lee C, Bennett E, Howell S, Tartaglia N. Hutaff-Lee C, et al. Among authors: howell s. Am J Med Genet C Semin Med Genet. 2019 Mar;181(1):126-134. doi: 10.1002/ajmg.c.31687. Epub 2019 Feb 14. Am J Med Genet C Semin Med Genet. 2019. PMID: 30767374 Free PMC article. Review.

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