Publications by authors named "Carole A Samango-Sprouse"

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The behavioral profile of 49,XXXXY and the potential impact of testosterone replacement therapy.
Carole A Samango-Sprouse, Mary P Hamzik, Eliana Gropman, Michaela R Brooks, Sherida Powell

Genet Med· July 2023

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The Effect of Hormonal Therapy on the Behavioral Outcomes in 47,XXY (Klinefelter Syndrome) between 7 and 12 Years of Age.
Mary P Hamzik, Andrea L Gropman, Michaela R Brooks, Sherida Powell, Teresa Sadeghin, Carole A Samango-Sprouse

Genes (Basel)· July 2023

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Novel Neurocognitive Profile in a Minority of Boys with 47,XXY (Klinefelter Syndrome).
Carole A Samango-Sprouse, Mary P Hamzik, Kosar Khaksari, Michaela R Brooks, Teresa Sadeghin

J Dev Behav Pediatr· December 2022

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Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister-Killian Syndrome and His Unaffected Twin.
Carole A Samango-Sprouse, Mary P Hamzik, Kenneth Rosenbaum, Kosar Khaksari, Francie Mitchell

Front Pediatr· March 2022

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Case Report: Infant With Congenital Adrenal Hyperplasia and 47,XXY.
Sophia Q Song, Andrea Gropman, Robert W Benjamin, Francie Mitchell, Michaela R Brooks, Carole A Samango-Sprouse

Front Genet· January 2022

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Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY.
Laura Tosi, Francie Mitchell, Grace F Porter, Leigh Ruland, Andrea Gropman, Carole A Samango-Sprouse

Am J Med Genet A· December 2021

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Evidence of intrauterine growth restriction and growth hormone deficiency in 49,XXXXY syndrome.
Debra R Counts, Christine Yu, Patricia C Lasutschinkow, Teresa Sadeghin, Andrea Gropman, Carole A Samango-Sprouse

Am J Med Genet A· December 2021

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Introduction: Comprehensive investigation into an international cohort of boys with 49,XXXXY.
Carole A Samango-Sprouse, Andrea L Gropman

Am J Med Genet A· December 2021

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Neurocognitive development and capabilities in boys with 49,XXXXY syndrome.
Andrea L Gropman, Grace F Porter, Patricia C Lasutschinkow, Teresa Sadeghin, Elizabeth S Tipton, Carole A Samango-Sprouse

Am J Med Genet A· December 2021

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Speech and language development in children with 49,XXXXY syndrome.
Carole A Samango-Sprouse, Patricia C Lasutschinkow, Michael McLeod, Grace F Porter, Sherida Powell

Am J Med Genet A· December 2021

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Neurodevelopmental outcome of prenatally diagnosed boys with 47,XXY (Klinefelter syndrome) and the potential influence of early hormonal therapy.
Carole A Samango-Sprouse, Selena L Tran, Patricia C Lasutschinkow, Teresa Sadeghin, Sherida Powell

Am J Med Genet A· August 2020

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Detection of maternal X chromosome abnormalities using single nucleotide polymorphism-based noninvasive prenatal testing.
Kimberly A Martin, Carole A Samango-Sprouse, Valerie Kantor, Rupin Dhamankar, Elizabeth Valenti

Am J Obstet Gynecol MFM· August 2020

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Behavioral phenotype of 49,XXXXY syndrome: Presence of anxiety-related symptoms and intact social awareness.
Patricia C Lasutschinkow, Andrea L Gropman, Grace F Porter, Teresa Sadeghin, Carole A Samango-Sprouse

Am J Med Genet A· May 2020

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A review of the intriguing interaction between testosterone and neurocognitive development in males with 47,XXY.
Carole A Samango-Sprouse, Christine Yu, Grace F Porter, Elizabeth S Tipton, Patricia C Lasutschinkow

Curr Opin Obstet Gynecol· April 2020

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Impact of early diagnosis and noninvasive prenatal testing (NIPT): Knowledge, attitudes, and experiences of parents of children with sex chromosome aneuploidies (SCAs).
Carole A Samango-Sprouse, Grace F Porter, Patricia C Lasutschinkow, Selena L Tran, Teresa Sadeghin

Prenat Diagn· March 2020

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Hormonal replacement therapy and its potential influence on working memory and competency/adaptive functioning in 47,XXY (Klinefelter syndrome).
Selena L Tran, Carole A Samango-Sprouse, Teresa Sadeghin, Sherida Powell, Andrea L Gropman

Am J Med Genet A· December 2019

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Update On The Clinical Perspectives And Care Of The Child With 47,XXY (Klinefelter Syndrome).
Carole A Samango-Sprouse, Debra R Counts, Selena L Tran, Patricia C Lasutschinkow, Grace F Porter

Appl Clin Genet· October 2019

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Identification of infants at risk for autism spectrum disorder and developmental language delay prior to 12 months.
Carole A Samango-Sprouse, Emily J Stapleton, Farhad Aliabadi, Robert Graw, Rebecca Vickers

Autism· April 2015

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Expanding the phenotypic profile of boys with 47, XXY: the impact of familial learning disabilities.
Carole A Samango-Sprouse, Emily J Stapleton, Francie L Mitchell, Teresa Sadeghin, Thomas P Donahue

Am J Med Genet A· June 2014

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Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47,XXY syndrome at 36 and 72 months of age.
Carole A Samango-Sprouse, Teresa Sadeghin, Francine L Mitchell, Teresa Dixon, Emily Stapleton

Am J Med Genet A· March 2013

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Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations.
Andrea Gropman, Carole A Samango-Sprouse

Am J Med Genet C Semin Med Genet· February 2013

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Introduction: past, present, and future care of individuals with XXY.
Carole A Samango-Sprouse, Andrea L Gropman

Am J Med Genet C Semin Med Genet· February 2013

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Is it all the X: familial learning dysfunction and the impact of behavioral aspects of the phenotypic presentation of XXY?
Carole A Samango-Sprouse, Emily Stapleton, Teresa Sadeghin, Andrea L Gropman

Am J Med Genet C Semin Med Genet· February 2013

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Musculoskeletal anomalies in a large cohort of boys with 49, XXXXY.
Courtney Sprouse, Laura Tosi, Emily Stapleton, Andrea L Gropman, Francie L Mitchell, Carole A Samango-Sprouse

Am J Med Genet C Semin Med Genet· February 2013

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Effects of short-course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndrome.
Carole A Samango-Sprouse, Andrea L Gropman, Teresa Sadeghin, Madison Kingery, Margaret Lutz-Armstrong

Acta Paediatr· June 2011

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