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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 22, 2013
Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variationsAndrea Gropman, Carole A Samango-Sprouse
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|January 30, 2013
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, et al.
American Journal of Medical Genetics. Part A|October 3, 2019
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, et al.
American Journal of Medical Genetics. Part A|February 22, 2020
Behavioral phenotype of 49,XXXXY syndrome: Presence of anxiety-related symptoms and intact social awarenessPatricia C Lasutschinkow, Andrea L Gropman, Grace F Porter, et al.
American Journal of Medical Genetics. Part A|July 4, 2020
Evidence of intrauterine growth restriction and growth hormone deficiency in 49,XXXXY syndromeDebra R Counts, Christine Yu, Patricia C Lasutschinkow, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 3, 2011
Effects of short-course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndromeCarole A Samango-Sprouse, Andrea L Gropman, Teresa Sadeghin, et al.
Journal of Developmental and Behavioral Pediatrics : JDBP|August 10, 2022
Novel Neurocognitive Profile in a Minority of Boys with 47,XXY (Klinefelter Syndrome)Carole A Samango-Sprouse, Mary P Hamzik, Kosar Khaksari, et al.
Current Opinion in Obstetrics & Gynecology|February 1, 2020
A review of the intriguing interaction between testosterone and neurocognitive development in males with 47,XXYCarole A Samango-Sprouse, Christine Yu, Grace F Porter, et al.
American Journal of Medical Genetics. Part A|January 25, 2013
Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47,XXY syndrome at 36 and 72 months of ageCarole A Samango-Sprouse, Teresa Sadeghin, Francine L Mitchell, et al.
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