T. Sadeghin

发表

The benefits and limitations of cell‐free DNA screening for 47, XXY (Klinefelter syndrome)

A. Gropman, C. Samango-Sprouse, Colleen Keen, 2017, Prenatal diagnosis.

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

A. Gropman, C. Samango-Sprouse, Teresa Sadeghin, 2019, American journal of medical genetics. Part A.

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

S. van Rijn, L. D. de Sonneville, C. Samango-Sprouse, 2018, American journal of medical genetics. Part A.

Positive effects of early androgen therapy on the behavioral phenotype of boys with 47,XXY

A. Gropman, C. Samango-Sprouse, P. Lawson, 2015, American journal of medical genetics. Part C, Seminars in medical genetics.

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

A. Gropman, C. Samango-Sprouse, Sophia Q. Song, 2021, Genetics in Medicine.

Impact of early diagnosis and noninvasive prenatal testing (NIPT): Knowledge, attitudes, and experiences of parents of children with sex chromosome aneuploidies (SCAs)

A. Gropman, C. Samango-Sprouse, Teresa Sadeghin, 2020, Prenatal diagnosis.

Neurocognitive development and capabilities in boys with 49,XXXXY syndrome

A. Gropman, C. Samango-Sprouse, Patricia C. Lasutschinkow, 2020, American journal of medical genetics. Part A.

Expanding the phenotypic profile of boys with 47, XXY: The impact of familial learning disabilities

A. Gropman, C. Samango-Sprouse, Emily J. Stapleton, 2014, American journal of medical genetics. Part A.

Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47,XXY syndrome at 36 and 72 months of age

A. Gropman, C. Samango-Sprouse, Emily J. Stapleton, 2013, American journal of medical genetics. Part A.

Effects of short‐course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndrome

A. Gropman, A. Rogol, C. Samango-Sprouse, 2011, Acta paediatrica.

Expanding the phenotypic profile of Kleefstra syndrome: A female with low‐average intelligence and childhood apraxia of speech

A. Gropman, C. Samango-Sprouse, P. Lawson, 2016, American journal of medical genetics. Part A.

Speech and language development in children with 49,XXXXY syndrome

A. Gropman, C. Samango-Sprouse, Patricia C. Lasutschinkow, 2020, American journal of medical genetics. Part A.

49,XXXXY syndrome: A study of neurological function in this uncommon X and Y chromosomal disorder

A. Gropman, C. Samango-Sprouse, F. Mitchell, 2020, American journal of medical genetics. Part A.

Evidence of intrauterine growth restriction and growth hormone deficiency in 49,XXXXY syndrome

A. Gropman, D. Counts, C. Samango-Sprouse, 2020, American journal of medical genetics. Part A.

Musculoskeletal abnormalities in a large international cohort of boys with 49,XXXXY

A. Gropman, L. Tosi, C. Samango-Sprouse, 2020, American journal of medical genetics. Part A.

Behavioral phenotype of 49,XXXXY syndrome: Presence of anxiety‐related symptoms and intact social awareness

A. Gropman, C. Samango-Sprouse, Patricia C. Lasutschinkow, 2020, American journal of medical genetics. Part A.

Neurodevelopmental variability in three young girls with a rare chromosomal disorder, 48, XXXX

A. Gropman, C. Samango-Sprouse, Colleen Keen, 2015, American journal of medical genetics. Part A.

Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister–Killian Syndrome and His Unaffected Twin

A. Gropman, Kosar Khaksari, C. Samango-Sprouse, 2022, Frontiers in Pediatrics.

Neurodevelopmental outcome of prenatally diagnosed boys with 47,XXY (Klinefelter syndrome) and the potential influence of early hormonal therapy

A. Gropman, C. Samango-Sprouse, F. Mitchell, 2020, American journal of medical genetics. Part A.

Identification of infants at risk for autism spectrum disorder and developmental language delay prior to 12 months

A. Gropman, C. Samango-Sprouse, Emily J. Stapleton, 2015, Autism : the international journal of research and practice.

Is it all the X: Familial learning dysfunction and the impact of behavioral aspects of the phenotypic presentation of XXY?

A. Gropman, C. Samango-Sprouse, Emily J. Stapleton, 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome

A. Gropman, A. Rogol, I. Fennoy, 2010, American journal of medical genetics. Part A.

Hormonal replacement therapy and its potential influence on working memory and competency/adaptive functioning in 47,XXY (Klinefelter syndrome)

A. Gropman, C. Samango-Sprouse, Selena L Tran, 2019, American journal of medical genetics. Part A.

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

A. Gropman, C. Samango-Sprouse, S. Powell, 2023, Genes.

Immunodeficiency in patients with 49,XXXXY chromosomal variation

J. Orange, C. Samango-Sprouse, M. Keller, 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

Musculoskeletal anomalies in a large cohort of boys with 49, XXXXY

A. Gropman, L. Tosi, C. Samango-Sprouse, 2013, American journal of medical genetics. Part C, Seminars in medical genetics.

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

A. Gropman, D. Counts, C. Samango-Sprouse, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Novel Neurocognitive Profile in a Minority of Boys with 47,XXY (Klinefelter Syndrome)

A. Gropman, Kosar Khaksari, C. Samango-Sprouse, 2022, Journal of developmental and behavioral pediatrics : JDBP.

Case Report: Infant With Congenital Adrenal Hyperplasia and 47,XXY

A. Gropman, C. Samango-Sprouse, F. Mitchell, 2022, Frontiers in Genetics.

Effects of short‐course androgen therapy on the neurodevelopmental profile of infants and children with 49,XXXXY syndrome

A. Gropman, A. Rogol, C. Samango-Sprouse, 2011, Acta paediatrica.