S. Howell

发表

Clinical developmental, neuropsychological, and social–emotional features of Turner syndrome

N. Tartaglia, C. Hutaff-Lee, E. Bennett, 2019, American journal of medical genetics. Part C, Seminars in medical genetics.

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

J. Gruen, S. Hosono, K. Hager, 2012, International Journal of Pediatric Endocrinology.

Clinical phenotype and management of individuals with mosaic monosomy X with Y chromosome material stratified by genital phenotype

C. Crerand, S. Davis, S. Howell, 2021, American journal of medical genetics. Part A.

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

J. Frazier, R. Boada, P. Zeitler, 2015, Journal of multidisciplinary healthcare.

Gender and Age Differences in Child Adjustment to Parental Separation

P. Portes, S. Howell, Joseph H. Brown, 1997 .

Eosinophilic esophagitis in individuals with sex chromosome aneuploidies: Clinical presentations and management implications

G. Furuta, S. Davis, N. Tartaglia, 2021, Molecular genetics & genomic medicine.

Supporting students with sex chromosome aneuploidies in educational settings: Results of a nationwide survey.

L. Pyle, R. Boada, S. Davis, 2021, Journal of school psychology.

Advances in the Interdisciplinary Care of Children with Klinefelter Syndrome.

S. Davis, P. Zeitler, N. Tartaglia, 2016, Advances in pediatrics.

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

J. Visootsak, N. Tartaglia, S. Howell, 2013, American journal of medical genetics. Part A.

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

P. Zeitler, N. Tartaglia, S. Howell, 2011, Acta paediatrica.

Diminished Ovarian Reserve in Girls and Adolescents with Trisomy X Syndrome

M. Cree‐Green, S. Davis, N. Tartaglia, 2020, Reproductive Sciences.

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

Kristen Wigby, N. Tartaglia, S. Howell, 2016, American journal of medical genetics. Part A.

Early neurodevelopmental and medical profile in children with sex chromosome trisomies: Background for the prospective eXtraordinarY babies study to identify early risk factors and targets for intervention

S. van Rijn, S. Davis, N. Tartaglia, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

ReviewA review of trisomy X ( 47 , XXX )

N. Tartaglia, S. Howell, Rebecca Wilson, 2015 .

A review of trisomy X (47,XXX)

N. Tartaglia, S. Howell, Rebecca Wilson, 2010, Orphanet journal of rare diseases.

Reviewof trisomy X (47,XXX)

N. Tartaglia, S. Howell, Rebecca Wilson, 2010 .

Current survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies

L. Pyle, R. Boada, S. Davis, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

Unique plasma metabolite signature for adolescents with Klinefelter syndrome reveals altered fatty acid metabolism

M. Kelsey, Peter Baker, S. Davis, 2021, medRxiv.

A mixed methods study of physical activity and quality of life in adolescents with Turner syndrome

S. Davis, S. Howell, Talia Thompson, 2019, American journal of medical genetics. Part A.

Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance

S. Davis, N. Tartaglia, S. Howell, 2021, medRxiv.

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

N. Tartaglia, S. Howell, J. Janusz, 2010, Pediatric endocrinology reviews : PER.

Exploring academic and character strengths in students with sex chromosome aneuploidies

S. Davis, S. Takamatsu, N. Tartaglia, 2021 .

Executive function in XXY: Comparison of performance‐based measures and rating scales

R. Boada, N. Tartaglia, S. Howell, 2020, American journal of medical genetics. Part C, Seminars in medical genetics.

“How Should I Tell my Child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies

N. Tartaglia, S. Howell, Lisa Cordeiro, 2015, Journal of Genetic Counseling.

The continued problem of URL decay: an updated analysis of health care management journal citations

Amber T Burtis, S. Howell, 2022, Journal of the Medical Library Association : JMLA.

The emotional journey of adapting to prenatally identified trisomy X.

S. Davis, S. Howell, Talia Thompson, 2023, Journal of Genetic Counseling.

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

P. Zeitler, N. Tartaglia, S. Howell, 2011, Acta paediatrica.

Noninvasive prenatal screening (NIPS) results for participants of the eXtraordinarY babies study: Screening, counseling, diagnosis, and discordance

S. Davis, N. Tartaglia, S. Howell, 2022, Journal of genetic counseling.