“How should I tell my child?” Disclosing the Diagnosis of Sex Chromosome Aneuploidies

per Dennis, Anna, Howell, Susan, Cordeiro, Lisa, Tartaglia, Nicole
Publicat a J Genet Couns (2014)

Chronic Urinary Tract Infection Due to Candida utilis

per Hazen, Kevin C., Theisz, Gordon W., Howell, Susan A.
Publicat 1999

Clinical Developmental, Neuropsychological, and Social-Emotional Features of Turner Syndrome

per Hutaff-Lee, Christa, Bennett, Elizabeth, Howell, Susan, Tartaglia, Nicole
Publicat a Am J Med Genet C Semin Med Genet (2019)

Timing of Diagnosis of 47,XXY and 48,XXYY: A Survey of Parent Experiences

per Visootsak, Jeannie, Ayari, Natalie, Howell, Susan, Lazarus, Joash, Tartaglia, Nicole
Publicat 2013

The Spectrum of the Behavioral Phenotype in Boys and Adolescents 47,XXY (Klinefelter Syndrome)

per Tartaglia, Nicole, Cordeiro, Lisa, Howell, Susan, Wilson, Rebecca, Janusz, Jennifer
Publicat 2010

SUN-263 Evidence for Diminished Ovarian Reserve in Youth with Trisomy X

per Davis, Shanlee, Howell, Susan, Serena, Dovey, Buyers, Eliza, Tartaglia, Nicole
Publicat a J Endocr Soc (2019)

A Mixed Methods Study of Physical Activity and Quality of Life in Adolescents with Turner Syndrome

per Thompson, Talia, Zieba, Briana, Howell, Susan, Karakash, William, Davis, Shanlee
Publicat a Am J Med Genet A (2019)

A review of trisomy X (47,XXX)

per Tartaglia, Nicole R, Howell, Susan, Sutherland, Ashley, Wilson, Rebecca, Wilson, Lennie
Publicat 2010

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

per Tartaglia, Nicole, Ayari, Natalie, Howell, Susan, D’Epagnier, Cheryl, Zeitler, Philip
Publicat 2011

Rapid Differentiation of Closely Related Candida Species and Strains by Pyrolysis-Mass Spectrometry and Fourier Transform-Infrared Spectroscopy

per Timmins, Éadaoin M., Howell, Susan A., Alsberg, Bjørn K., Noble, William C., Goodacre, Royston
Publicat 1998

Advances in the interdisciplinary care of children with Klinefelter syndrome

per Davis, Shanlee, Howell, Susan, Wilson, Rebecca, Tanda, Tanea, Ross, Judy, Zeitler, Philip, Tartaglia, Nicole
Publicat a Adv Pediatr (2016)

Expanding the Phenotype of Triple X Syndrome: A Comparison of Prenatal Versus Postnatal Diagnosis

per Wigby, Kristen, D’Epagnier, Cheryl, Howell, Susan, Reicks, Amy, Wilson, Rebecca, Cordeiro, Lisa, Tartaglia, Nicole
Publicat a Am J Med Genet A (2016)

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

per Thompson, Talia, Howell, Susan, Davis, Shanlee, Wilson, Rebecca, Janusz, Jennifer, Boada, Richard, Pyle, Laura, Tartaglia, Nicole
Publicat a Am J Med Genet C Semin Med Genet (2020)

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

per Hager, Karl, Jennings, Kori, Hosono, Seiyu, Howell, Susan, Gruen, Jeffrey R, Tartaglia, Nicole R, Rinder, Henry M
Publicat 2012

Diminished ovarian reserve in girls and adolescents with Trisomy X Syndrome

per Davis, Shanlee M, Soares, Katelyn, Howell, Susan, Cree-Green, Melanie, Buyers, Eliza, Johnson, Joshua, Tartaglia, Nicole R
Publicat a Reprod Sci (2020)

Clinical Phenotype and Management of Individuals with Mosaic Monosomy X with Y Chromosome Material Stratified by Genital Phenotype

per Guzewicz, Lindsey, Howell, Susan, Crerand, Canice E., Umbaugh, Hailey, Nokoff, Natalie J, Barker, Jennifer, Davis, Shanlee M
Publicat a Am J Med Genet A (2021)

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

per Tartaglia, Nicole, Howell, Susan, Wilson, Rebecca, Janusz, Jennifer, Boada, Richard, Martin, Sydney, Frazier, Jacqueline B, Pfeiffer, Michelle, Regan, Karen, McSwegin, Sarah, Zeitler, Philip
Publicat a J Multidiscip Healthc (2015)

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

per Tartaglia, Nicole, Howell, Susan, Davis, Shanlee, Kowal, Karen, Tanda, Tanea, Brown, Mariah, Boada, Cristina, Alston, Amanda, Crawford, Leah, Thompson, Talia, van Rijn, Sophie, Wilson, Rebecca, Janusz, Jennifer, Ross, Judith
Publicat a Am J Med Genet C Semin Med Genet (2020)