Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Alicia A Romano"'
Autor:
Alicia B. Romano, Ashley B. Heim, Aspen E. King, Cara F. Smith, Emily A. Holt, Emily A. Royse, Tanner M. Harvey, David O. Lyons, Tyler Sherman
Publikováno v:
Journal of Biological Education. 55:306-320
Formative assessments have been shown to improve student success; however, the format in which these assessments are implemented has not been well researched. In this study, individual Anat...
Autor:
David Atkin, Kimberly A. Neuendorf, Clare Gross, George B. Ray, Jill E. Rudd, Alicia Faith Romano
Publikováno v:
Journal of Family Communication. 19:243-260
This study examined conflict, parenting communication style, and attitudes regarding the parent-child relationship for a marginalized special population: incarcerated mothers and their children. Br...
Autor:
Petur Benedikt Juliusson, Alicia A Romano, Judith L. Ross, Tilman R Rohrer, Bradley S. Miller, Michel Polak, Jennifer Abuzzahab, Lars Sävendahl, Vlady Ostrow, Alberto Pietropoli, Joanne C. Blair, Anna Camilla Birkegård, Philippe Backeljauw, Jovanna Dahlgren
Publikováno v:
Hormone Research in Paediatrics
Introduction: Few data exist on long-term growth hormone (GH) treatment in patients with Noonan syndrome (NS). Objective: To evaluate the effectiveness and safety of GH treatment in NS in clinical practice. Methods: Height gain, near-adult height (NA
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3d0f20ffbe69935eba53f54eb279c2a
https://hdl.handle.net/11250/2992045
https://hdl.handle.net/11250/2992045
Autor:
Petur Benedikt Juliusson, Alicia A Romano, Jo Blair, Alberto Pietropoli, Jovanna Dahlgren, Jennifer Abuzzahab
Publikováno v:
Endocrine Abstracts.
Autor:
Alicia A, Romano
Publikováno v:
Pediatric endocrinology reviews : PER. 16(Suppl 2)
Short stature is a common characteristic of Noonan Syndrome (NS), a genetic condition caused by mutations affecting the RAS / mitogen-activated protein kinase (MAPK) cascade. Growth hormone (GH) has been used to normalize childhood growth and increas
Autor:
Max Benn, Carl I. Thompson, Richard A Noto, W Weiler, James Haigney, Tara Patale, Robert Potenza, Zeyad El-Naghy, Liam McGuirk, Alicia A Romano, Michael S. Tenner, Nicholas Andrew Krasnow
Publikováno v:
Journal of the Endocrine Society
Background: We have previously demonstrated that short children with Idiopathic Short Stature (ISS), Growth Hormone Deficiency (GHD), and their short siblings have significantly diminished pituitary volumes (PV) compared to normal children. In compar
Autor:
Jennifer J, Bell, Barbara, Lippe, Alicia A, Romano, Joseph T, Cernich, Rita D, Swinford, Dalia, Moawad
Publikováno v:
Pediatric endocrinology reviews : PER. 16(2)
The National Cooperative Growth Study (NCGS) data are reviewed from 1985-2010 to report on final demographic, efficacy, and safety findings, and to illustrate the value of long-term, real-world follow-up to physicians and patients.The NCGS was a mult
Publikováno v:
Journal of Blood Medicine
Diane J Nugent,1 Alicia A Romano,2 Shreya Sabharwal,3 David L Cooper3 1Center for Inherited Bleeding Disorders, Children’s Hospital of Orange County, Orange, CA, USA; 2Department of Pediatrics, New York Medical College, Valhalla, NY, USA; 3Medical
Autor:
Jacqueline A. Noonan, Clifford M. Takemoto, Wanda Robinson, Judith Allanson, Alicia A Romano, Bruce D. Gelb, Jovanna Dahlgren, Mary Ella M Pierpont, Bryan D. Hall, Amy E. Roberts
Publikováno v:
Pediatrics. 126:746-759
Noonan syndrome (NS) is a common, clinically and genetically heterogeneous condition characterized by distinctive facial features, short stature, chest deformity, congenital heart disease, and other comorbidities. Gene mutations identified in individ
Autor:
Alicia A Romano, Joan R. Jacobs, Barbara Lippe, D. Aaron Davis, Joanne Julius Hunold, Ken Dana, Bert Bakker
Publikováno v:
The Journal of clinical endocrinology and metabolism. 94(7)
Noonan syndrome (NS) is a heterogeneous genetic disorder characterized by short stature.The National Cooperative Growth Study (NCGS), a postmarketing observational study of recombinant human GH (rhGH)-treated children, includes a large cohort of chil