Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Nina N, Sainath"'
Autor:
Nina N, Sainath, Christina, Bales, Jefferson N, Brownell, Octavia, Pickett-Blakely, Aisha, Sattar, Virginia A, Stallings
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 75:36-41
Patients with short bowel syndrome (SBS) can have a high morbidity rate. To minimize morbidity, enteral autonomy is the primary goal in clinical management of patients with SBS. This is often difficult to achieve because of significant malabsorption.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a51bd084206ec85b337dd54da609c6f
https://doi.org/10.1097/mpg.0000000000003465
https://doi.org/10.1097/mpg.0000000000003465
Publikováno v:
Journal of Cystic Fibrosis. 18:135-143
Background In patients with cystic fibrosis (CF), ivacaftor treatment results in significant weight gain and the impact on diet has not been explored. Methods A study in 22 subjects (6.1–61.6 years) compared diet, energy balance, weight gain, and b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac438dcb6477dd8f7652ee6246a8deb9
https://doi.org/10.1016/j.jcf.2018.06.004
https://doi.org/10.1016/j.jcf.2018.06.004
Autor:
Laurie E. Cohen, Joshua H. Gordon, Catherine M. Gordon, Mark W. Kieran, Erica Popovsky, Henry A. Feldman, Nina N. Sainath
Publikováno v:
Pediatric Blood & Cancer. 58:959-963
Background Childhood cancer survivors are at high risk for reduced bone mineral density (BMD). Our objective was to determine whether post-pubertal adolescent survivors of brain tumors, whose tumor or treatments placed them at risk for pituitary horm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1907077f23514d3c54e8183d31ffd0f9
https://doi.org/10.1002/pbc.23300
https://doi.org/10.1002/pbc.23300
Publikováno v:
The Journal of Pediatrics. 201:229-237.e4
To determine if ivacaftor treatment results in weight gain and improved pulmonary function in people with cystic fibrosis transmembrane conductance regulator gating mutations.Children and adults with cystic fibrosis and at least 1 cystic fibrosis tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd799fd2130cffdce848e8a4222e00a3
https://doi.org/10.1016/j.jpeds.2018.05.018
https://doi.org/10.1016/j.jpeds.2018.05.018
Autor:
Virginia A. Stallings, Nina N. Sainath, Joan I. Schall, J. Samuel, Chiara Bertolaso, Carolyn McAnlis, E. Karalunas, A. Hyczko
Publikováno v:
Journal of Cystic Fibrosis. 15:S101-S102
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f0c4b6aeed7d09edf7b8b74ac751c14a
https://doi.org/10.1016/s1569-1993(16)30437-4
https://doi.org/10.1016/s1569-1993(16)30437-4
Autor:
Stallings VA; Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA; Department of Pediatrics, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA. Electronic address: stallingsv@email.chop.edu., Sainath N; Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA., Oberle M; Division of Endocrinology, Children's Hospital of Philadelphia, Philadelphia, PA., Bertolaso C; Universita La Sapienza-Policlinico, Rome, Italy., Schall JI; Division of Gastroenterology, Hepatology and Nutrition, Children's Hospital of Philadelphia, Philadelphia, PA.
Publikováno v:
The Journal of pediatrics [J Pediatr] 2018 Oct; Vol. 201, pp. 229-237.e4. Date of Electronic Publication: 2018 Jul 18.
Autor:
Dams-Kozlowska H; Department of Biomedical Engineering, Tufts University, 4 Colby St., Rm. 153, Medford, MA 02155, USA., Sainath N, Kaplan DL
Publikováno v:
Applied microbiology and biotechnology [Appl Microbiol Biotechnol] 2008 Mar; Vol. 78 (4), pp. 677-83. Date of Electronic Publication: 2008 Feb 01.