Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Theresa Newlove"'
Publikováno v:
Paediatric anaesthesiaREFERENCES.
Autor:
Andrea Chapman, Theresa Newlove, Amrit K. Dhariwal, Katelynn E. Boerner, Elizabeth A. Stanford, Katherine Edwards, Katherine E. Green
Publikováno v:
Journal of Pediatric Psychology. 45:156-169
ObjectivesPain and other physical symptoms commonly co-occur in childhood. There is debate about the relevance of somatization in understanding pain. The present review critically appraised and synthesized the extant literature on the relationship be
Autor:
Alam Lakhani, Carlie Penner, Theresa Newlove, Kevan Jacobson, Matthew Smyth, Kathi Evans, Justin M. Chan
Publikováno v:
The Journal of pediatrics. 238
OBJECTIVES To evaluate quality of life (QoL) in a large cohort of pediatric patients with inflammatory bowel disease (IBD) and to identify the clinical factors that influence QoL. STUDY DESIGN This cross-sectional study analyzes a quality improvement
Autor:
Christian L Petersen, Matthias Görges, Evgenia Todorova, Nicholas C West, Theresa Newlove, J Mark Ansermino
BACKGROUND Deep diaphragmatic breathing, also called belly breathing, is a popular behavioral intervention that helps children cope with anxiety, stress, and their experience of pain. Combining physiological monitoring with accessible mobile technolo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b1f3a92cbd474e939a0c9c64d0c3efb0
https://doi.org/10.2196/preprints.16639
https://doi.org/10.2196/preprints.16639
Autor:
Nicholas West, Evgenia V Todorova, J. Mark Ansermino, Christian L. Petersen, Matthias Görges, Theresa Newlove
Publikováno v:
JMIR Perioperative Medicine
Background Deep diaphragmatic breathing, also called belly breathing, is a popular behavioral intervention that helps children cope with anxiety, stress, and their experience of pain. Combining physiological monitoring with accessible mobile technolo
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:AB56
Autor:
Amit P. Bhavsar, Joy Yaplito-Lee, Casper Shyr, Anupam Chakrapani, Anna Lehman, Hilary Vallance, Theresa Newlove, Marion B. Coulter-Mackie, Mary Anne Preece, Graham Sinclair, Hien Nguyen, Colin J. D. Ross, Virginie Bernard, Wyeth W. Wasserman, Ramona Salvarinova, James Pitt, William S. Sly, Abdul Waheed, Henry Ukpeh, Saikat Santra, Patrice Eydoux, Lin-Hua Zhang, Clara D.M. van Karnebeek, Sylvia Stockler-Ipsiroglu, Gabriella Horvath, Sarah Ball
Publikováno v:
American journal of human genetics, 94(3), 453-461. Cell Press
Four children in three unrelated families (one consanguineous) presented with lethargy, hyperlactatemia, and hyperammonemia of unexplained origin during the neonatal period and early childhood. We identified and validated three different CA5A alterat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50d70abe269347ebb8f27da6703d95ae
https://pure.amc.nl/en/publications/mitochondrial-carbonic-anhydrase-va-deficiency-resulting-from-ca5a-alterations-presents-with-hyperammonemia-in-early-childhood(7d7feb0b-00e9-418f-bda0-ef6e1a2763b7).html
https://pure.amc.nl/en/publications/mitochondrial-carbonic-anhydrase-va-deficiency-resulting-from-ca5a-alterations-presents-with-hyperammonemia-in-early-childhood(7d7feb0b-00e9-418f-bda0-ef6e1a2763b7).html
Autor:
Vincenzo Leuzzi, Helena Caldeira Araújo, G. Christoph Korenke, K. T. Verbruggen, Vassiliki Konstantopoulou, Vassili Valayannopoulos, Goknur Haliloglu, Saadet Mercimek-Mahmutoglu, Aizeddin A. Mhanni, Sylvia Stockler-Ipsiroglu, Brad Angle, Michael T. Geraghty, Jennifer MacKenzie, Bruce A. Barshop, Andrew P. Morris, Andrea Schlune, Andreas Schulze, Clara D.M. van Karnebeek, Francjan J. van Spronsen, Iris Marquart, Bruno Maranda, Deborah L. Renaud, William L. Nyhan, Grant A. Mitchell, Nataliya Yuskiv, Turgay Coşkun, Christiane Grolik, Luísa Diogo, Theresa Newlove, Nicola Longo, Alina Levtova, Fernando Scaglia
Publikováno v:
Molecular genetics and metabolism, 111(1), 16-25. Academic Press Inc.
Molecular Genetics and Metabolism, 111(1), 16-25. ACADEMIC PRESS INC ELSEVIER SCIENCE
Molecular Genetics and Metabolism, 111(1), 16-25. ACADEMIC PRESS INC ELSEVIER SCIENCE
We collected data on 48 patients from 38 families with guanidinoacetate methyltransferase (GAMT) deficiency. Global developmental delay/intellectual disability (DD/ID) with speech/language delay and behavioral problems as the most affected domains wa
Publikováno v:
Journal of Personality Disorders. 7:329-341
We investigated personality disorder (PD) in court- and self-referred wife assaulters using the Millon Clinical Multiaxial In-ventory-II (MCMI-II-Millon, 1987) and the Personality Disorder Examination (PDE —Loranger, 1988). MCMI-II results indicate
Autor:
Jean Paul Collet, Vanessa Edgar, Mary Dunbar, Clara D.M. van Karnebeek, Sravan Jaggumantri, Michael A. Sargent, Rajavel Elango, Sylvia Stockler-Ipsiroglu, Cristina Mignone, Theresa Newlove
Publikováno v:
Pediatric neurology, 53(4), 360-363. Elsevier Inc.
Background Creatine transporter (SLC6A8) deficiency is an X-linked inborn error of metabolism characterized by cerebral creatine deficiency, behavioral problems, seizures, hypotonia, and intellectual developmental disability. A third of patients are