Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Caroline Oren"'
Autor:
David McCormick, Steven L. Kugler, Deb K. Pal, Jacqueline Taylor, Jennifer Crosbie, Tara Clarke, Steven M. Wolf, Russell Schachar, John Trounce, Cigdem I. Akman, Elaine C. Wirrell, Michael D. Wilson, David E. Mandelbaum, Laura Addis, Roberto Caraballo, Lisa J. Strug, Stéphane Auvin, Paul Arnold, Caroline Oren, Maria Kinali, Naim Panjwani, Patricia McGoldrick
Publikováno v:
Annals of Clinical and Translational Neurology
Objective Rolandic epilepsy is a common genetic focal epilepsy of childhood characterized by centrotemporal sharp waves on electroencephalogram. In previous genome‐wide analysis, we had reported linkage of centrotemporal sharp waves to chromosome 1
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d37dbe2495d7ef0609a1afbb7f3fb6b5
http://europepmc.org/articles/PMC4931716
http://europepmc.org/articles/PMC4931716
Autor:
David McCormick, Tara Clarke, Shan Tang, Rajesh Gupta, Steven L. Kugler, Lisa J. Strug, Marisa Pina, Sushma Goyal, Cigdem I. Akman, Caroline Oren, Anna B. Smith, John Trounce, Elaine Hughes, Hannah Cockerill, Steven M Wolf, John Jackman, David E. Mandelbaum, Kumudini Gomez, Colm J. McGinnity, Zaloa Agirre-Arrizubieta, Patricia McGoldrick, Nicola Jolleff, Jacqueline Taylor, Yaiza Hernández Vega, David Scott, Deb K. Pal
Publikováno v:
Epilepsy & Behavior. 53:174-179
Objective The high prevalence and impact of neurodevelopmental comorbidities in childhood epilepsy are now well known, as are the increased risks and familial aggregation of reading disability (RD) and speech sound disorder (SSD) in rolandic epilepsy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a2946e77f34f7b7d901a846353303b6
https://doi.org/10.1016/j.yebeh.2015.10.016
https://doi.org/10.1016/j.yebeh.2015.10.016
Autor:
Joanna F. Flatt, Mehul T. Dattani, Caroline Oren, Benjamin Jacobs, Gordon W. Stewart, Stephanie Grunewald, Evelien Gevers, Waleed M. Bawazir, Ai Leen Ang, Lesley J. Bruce
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 97:E987-E993
GLUT1 (glucose transporter 1) deficiency syndrome is a well-known presentation in pediatric practice. Very rare mutations not only disable carbohydrate transport but also cause the red cell membrane to be constitutively permeant to monovalent cations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e2c121d1a176b83fd525ef5713fb4b0
https://doi.org/10.1210/jc.2012-1399
https://doi.org/10.1210/jc.2012-1399
Autor:
Praveen, Saroey, Joanne, Beckmann, Qureshi, Maharukh, Gabriel, Conder, Caroline, Oren, Bhanu, Williams
Publikováno v:
Archives of disease in childhood. 97(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::506f88510f32ac800b7942c8fc9a5167
https://pubmed.ncbi.nlm.nih.gov/22143904
https://pubmed.ncbi.nlm.nih.gov/22143904
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 20(6)
Morbidity after paediatric epidural anaesthesia is unusual. We report a case of transient motor nerve root block in an eleven years old girl receiving epidural analgesia postoperatively following anterior instrumented spinal fusion for scoliosis. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3d42702b1443ff0165a98b87ad456e95
https://pubmed.ncbi.nlm.nih.gov/20642973
https://pubmed.ncbi.nlm.nih.gov/20642973
Autor:
Caroline Oren, Praveen Saroey, Gabriel Conder, Bhanu Williams, Qureshi Maharukh, Joanne Beckmann
Publikováno v:
Archives of Disease in Childhood. 97:458-458
A 5-year-old Romanian girl presented with a 1-week history of abdominal pain and distension and a 1-day history of fever. She was systemically well but had nodular hepatomegaly measuring 12 cm below the costal margin. On ultrasound and MRI, there wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a17d36707d68acee57fe8f869585fda6
https://doi.org/10.1136/archdischild-2011-301010
https://doi.org/10.1136/archdischild-2011-301010
Autor:
Panjwani, Naim1, Wilson, Michael D.1,2, Addis, Laura3,4, Crosbie, Jennifer5,6, Wirrell, Elaine7, Auvin, Stéphane8, Caraballo, Roberto H.9, Kinali, Maria10, McCormick, David11, Oren, Caroline12, Taylor, Jacqueline13, Trounce, John14, Clarke, Tara15, Akman, Cigdem I.16, Kugler, Steven L.17, Mandelbaum, David E.18, McGoldrick, Patricia19, Wolf, Steven M.19, Arnold, Paul5,6,20, Schachar, Russell5,6
Publikováno v:
Annals of Clinical & Translational Neurology. Jul2016, Vol. 3 Issue 7, p512-522. 11p.
Autor:
Addis, Laura, Sproviero, William, Thomas, Sanjeev V., Caraballo, Roberto H., Newhouse, Stephen J., Gomez, Kumudini, Hughes, Elaine, Kinali, Maria, McCormick, David, Hannan, Siobhan, Cossu, Silvia, Taylor, Jacqueline, Akman, Cigdem I., Wolf, Steven M., Mandelbaum, David E., Gupta, Rajesh, van der Spek, Rick A., Pruna, Dario, Pal, Deb K.
Publikováno v:
Journal of Medical Genetics; Sep2018, Vol. 55 Issue 9, p607-616, 10p
Autor:
Martinos, Marina M., Pujar, Suresh, Gillberg, Christopher, Cortina‐Borja, Mario, Neville, Brian G. R., De Haan, Michelle, Scott, Rod C., Chin, Richard F. M., Cortina-Borja, Mario
Publikováno v:
Developmental Medicine & Child Neurology; Apr2018, Vol. 60 Issue 4, p409-416, 8p
Autor:
Eltze, Christin M., Chong, Wui K., Cox, Tim, Whitney, Andrea, Cortina‐Borja, Mario, Chin, Richard F. M., Scott, Rod C., Cross, J. Helen
Publikováno v:
Epilepsia (Series 4); Mar2013, Vol. 54 Issue 3, p437-445, 9p