Zobrazeno 1 - 10
of 19
pro vyhledávání: '"59"'
Autor:
Barış Altay, Bora Irer, Volkan Sen, Serdar Kalemci, Fuat Kizilay, Ozgur Cogulu, Deniz Özalp Kızılay, Adnan Şimşir
Publikováno v:
Neurourology and Urodynamics. 39:833-840
Aims In children with Down syndrome (DS) which causes cognitive impairment and intellectual disability (ID), dysfunctional voiding is proposed to be more common than in the normal population. In this study, we aimed to compare the voiding symptoms of
Autor:
Francine Blei, Beth A. Drolet, Ilona J. Frieden, Maria‐Laura Cossio, Maria C. Garzon, Julie Powell, Mohit Maheshwari, Dawn H. Siegel, Denise W. Metry, Olivia M. T. Davies, Christine T. Lauren, Nicole S. Stefanko, Catherine McCuaig, Sumaiya S. Salman
Publikováno v:
Pediatric Dermatology. 36:618-622
Background Awareness of PHACE syndrome has increased; however, little information exists regarding its natural history, especially in patients over the age of 18. We aim to describe the natural history of PHACE to enhance clinical management and coun
Autor:
Elizabeth Perry Caldwell
Publikováno v:
Journal for Specialists in Pediatric Nursing. 25
PURPOSE After patients with sickle cell disease (SCD) transfer from pediatric care to adult care, significant morbidity and mortality occurs. There are many possible contributors to the success or failure of this transition. One hypothesis is that he
Autor:
Kirsty Vickerman, Christopher D. Graham, Steven Kemp, Markus Reuber, Hayley Kitchingman, Rebecca Chan
Publikováno v:
Kemp, S, Graham, C D, Chan, R, Kitchingman, H, Vickerman, K & Reuber, M 2018, ' The frequency and management of seizures during psychological treatment among patients with psychogenic nonepileptic seizures and epilepsy ', Epilepsia, vol. 59, no. 4, pp. 844-853 . https://doi.org/10.1111/epi.14040
OBJECTIVE: Growing evidence suggests that psychological treatments are effective for improving outcomes in both epilepsy and psychogenic nonepileptic seizures (PNES). However, the risk of in-session seizures may cause concerns about safety and about
Autor:
Charlotte Simister, Parag Sayal, Yehani Wedatilake, Elaine Murphy, Aidan Ryan, Adrian T. H. Casey, Aoife M. Waters, Robin H. Lachmann, Ulpee Darbar, Annalisa Sechi, Douglas Chesher, Michael J Oddy
Publikováno v:
Journal of Inherited Metabolic Disease
X-linked hypophosphatemia (XLH) is the most common monogenic disorder causing hypophosphatemia. This case-note review documents the clinical features and the complications of treatment in 59 adults (19 male, 40 female) with XLH. XLH is associated wit
Autor:
Wenbo Wang, Xunwu Meng, Ou Wang, Weibo Xia, Yan Jiang, Xiaoping Xing, Mei Li, Jing Kong, Min Nie
Publikováno v:
Clinical Endocrinology. 87:865-873
Objective Primary hyperparathyroidism (PHPT) in children is thought to be extremely rare. Our study aimed to summarize the clinical characteristics and the molecular genetics in patients with pediatric PHPT in China. Design Retrospective observationa
Autor:
Hiroshi Koga, Takahito Ninomiya
Publikováno v:
Pediatrics International. 59:578-582
Backgound Urethral prolapse (UP) in children is a rare condition and has commonly been reported in Black girls. The aim of this study was to elucidate the status of medical management for UP in Japanese children. Methods A secondary data analysis was
Autor:
Phillip L. Pearl, Iván Sánchez Fernández, Ersida Buraniqi, Arnold J. Sansevere, Réjean M. Guerriero, Tobias Loddenkemper, Robert C. Tasker
Publikováno v:
Epilepsia. 58:420-428
SummaryObjective To identify factors associated with in-hospital mortality in neonates and children undergoing continuous electroencephalography (cEEG) monitoring in the intensive care unit (ICU). Methods We performed a retrospective observational st
Autor:
Jane S Chen, Portia Kamthunzi, J. Brett Heimlich, Irving F. Hoffman, Khadija Paseli, Satish Gopal, Nigel S. Key, Kenneth I. Ataga, Wiza Kumwenda, Hillary M. Topazian, Isobel Kambalame, Tisungane Mvalo, Noel Mumba, Graham Ellis, Katherine D. Westmoreland, Gerald Tegha, Pilirani Mafunga, Msandeni Chiume
Publikováno v:
Pediatr Blood Cancer
INTRODUCTION Sickle cell disease (SCD) is among the most common inherited hematologic diseases in sub-Saharan Africa (SSA). Historically, hydroxyurea administration in SSA has been restricted due to limited region-specific evidence for safety and eff
Autor:
Muneer H. Al Bagshi, Sameera Al Afghani, Ahmed M. Al-Suliman, Abdulrahman Alsultan, Wasil Jastaniah, Zaki Nasserullah, Mohammed K. Alabdulaali
Publikováno v:
Pediatric Transplantation. 20:831-835
Allogeneic HSCT is the only curative treatment for SCD. In this study, we estimated the number of Saudi patients with SCD who are candidates for HSCT. We used the presence of overt stroke, recurrent ACS, and frequent severe pain crisis as indications