Search Results
School of Medicine, Western Sydney University, Sydney, Australia
Search for other papers by Prishila Fookeerah in
Google Scholar
PubMed
Westmead Clinical School, University of Sydney, Sydney, Australia
Search for other papers by Winny Varikatt in
Google Scholar
PubMed
Westmead Clinical School, University of Sydney, Sydney, Australia
Search for other papers by Meena Shingde in
Google Scholar
PubMed
Department of Neurosurgery, Westmead Hospital, Sydney, Australia
Search for other papers by Mark A J Dexter in
Google Scholar
PubMed
School of Medicine, Western Sydney University, Sydney, Australia
Search for other papers by Mark McLean in
Google Scholar
PubMed
patients harbouring these tumours was 44 years (range 24–71 years). There were six male and three female patients. The mean maximum tumour diameter on imaging at diagnosis was 20.9 mm (range 8–38). The mean follow-up duration was 62.5 months (range 12
Fuzong Clinical Medical College of Fujian Medical University, Fuzhou, China
Search for other papers by Kunzhe Lin in
Google Scholar
PubMed
Search for other papers by Lingling Lu in
Google Scholar
PubMed
Search for other papers by Zhijie Pei in
Google Scholar
PubMed
Search for other papers by Shuwen Mu in
Google Scholar
PubMed
Search for other papers by Shaokuan Huang in
Google Scholar
PubMed
Department of Neurosurgery, 900th Hospital, Fuzhou, China
Search for other papers by Shousen Wang in
Google Scholar
PubMed
.2 ± 12.9 Sex Male 146 Female 139 Tumor size, cm 3 6.6 ± 6.4 Tumor height, mm 25.7 ± 8.5 Pathological tumor type Gonadotropinoma 93 Null cell adenoma 78 PRL cell adenoma 41
Division of Endocrinology, Mid and South Essex NHS Trust, Broomfield, UK
Search for other papers by Saroj Kumar Sahoo in
Google Scholar
PubMed
Search for other papers by Jayakrishnan C Menon in
Google Scholar
PubMed
Search for other papers by Nidhi Tripathy in
Google Scholar
PubMed
Search for other papers by Monalisa Nayak in
Google Scholar
PubMed
Search for other papers by Subhash Yadav in
Google Scholar
PubMed
/L), TSH (reference range 0.4–4 mIU/L), DHEAS (reference range: male 2.4–13.4 µmol/L, female (5–24 years) 1.8–11.0 µmol/L, female (25–45 years) 1.7–9.2 µmol/L, female (>45 years) 0.5–6.9 µmol/L) and plasma ACTH (reference range 1.6–13.9 pmol/L) were also
Department of Clinical Research, University of Basel, Basel, Switzerland
Search for other papers by Cihan Atila in
Google Scholar
PubMed
Department of Clinical Research, University of Basel, Basel, Switzerland
Search for other papers by Sophie Monnerat in
Google Scholar
PubMed
Search for other papers by Roland Bingisser in
Google Scholar
PubMed
Search for other papers by Martin Siegemund in
Google Scholar
PubMed
Search for other papers by Maurin Lampart in
Google Scholar
PubMed
Search for other papers by Marco Rueegg in
Google Scholar
PubMed
Search for other papers by Núria Zellweger in
Google Scholar
PubMed
Search for other papers by Stefan Osswald in
Google Scholar
PubMed
Search for other papers by Katharina Rentsch in
Google Scholar
PubMed
Department of Clinical Research, University of Basel, Basel, Switzerland
Search for other papers by Mirjam Christ-Crain in
Google Scholar
PubMed
University Center of Cardiovascular Science & Department of Cardiology, University Heart and Vascular Center Hamburg, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
German Center for Cardiovascular Research (DZHK), Partner Site Hamburg–Kiel–Lübeck, Hamburg, Germany
Search for other papers by Raphael Twerenbold in
Google Scholar
PubMed
respiratory infections. The median (IQR) age was 57 years (43, 70), and 280 (56%) were female. Hyponatremia prevalence was 21% in the pooled group, 28% in patients with COVID-19, 12% in other viral respiratory infections, and 30% in bacterial respiratory
Department of Pediatric Endocrinology, Wilhelmina Children’s Hospital, University Medical Center, Lundlaan, EA Utrecht, The Netherlands
Search for other papers by I M A A van Roessel in
Google Scholar
PubMed
Department of Pediatric Endocrinology, Wilhelmina Children’s Hospital, University Medical Center, Lundlaan, EA Utrecht, The Netherlands
Search for other papers by J E Gorter in
Google Scholar
PubMed
Department of Pediatric Endocrinology, Wilhelmina Children’s Hospital, University Medical Center, Lundlaan, EA Utrecht, The Netherlands
Search for other papers by B Bakker in
Google Scholar
PubMed
Wilhelmina Children’s Hospital, University Medical Center, Lundlaan, EA Utrecht, The Netherlands
Search for other papers by M M van den Heuvel-Eibrink in
Google Scholar
PubMed
Department of Radiology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
Search for other papers by M H Lequin in
Google Scholar
PubMed
Search for other papers by J van der Lugt in
Google Scholar
PubMed
Search for other papers by L Meijer in
Google Scholar
PubMed
Search for other papers by A Y N Schouten-van Meeteren in
Google Scholar
PubMed
Department of Pediatric Endocrinology, Wilhelmina Children’s Hospital, University Medical Center, Lundlaan, EA Utrecht, The Netherlands
Search for other papers by H M van Santen in
Google Scholar
PubMed
included in this study (Supplementary Table 1). Of them, 49.1% (79/161) were female and the median age at diagnosis of the supratentorial midline LGG was 4.7 years (range: 0.1–17.9). Of all patients, 75.0% (111/148) had experienced one or more tumor
National Center for Children’s Health, Beijing, China
Search for other papers by Yi Wang in
Google Scholar
PubMed
Search for other papers by Yingying Xu in
Google Scholar
PubMed
Search for other papers by Rongrong Xie in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Bingyan Cao in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Yuan Ding in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Jiayun Guo in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Xiaoqiao Li in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Xiaolin Ni in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Zheng Yuan in
Google Scholar
PubMed
Search for other papers by Linqi Chen in
Google Scholar
PubMed
Search for other papers by Liyang Liang in
Google Scholar
PubMed
National Center for Children’s Health, Beijing, China
Search for other papers by Chunxiu Gong in
Google Scholar
PubMed
’s Hospital, Capital Medical University. Written informed consent was obtained from the parents or legal guardians of the patients. Results Patient characteristics Sixteen patients (male:female ratio, 8:8) were diagnosed with ROHHAD syndrome over
Division of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands
Search for other papers by J Van Schaik in
Google Scholar
PubMed
Department of Exercise Physiology, Child Development & Exercise Center, Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
Search for other papers by M Burghard in
Google Scholar
PubMed
Department of Radiology, Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
Search for other papers by M H Lequin in
Google Scholar
PubMed
Department of Radiology, Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
Search for other papers by E A van Maren in
Google Scholar
PubMed
Search for other papers by A M van Dijk in
Google Scholar
PubMed
Department of Exercise Physiology, Child Development & Exercise Center, Wilhelmina Children’s Hospital, University Medical Center Utrecht, Utrecht, The Netherlands
Search for other papers by T Takken in
Google Scholar
PubMed
Search for other papers by L B Rehorst-Kleinlugtenbelt in
Google Scholar
PubMed
Division of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands
Search for other papers by B Bakker in
Google Scholar
PubMed
Search for other papers by L Meijer in
Google Scholar
PubMed
Search for other papers by E W Hoving in
Google Scholar
PubMed
Institute of Mathematics, Leiden University, Leiden, The Netherlands
Search for other papers by M Fiocco in
Google Scholar
PubMed
Search for other papers by A Y N Schouten-van Meeteren in
Google Scholar
PubMed
Division of Pediatric Oncology, University Medical Centre Groningen, Groningen, The Netherlands
Search for other papers by W J E Tissing in
Google Scholar
PubMed
Division of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands
Search for other papers by H M van Santen in
Google Scholar
PubMed
. Analyses were performed by using SPSS version 25.0. Results Patient characteristics Among the 67 children with suspected HD and weight gain or obesity, 38 (56.7%) were female. Mean age at brain injury diagnosis was 6.8 years ± 4.2 and mean age
Department of Infectious Diseases, Copenhagen University Hospital – Amager and Hvidovre, Hvidovre, Denmark
Search for other papers by Clara Lundetoft Clausen in
Google Scholar
PubMed
Search for other papers by Trine Holm Johannsen in
Google Scholar
PubMed
Search for other papers by Niels Erik Skakkebæk in
Google Scholar
PubMed
Search for other papers by Hanne Frederiksen in
Google Scholar
PubMed
Centre for Physical Activity Research, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Search for other papers by Camilla Koch Ryrsø in
Google Scholar
PubMed
Search for other papers by Arnold Matovu Dungu in
Google Scholar
PubMed
Search for other papers by Maria Hein Hegelund in
Google Scholar
PubMed
Search for other papers by Daniel Faurholt-Jepsen in
Google Scholar
PubMed
Centre for Physical Activity Research, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Search for other papers by Rikke Krogh-Madsen in
Google Scholar
PubMed
Centre for Physical Activity Research, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
Search for other papers by Birgitte Lindegaard in
Google Scholar
PubMed
Center for Clinical Research and Prevention, Copenhagen University Hospital – Bispebjerg and Frederiksberg, Copenhagen, Denmark
Search for other papers by Allan Linneberg in
Google Scholar
PubMed
Search for other papers by Line Lund Kårhus in
Google Scholar
PubMed
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
Search for other papers by Anders Juul in
Google Scholar
PubMed
Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark
Search for other papers by Thomas Benfield in
Google Scholar
PubMed
hormones. To our knowledge, this study provides novel insight regarding a significant association between the suppression of female pituitary hormones and morbidity in COVID-19. When we compare the results of the mortality analysis in the second cohort
Search for other papers by Lingjuan Li in
Google Scholar
PubMed
Search for other papers by Jing Qin in
Google Scholar
PubMed
Search for other papers by Lin Ren in
Google Scholar
PubMed
Search for other papers by Shiyuan Xiang in
Google Scholar
PubMed
National Center for Neurological Disorders, Shanghai, China
Shanghai Clinical Medical Center of Neurosurgery, Shanghai, China
Neurosurgical Institute of Fudan University, Shanghai, China
Shanghai Key Laboratory of Medical Brain Function and Restoration and Neural Regeneration, Fudan University, Shanghai, China
Search for other papers by Xiaoyun Cao in
Google Scholar
PubMed
Search for other papers by Xianglan Zheng in
Google Scholar
PubMed
Search for other papers by Zhiwen Yin in
Google Scholar
PubMed
National Center for Neurological Disorders, Shanghai, China
Shanghai Clinical Medical Center of Neurosurgery, Shanghai, China
Neurosurgical Institute of Fudan University, Shanghai, China
Shanghai Key Laboratory of Medical Brain Function and Restoration and Neural Regeneration, Fudan University, Shanghai, China
Search for other papers by Nidan Qiao in
Google Scholar
PubMed
prolonged postoperative hypernatremia Gender 0.006 Male Reference Female 3.01 1.39 6.75 Stalk preserved 0.028 Yes Reference No 1.86 1.10 3.37 Puget classification
Search for other papers by Kevin C J Yuen in
Google Scholar
PubMed
Search for other papers by Gudmundur Johannsson in
Google Scholar
PubMed
Search for other papers by Ken K Y Ho in
Google Scholar
PubMed
Search for other papers by Bradley S Miller in
Google Scholar
PubMed
Search for other papers by Ignacio Bergada in
Google Scholar
PubMed
Search for other papers by Alan D Rogol in
Google Scholar
PubMed
continuing GH therapy is indicated. GH therapy does not provide any height benefit after the attainment of skeletal maturity due to epiphyseal closure (bone age ~15 years in females, ~17 years in males). However, continued GH therapy during the transition