Results 141 to 150 of about 59,066 (338)

Prognosis of Dysphagia in Pediatric Patients With Vocal Fold Immobility

Otolaryngology–Head and Neck Surgery, EarlyView.
Abstract Objective This study aims to determine the incidence and prognosis of dysphagia in pediatric patients with true vocal fold (TVF) immobility or hypomobility. Study Design A single‐center retrospective chart review. Setting A single‐institution tertiary‐care center.
Rachel Georgopoulos, Khashayar Arianpour, Samantha Anne   +2 more
wiley   +1 more source

Minimizing skull defects in retrosigmoid approach: precision mapping of the sigmoid sinus with mastoid emissary vein canal

Ukrainian Neurosurgical Journal
Objective. The retrosigmoid approach is a commonly used cranial approach to the cerebellopontine angle lesions, vascular and nerve pathologies.
Artem V. Rozumenko, Mykola V. Yehorov, Vasyl V. Shust, Dmytro M. Tsiurupa, Anton M. Dubrovka, Petro M. Onishchenko, Volodymyr O. Fedirko   +6 more
doaj   +1 more source

An Arbitrary-Modal Fusion Network for Volumetric Cranial Nerves Tract Segmentation [PDF]

arXiv
The segmentation of cranial nerves (CNs) tract provides a valuable quantitative tool for the analysis of the morphology and trajectory of individual CNs. Multimodal CNs tract segmentation networks, e.g., CNTSeg, which combine structural Magnetic Resonance Imaging (MRI) and diffusion MRI, have achieved promising segmentation performance.
arxiv  

Optimized Cranial Bandeau Remodeling [PDF]

arXiv, 2019
Craniosynostosis, a condition affecting 1 in 2000 infants, is caused by premature fusing of cranial vault sutures, and manifests itself in abnormal skull growth patterns. Left untreated, the condition may lead to severe developmental impairment. Standard practice is to apply corrective cranial bandeau remodeling surgery in the first year of the infant ...
arxiv  

Paragangliomas and paraganglioma syndromes [PDF]

, 2007
Paragangliomas are rare tumors of neural crest origin.
Davidoff, J., De Bleser, R.
core   +2 more sources

Wilms Tumor in Children with AMER1/WTX Germline Pathogenic Variants: A Multicenter Case Series

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background 10–15% of children with Wilms tumor (WT) have predisposing genetic syndromes. Somatic mutations are frequently identified; however, germline pathogenic variants in AMER1 are much less prevalent and are associated with osteopathia striata with cranial sclerosis (OSCS).
Insiyah Campwala, Jaclyn Schienda, Andrew J. Murphy, Basil Hashimi, Taylor Perry, Nicholas Cost, Junne Kamihara, Elizabeth A. Mullen, Teresa Santiago, Marcus M. Malek   +9 more
wiley   +1 more source

Treatment‐Related Risk Factors for Diabetes Mellitus in Childhood Cancer Survivors—A Case‐Cohort Study Within Adult Life After Childhood Cancer in Scandinavia (ALiCCS)

Pediatric Blood &Cancer, EarlyView.
ABSTRACT The aim was to identify treatment‐related risk factors for diabetes in 5‐year survivors of childhood cancer (CCS). This case‐cohort study within Adult Life after Childhood Cancer in Scandinavia (ALiCCS) included 140 CCS with diabetes and a subcohort of 390 randomly selected CCS.
Line Kenborg, Peter H. Asdahl, Smita Bhatia, Jane Christensen, Thorgerdur Gudmundsdottir, Lars Hjorth, Rebecca Howell, Anja Krøyer, Morten Jørgensen, Michael R. T. Laursen, Yasmin Lassen‐Ramshad, Sofie de fine Licht, Thomas Tjørnelund Nielsen, Catherine Rechnitzer, Susan A. Smith, Thomas Wiebe, Henrik Hasle, Anna S. Holmqvist, the ALiCCS study group   +18 more
wiley   +1 more source

Osteoblastoma of the Lateral Skull Base: Work-Up, Surgical Management, and a Review of the Literature”

Journal of Neurological Surgery Reports, 2013
Objectives To describe the work-up and surgical management of an osteoblastoma involving the lateral skull base. Typically occurring in the spine or long bones, osteoblastomas of the craniofacial skeleton are exceedingly rare and infrequently reported. A
Craig Miller, Rihan Khan, G. Michael Lemole Jr., Abraham Jacob   +3 more
doaj   +1 more source

Clinical Outcome and Risk Factors for Progression of Prenatally Diagnosed Fetal Ventriculomegaly: A Retrospective Multicenter Study

Prenatal Diagnosis, EarlyView.
ABSTRACT Objective To investigate the clinical outcome of fetuses with ventriculomegaly (VM), and to identify risk factors for progression of fetal VM in order to improve prenatal counseling. This was a multicenter, retrospective cohort study, comprising 229 cases with VM.
Anouk Moens, Zoe Albersnagel, Marieke B. Veenhof, Phebe N. Adama van Scheltema, Esther Sikkel, Mariëtte J. V. Hoffer, Brigitte H. W. Faas, Dineke Westra, Ilse Feenstra, Emilia K. Bijlsma, Gijs W. E. Santen, Corrie E. Erasmus, Cacha M. P. C. D. Peeters‐Scholte   +12 more
wiley   +1 more source

Horner syndrome in a pediatric patient

Pediatric Investigation, EarlyView.
Horner syndrome (HS) is a rare neurological disorder arising from disruption of the oculosympathetic pathway. paediatric HS is uncommon and may be congenital, however it is imperative that underlying sinister causes are excluded. ABSTRACT Introduction Horner syndrome (HS) is a rare neurological disorder arising from disruption of the oculosympathetic ...
Devansh Tandon, Matthew Azzopardi, Dominic Fenn, Mira Parmar, Saurabh Jain   +4 more
wiley   +1 more source