Results 41 to 50 of about 1,421,260 (161)

Contrast‐Enhanced Ultrasound in the Diagnosis of Parotid Gland Castleman Disease in a Child

Journal of Clinical Ultrasound, EarlyView.
A 16‐year‐old girl with slowly progressive painless right parotid swelling. MRI demonstrated a T2‐hyperintense, markedly enhancing lesion suggestive of a vascular malformation. Fine‐needle aspiration yielded nonspecific lymphoid tissue. CEUS demonstrated rapid homogeneous enhancement of a hypervascular solid mass, raising suspicion for Castleman ...
Sruthilatha Sakthi Velavan, Shanelle De Lancy, Diane W. Chen, Boaz Karmazyn   +3 more
wiley   +1 more source

Supporting mental health conversations among youth with neurodevelopmental disorders through digital storytelling: A co‐produced study

JCPP Advances, EarlyView.
Abstract Background Youth (aged 15–24 years) diagnosed with neurodevelopmental disorders (NDD) experience higher rates of co‐occurring mental health challenges and disparities in receiving timely care. A significant barrier to support is a lack of guidance for healthcare professionals (HCPs) on delivering conversations about co‐occurring mental health ...
Patrick Jachyra, Yona Lunsky, Andrada Cretu, Elim Chan, Noah Barnett, Michael Barnett, Sheldon Gaboury, Cathy Gaboury, Austin Cosgrove, Susan Cosgrove, Claudine Aquino‐Evangelista, Carla Southward, Evdokia Anagnostou   +12 more
wiley   +1 more source

Shaping the research agenda of pediatric gastroenterology, hepatology, and nutrition: The proposal from an Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) expert group

JPGN Reports, EarlyView.
Abstract The Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) recognized the need to define research priorities and identify knowledge gaps to guide future investigations in pediatric digestive health. Following international examples, SIGENP aimed to provide a structured framework that aligns scientific innovation with ...
Carlo Agostoni, Daniele Alberti, Renata Auricchio, Maria Elisabetta Baldassarre, Osvaldo Borrelli, Matteo Bramuzzo, Teresa Capriati, Carlo Catassi, Sabrina Cenni, Marco Crocco, Salvatore Cucchiara, Luigi Dall'Oglio, Paola De Angelis, Marco Deganello Saccomani, Fabiola Di Dato, Angelo Di Giorgio, Antonella Diamanti, Valeria Dipasquale, Enrico Felici, Ruggiero Francavilla, Valentina Giorgio, Luigi Greco, Raffaele lorio, Flavio Labriola, Paolo Lionetti, Elena Lionetti, Giuseppe Maggiore, Monica Malamisura, Claudia Mandato, Antonio Marseglia, Emanuele Nicastro, Lorenzo Norsa, Salvatore Oliva, Licia Pensabene, Elena Sofia Pieri, Paolo Quitadamo, Giusy Ranucci, Sara Renzo, Claudio Romano, Silvia Salvatore, Luca Scarallo, Maria Immacolata Spagnuolo, Annamaria Staiano, Caterina Strisciuglio, Renato Tambucci, Riccardo Troncone, Pietro Vajro   +46 more
wiley   +1 more source

FDG PET-MRI evaluation of synchronous gallbladder adenocarcinoma and POEMS syndrome

Radiology Case Reports, 2022
POEMS syndrome is a rare paraneoplastic syndrome associated with a plasma cell proliferative disorder. Gallbladder adenocarcinoma is a rare malignancy, with no association with POEMS syndrome.
Fatemeh Ataei, MD, Akash Sharma, MD, Rupert Stanborough, MD, Ephraim E. Parent, MD, PhD   +3 more
doaj   +1 more source

Alcohol Misuse Link to POEMS Syndrome in a Patient [PDF]

, 2017
Previously called Crow–Fukase syndrome, POEMS syndrome is characterized by poly-neuropathy, osteo-sclerotic myeloma, organomegaly, endocrinopathy, monoclonal plasma cell disorder, and skin changes.
Cohen, Lawrence B., Neuman, Manuela G., Lawrence Cohen, Susan Goodwin, Goodwin, Susan E., John Neary, Neary, John, Manuela Neuman   +7 more
core   +1 more source

Anthropometric patterns in children with moderate‐to‐severe atopic dermatitis: Cross‐sectional insights from the TREATkids cohort

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary Background and objectives The relationship between atopic dermatitis (AD), weight, height, and body mass index (BMI) in children and adolescents and the impact of systemic treatments is controversial. We report the distribution of weight, height, and BMI in the German TREATkids cohort compared to a standardized German cohort (Kromeyer‐Hauschild)
Barbara Kind, Doreen Siegels, Hagen Ott, Susanne Abraham, René Sachse, Katharina Lönnecke, Inken Harder, Annice Heratizadeh, Katja Nemat, Christian Vogelberg, Dora Stölzl, Ines Gellhaus, Susanne Lau, Mehrak Yoosefi Moridani, Thomas Werfel, Stephan Weidinger, Jochen Schmitt, the TREATgermany study group   +17 more
wiley   +1 more source

Case report: POEMS syndrome in childhood

, 2008
POEMS syndrome is a rare multisystem disorder, which is characterized by polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes.
Hatipoglu, Sami, Dogan, Oner, Salihoglu, Bahar, Sevketoglu, Esra, Ayan, Inci   +4 more
core   +1 more source

A case of recurrent pleural effusion: tuberculous pleurisy or other disease? A case report

BMC Geriatrics
Background POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes) is a paraneoplastic syndrome caused by a plasma cell proliferative disorder.
Yuanhao Ji, Jinsun Yang
doaj   +1 more source

Emerging Resistance in the Digital Transformation of Public Transport: Older Passengers With Dementia and Experiences of Ecobiographical Disruption

Information Systems Journal, EarlyView.
ABSTRACT The digital transformation of public transport is prone to resistance. Among the discontents of such transformation, older people and those living with cognitive impairments are repeatedly identified. Stereotypes assuming their innate resistance to technological change are widespread, but research shows that older people with dementia can have
James Rupert Fletcher
wiley   +1 more source

Pentraxin-3 and VEGF in POEMS syndrome: a 2-year longitudinal study.

, 2014
Circulating Pentraxin 3 (PTX3) and vascular endothelial growth factor (VEGF) levels were measured longitudinally (mean follow-up 2 years) by ELISA in 6 patients with polyneuropathy, organomegaly, endocrinopathy, M-protein, skin changes (POEMS) syndrome ...
Lessi, F., Lauria G, Cavallaro, T., Scarlato M, Lessi F, Cavallaro T, Campagnolo, M., Manfredi AA, Lucchetta, M., Briani, C., Adami, F., Cabrini I, Ferrari S, DALLA TORRE, CHIARA, ADAMI, FAUSTO, Morbin M, Cabrini, I., Torre, C. D., Ferrari, S., Campagnolo M, BRIANI, CHIARA, Lucchetta M, Scarlato, M., Manfredi, A. A., Morbin, M., G. LAURIA PINTER, Lauria G., Lessi F., Scarlato M., Briani C., Lucchetta M., Morbin M., Adami F, Torre CD, CABRINI, Ilaria, Campagnolo M., Dalla Torre C., Briani C, Manfredi A. A., CAVALLARO, Tiziana, FERRARI, Sergio, Adami F., MANFREDI , ANGELO ANDREA M. A.   +42 more
core   +2 more sources