Results 251 to 260 of about 75,210 (379)

Outcomes following feeding gastrostomy (FG) insertion in patients with learning disability: a retrospective cohort study using the health improvement network (THIN) database [PDF]

, 2019
Philip Harvey, Tom Thomas, Joht Singh Chandan, Neeraj Bhala, Krishnarajah Nirantharakumar, Nigel Trudgill   +5 more
openalex   +1 more source

Healthcare Utilisation and Barriers and Facilitators of Healthcare Access for Young People With Intellectual Disability: A Systematic Review

Journal of Intellectual Disability Research, Volume 70, Issue 2, Page 130-161, February 2026.
ABSTRACT Background Young people with intellectual disability may exhibit poorer general health, higher mortality rates and greater limitations from physical or mental illnesses compared to the general population. It is important to understand how this may relate to healthcare utilisation, including factors influencing healthcare access for young ...
Felicia Kreps, Shalini Wijekulasuriya, Yvonne Zurynski, Rebecca Mitchell   +3 more
wiley   +1 more source

Unusual Complication of Percutaneous Gastrostomy Tube Replacement. [PDF]

ACG Case Rep J
Liang SR, Ketwaroo G, Njei B, Ogurick A, Rabiee A, Protiva P.   +5 more
europepmc   +1 more source

Quantification of head and neck cancer patients' anatomical changes during radiotherapy: Toward the prediction of replanning need

Journal of Applied Clinical Medical Physics, Volume 27, Issue 1, January 2026.
Abstract Background Head and neck cancer (HNC) patients undergoing radiotherapy (RT) may experience anatomical changes during treatment, which can compromise the validity of the initial treatment plan, necessitating replanning. However, ad hoc replanning disrupts clinical workflows and increases workload.
Odette Rios‐Ibacache, James Manalad, Kayla O'Sullivan‐Steben, Emily Poon, Luc Galarneau, Julia Khriguian, George Shenouda, John Kildea   +7 more
wiley   +1 more source

Gastropexy device impaction in children with push percutaneous endoscopic gastrostomy. [PDF]

Sci Rep
Viart J, Antoine M, Aumar M, Tran LC, Guimber D, Coopman S, Saingier C, Leroy M, Ley D, Gottrand F.   +9 more
europepmc   +1 more source

ANAESTHETIC MANAGEMENT OF A CHILD WITH OTAHARA SYNDROME PLANNED FOR LAPAROSCOPIC FUNDOPLICATION, FEEDING GASTROSTOMY AND UMBILICAL HERNIA REPAIR -A CASE REPORT. [PDF]

Dr Madhava Pai K, Daniela Maldonado J, Ashley R. Dennison   +2 more
openalex   +1 more source

Characteristics of Cerebral Palsy in the Midwestern US

Annals of Clinical and Translational Neurology, Volume 13, Issue 1, Page 21-35, January 2026.
ABSTRACT Objective Cerebral palsy (CP) is the most common lifelong motor disability worldwide. Yet, data is limited on how CP manifests in the US. Our objective was to characterize and determine factors affecting functional outcomes in a large population of young people with CP in the Midwestern US.
Susie Kim, Kelsey Steffen, Lauren Gottschalk‐Henneberry, Jennifer Miros, Amy Robichaux‐Viehoever, Karen Taca, Bhooma R. Aravamuthan   +6 more
wiley   +1 more source

Safety and feasibility of tracheostomy and gastrostomy home replacement: a five-year experience from a palliative care center. [PDF]

Front Pediatr
Burlo F, Bortolin I, Grasso DL, Oveglia A, Barbi E, De Zen L, Taucar V, Peri F.   +7 more
europepmc   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

Annals of Clinical and Translational Neurology, Volume 13, Issue 1, Page 108-121, January 2026.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco, Mònica Roldán, Yalda Jamshidi, Ioannis Georvasilis, Rocío Jadraque Rodríguez, Reza Boostani, Ali Shoeibi, Lluís Armengol, Anna Codina, Ehsan Ghayoor Karimiani, Cristina Hernando‐Davalillo, Loreto Martorell, María Luisa Ramírez Almaraz, Jordi Muchart, Carlos Ortez, Andrés Nascimento, Roser Urreizti, Daniel Natera‐de Benito, Mercedes Serrano   +18 more
wiley   +1 more source

Growth Differentiation Factor 15 Elevation in the Central Nervous System Is Associated With Failure to Thrive in Alexander Disease

Annals of Clinical and Translational Neurology, Volume 13, Issue 1, Page 144-156, January 2026.
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann, Michelle M. Sonsalla, Cora Luzinski, Fernando Zacahua, David A. Harris, Dudley W. Lamming, Albee Messing   +6 more
wiley   +1 more source