Results 171 to 180 of about 70,134 (376)

Robotic surgery for paediatric neurogenic lower urinary tract dysfunction: a systematic review

open access: yesBJU International, Volume 135, Issue 4, Page 557-566, April 2025.
Objective To evaluate in a systematic review the outcomes, benefits, and limitations of robot‐assisted surgeries for paediatric neurogenic lower urinary tract dysfunction (LUTD), as robot‐assisted techniques have emerged as a potential alternative, offering enhanced precision, dexterity, and visualisation.
Ihtisham Ahmad   +6 more
wiley   +1 more source

Development and Content Validity of the International Association for Disability and Oral Health Universal Case Mix Tool: A Consensus Study

open access: yesCommunity Dentistry and Oral Epidemiology, EarlyView.
ABSTRACT Objectives To develop the International Association for Disability and Oral Health Universal Case Mix Tool (iADH UCMT) that rates case complexity in the delivery of oral healthcare. Methods A modified e‐Delphi survey sought consensus on the content of a universal Case Mix Tool to rate the degree of adaptation over and above that required for ...
Caoimhin Mac Giolla Phadraig   +4 more
wiley   +1 more source

Advantages of Percutaneous Endoscopic Gastrostomy Tube Placement in Patients with Head and Neck Cancer who Receive Radiation as Part of Their Treatment [PDF]

open access: yes, 2018
The use of percutaneous endoscopic gastrostomy tubes as an intervention strategy in head and neck cancer was investigated in this retrospective chart review.
Thul, Nevin
core   +1 more source

Biallelic FGF4 Variants Linked to Thoracic Dystrophy and Respiratory Insufficiency

open access: yesClinical Genetics, EarlyView.
We report three people from two unrelated families with a clinical diagnosis of thoracic dystrophy characterized by short or missing ribs, narrow chest, and respiratory insufficiency. Affected people each have rare, biallelic, predicted deleterious missense substitutions in FGF4, a gene known to be essential for the formation of the thoracic skeleton ...
Laura M. Watts   +8 more
wiley   +1 more source

Production and Functional Verification of 8‐Gene (GGTA1, CMAH, β4GalNT2, hCD46, hCD55, hCD59, hTBM, hCD39)‐Edited Donor Pigs for Xenotransplantation

open access: yesCell Proliferation, EarlyView.
Schematic representation of generation of 8‐gene‐edited cloned pigs and their verification by pig to non‐human primate kidney xenotransplantation. ABSTRACT Gene‐edited (GE) pig‐to‐human xenotransplantation continues to make breakthroughs, but which kind of gene combination is suitable for organ‐specific transplantation remains unclear.
Jiaoxiang Wang   +23 more
wiley   +1 more source

Post-acute care and secondary prevention after ischaemic stroke [PDF]

open access: yes, 2011
Higgins, P.   +3 more
core   +1 more source

Comparison of fully versus partially covered metal stents in endoscopic ultrasound‐guided hepaticogastrostomy for malignant biliary obstruction (with video)

open access: yesDigestive Endoscopy, Volume 37, Issue 5, Page 532-540, May 2025.
Background Endoscopic ultrasound‐guided hepaticogastrostomy (EUS‐HGS) using a fully covered metal stent (FCMS) or partially covered metal stent (PCMS) is performed to manage unresectable malignant biliary obstruction (MBO) following unsuccessful endoscopic retrograde cholangiopancreatography.
Sung Hyun Cho   +4 more
wiley   +1 more source

Cerebral palsy and perinatal mortality in children born in Norway to immigrant mothers

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Plain language summary: https://onlinelibrary.wiley.com/doi/10.1111/dmcn.16271 Abstract Aim To compare the prevalence and clinical characteristics of cerebral palsy (CP), and perinatal mortality, in children born to non‐immigrant mothers with children born to immigrant mothers. Method This was a registry‐based cross‐sectional study.
Maria Wiedswang Sigholt   +5 more
wiley   +1 more source

Rare dysfunctional SCN2A variants are associated with malformation of cortical development

open access: yesEpilepsia, Volume 66, Issue 3, Page 914-928, March 2025.
Abstract Objective SCN2A encodes the voltage‐gated sodium (Na+) channel α subunit NaV1.2, which is important for the generation and forward and back propagation of action potentials in neurons. Genetic variants in SCN2A are associated with a spectrum of neurodevelopmental disorders.
Jérôme Clatot   +19 more
wiley   +1 more source

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