Results 131 to 140 of about 4,837 (273)

Endoscopic Ultrasound‐Guided Ethanol Ablation for Benign Insulinoma: A Single‐Centre Experience and Literature Review

open access: yesClinical Endocrinology, EarlyView.
ABSTRACT Objectives Insulinoma is a predominantly benign pancreatic neuroendocrine tumour that is traditionally managed surgically. However, surgical invasiveness and anaesthesia‐related risks limit its applicability in selected patients. Endoscopic ultrasound (EUS)‐guided ethanol ablation has emerged as a minimally invasive alternative.
Yuchao Wu   +15 more
wiley   +1 more source

Paciente con enfermedad de Crohn y convulsiones por hipomagnesemia [PDF]

open access: yes, 2007
Se trata de un paciente con enfermedad de Crohn y afectación intestinal extensa por su enfermedad, que presenta episodios repetidos de convulsiones generalizadas.
Fernández-Rodríguez,E.   +1 more
core  

Pharmacological and non‐pharmacological interventions for managing sleep disorders in children with cerebral palsy: A systematic review

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
xxxxxx Aim To systematically review the effectiveness, safety, and economic evidence of pharmacological and non‐pharmacological interventions for sleep disorders in children with cerebral palsy (CP). Method Databases including MEDLINE, Embase, CENTRAL (the Cochrane Library), International Clinical Trials Registry Platform of the World Health ...
Nishant Jaiswal   +11 more
wiley   +1 more source

Las convulsiones y la epilepcia

open access: yes, 2010
¿Qué es la epilepsia?/Causas de epilepsia/Métodos de diagnostico/Tratamiento/Consideraciones psicosociales/Nuevas terapias/Recomendaciones en caso de presentarse una convulsión.
Takeuchi Tan, Yuri   +2 more
openaire   +1 more source

Comportamiento de la mutación mtDNA A3243G en dos familias antioqueñas de pacientes diagnosticados con el síndrome MELAS

open access: yesIatreia, 2010
Introducción: mutaciones en mtDNA causan citopatias mitocondriales, la más común de ellas es el síndrome MELAS; la transición A3243G en tRNA de leucina (tRNALeu) se presenta en 80% de pacientes.
María Victoria Parra Marín   +4 more
doaj  

Perinatal, socioenvironmental, and neurological factors to predict motor delay in infants born preterm

open access: yesDevelopmental Medicine &Child Neurology, EarlyView.
Abstract Aim To determine the best combination of perinatal characteristics, socioenvironmental factors, and neurological examination at term‐equivalent age for identifying motor delay at 3 months 2 weeks corrected age in infants born preterm between 29 weeks and 36 weeks of gestation.
Melanie Gagnon   +8 more
wiley   +1 more source

Newly identified human aminoacyl‐tRNA synthetase complex interacting multifunctional protein 2 (AIMP2) loss‐of‐function mutations cause neurodevelopmental defects linked to cell death in a zebrafish model

open access: yesThe FEBS Journal, EarlyView.
Human AIMP2 mutations lead to severe neurodevelopmental defects and brain atrophy. Using patient‐derived fibroblasts from two individuals, we show decreased AIMP2 protein levels and overall protein synthesis. In a zebrafish loss‐of‐function model, the lack of AIMP2 leads to an increase in cell death and results in smaller brains.
Patrick Mullen   +10 more
wiley   +1 more source

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