Hypertensive encephalopathy in children with malignant disease

POLG1 manifestations in childhood.

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DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis.

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Insufficient energy and nutrient intake in children with motor disability.

Acta paediatrica (Oslo, Norway : 1992)·2009

High-dose vitamin D supplementation in children with cerebral palsy or neuromuscular disorder.

Neuropediatrics·2007

Cerebroretinal microangiopathy with calcifications and cysts.

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Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients.

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Brain Abscess as the Initial Manifestation of Hereditary Hemorrhagic Telangiectasia in a Child.

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Autonomic-Related Symptoms and Their Link to Autonomic Function and Post-concussion Symptoms in Youth Post-concussion.

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Continuous Electroencephalographic Characterization of Late Seizures in Traumatic Brain Injury With a Biphasic Clinical Course and Late Reduced Diffusion: A Case Series.

Pediatric neurology·2026

Clinical Utility and Measurement Properties of Balance Measures in Duchenne Muscular Dystrophy: A Scoping Review.

Pediatric neurology·2026

The Effect of Inspiratory Muscle Training on Respiratory Parameters, Trunk Control, Gait, and Functional Independence in Children With Cerebral Palsy: A Randomized Controlled Trial.

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Congenital heart diseases involving congenitally diseased pulmonary valve phenotypes: Novel insights into the health care burden across the life course.

JTCVS open·2026

Rhabdomyosarcoma in Children: A Retrospective Analysis of 12 Cases.

Cureus·2026

Development and Validation of a Prediction Model for Early ARDS in Children with Sepsis in the PICU: A Multicenter Retrospective Cohort Study.

Journal of multidisciplinary healthcare·2026

The silent zone of paediatric asthma: integrating small airway dysfunction assessment into clinical practice.

EClinicalMedicine·2026

Characteristics and outcomes of pediatric extracorporeal cardiopulmonary resuscitation (E-CPR): a nationwide retrospective analysis from the French pediatric ECMO Network.

Annals of intensive care·2026

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Molecular genetics and metabolism reports·2026

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Hypertensive encephalopathy in children with malignant disease

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POLG1 manifestations in childhood.

DARS2 mutations in mitochondrial leucoencephalopathy and multiple sclerosis.

Insufficient energy and nutrient intake in children with motor disability.

High-dose vitamin D supplementation in children with cerebral palsy or neuromuscular disorder.

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Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients.

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Hypertensive encephalopathy in children with malignant disease

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