Ana Salas-Camacho

Madrid, MD 28040, Spain

Last Updated: 09/26/2026

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Found 33 publications

Beyond Maximum Haemorrhage Grade: Serial Cranial Ultrasound Phenotyping Refines Developmental Risk Stratification After Intraventricular Haemorrhage in Very Preterm Infants.

Beyond Maximum Haemorrhage Grade: Serial Cranial Ultrasound Phenotyping Refines Developmental Risk Stratification After Intraventricular Haemorrhage in Very Preterm Infants.

Journal: Journal of clinical medicine
Published: June 19, 2026

Three-Domain Serial Cranial Ultrasound Phenotypes and Outcomes in Very Preterm Infants with Severe Brain Injury: A Single-Center Cohort Study.

Three-Domain Serial Cranial Ultrasound Phenotypes and Outcomes in Very Preterm Infants with Severe Brain Injury: A Single-Center Cohort Study.

Journal: Children (Basel, Switzerland)
Published: May 17, 2026

The transition of patients with neuromuscular diseases: recommendations of the Spanish Society of Pediatric Neurology and the Spanish Society of Neurology. Endorsed by SENEP, SEN, and ASEM.

The transition of patients with neuromuscular diseases: recommendations of the Spanish Society of Pediatric Neurology and the Spanish Society of Neurology. Endorsed by SENEP, SEN, and ASEM.

Journal: Neurologia
Published: February 05, 2025

Delphi study on epidemiology, clinical management, disease burden, and treatment of paediatric patients with Duchenne muscular dystrophy in Spain.

Delphi study on epidemiology, clinical management, disease burden, and treatment of paediatric patients with Duchenne muscular dystrophy in Spain.

Journal: Neurologia
Published: December 24, 2024

Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies.

Rapid Molecular Diagnosis of Genetically Inherited Neuromuscular Disorders Using Next-Generation Sequencing Technologies.

Journal: Journal of clinical medicine
Published: March 01, 2022

First female with Allan-Herndon-Dudley syndrome and partial deletion of X-inactivation center.

First female with Allan-Herndon-Dudley syndrome and partial deletion of X-inactivation center.

Journal: Neurogenetics
Published: April 03, 2021

New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy.

New genotype-phenotype correlations in a large European cohort of patients with sarcoglycanopathy.

Journal: Brain : a journal of neurology
Published: March 15, 2020

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.

Journal: Medicina clinica
Published: September 07, 2018

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.

Journal: Neurologia
Published: September 06, 2018

Autosomal dominant distal myopathy with nemaline rods due to p.Glu197Asp mutation in ACTA1.

Autosomal dominant distal myopathy with nemaline rods due to p.Glu197Asp mutation in ACTA1.

Journal: Neuromuscular disorders : NMD
Published: August 23, 2018

Steroids for familial acute necrotizing encephalopathy: A future investment?

Steroids for familial acute necrotizing encephalopathy: A future investment?

Journal: Clinical neurology and neurosurgery
Published: November 05, 2017

Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review.

Hydrocephalus in pyridoxine-dependent epilepsy: New case and literature review.

Journal: Brain & development
Published: October 05, 2017
Showing 1-12 of 33

Last Updated: 09/26/2026