Luis Solana-Gutierrez
Nino Jesus, MD, Spain
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 23 publications
Craniofacial features of POLR3-related leukodystrophy caused by biallelic variants in POLR3A, POLR3B and POLR1C.
Journal: Journal of medical genetics
Published: February 16, 2023
Value of Thyroid Peroxidase Antibodies in Neuroimmune Diseases: Analysis of Interference During Treatment with Intravenous Immunoglobulins.
Journal: Laboratory medicine
Published: March 21, 2022
The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1.
Journal: Clinical genetics
Published: December 20, 2021
Classic Ketogenic Diet and Modified Atkins Diet in SLC2A1 Positive and Negative Patients with Suspected GLUT1 Deficiency Syndrome: A Single Center Analysis of 18 Cases.
Journal: Nutrients
Published: January 15, 2021
Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy.
Journal: Brain : a journal of neurology
Published: December 22, 2020
Delineating the neurological phenotype in children with defects in the ECHS1 or HIBCH gene.
Journal: Journal of inherited metabolic disease
Published: April 03, 2020
Opsoclonus-myoclonus syndrome: Experience in a tertiary hospital in the last 12 years
Journal: Anales de pediatria
Published: October 05, 2019
Tocilizumab in pediatric refractory status epilepticus and acute epilepsy: Experience in two patients.
Journal: Journal of neuroimmunology
Published: September 28, 2019
Opsoclonus-myoclonus syndrome: Clinical characteristics, therapeutic considerations, and prognostic factors in a Spanish paediatric cohort.
Journal: Neurologia
Published: September 24, 2019
Opsoclonus-myoclonus syndrome: clinical characteristics, therapeutic considerations, and prognostic factors in a Spanish paediatric cohort.
Journal: Neurologia
Published: September 24, 2019
Last Updated: 09/26/2026