Carmen M. Burloiu

Bucharest, B 041914, Romania

Last Updated: 09/26/2026

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Found 10 publications

Brain Matters in Duchenne Muscular Dystrophy: DMD Mutation Sites and Their Association with Neurological Comorbidities Through Isoform Impairment.

Brain Matters in Duchenne Muscular Dystrophy: DMD Mutation Sites and Their Association with Neurological Comorbidities Through Isoform Impairment.

Journal: Genes

Published: November 30, 2025

Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective Study.

Duchenne and Becker Muscular Dystrophies in Romania: a 10-year Retrospective Study.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: May 23, 2025

Age-Onset-Related Particularities of Pediatric MS-Understanding the Spectrum: A Tertiary Center Experience.

Age-Onset-Related Particularities of Pediatric MS-Understanding the Spectrum: A Tertiary Center Experience.

Journal: Diseases (Basel, Switzerland)

Published: April 15, 2025

Overtime Challenges of Diagnosis and Treatment in Two Pediatric Patients with Extensive Cerebral Tumefactive Lesions Indicative of Baló's Type Multiple Sclerosis.

Overtime Challenges of Diagnosis and Treatment in Two Pediatric Patients with Extensive Cerebral Tumefactive Lesions Indicative of Baló's Type Multiple Sclerosis.

Journal: Children (Basel, Switzerland)

Published: April 14, 2025

Pediatric-Onset Multiple Sclerosis (POMS) and Epilepsy: Exploring Etiological Complexity-Outcomes from a Single-Center Experience.

Pediatric-Onset Multiple Sclerosis (POMS) and Epilepsy: Exploring Etiological Complexity-Outcomes from a Single-Center Experience.

Journal: Children (Basel, Switzerland)

Published: April 14, 2025

Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies-Data from a Romanian Cohort.

Phenotypic and Genotypic Spectrum of Early-Onset Developmental and Epileptic Encephalopathies-Data from a Romanian Cohort.

Journal: Genes

Published: May 09, 2022

A case of Bardet-Biedl syndrome caused by a recurrent variant in BBS12: A case report.

A case of Bardet-Biedl syndrome caused by a recurrent variant in BBS12: A case report.

Journal: Biomedical reports

Published: August 03, 2021

Neurofibromatosis type 1 associated with moyamoya syndrome. Case report and review of the literature.

Neurofibromatosis type 1 associated with moyamoya syndrome. Case report and review of the literature.

Journal: Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie

Published: October 29, 2019

Ketogenic Diet in Patients with GLUT1 Deficiency Syndrome.

Ketogenic Diet in Patients with GLUT1 Deficiency Syndrome.

Journal: Maedica

Published: September 17, 2019

Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea.

Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea.

Journal: American journal of human genetics

Published: April 04, 2016

Showing 1-10 of 10

Last Updated: 09/26/2026