Glut1 Ds | List of Frontiers open access articles

Case Report

Published on 28 Jan 2021

A Challenging Diagnosis of Atypical Glut1-DS: A Case Report and Literature Review

in Neuromuscular Disorders and Peripheral Neuropathies

Miaomiao Yu
Jing Miao
Yudan Lv
Xue Wang
Wuqiong Zhang
Na Shao
Hongmei Meng

Frontiers in Neurology

doi 10.3389/fneur.2020.549331

6,683 views
6 citations

Original Research

Published on 13 Nov 2024

Epileptiform activity in brain organoids derived from patient with Glucose Transporter 1 Deficiency Syndrome

in Neurodegeneration

Y. Müller
L. Lengacher
F. Friscourt
C. Quairiaux
L. Stoppini
P. J. Magistretti
S. Lengacher
C. Finsterwald

Frontiers in Neuroscience

doi 10.3389/fnins.2024.1498801

4,948 views
5 citations

Case Report

Published on 22 Nov 2021

Clinical and Genetic Characteristics of Chinese Children With GLUT1 Deficiency Syndrome: Case Report and Literature Review

in Genetics of Common and Rare Diseases

Qingqing Hu
Yuechi Shen
Tangfeng Su
Yan Liu
Sanqing Xu

Frontiers in Genetics

doi 10.3389/fgene.2021.734481

6,169 views
14 citations

Original Research

Published on 16 May 2024

Analysis of dietary fats intake and lipid profile in Chilean patients with glucose transport type 1 deficiency syndrome: similarities and differences with the reviewed literature

in Clinical Nutrition

María Florencia Salazar
María Jesús Leal-Witt
Valentina Parga
Carolina Arias
Verónica Cornejo

Frontiers in Nutrition

doi 10.3389/fnut.2024.1390799

2,595 views

Case Report

Published on 31 May 2021

CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report

in Epilepsy

Chiara Scoppola
Giorgio Magli
Marta Conti
Maria Fadda
Giovanni M. Luzzu
Delia M. Simula
Alessandra Carta
Stefano Sotgiu
Susanna Casellato

Frontiers in Neurology

doi 10.3389/fneur.2021.679354

5,276 views
10 citations

Brief Research Report

Published on 23 Jun 2020

A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies

in Neurogenetics

Olimpia Musumeci
Edoardo Ferlazzo
Carmelo Rodolico
Antonio Gambardella
Monica Gagliardi
Umberto Aguglia
Antonio Toscano

Frontiers in Neurology

doi 10.3389/fneur.2020.00514

5,360 views
5 citations

Articles

A Challenging Diagnosis of Atypical Glut1-DS: A Case Report and Literature Review

Epileptiform activity in brain organoids derived from patient with Glucose Transporter 1 Deficiency Syndrome

Clinical and Genetic Characteristics of Chinese Children With GLUT1 Deficiency Syndrome: Case Report and Literature Review

Analysis of dietary fats intake and lipid profile in Chilean patients with glucose transport type 1 deficiency syndrome: similarities and differences with the reviewed literature

CACNA1A-Linked Hemiplegic Migraine in GLUT 1 Deficiency Syndrome: A Case Report

A Family With a Complex Phenotype Caused by Two Different Rare Metabolic Disorders: GLUT1 and Very-Long-Chain Fatty Acid Dehydrogenase (VLCAD) Deficiencies