Clinical Variability of GLUT1DS
Investigators from Pavia, Rho, Brescia and Milan, Italy, studied 22 patients diagnosed with GLUT1 deficiency syndrome (GLUT1DS) to document clinical or genetic differences between patients with familial <em>SLC2A1</em> gene mutations (n=11) and those with sporadic mutations (n=11).
Saved in:
Main Authors: | Anastasia Martinez-Esteve Melnikova (Author), Christian M Korff (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
2015-02-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Characterization of Speech and Language Phenotype in GLUT1DS
by: Martina Paola Zanaboni, et al.
Published: (2021) -
Timing of Ketogenic Dietary Therapy (KDT) Introduction and Its Impact on Cognitive Profiles in Children with Glut1-DS-A Preliminary Study
by: Martina Barthold, et al.
Published: (2023) -
Expanding Genetic and Clinical Spectrum of GLUT1D
by: J Gordon Millichap
Published: (2010) -
Peritoneal expression of SGLT-2, GLUT1 and GLUT3 in peritoneal dialysis patients
by: Severin Schricker, et al.
Published: (2021) -
GLUT-1 Expression in Breast Cancer
by: Oguzhan OKCU, et al.
Published: (2022)