Publications by authors named "Axel Panzer"

Claim this Profile
C
Characterization of the Epileptogenic Phenotype and Response to Antiseizure Medications in Lissencephaly Patients.
Christiane R Proepper, Sofia M Schuetz, Lisa-Maria Schwarz, Katja von Au, Thomas Bast, Axel Panzer

Neuropediatrics· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
U
Use of Sodium Channel Blockers in the Thr226Met Pathologic Variant of SCN1A: A Case Report.
Brenda Carolina Nájera-Chávez, Lea Seeber, Klaus Goldhahn, Axel Panzer

Neuropediatrics· December 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in plasticity-related-gene-1 (PRG-1) protein contribute to hippocampal seizure susceptibility and modify epileptic phenotype.
Ellen Knierim, Johannes Vogt, Michael Kintscher, Alexey Ponomarenko, Jan Baumgart, Axel Panzer

Cereb Cortex· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SIGLEC1 (CD169) as a potential diagnostical screening marker for monogenic interferonopathies.
Banu Orak, Gonza Ngoumou, Frédéric Ebstein, Barbara Zieba, Carl Christoph Goetzke, Axel Panzer

Pediatr Allergy Immunol· April 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Leukoencephalopathy with calcifications and cysts: Genetic and phenotypic spectrum.
Yanick J Crow, Heather Marshall, Gillian I Rice, Luis Seabra, Emma M Jenkinson, Axel Panzer

Am J Med Genet A· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Clinical features and blood iron metabolism markers in children with beta-propeller protein associated neurodegeneration.
Anezka Belohlavkova, Katalin Sterbova, Cornelia Betzler, Stuve Burkhard, Axel Panzer

Eur J Paediatr Neurol· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Severity Assessment in CDKL5 Deficiency Disorder.
Scott Demarest, Elia M Pestana-Knight, Heather E Olson, Jenny Downs, Eric D Marsh, Axel Panzer

Pediatr Neurol· August 2019

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, Carolina Uggenti, Anthony Oojageer, Axel Panzer

Nat Genet· January 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts.
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, Carolina Uggenti, Anthony Oojageer, Axel Panzer

Nat Genet· October 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Febrile infection-related epilepsy syndrome (FIRES): a nonencephalitic encephalopathy in childhood.
Andreas van Baalen, Martin Häusler, Rainer Boor, Axel Rohr, Jürgen Sperner, Axel Panzer

Epilepsia· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Wilhelmina G Leen, Joerg Klepper, Marcel M Verbeek, Maike Leferink, Tom Hofste, Axel Panzer

Brain· March 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis