Darius Ebrahimi‐Fakhari - AILBRY

Results for 'Darius Ebrahimi‐Fakhari' :

Restoring impaired protein metabolism in Parkinson's disease — TFEB‐mediated autophagy as a novel therapeutic target

Publication Year: 2013

DOI: https://doi.org/10.1002/mds.25601

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
- Lara Wahlster
Autophagy and neurodegeneration — genetic findings in SENDA syndrome, a subtype of neurodegeneration with brain iron accumulation, provide a novel link

Publication Year: 2013

DOI: https://doi.org/10.1002/mds.25563

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

Publication Year: 2017

DOI: https://doi.org/10.1002/mds.27045

Abstract:

Authors:
- Connie Marras
- Anthony E. Lang
- Bart P.C. van de Warrenburg
- Carolyn M. Sue
- Sarah J. Tabrizi
- Lars Bertram
- Saadet Mercimek‐Mahmutoglu
- Darius Ebrahimi‐Fakhari
- Thomas T. Warner
- Alexandra Dürr
- Birgit Assmann
- Katja Lohmann
- Vladimir Kostić
- Christine Klein
Parkinson's disease: A disorder of axonal mitophagy?

Publication Year: 2014

DOI: https://doi.org/10.1002/mds.26047

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
- Lara Wahlster
- Mustafa Şahin
Reply letter to Jinnah “Locus pocus” and Albanese “Complex dystonia is not a category in the new 2013 consensus classification”: Necessary evolution, no magic!

Publication Year: 2016

DOI: https://doi.org/10.1002/mds.26763

Abstract:

Authors:
- Christine Klein
- Anthony E. Lang
- Bart P.C. van de Warrenburg
- Carolyn M. Sue
- Sarah J. Tabrizi
- Lars Bertram
- Saadet Mercimek‐Mahmutoglu
- Darius Ebrahimi‐Fakhari
- Thomas T. Warner
- Alexandra Dürr
- Birgit Assmann
- Vladimir Kostić
- Katja Lohmann
- Connie Marras
Linking mitochondrial dysfunction to neurodegeneration in lysosomal storage diseases

Publication Year: 2017

DOI: https://doi.org/10.1007/s10545-017-0048-0

Abstract:

Authors:
- Afshin Saffari
- Stefan Kölker
- Georg F. Hoffmann
- Darius Ebrahimi‐Fakhari
Novel and de novo point and large microdeletion mutation in <i>PRRT2</i>‐related epilepsy

Publication Year: 2020

DOI: https://doi.org/10.1002/brb3.1597

Abstract:

Authors:
- Yang Li
- Cuiping You
- Shiyan Qiu
- Xiaofan Yang
- Yufen Li
- Feng Liu
- Dongqing Zhang
- Yue Niu
- XU Li-yun
- Na Xu
- Xia Li
- Fang Luo
- Jun‐Li Yang
- Baomin Li
International electives in the final year of German medical school education--a student's perspective.

Publication Year: 2014

DOI: https://doi.org/10.3205/zma000918

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
- Mridul Agrawal
- Lara Wahlster
Modeling Parkinson's disease in a dish — A story of yeast and men

Publication Year: 2013

DOI: https://doi.org/10.1002/mds.25781

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
- Lara Wahlster
EPG5 Variants with Modest Functional Impact Result in an Ameliorated and Primarily Neurological Phenotype in a 3.5-Year-Old Patient with Vici Syndrome

Publication Year: 2019

DOI: https://doi.org/10.1055/s-0039-1692129

Abstract:

Authors:
- Megan Kane
- Jiajun Zhao
- Julie A. Muskett
- Amelia Diplock
- Siddharth Srivastava
- Natalie Hauser
- John F. Deeken
- John E. Niederhuber
- Wendy E. Smith
- Thierry Vilboux
- Darius Ebrahimi‐Fakhari
Tuberous Sclerosis Complex Associated Neuropsychiatric Disorders and Parental Stress: Findings from a National, Prospective TSC Surveillance Study

Publication Year: 2019

DOI: https://doi.org/10.1055/s-0039-1693042

Abstract:

Authors:
- Daniel Ebrahimi‐Fakhari
- Justine Hussong
- Marina Flotats‐Bastardas
- Darius Ebrahimi‐Fakhari
- Michael Zemlin
- Alexander von Gontard
- Sascha Meyer
Adaptor Protein Complex 4 Deficiency: A Paradigm of Complex Hereditary Spastic Paraplegia Associated With Defective Protein Trafficking (S19.009)

Publication Year: 2019

DOI: https://doi.org/10.1212/wnl.92.15_supplement.s19.009

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
- Robert Behne
- Julian Teinert
- Miriam Wimmer
- Amelia Diplock
- Erin Carmody
- Kira A. Dies
- Pin-Fang Chen
- Elizabeth D. Buttermore
- Mustafa Şahin
Resident and Fellow Section in Neuropediatrics

Publication Year: 2018

DOI: https://doi.org/10.1055/s-0038-1666857

Abstract:

Authors:
- Darius Ebrahimi‐Fakhari
- Bernd A. Neubauer
- Barbara Plecko
- Nicole I. Wolf
Invitation and Welcome to the 43rd Annual Meeting of the Society for Neuropediatrics

Publication Year: 2017

DOI: https://doi.org/10.1055/s-0037-1601319

Abstract:

Authors:
- Andreas Hahn
- Bernd A. Neubauer
Contents

Publication Year: 2015

DOI: https://doi.org/10.1016/s0031-3955(15)00058-9

Abstract:

Authors:
- Authors not available

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AILBRY - Article Search

Results for 'Darius Ebrahimi‐Fakhari' :

Restoring impaired protein metabolism in Parkinson's disease — TFEB‐mediated autophagy as a novel therapeutic target

Autophagy and neurodegeneration — genetic findings in SENDA syndrome, a subtype of neurodegeneration with brain iron accumulation, provide a novel link

Nomenclature of genetic movement disorders: Recommendations of the International Parkinson and Movement Disorder Society task force

Parkinson's disease: A disorder of axonal mitophagy?

Reply letter to Jinnah “Locus pocus” and Albanese “Complex dystonia is not a category in the new 2013 consensus classification”: Necessary evolution, no magic!

Linking mitochondrial dysfunction to neurodegeneration in lysosomal storage diseases

Novel and de novo point and large microdeletion mutation in <i>PRRT2</i>‐related epilepsy

International electives in the final year of German medical school education--a student's perspective.

Modeling Parkinson's disease in a dish — A story of yeast and men

EPG5 Variants with Modest Functional Impact Result in an Ameliorated and Primarily Neurological Phenotype in a 3.5-Year-Old Patient with Vici Syndrome

Tuberous Sclerosis Complex Associated Neuropsychiatric Disorders and Parental Stress: Findings from a National, Prospective TSC Surveillance Study

Adaptor Protein Complex 4 Deficiency: A Paradigm of Complex Hereditary Spastic Paraplegia Associated With Defective Protein Trafficking (S19.009)

Resident and Fellow Section in Neuropediatrics

Invitation and Welcome to the 43rd Annual Meeting of the Society for Neuropediatrics

Contents

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