Thomas Klopstock

About Thomas Klopstock

Thomas Klopstock, With an exceptional h-index of 88 and a recent h-index of 61 (since 2020), a distinguished researcher at Ludwig-Maximilians-Universität München, specializes in the field of mitochondrial disorders.

His recent articles reflect a diverse array of research interests and contributions to the field:

Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial

Natural history of mitochondrial optic neuropathies

Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

Phenotype and natural history of mitochondrial membrane protein-associated neurodegeneration

New insights into idebenone therapy in relation to NQO1

Recommendations for optimal interdisciplinary management and healthcare settings for patients with rare neurological diseases

FARS‐ADL across Ataxias: Construct Validity, Sensitivity to Change, and Minimal Important Change

Thomas Klopstock Information

University

Position

Dept. of Neurology

Citations(all)

35279

Citations(since 2020)

16803

Cited By

25242

hIndex(all)

88

hIndex(since 2020)

61

i10Index(all)

272

i10Index(since 2020)

225

Email

University Profile Page

Ludwig-Maximilians-Universität München

Google Scholar

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Thomas Klopstock Skills & Research Interests

mitochondrial disorders

Top articles of Thomas Klopstock

Title

Journal

Author(s)

Publication Date

Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial

Cell Reports Medicine

Patrick Yu-Wai-Man

Valerio Carelli

Nancy J Newman

Magda Joana Silva

Aki Linden

...

2024/2/29

Natural history of mitochondrial optic neuropathies

Acta Ophthalmologica

Thomas Klopstock

2024/1

Management of seizures in patients with primary mitochondrial diseases: consensus statement from the InterERNs Mitochondrial Working Group

European Journal of Neurology

Michelangelo Mancuso

Maria T Papadopoulou

Yi Shiau Ng

Anna Ardissone

Marcello Bellusci

...

2024/4/4

Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy

Cell Reports Medicine

Serena Jasmine Aleo

Valentina Del Dotto

Martina Romagnoli

Claudio Fiorini

Giada Capirossi

...

2024/2/20

Phenotype and natural history of mitochondrial membrane protein-associated neurodegeneration

Brain

Vassilena Iankova

Peter Sparber

Mohammad Rohani

Petr Dusek

Boriana Büchner

...

2024/4

New insights into idebenone therapy in relation to NQO1

Acta Ophthalmologica

Chiara La Morgia

Serena Jasmine Aleo

Valentina Del Dotto

Martina Romagnoli

Claudio Fiorini

...

2024/1

Recommendations for optimal interdisciplinary management and healthcare settings for patients with rare neurological diseases

Orphanet Journal of Rare Diseases

Holm Graessner

Carola Reinhard

Tobias Bäumer

Annette Baumgärtner

Knut Brockmann

...

2024/2/13

FARS‐ADL across Ataxias: Construct Validity, Sensitivity to Change, and Minimal Important Change

Movement Disorders

Andreas Traschütz

Zofia Fleszar

Holger Hengel

Thomas Klockgether

Friedrich Erdlenbruch

...

2024/3/20

Effects of tofersen treatment in patients with SOD1-ALS in a “real-world” setting–a 12-month multicenter cohort study from the German early access program

Eclinicalmedicine

Maximilian Wiesenfarth

Johannes Dorst

David Brenner

Zeynep Elmas

Özlem Parlak

...

2024/3/1

Current management of primary mitochondrial disorders in EU countries: the European Reference Networks survey

Journal of Neurology

Michelangelo Mancuso

Piervito Lopriore

Costanza Lamperti

Thomas Klopstock

Shamima Rahman

...

2024/2

A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy

Nature Genetics

Karla P Figueroa

Caspar Gross

Elena Buena-Atienza

Sharan Paul

Mandi Gandelman

...

2024/4/29

Predictors of Survival in Friedreich's Ataxia: A Prospective Cohort Study

Movement Disorders

Elisabetta Indelicato

Kathrin Reetz

Sarah Maier

Wolfgang Nachbauer

Matthias Amprosi

...

2024/3

Long‐term efficacy of idebenone in patients with Leber hereditary optic neuropathy according to age at symptom onset and disease phase: Results from the LEROS study

Acta Ophthalmologica

Xavier Llòria

Patrick Yu‐Wai‐Man

Valerio Carelli

Livia Tomasso

Thomas Klopstock

2024/1

Assessing Clinically Relevant Recovery of Visual Acuity Over Time in Patients with Leber Hereditary Optic Neuropathy Treated with Idebenone: Results from the LEROS Study (S40. 001)

Nancy Newman

Patrick Yu-Wai-Man

Valerio Carelli

Xavier Llòria

Thomas Klopstock

2024/4/14

Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias

The American Journal of Human Genetics

Paulina Cunha

Emilien Petit

Marie Coutelier

Giulia Coarelli

Caterina Mariotti

...

2023/7/6

Treatment with lenadogene nolparvovec gene therapy results in sustained visual improvement in m. 11778G> A MT-ND4-LHON patients: the RESTORE study

Investigative Ophthalmology & Visual Science

Patrick Yu-Wai-Man

Nancy J Newman

Biousse Valérie

Valerio Carelli

Mark L Moster

...

2023/6/1

Patient and caregiver experiences with pantothenate kinase-associated neurodegeneration (PKAN): results from a patient community survey

Orphanet Journal of Rare Diseases

Thomas Klopstock

Saadet Mercimek-Andrews

Agnieszka Jurecka

Patricia Wood

Maciej Cwyl

...

2023/8/31

Longitudinal changes of SARA scale in Friedreich ataxia: Strong influence of baseline score and age at onset

Annals of Clinical and Translational Neurology

Luca Porcu

Mario Fichera

Lorenzo Nanetti

Eliana Rulli

Paola Giunti

...

2023/11

Protocol: Patient-reported, health economic and psychosocial outcomes in patients with Friedreich ataxia (PROFA): protocol of an observational study using momentary data …

BMJ Open

Maresa Buchholz

Niklas Weber

Stephanie Borel

Sabrina Sayah

Feng Xie

...

2023

Long-term Follow-up of m. 11778G> A MT-ND4-LHON Patients Treated with Lenadogene Nolparvovec Ocular Gene Therapy: the RESTORE Study (S12. 004)

Valerie Biousse

Nancy Newman

Patrick Yu-Wai-Man

Valerio Carelli

Mark Moster

...

2023/4/25

See List of Professors in Thomas Klopstock University(Ludwig-Maximilians-Universität München)