J. Wolf

发表

[Causes of death in amyotrophic lateral sclerosis : Results from the Rhineland-Palatinate ALS registry].

J. Wöhrle, M. Maschke, A. Grau, 2017, Der Nervenarzt.

Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study

A. Ludolph, J. Grosskreutz, J. Dorst, 2022, Scientific Reports.

Lithium and ECT – Concurrent use still demands attention: Three case reports

A. Sartorius, F. Henn, J. Wolf, 2005, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Use and subjective experience of the impact of motor-assisted movement exercisers in people with amyotrophic lateral sclerosis: a multicenter observational study

A. Ludolph, J. Grosskreutz, J. Dorst, 2022, Scientific Reports.

Recent Surgery or Invasive Procedures and the Risk of Stroke

H. Becher, A. Grau, F. Buggle, 2014, Cerebrovascular Diseases.

Remote digital assessment of amyotrophic lateral sclerosis functional rating scale – a multicenter observational study

S. Petri, J. Grosskreutz, A. Rödiger, 2022, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Incidence of amyotrophic lateral sclerosis in Rhineland-Palatinate, Germany

H. Becher, J. Wöhrle, M. Maschke, 2014, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Peripheral neuropathy as initial manifestation of primary systemic vasculitides

A. Grau, J. Wolf, F. Palm, 2013, Journal of Neurology.

Variability and prognostic relevance of different phenotypes in amyotrophic lateral sclerosis — Data from a population-based registry

J. Wöhrle, M. Maschke, A. Grau, 2014, Journal of the Neurological Sciences.

Hot-spot KIF5A mutations cause familial ALS

H. Braak, T. Meitinger, T. Strom, 2018, Brain : a journal of neurology.

Provision of assistive technology devices among people with ALS in Germany: a platform-case management approach

S. Petri, A. Ludolph, J. Grosskreutz, 2018, Amyotrophic lateral sclerosis & frontotemporal degeneration.

ALSgeneScanner: a pipeline for the analysis and interpretation of DNA sequencing data of ALS patients

Berg, S. Newhouse, A. Al-Chalabi, 2019, Amyotrophic lateral sclerosis & frontotemporal degeneration.

The role of de novo mutations in the development of amyotrophic lateral sclerosis

Annelot M. Dekker, Raymond D. Schellevis, S. Pulit, 2017, Human mutation.

Management of oral anticoagulation after cardioembolic stroke and stroke survival data from a population based stroke registry (LuSSt)

H. Becher, A. Grau, J. Wolf, 2014, BMC Neurology.

Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers’ Lives

S. Petri, A. Ludolph, D. Zeller, 2021, Brain sciences.

A Nation-Wide, Multi-Center Study on the Quality of Life of ALS Patients in Germany

S. Petri, A. Ludolph, D. Zeller, 2021, Brain sciences.

Factors predicting one-year mortality in amyotrophic lateral sclerosis patients – data from a population-based registry

J. Wöhrle, M. Maschke, A. Grau, 2014, BMC Neurology.

Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study

S. Petri, A. Ludolph, D. Czell, 2015, Journal of Neurology.

Clozapine-induced lupus erythematosus.

A. Sartorius, F. Henn, J. Wolf, 2004, Journal of clinical psychopharmacology.

Factors Predicting Survival in ALS Patients - Data from a Population-Based Registry in Rhineland-Palatinate, Germany

J. Wöhrle, M. Maschke, A. Grau, 2015, Neuroepidemiology.

Frequency of C9orf72 and SOD1 mutations in 302 sporadic ALS patients from three German ALS centers

P. Andersen, Jochen H Weishaupt, J. Wolf, 2023, Amyotrophic lateral sclerosis & frontotemporal degeneration.

July 2017 ENCALS statement on edaravone

A. Al-Chalabi, P. Andersen, A. Chiò, 2017, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Safety and Effectiveness of Long-term Intravenous Administration of Edaravone for Treatment of Patients With Amyotrophic Lateral Sclerosis.

S. Petri, A. Ludolph, J. Grosskreutz, 2022, JAMA neurology.

Intracerebral haemorrhage in a population-based stroke registry (LuSSt): incidence, aetiology, functional outcome and mortality

H. Becher, A. Grau, J. Wolf, 2013, Journal of Neurology.

Clinical and genetic features of amyotrophic lateral sclerosis patients with C9orf72 mutations

D. Lulé, S. Petri, J. Grosskreutz, 2023, Brain communications.

Etiology, Risk Factors and Sex Differences in Ischemic Stroke in the Ludwigshafen Stroke Study, a Population-Based Stroke Registry

H. Becher, M. Hennerici, A. Grau, 2011, Cerebrovascular Diseases.

Prognostic factors in ALS: a comparison between Germany and China

A. Winkler, J. Dreyhaupt, S. Petri, 2019, Journal of Neurology.

Economic evaluation of Motor Neuron Diseases: a nationwide cross-sectional analysis in Germany

S. Petri, D. Zeller, J. Dorst, 2023, Journal of Neurology.

Rare genetic variation in UNC13A may modify survival in amyotrophic lateral sclerosis

C. Lewis, J. Powell, A. Al-Chalabi, 2016, Amyotrophic lateral sclerosis & frontotemporal degeneration.