Martin Mücke

ORCID: 0000-0002-9275-9035
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About
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Research Areas
  • Pain Management and Opioid Use
  • Pain Mechanisms and Treatments
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Palliative Care and End-of-Life Issues
  • Genomics and Rare Diseases
  • Cannabis and Cannabinoid Research
  • Childhood Cancer Survivors' Quality of Life
  • Cancer survivorship and care
  • Pharmacological Effects and Toxicity Studies
  • Mast cells and histamine
  • Botulinum Toxin and Related Neurological Disorders
  • Pancreatic and Hepatic Oncology Research
  • Food Allergy and Anaphylaxis Research
  • Inflammatory Myopathies and Dermatomyositis
  • Neurogenetic and Muscular Disorders Research
  • Child and Adolescent Psychosocial and Emotional Development
  • Anxiety, Depression, Psychometrics, Treatment, Cognitive Processes
  • Hereditary Neurological Disorders
  • Nutrition and Health in Aging
  • Psychiatric care and mental health services
  • Pediatric Pain Management Techniques
  • Urticaria and Related Conditions
  • Musculoskeletal pain and rehabilitation
  • Opioid Use Disorder Treatment
  • Pain Management and Placebo Effect

RWTH Aachen University
2022-2024

University Hospital Bonn
2015-2024

Universitätsklinikum Aachen
2022-2024

University of Bonn
2016-2024

Medizinische Hochschule Hannover
2023

Centrum für Integrierte Onkologie
2017-2022

Helmholtz Centre for Infection Research
2022

Ostfalia University of Applied Sciences
2022

Luisenhospital Aachen
2022

University of Basel
2019

Background Worldwide approximately 7,000 rare diseases have been identified. Accordingly, 4 million individuals live with a disease in Germany. The mean time to diagnosis is about 6 years and patients receive several incorrect diagnoses during this time. A multiplicity of factors renders diagnosing extremely difficult. Detection shared phenomena among different could assist the diagnostic process. In order explore demand for support obtain commonalities patients, nationwide Delphi survey...

10.1371/journal.pone.0172532 article EN cc-by PLoS ONE 2017-02-24
Axel Schmidt Magdalena Danyel Kathrin Grundmann Theresa Brunet Hannah Klinkhammer and 95 more Tzung‐Chien Hsieh Hartmut Engels Sophia Peters Alexej Knaus Shahida Moosa Luisa Averdunk Felix Boschann Henrike L. Sczakiel Sarina Schwartzmann Martin A. Mensah Jean Tori Pantel Manuel Holtgrewe Annemarie Bösch Claudia Weiß Natalie Weinhold Aude‐Annick Suter Corinna Stoltenburg Julia Neugebauer Tillmann Kallinich Angela M. Kaindl Susanne Holzhauer Christoph Bührer Philip Bufler Uwe Kornak Claus‐Eric Ott Markus Schülke Huu Phuc Nguyen Sabine Hoffjan Corinna Grasemann Tobias Rothoeft Folke Brinkmann Nora Matar Sugirthan Sivalingam Claudia Perne Elisabeth Mangold Martina Kreiß Kirsten Cremer Regina C. Betz Martin Mücke Lorenz Grigull Thomas Klockgether Isabel Spier André Heimbach Tim Bender Fabian Brand Christiane Stieber Alexandra Marzena Morawiec Pantelis Karakostas Valentin Sebastian Schäfer Sarah Bernsen Patrick Weydt Sergio Castro‐Gomez Ahmad Aziz Marcus Grobe‐Einsler Okka Kimmich Xenia Kobeleva Demet Önder Hellen Lesmann Sheetal Kumar Paweł Tacik Meghna Ahuja Basin Pietro Incardona Min Ae Lee‐Kirsch Reinhard Berner Catharina Schuetz Julia Körholz Tanita Kretschmer Nataliya Di Donato Evelin Schröck A. Heinen Ulrike Reuner Amalia-Mihaela Hanßke Frank J. Kaiser Eva Manka Martin Munteanu Alma Kuechler Cordula Kiewert Raphael Hirtz Elena Schlapakow Christian Schlein Jasmin Lisfeld Christian Kubisch Theresia Herget Maja Hempel Christina Weiler‐Normann Kurt Ullrich Christoph Schramm Cornelia Rudolph Franziska Rillig Maximilian Groffmann Ania C. Muntau Alexandra Tibelius Eva Maria Christina Schwaibold Christian P. Schaaf Michal Zawada

Abstract Individuals with ultrarare disorders pose a structural challenge for healthcare systems since expert clinical knowledge is required to establish diagnoses. In TRANSLATE NAMSE, 3-year prospective study, we evaluated novel diagnostic concept based on multidisciplinary expertise in Germany. Here present the systematic investigation of phenotypic and molecular genetic data 1,577 patients who had undergone exome sequencing were partially analyzed next-generation phenotyping approaches....

10.1038/s41588-024-01836-1 article EN cc-by Nature Genetics 2024-07-22

<b>Purpose:</b> Evaluation of ultrasound-guided high-intensity focused ultrasound (HIFU) used for the first time in Germany patients with inoperable pancreatic cancer reduction tumor volume and relief tumor-associated pain. <b>Materials Methods:</b> 15 locally advanced tumor-related pain symptoms were treated by HIFU (n = 6 UICC stage III, n 9 IV). 13 underwent simultaneous standard chemotherapy. Ablation was performed using JC system (Chongqing, China HAIFU Company) an ultrasonic device...

10.1055/s-0042-105517 article EN RöFo - Fortschritte auf dem Gebiet der Röntgenstrahlen und der bildgebenden Verfahren 2016-06-07

Pancreatic cancer (PaC) is a life-limiting tumor with wide range of incapacitating symptoms such as pain in more than 80 % patients. This prospective interventional study addresses the clinical effectiveness ultrasound-guided high-intensity focused ultrasound (HIFU) treatment for patients advanced-stage PaC, including perception, size and survival benefit. 50 late-stage PaC underwent HIFU. Clinical assessment included evaluation volume by imaging burden (pain severity, sensation,...

10.1055/a-0591-3386 article DE Ultraschall in der Medizin - European Journal of Ultrasound 2018-04-17
Axel Schmidt Magdalena Danyel Kathrin Grundmann Theresa Brunet Hannah Klinkhammer and 95 more Tzung‐Chien Hsieh Hartmut Engels Sophia Peters Alexej Knaus Shahida Moosa Luisa Averdunk Felix Boschann Henrike L. Sczakiel Sarina Schwartzmann Martin A. Mensah Jean Tori Pantel Manuel Holtgrewe Annemarie Bösch Claudia Weiß Natalie Weinhold Aude‐Annick Suter Corinna Stoltenburg Julia Neugebauer Tillmann Kallinich Angela M. Kaindl Susanne Holzhauer Christoph Bührer Philip Bufler Uwe Kornak Claus‐Eric Ott Markus Schülke Huu Phuc Nguyen Sabine Hoffjan Corinna Grasemann Tobias Rothoeft Folke Brinkmann Nora Matar Sugirthan Sivalingam Claudia Perne Elisabeth Mangold Martina Kreiß Kirsten Cremer Regina C. Betz Tim Bender Martin Mücke Lorenz Grigull Thomas Klockgether Spier Isabel Heimbach André Bender Tim Fabian Brand Christiane Stieber Alexandra Marzena Morawiec Pantelis Karakostas Valentin Sebastian Schäfer Sarah Bernsen Patrick Weydt Sergio Castro‐Gomez Ahmad Aziz Marcus Grobe‐Einsler Okka Kimmich Xenia Kobeleva Demet Önder Hellen Lesmann Sheetal Kumar Paweł Tacik Min Ae Lee‐Kirsch Reinhard Berner Catharina Schuetz Julia Körholz Tanita Kretschmer Nataliya Di Donato Evelin Schröck A. Heinen Ulrike Reuner Amalia-Mihaela Hanßke Frank J. Kaiser Eva Manka Martin Munteanu Alma Kuechler Cordula Kiewert Raphael Hirtz Elena Schlapakow Christian Schlein Jasmin Lisfeld Christian Kubisch Theresia Herget Maja Hempel Christina Weiler‐Normann Kurt Ullrich Christoph Schramm Cornelia Rudolph Franziska Rillig Maximilian Groffmann Ania C. Muntau Alexandra Tibelius Eva Maria Christina Schwaibold Christian P. Schaaf Michal Zawada Lilian Kaufmann

Abstract Most individuals with rare diseases initially consult their primary care physician. For a subset of diseases, efficient diagnostic pathways are available. However, ultra-rare often require both expert clinical knowledge and comprehensive genetic diagnostics, which poses structural challenges for public healthcare systems. To address these within Germany, novel structured concept, based on multidisciplinary expertise at established university hospital centers (CRDs), was evaluated in...

10.1101/2023.04.19.23288824 preprint EN cc-by-nd medRxiv (Cold Spring Harbor Laboratory) 2023-04-25
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