Article
Clinical Neurology
Marta Bellofatto, Alessandro Bertini, Irene Tramacere, Fiore Manganelli, Gian Maria Fabrizi, Angelo Schenone, Lucio Santoro, Tiziana Cavallaro, Marina Grandis, Stefano C. Previtali, Yuri Falzone, Isabella Allegri, Luca Padua, Costanza Pazzaglia, Daniela Calabrese, Paola Saveri, Aldo Quattrone, Paola Valentino, Stefano Tozza, Luca Gentile, Massimo Russo, Anna Mazzeo, Giuseppe Vita, Sylvie Piacentini, Chiara Pisciotta, Davide Pareyson
Summary: This study investigated fatigue in CMT patients and found that 36% of the patients experienced abnormal fatigue. Abnormal fatigue was correlated with disease severity, anxiety, depression, sleepiness, and obesity. Therefore, the management of CMT patients should involve treating fatigue and addressing other factors such as anxiety, depression, sleepiness, and obesity.
EUROPEAN JOURNAL OF NEUROLOGY
(2023)
Article
Clinical Neurology
Marta Bellofatto, Alessandro Bertini, Irene Tramacere, Fiore Manganelli, Gian Maria Fabrizi, Angelo Schenone, Lucio Santoro, Tiziana Cavallaro, Marina Grandis, Stefano C. Previtali, Yuri Falzone, Isabella Allegri, Luca Padua, Costanza Pazzaglia, Daniela Calabrese, Paola Saveri, Aldo Quattrone, Paola Valentino, Stefano Tozza, Luca Gentile, Massimo Russo, Anna Mazzeo, Giuseppe Vita, Sylvie Piacentini, Chiara Pisciotta, Davide Pareyson
Summary: This study investigated the presence of fatigue and its correlations in Charcot-Marie-Tooth disease (CMT). The results showed that 36% of the patients had abnormal fatigue, which was correlated with disease severity, anxiety, depression, sleepiness, and obesity. Therefore, the management of CMT patients should include treatment for fatigue and its different generators.
EUROPEAN JOURNAL OF NEUROLOGY
(2022)
Article
Health Care Sciences & Services
Jihyun Park, So Young Joo, Byung-Ok Choi, Dae-Hyun Kim, Jong Bum Park, Jong Weon Lee, Deog Young Kim
Summary: This study evaluated the characteristics of gait patterns in CMT1A patients and classified them according to disease severity. The results showed significant differences in gait parameters between CMT1A patients and healthy controls, as well as variations in gait patterns within different severity groups.
JOURNAL OF PERSONALIZED MEDICINE
(2023)
Article
Clinical Neurology
Marta Bellofatto, Luca Gentile, Alessandro Bertini, Irene Tramacere, Fiore Manganelli, Gian Maria Fabrizi, Angelo Schenone, Lucio Santoro, Tiziana Cavallaro, Marina Grandis, Stefano Previtali, Marina Scarlato, Isabella Allegri, Luca Padua, Costanza Pazzaglia, Flavio Villani, Eleonora Cavalca, Paola Saveri, Aldo Quattrone, Paola Valentino, Stefano Tozza, Massimo Russo, Anna Mazzeo, Giuseppe Vita, Sylvie Piacentini, Giuseppe Didato, Chiara Pisciotta, Davide Pareyson, CMT Network
Summary: This study investigated the presence of sleep abnormalities in Charcot-Marie-Tooth disease (CMT) patients and their correlation with disease severity and characteristics. The results showed that CMT patients had poor sleep quality and daytime somnolence, which were associated with anxiety, depression, and fatigue.
JOURNAL OF NEUROLOGY
(2023)
Review
Biochemistry & Molecular Biology
Marina Stavrou, Irene Sargiannidou, Elena Georgiou, Alexia Kagiava, Kleopas A. Kleopa
Summary: CMT disease is a genetically heterogeneous disorder affecting the peripheral nerves, with diverse molecular genetic mechanisms discovered over the past three decades. There are currently various treatment approaches in preclinical testing and clinical trials, including disease-specific targeted therapies and treatments targeting common pathways shared by different CMT types. As promising treatments advance to clinical translation, optimizing outcome measures, novel biomarkers, and appropriate trial designs are crucial to facilitate successful testing and validation of novel treatments for CMT patients.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
(2021)
Review
Clinical Neurology
Miaomiao Ma, Yao Li, Shimiao Dai, Ming Chu, Litao Sun, Longjian Liu, Ji-Chang Zhou
Summary: Charcot-Marie-Tooth disease and related inherited peripheral neuropathies (CMT & RIPNs) cause significant suffering and burden to patients, but there is a lack of comprehensive understanding of their global prevalence rates. Further epidemiological studies with well-defined diagnostic criteria are needed to improve the assessment of prevalence and raise awareness for better healthcare support.
JOURNAL OF NEUROLOGY
(2023)
Article
Orthopedics
Sergio Tejero, Juan Chans-Veres, Andres Carranza-Bencano, Ahmed E. Galhoum, Daniel Poggio, Victor Valderrabano, Mario Herrera-Perez
Summary: The study aimed to compare functional outcomes, quality of life, and complications in two groups of Charcot-Marie-Tooth (CMT) patients based on the type of surgical operations. Patients who underwent joint preserving surgery showed better functional improvement and lower rates of complications compared to those who underwent joint sacrificing surgery. Early surgical intervention may be beneficial in delaying or preventing extensive reconstructive procedures in CMT patients.
INTERNATIONAL ORTHOPAEDICS
(2021)
Article
Clinical Neurology
Eduardo Boiteux Uchoa Cavalcanti, Savana Camilla de Lima Santos, Carlos Eduardo Speck Martins, Daniel Rocha de Carvalho, Isabela Maria Pinto de Oliveira Rizzo, Maria Cristina Del Negro Barroso Freitas, Denise da Silva Freitas, Francineide Sadala de Souza, Altamir Monteiro Junior, Osvaldo Jose Moreira do Nascimento
Summary: This study aimed to describe the clinical, genetic, and epidemiological features of Charcot-Marie-Tooth disease (CMT) in Brazilian patients from a tertiary center, and to compare the data with previously published findings. The study found that the first decade of life was the most common period of disease onset in CMT patients, with PMP22, GJB1, and other genes being common causative genes. The study provides further insights into the frequency of CMT subtypes in a Brazilian clinical-based population and emphasizes the importance of rarer and previously undiagnosed variants in clinical practice.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
(2021)
Article
Neurosciences
Juliana Cardoso, Cyntia R. J. Alves de Baptista, Cristina D. Sartor, Adriana H. Nascimento Elias, Wilson Marques Junior, Edson Z. Martinez, Isabel C. N. Sacco, Ana Claudia Mattiello-Sverzut
Summary: This study compared the dynamic plantar pressure patterns in children and adolescents with and without CMT, finding clear changes in most dynamic plantar pressure variables for children with CMT and changes mainly in contact area and contact time for adolescents with CMT. Associations were found between supinated foot posture, dorsiflexion ROM, and plantar flexion IMS in CMT patients, which can be useful for guiding rehabilitation therapies.
Article
Clinical Neurology
Zhongbo Chen, Reza Maroofian, A. Nazli Basak, Leena Shingavi, Mert Karakaya, Stephanie Efthymiou, Emil K. Gustavsson, Leyla Meier, Kiran Polavarapu, Seena Vengalil, Veeramani Preethish-Kumar, Bevinahalli N. Nandeesh, Nalan Gokce Gunes, Onur Akan, Fatma Candan, Bertold Schrank, Stephan Zuchner, David Murphy, Mahima Kapoor, Mina Ryten, Brunhilde Wirth, Mary M. Reilly, Atchayaram Nalini, Henry Houlden, Payam Sarraf
Summary: Pathogenic variants in PLEKHG5 have been reported in patients with autosomal recessive intermediate Charcot-Marie-Tooth disease and spinal muscular atrophy. The study identified novel biallelic variants in PLEKHG5 in 13 individuals from nine families, showing variable disease severity and age of onset. The findings suggest PLEKHG5-associated neuropathies as an important differential diagnosis in non-5q spinal muscular atrophy cases, expanding the understanding of the disease spectrum.
EUROPEAN JOURNAL OF NEUROLOGY
(2021)
Article
Clinical Neurology
Silvia Cipriani, Marta Guerrero-Valero, Stefano Tozza, Edward Zhao, Veith Vollmer, Danique Beijer, Matt Danzi, Cristina Rivellini, Dejan Lazarevic, Giovanni Battista Pipitone, Bianca Rose Grosz, Costanza Lamperti, Stefania Bianchi Marzoli, Paola Carrera, Marcella Devoto, Chiara Pisciotta, Davide Pareyson, Marina Kennerson, Stefano C. Previtali, Stephan Zuchner, Steven S. Scherer, Fiore Manganelli, Martin Bahler, Alessandra Bolino
Summary: The study identified that novel or very rare variants in the MYO9B gene are associated with CMT2 and isolated OA. Functional studies showed that variants in MYO9B impair protein expression level and motor activity, indicating its essential role in peripheral and central nervous system axons.
EUROPEAN JOURNAL OF NEUROLOGY
(2023)
Article
Multidisciplinary Sciences
Hyun Su Kim, Ji Hyun Lee, Young Cheol Yoon, Min Jae Cha, Soo Hyun Nam, Hye Mi Kwon, Seonwoo Kim, Hojeong Won, Byung-Ok Choi
Summary: The study found that CMT1A patients had significantly higher fat fraction and larger cross-sectional area of the sciatic nerve compared to controls. The cross-sectional area at level 3 correlated positively with CMTNSv2, suggesting its potential as an imaging marker for clinical severity.
SCIENTIFIC REPORTS
(2021)
Article
Clinical Neurology
Luce Barbat du Closel, Nathalie Bonello-Palot, Yann Pereon, Andoni Echaniz-Laguna, Jean Philippe Camdessanche, Aleksandra Nadaj-Pakleza, Jean-Baptiste Chanson, Simon Frachet, Laurent Magy, Julien Cassereau, Pascal Cintas, Ariane Choumert, Perrine Devic, Sarah Leonard Louis, Robinson Gravier Dumonceau, Emilien Delmont, Emmanuelle Salort-Campana, Francoise Bouhour, Philippe Latour, Tanya Stojkovic, Shahram Attarian
Summary: This study investigated the clinical presentation of patients with CMTX1 and found that women usually have milder clinical symptoms compared to men. The study also identified two subgroups of women over the age of 48, with one group showing similar disease progression to men.
EUROPEAN JOURNAL OF NEUROLOGY
(2023)
Article
Engineering, Biomedical
Bente E. Bloks, Lise M. Wilders, Jan Willem K. Louwerens, Alexander C. Geurts, Jorik Nonnekes, Noel L. W. Keijsers
Summary: This study aimed to understand the plantar pressure situation of patients with hereditary motor and sensory neuropathies (HMSN) and propose a quantitative outcome measure for the evaluation of surgical interventions. Plantar pressure measurements of 52 HMSN patients and 586 healthy controls were evaluated, revealing differences in plantar pressure patterns among different foot deformity categories. It was suggested to use root mean square deviations (RMSD) in combination with the fifth metatarsal head pressure ratio as outcome measures for evaluating surgical interventions in HMSN patients.
JOURNAL OF NEUROENGINEERING AND REHABILITATION
(2023)
Review
Clinical Neurology
Alessandra Bolino, Maurizio D'Antonio
Summary: Charcot-Marie-Tooth (CMT) neuropathies, despite a large number of identified causative genes, lack effective therapeutic options. However, recent advances in understanding disease mechanisms, animal modeling, and gene and molecular therapies have greatly improved the prospects of treating CMT, with several strategies progressing towards clinical trials.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
(2023)
Article
Clinical Neurology
Samuel Arends, Judith Drenthen, Peter van den Bergh, Hessel Franssen, Robert D. M. Hadden, Badrul Islam, Satoshi Kuwabara, Ricardo C. Reisin, Nortina Shahrizaila, Hiroshi Amino, Giovanni Antonini, Shahram Attarian, Claudia Balducci, Fabio Barroso, Tulio Bertorini, Davide Binda, Thomas H. Brannagan, Jan Buermann, Carlos Casasnovas, Guido Cavaletti, Chi-Chao Chao, Mazen M. Dimachkie, Ernesto A. Fulgenzi, Giuliana Galassi, Gerardo Gutierrez Gutierrez, Thomas Harbo, Hans-Peter Hartung, Sung-Tsang Hsieh, Lynette Kiers, Helmar C. Lehmann, Fiore Manganelli, Girolama A. Marfia, Giorgia Mataluni, Julio Pardo, Yann Pereon, Yusuf A. Rajabally, Lucio Santoro, Yukari Sekiguchi, Beth Stein, Mark Stettner, Antonino Uncini, Christine Verboon, Camiel Verhamme, Michal Vytopil, Waqar Waheed, Min Wang, Sasha Zivkovic, Bart C. Jacobs, David R. Cornblath
Summary: This study investigated the heterogeneity of electrodiagnostic (EDx) studies in Guillain-Barre syndrome (GBS) patients collected as part of the International GBS Outcome Study (IGOS). The results showed extensive variation in the clinical practice of EDx among IGOS centers across different regions. This diversity is likely to be present in other neuromuscular disorders and centers, emphasizing the need for standardization of EDx in future multinational GBS studies.
CLINICAL NEUROPHYSIOLOGY
(2022)
Article
Clinical Neurology
Jia Lun Lim, Katja Lohmann, Ai Huey Tan, Yi Wen Tay, Khairul Azmi Ibrahim, Zariah Abdul Aziz, Ahmad Shahir Mawardi, Santhi Datuk Puvanarajah, Thien Thien Lim, Irene Looi, Joshua Chin Ern Ooi, Yuen Kang Chia, Kalai Arasu Muthusamy, Peter Bauer, Arndt Rolfs, Christine Klein, Azlina Ahmad-Annuar, Shen-Yang Lim
Summary: The study in Malaysia on GBA variants revealed a higher rate of GBA mutations among early-onset PD patients, especially across three different ethnicities. Additionally, the study explored the severe disease progression and spine posture abnormalities in GBA variant carriers.
JOURNAL OF NEURAL TRANSMISSION
(2022)
Letter
Clinical Neurology
Cheng-Yin Tan, Tsun-Haw Toh, Yen-Fa Toh, Kum-Thong Wong, Nortina Shahrizaila, Khean-Jin Goh
Article
Biochemistry & Molecular Biology
Lisa J. Ewans, Andre E. Minoche, Deborah Schofield, Rupendra Shrestha, Clare Puttick, Ying Zhu, Alexander Drew, Velimir Gayevskiy, George Elakis, Corrina Walsh, Lesley C. Ades, Alison Colley, Carolyn Ellaway, Carey-Anne Evans, Mary-Louise Freckmann, Linda Goodwin, Anna Hackett, Benjamin Kamien, Edwin P. Kirk, Michelle Lipke, David Mowat, Elizabeth Palmer, Sulekha Rajagopalan, Anne Ronan, Rani Sachdev, William Stevenson, Anne Turner, Meredith Wilson, Lisa Worgan, Marie-Christine Morel-Kopp, Michael Field, Michael F. Buckley, Mark J. Cowley, Marcel E. Dinger, Tony Roscioli
Summary: Whole genome sequencing (WGS) has a higher diagnostic rate compared to whole exome sequencing (WES) in suspected Mendelian disorder cases. However, the specific diagnostic yield and associated costs are still uncertain. This study investigates the differences in diagnostic and cost outcomes between WGS and WES in a cohort of families with suspected Mendelian disorders. The results show that WGS diagnosed 34% of WES-negative families, but subsequent WES reanalysis would have diagnosed 18% of these families, resulting in a WGS-specific diagnostic yield of 19% for the remaining families. The cost of WGS for additional diagnoses is higher compared to WES reanalysis.
EUROPEAN JOURNAL OF HUMAN GENETICS
(2022)
Article
Clinical Neurology
Samuel Arends, Judith Drenthen, Peter Y. K. van den Bergh, Robert D. M. Hadden, Nortina Shahrizaila, Mazen M. Dimachkie, Gerardo Gutierrez Gutierrez, Hans Katzberg, Lynette Kiers, Helmar C. Lehmann, Yann Pereon, Ricardo C. Reisin, Antonino Uncini, Camiel Verhamme, Wagar Waheed, David R. Cornblath, Bart C. Jacobs
Summary: This study investigated how neuromuscular EDx experts approach key aspects of GBS subtyping in practice and compared previously published EDx criteria for GBS. The study found extensive variability in the practical use of EDx criteria, potentially reducing the reproducibility of GBS subtyping.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
(2022)
Article
Clinical Neurology
Eng Tah Goh, Christine Lock, Audrey Jia Luan Tan, Bee Ling Tan, Sai Liang, Robin Pillay, Sumeet Kumar, Azlina Ahmad-Annuar, Vairavan Narayanan, Janell Kwok, Yi Jayne Tan, Adeline S. L. Ng, Eng King Tan, Zofia Czosnyka, Marek Czosnyka, John D. Pickard, Nicole C. Keong
Summary: This study aims to evaluate clinical responses after ventriculo-peritoneal shunt (VPS) in a cohort of patients with coexisting NPH and neurodegenerative disease. The results showed that after VPS insertion, Classic NPH patients had significantly improved cognition compared to Complex NPH patients. Improvement in gait and urinary symptoms did not differ between the groups.
FRONTIERS IN NEUROLOGY
(2022)
Article
Biochemistry & Molecular Biology
Kamariah Ibrahim, Azlina Ahmad-Annuar
Summary: This article discusses the low awareness of using publicly available research data sets for undergraduate training in certain parts of the world. It highlights the need to strengthen awareness of reusing public data sets as tools for research, especially in the context of the COVID-19 pandemic and the shift towards big data-driven research in the life sciences.
BIOCHEMISTRY AND MOLECULAR BIOLOGY EDUCATION
(2022)
Article
Clinical Neurology
Sonja E. Leonhard, Annemiek A. van der Eijk, Henning Andersen, Giovanni Antonini, Samuel Arends, Shahram Attarian, Fabio A. Barroso, Kathleen J. Bateman, Manou R. Batstra, Luana Benedetti, Bianca van den Berg, Peter Van den Bergh, Jan Burmann, Mark Busby, Carlos Casasnovas, David R. Cornblath, Amy Davidson, Alex Y. Doets, Pieter A. van Doorn, Charlotte Dornonville de la Cour, Thomas E. Feasby, Janev Fehmi, Tania Garcia-Sobrino, Jonathan M. Goldstein, Kenneth C. Gorson, Volkan Granit, Robert D. M. Hadden, Thomas Harbo, Hans-Peter Hartung, Imran Hasan, Jakob Holbech, James K. L. Holt, Israt Jahan, Zhahirul Islam, Summer Karafiath, Hans D. Katzberg, Ruud P. Kleyweg, Noah Kolb, Krista Kuitwaard, Motoi Kuwahara, Susumu Kusunoki, Linda W. G. Luijten, Satoshi Kuwabara, Edward Lee Pan, Helmar C. Lehmann, Marijke Maas, Lorena Martin-Aguilar, James Al Miller, Quazi Deen Mohammad, Soledad Monges, Velina Nedkova-Hristova, Eduardo Nobile-Orazio, Julio Pardo, Yann Pereon, Luis Querol, Ricardo Reisin, Wouter Van Rijs, Simon Rinaldi, Rhys C. Roberts, Joyce Roodbol, Nortina Shahrizaila, Soren Hein Sindrup, Beth Stein, Tan Cheng-Yin, Hatice Tankisi, Anne P. Tio-Gillen, Maria J. Sedano Tous, Christine Verboon, Frederique H. Vermeij, Leo H. Visser, Ruth Huizinga, Hugh J. Willison, Bart C. Jacobs
Summary: This study analyzed the role of infections in Guillain-Barre syndrome (GBS) and their association with clinical features and disease severity. The distribution of infections varied across geographical regions, but the association between infection and clinical phenotype differed. Coinfections were common, highlighting the importance of broad serologic testing. Infections were also found to have prognostic value for GBS outcome.
Article
Multidisciplinary Sciences
Eva-Juliane Vollstedt, Harutyun Madoev, Anna Aasly, Azlina Ahmad-Annuar, Bashayer Al-Mubarak, Roy N. Alcalay, Victoria Alvarez, Ignacio Amorin, Grazia Annesi, David Arkadir, Soraya Bardien, Roger A. Barker, Melinda Barkhuizen, A. Nazli Basak, Vincenzo Bonifati, Agnita Boon, Laura Brighina, Kathrin Brockmann, Andrea Carmine Belin, Jonathan Carr, Jordi Clarimon, Mario Cornejo-Olivas, Leonor Correia Guedes, Jean-Christophe Corvol, David Crosiers, Joana Damasio, Parimal Das, Patricia de Carvalho Aguiar, Anna De Rosa, Jolanta Dorszewska, Sibel Ertan, Rosangela Ferese, Joaquim Ferreira, Emilia Gatto, Gencer Genc, Nir Giladi, Pilar Gomez-Garre, Hasmet Hanagasi, Nobutaka Hattori, Faycal Hentati, Dorota Hoffman-Zacharska, Sergey N. Illarioshkin, Joseph Jankovic, Silvia Jesus, Valtteri Kaasinen, Anneke Kievit, Peter Klivenyi, Vladimir Kostic, Dariusz Koziorowski, Andrea A. Kuehn, Anthony E. Lang, Shen-Yang Lim, Chin-Hsien Lin, Katja Lohmann, Vladana Markovic, Mika Henrik Martikainen, George Mellick, Marcelo Merello, Lukasz Milanowski, Pablo Mir, Oezguer oeztop-cakmak, Marcia Mattos Goncalves Pimentel, Teeratorn Pulkes, Andreas Puschmann, Ekaterina Rogaeva, Esther M. Sammler, Maria Skaalum Petersen, Matej Skorvanek, Mariana Spitz, Oksana Suchowersky, Ai Huey Tan, Pichet Termsarasab, Avner Thaler, Vitor Tumas, Enza Maria Valente, Bart van de Warrenburg, Caroline H. Williams-Gray, Ruey-Mei Wu, Baorong Zhang, Alexander Zimprich, Justin Solle, Shalini Padmanabhan, Christine Klein
Summary: Parkinson's disease is a rapidly growing neurodegenerative disorder that affects approximately 7 million people worldwide. The majority of research on monogenic Parkinson's disease is focused on patients of European White ancestry, leaving a significant knowledge gap in underrepresented populations. To address this, a global network of centers working on monogenic Parkinson's disease has been established to facilitate collaborative research and the development of new therapies. An interactive map and online tool have also been developed to enable quick access to available resources and promote collaboration. This initiative aims to fill the knowledge gap and impact the treatment of monogenic and potentially idiopathic Parkinson's disease patients.
Article
Clinical Neurology
Ai Huey Tan, Mario Cornejo-Olivas, Njideka Okubadejo, Pramod Kumar Pal, Gerard Saranza, Paula Saffie-Awad, Azlina Ahmad-Annuar, Artur F. Schumacher-Schuh, Kigocha Okeng'o, Ignacio F. Mata, Emilia M. Gatto, Shen-Yang Lim
MOVEMENT DISORDERS CLINICAL PRACTICE
(2023)
Article
Clinical Neurology
Matthew Silsby, Con Yiannikas, Alessandro F. Fois, Marina L. Kennerson, Matthew C. Kiernan, Victor S. C. Fung, Steve Vucic
Summary: Neuropathic tremor is a common clinical feature in CMT1A, with distinct characteristics compared to essential tremor. Upper limb tremors were postural and kinetic, while lower limb tremors were postural and orthostatic. The frequency of upper limb tremors varied along the limb, with a lower frequency distally and a higher frequency proximally. Lower limb tremors had a consistent frequency and were unaffected by fatigue. Postural lower limb tremor was associated with imbalance.
JOURNAL OF NEUROLOGY
(2023)
Meeting Abstract
Clinical Neurology
A. M. Dy Closas, A. H. Tan, J. L. Lim, Y. W. Tay, A. Ahmad-Annuar, K. Lohmann, C. Klein, C. Y. Cham, K. A. Muthusamy, S. Y. Lim
MOVEMENT DISORDERS
(2023)
Meeting Abstract
Clinical Neurology
Ling Yi Lee, Cheng Yin Tan, Kum Thong Wong, Khean-Jin Goh, Nortina Shahrizaila
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
(2022)
Meeting Abstract
Clinical Neurology
Samuel Arends, Judith Drenthen, Peter Van den Bergh, Robert Hadden, Nortina Shahrizaila, Davide Binda, Thomas Brannagan, Carlos Casasnovas, Mazen Dimachkie, Ernesto Fulgenzi, Gerardo Gutierrez-Gutierrez, Sung-Tsang Hsieh, Hans Katzberg, Lynette Kiers, Helmar Lehmann, Girolama Marfia, Giorgia Mataluni, Julio Pardo-Fernandez, Yann Pereon, Yukari Sekiguchi, Antonino Uncini, Camiel Verhamme, Waqar Waheed, Min Wang, Bart Jacobs, David Cornblath
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
(2022)
Review
Neurosciences
Jonathan Cole, Anita Kamondi, Paulo Teixeira Kimaid, Nortina Shahrizaila
Summary: This paper presents the results of the first survey on training and education conducted by the regional chapters of the International Federation of Clinical Neurophysiology. The survey reveals significant differences in training durations and competency testing among different countries.
CLINICAL NEUROPHYSIOLOGY PRACTICE
(2022)