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For: Ho G, Cardamone M, Farrar M. Congenital and childhood myotonic dystrophy: Current aspects of disease and future directions. World J Clin Pediatr 2015; 4(4): 66-80 [PMID: 26566479 DOI: 10.5409/wjcp.v4.i4.66]
URL: https://www.wjgnet.com/2219-2808/full/v4/i4/66.htm
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Number Citing Articles
1
Federica S. Ricci, Martina Vacchetti, Chiara Brusa, Rossella D'Alessandro, Paola La Rosa, Gianluca Martone, Chiara Davico, Benedetto Vitiello, Tiziana E. Mongini. Cognitive, neuropsychological and emotional-behavioural functioning in a sample of children with myotonic dystrophy type 1. European Journal of Paediatric Neurology 2022; 39 doi: 10.1016/j.ejpn.2022.05.008
2
Barbora Červenková. Congenital Myotonic Dystrophy in the Neonatal Period -. Listy klinické logopedie 2023; 7(1) doi: 10.36833/lkl.2023.008
3
Nathaniël B. Rasing, Willianne van de Geest-Buit, On Ying A. Chan, Karlien Mul, Anke Lanser, Corrie E. Erasmus, Jan T. Groothuis, Judith Holler, Koen J. A. O. Ingels, Bart Post, Ietske Siemann, Nicol C. Voermans. Psychosocial functioning in patients with altered facial expression: a scoping review in five neurological diseases. Disability and Rehabilitation 2024; 46(17) doi: 10.1080/09638288.2023.2259310
4
Antonella Lo Mauro, Andrea Aliverti. Physiology of respiratory disturbances in muscular dystrophies. Breathe 2016; 12(4) doi: 10.1183/20734735.012716
5
Lleimi Alarcón-Pérez, Cristina Pastor-Laín, Lourdes Barragán-González, Claudia Sarrais-Polo, María T. López-Gil, Ignacio Mantilla-Martínez. Management of anesthesia in a pediatric patient with myotonic dystrophy type 1. Case report. Colombian Journal of Anesthesiology 2018; 46(1) doi: 10.1097/CJ9.0000000000000013
6
Sonal Malhotra, Aristotle Asis, Daniel Glaze. Sleep Medicine. 2023;  doi: 10.1007/978-3-031-30010-3_14
7
Progressive Brain Disorders in Childhood. 2017;  doi: 10.1017/9781107323704.055
8
Gerardo Gutiérrez Gutiérrez, Jordi Díaz-Manera, Míriam Almendrote, Sharona Azriel, José Eulalio Bárcena, Pablo Cabezudo García, Ana Camacho Salas, Carlos Casanova Rodríguez, Ana María Cobo, Patricia Díaz Guardiola, Roberto Fernández-Torrón, María Pía Gallano Petit, Pablo García Pavía, María Gómez Gallego, Antonio José Gutiérrez Martínez, Ivonne Jericó, Solange Kapetanovic García, Adolfo López de Munaín Arregui, Loreto Martorell, Germán Morís de la Tassa, Raúl Moreno Zabaleta, José Luis Muñoz-Blanco, Juana Olivar Roldán, Samuel Ignacio Pascual Pascual, Rafael Peinado Peinado, Helena Pérez, Juan José Poza Aldea, María Rabasa, Alba Ramos, Alfredo Rosado Bartolomé, Miguel Ángel Rubio Pérez, Jon Andoni Urtizberea, Gustavo Zapata-Wainberg, Eduardo Gutiérrez-Rivas. Guía clínica para el diagnóstico y seguimiento de la distrofia miotónica tipo 1, DM1 o enfermedad de Steinert. Medicina Clínica 2019; 153(2) doi: 10.1016/j.medcli.2018.10.028
9
Samantha LoRusso, Benjamin Weiner, W. David Arnold. Myotonic Dystrophies: Targeting Therapies for Multisystem Disease. Neurotherapeutics 2018; 15(4) doi: 10.1007/s13311-018-00679-z
10
Stella Lanni, Christopher E. Pearson. Molecular genetics of congenital myotonic dystrophy. Neurobiology of Disease 2019; 132 doi: 10.1016/j.nbd.2019.104533
11
Molly White. Patient Input to Inform the Development of Central Nervous System Outcome Measures in Myotonic Dystrophy. Therapeutic Innovation & Regulatory Science 2020; 54(5) doi: 10.1007/s43441-020-00117-3
12
I. Lambert, A. Sevy. Hypersomnolence secondaire à une dystrophie myotonique de type 1 sans myotonie clinique. Médecine du Sommeil 2018; 15(2) doi: 10.1016/j.msom.2018.03.001
13
James D. Thomas, Łukasz J. Sznajder, Olgert Bardhi, Faaiq N. Aslam, Zacharias P. Anastasiadis, Marina M. Scotti, Ichizo Nishino, Masayuki Nakamori, Eric T. Wang, Maurice S. Swanson. Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy. Genes & Development 2017; 31(11) doi: 10.1101/gad.300590.117
14
Ambika G. Chidambaram, Sanjay Jhawar, Craig M. McDonald, Kiran Nandalike. Sleep Disordered Breathing in Children with Neuromuscular Disease. Children 2023; 10(10) doi: 10.3390/children10101675
15
Patricia Furlong, Ashish Dugar, Molly White. Patient engagement in clinical trial design for rare neuromuscular disorders: impact on the DELIVER and ACHIEVE clinical trials. Research Involvement and Engagement 2024; 10(1) doi: 10.1186/s40900-023-00535-1
16
Catherine Morgan, Michael E. Msall. Developmental and Behavioral Pediatrics. 2018;  doi: 10.1542/9781610021357-14
17
Omay Lee, Mary Porteous. Genetic testing and reproductive choice in neurological disorders. Practical Neurology 2017; 17(4) doi: 10.1136/practneurol-2017-001619
18
Fernando Suárez-Obando, Adriana Ordóñez-Vásquez, Luisa Fernanda Suárez Ordóñez, Juan Carlos Prieto. Métodos diagnósticos moleculares en enfermedades neuromusculares y neurodegenerativas de origen genético. Pediatría 2024; 57(1) doi: 10.14295/rp.v57i1.497
19
Dhvani H. Kuntawala, Rui Vitorino, Ana C. Cruz, Filipa Martins, Sandra Rebelo. Multisystem Symptoms in Myotonic Dystrophy Type 1: A Management and Therapeutic Perspective. International Journal of Molecular Sciences 2025; 26(11) doi: 10.3390/ijms26115350
20
Heather R. Gilbreath. Common Neuromuscular Disorders in Pediatrics. Physician Assistant Clinics 2016; 1(4) doi: 10.1016/j.cpha.2016.05.002
21
Robin Miralles, Deepa Panjwani. Emerging Topics and Controversies in Neonatology. 2020;  doi: 10.1007/978-3-030-28829-7_5
22
Thiéry De Serres-Bérard, Marion Pierre, Mohamed Chahine, Jack Puymirat. Deciphering the mechanisms underlying brain alterations and cognitive impairment in congenital myotonic dystrophy. Neurobiology of Disease 2021; 160 doi: 10.1016/j.nbd.2021.105532
23
Howard B. Panitch. Kendig's Disorders of the Respiratory Tract in Children. 2019;  doi: 10.1016/B978-0-323-44887-1.00021-3
24
Rebecca Folkerth. Perinatal Neuropathology. 2021;  doi: 10.1017/9781316671863.056
25
Sithara Ramdas, Sandeep Jayawant. Advances in neuromuscular disorders – an update. Paediatrics and Child Health 2017; 27(6) doi: 10.1016/j.paed.2017.02.009
26
Ahamodur Choudhury, Abdul Rahyead, Jochen Kammermeier, Mohamed Mutalib. The Use of Pyridostigmine in a Child With Chronic Intestinal Pseudo-Obstruction. Pediatrics 2018; 141(Supplement_5) doi: 10.1542/peds.2017-0007
27
Rie Asayama, Kaori Tanaka‐Nishikubo, Keiko Tanaka, Naohito Hato. High‐Resolution Pharyngeal Manometry Assessment of Swallowing in Asymptomatic Myotonic Dystrophy. Laryngoscope Investigative Otolaryngology 2025; 10(4) doi: 10.1002/lio2.70209
28
Slavica Ostojić, Gordana Kovačević, Giovanni Meola, Jovan Pešović, Dušanka Savić-Pavićević, Miloš Brkušanin, Ružica Kravljanac, Marina Perić, Jelena Martić, Katarina Pejić, Snežana Ristić, Stojan Perić. Main features and disease outcome of congenital myotonic dystrophy - experience from a single tertiary center. Neuromuscular Disorders 2024; 40 doi: 10.1016/j.nmd.2024.05.002
29
Louise Hartley, Laura Hyrapetian. Reference Module in Neuroscience and Biobehavioral Psychology. 2025;  doi: 10.1016/B978-0-323-95702-1.00418-8
30
Scott R. Auerbach, Carol Wittlieb-Weber. Heart Failure in the Child and Young Adult. 2026;  doi: 10.1016/B978-0-443-13279-7.00044-4
31
Melissa Borrelli, Gaetano Terrone, Roberto Evangelisti, Flora Fedele, Adele Corcione, Francesca Santamaria. Respiratory phenotypes of neuromuscular diseases: A challenging issue for pediatricians. Pediatrics & Neonatology 2023; 64(2) doi: 10.1016/j.pedneo.2022.09.016
32
Yuu Uchio, Masaya Zushi, Kaho Nakamura, Naoko Shima, Tetsuo Ikai. A Case of Congenital Myotonic Dystrophy with Rehabilitation Intervention in the Neonatal Intensive Care Unit. The Japanese Journal of Rehabilitation Medicine 2024; 61(2) doi: 10.2490/jjrmc.23003
33
Yuhei Hasuike, Hideki Mochizuki, Masayuki Nakamori. Cellular Senescence and Aging in Myotonic Dystrophy. International Journal of Molecular Sciences 2022; 23(4) doi: 10.3390/ijms23042339
34
Howard B Panitch. Respiratory Implications of Pediatric Neuromuscular Disease. Respiratory Care 2017; 62(6) doi: 10.4187/respcare.05250
35
Maya Braun, Shachar Shoshani, Joana Teixeira, Anna Mellul Shtern, Maya Miller, Zvi Granot, Sylvia E.J. Fischer, Susana M.D. A. Garcia, Yuval Tabach. Asymmetric inheritance of RNA toxicity in C. elegans expressing CTG repeats. iScience 2022; 25(5) doi: 10.1016/j.isci.2022.104246
36
Evan M. Pucillo, Deanna L. Dibella, Man Hung, Jerry Bounsanga, Becky Crockett, Melissa Dixon, Russell J. Butterfield, Craig Campbell, Nicholas E. Johnson. Physical function and mobility in children with congenital myotonic dystrophy. Muscle & Nerve 2017; 56(2) doi: 10.1002/mus.25482
37
Claire Johnson, Kathleen E. Langbehn, Jeffrey D. Long, David Moser, Stephen Cross, Laurie Gutmann, Peggy C. Nopoulos, Ellen van der Plas. Encoding of facial expressions in individuals with adult-onset myotonic dystrophy type 1. Journal of Clinical and Experimental Neuropsychology 2020; 42(9) doi: 10.1080/13803395.2020.1826410
38
Kathryn Kinser. Radiopaedia.org. 2019;  doi: 10.53347/rID-66131
39
Yanan Zhang, Bailey Wallace, Bo Cai, Nicholas Johnson, Emma Ciafaloni, Yedatore Swamy Venkatesh, Christina Westfield, Suzanne McDermott. Latent factors underlying the symptoms of adult-onset myotonic dystrophy type 1 during the clinical course. Orphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03359-8
40
Tohru Matsuura. Myotonic Dystrophy. 2018;  doi: 10.1007/978-981-13-0508-5_1
41
Vesna Martić-Popović, Marina Nikolić. Myotonic dystrophy type I with a special focus on clinical significance in pregnancy. Timocki medicinski glasnik 2026; 51(1) doi: 10.5937/tmg2601072M
42
John E Pascoe, Alexander Zygmunt, Zarmina Ehsan, Neepa Gurbani. Sleep in pediatric neuromuscular disorders. Seminars in Pediatric Neurology 2023; 48 doi: 10.1016/j.spen.2023.101092
43
Göknur Haliloğlu, Gianina Ravenscroft. The evolving genetic landscape of neuromuscular fetal akinesias. Journal of Neuromuscular Diseases 2025; 12(5) doi: 10.1177/22143602251339357
44
Mousa Ahmadpour‐kacho, Yadollah Zahed Pasha, Samira Pournajaf. A couple of the first cousins born with hypotonia and maternal polyhydramnios. Clinical Case Reports 2024; 12(2) doi: 10.1002/ccr3.8503
45
Oscar J. Wambuguh. Research Anthology on Pediatric and Adolescent Medicine. 2022;  doi: 10.4018/978-1-6684-5360-5.ch009
46
Tiyasha De, Pooja Sharma, Bharathram Upilli, A. Vivekanand, Shreya Bari, Akhilesh Kumar Sonakar, Achal Kumar Srivastava, Mohammed Faruq. Spinocerebellar ataxia type 27B (SCA27B) in India: insights from a large cohort study suggest ancient origin. Neurogenetics 2024; 25(4) doi: 10.1007/s10048-024-00770-y
47
Laurène M. André, Remco T.P. van Cruchten, Marieke Willemse, Karel Bezstarosti, Jeroen A.A. Demmers, Ellen L. van Agtmaal, Derick G. Wansink, Bé Wieringa. Recovery in the Myogenic Program of Congenital Myotonic Dystrophy Myoblasts after Excision of the Expanded (CTG)n Repeat. International Journal of Molecular Sciences 2019; 20(22) doi: 10.3390/ijms20225685
48
Kosuke Shigematsu, Yukiko Mikami, Mamiko Shinsaka, Masanobu Kinoshita, Yasushi Takai. Congenital Phenotypes and DMPK CTG Repeat Number in Mothers/Children with Myotonic Dystrophy Type 1. OBM Genetics 2023; 7(01) doi: 10.21926/obm.genet.2301179
49
Bryan P. Fitzgerald, Kelly M. Conn, Joanne Smith, Andrew Walker, Amy L. Parkhill, James E. Hilbert, Elizabeth A. Luebbe, Richard T. Moxley III. Medication adherence in patients with myotonic dystrophy and facioscapulohumeral muscular dystrophy. Journal of Neurology 2016; 263(12) doi: 10.1007/s00415-016-8300-3
50
E.O. Ivanova, A.N. Moskalenko, E.Y. Fedotova, S.A. Kurbatov, S.N. Illarioshkin. Myotonic dystrophy: genetics and clinical polymorphism . Annals of Clinical and Experimental Neurology 2019; 13(1) doi: 10.25692/ACEN.2019.1.2
51
Jennifer C. Keene, Ulrike Mietzsch, Niranjana Natarajan. Hypotonia in the Neonatal Intensive Care Unit. Clinics in Perinatology 2025; 52(2) doi: 10.1016/j.clp.2025.02.013
52
E. K. Erokhina, E. A. Melnik, D. V. Vlodavets. Clinical characteristics of different forms of myotonic dystrophy type 1. Russian Journal of Child Neurology 2023; 18(1) doi: 10.17650/2073-8803-2023-18-1-22-37
53
Alex S. García-Gutiérrez, Adriana E. Pérez-Padilla, Jose E. Leon-Rojas, Edison Ramos-Gonzales, Iván Ramírez, María B. Trujillo. Complicated Traumatic Nerve Injury Treated with Tendon Transfers in a Patient with Myotonic Dystrophy. JBJS Case Connector 2021; 11(2) doi: 10.2106/JBJS.CC.21.00100
54
Examining the Causal Relationship Between Genes, Epigenetics, and Human Health. Advances in Bioinformatics and Biomedical Engineering 2019;  doi: 10.4018/978-1-5225-8066-9.ch017
55
Larry D. Purnell, Eric A. Fenkl. Handbook for Culturally Competent Care. 2019;  doi: 10.1007/978-3-030-21946-8_14
56
Laia Brunet Garcia, Ankita Hajra, Ella Field, Joseph Wacher, Helen Walsh, Gabrielle Norrish, Adnan Manzur, Francesco Muntoni, Pinki Munot, Stephanie Robb, Rosaline Quinlivan, Mariacristina Scoto, Giovanni Baranello, Anna Sarkozy, Luke Starling, Juan Pablo Kaski, Elena Cervi. Cardiac Manifestations of Myotonic Dystrophy in a Pediatric Cohort. Frontiers in Pediatrics 2022; 10 doi: 10.3389/fped.2022.910660
57
Heather A. Hayes, Deanna Dibella, Rebecca Crockett, Melissa Dixon, Russel J. Butterfield, Nicholas E. Johnson. Stepping Activity in Children With Congenital Myotonic Dystrophy. Pediatric Physical Therapy 2018; 30(4) doi: 10.1097/PEP.0000000000000537
58
Rosemary Rogers, Kelly Moyer, Kenneth J. Moise. Congenital myotonic dystrophy: An overlooked diagnosis not amenable to detection by sequencing. Prenatal Diagnosis 2022; 42(2) doi: 10.1002/pd.6105
59
Vamsi Krishna Murthy Ginjupalli, Jean-Baptiste Reisqs, Michael Cupelli, Mohamed Chahine, Mohamed Boutjdir. Cardiac Involvement in Myotonic Dystrophy Type 1: Mechanisms, Clinical Perspectives, and Emerging Therapeutic Strategies. International Journal of Molecular Sciences 2025; 26(22) doi: 10.3390/ijms262210992
60
Sameera Vattipalli, Girija Prasad Rath, Umeshkumar Athiraman. Fundamentals of Pediatric Neuroanesthesia. 2021;  doi: 10.1007/978-981-16-3376-8_35
61
C. Sarret, B. Khalili, B. Pontier, F. Laffargue. Quand suspecter une maladie musculaire chez l’enfant ?. Perfectionnement en Pédiatrie 2018; 1(3) doi: 10.1016/j.perped.2018.07.006
62
Kristofoor E. Leeuwenberg, Johanna E. Bruijnes, llse Karnebeek, Fran Smulders, Sandra Altena-Rensen, Caroline M.L. Gorissen-Brouwers, Sylvia Klinkenberg, Catharina G. Faber, Hilde Braakman, Karlien Mul. The blind men and the elephant: recognising the multisystem symptoms of myotonic dystrophy type 1. Orphanet Journal of Rare Diseases 2025; 20(1) doi: 10.1186/s13023-025-03920-z
63
Anwar Baban, Valentina Lodato, Giovanni Parlapiano, Corrado di Mambro, Rachele Adorisio, Enrico Silvio Bertini, Carlo Dionisi-Vici, Fabrizio Drago, Diego Martinelli. Myocardial and Arrhythmic Spectrum of Neuromuscular Disorders in Children. Biomolecules 2021; 11(11) doi: 10.3390/biom11111578
64
Valeria Dipasquale, Rossella Morello, Claudio Romano. Gastrointestinal and nutritional care in pediatric neuromuscular disorders. World Journal of Clinical Pediatrics 2023; 12(4): 197-204 doi: 10.5409/wjcp.v12.i4.197
65
Stephan Wenninger, Federica Montagnese, Benedikt Schoser. Core Clinical Phenotypes in Myotonic Dystrophies. Frontiers in Neurology 2018; 9 doi: 10.3389/fneur.2018.00303
66
Kiera N. Berggren, Man Hung, Melissa M. Dixon, Jerry Bounsanga, Becky Crockett, Mary D. Foye, Yushan Gu, Craig Campbell, Russell J. Butterfield, Nicholas E. Johnson. Orofacial strength, dysarthria, and dysphagia in congenital myotonic dystrophy. Muscle & Nerve 2018; 58(3) doi: 10.1002/mus.26176
67
Irina V. Grishchenko, Yana V. Purvinsh, Dmitry V. Yudkin. Mechanisms of Genome Protection and Repair. Advances in Experimental Medicine and Biology 2020; 1241 doi: 10.1007/978-3-030-41283-8_7
68
M. De Antonio, C. Dogan, D. Hamroun, M. Mati, S. Zerrouki, B. Eymard, S. Katsahian, G. Bassez. Unravelling the myotonic dystrophy type 1 clinical spectrum: A systematic registry-based study with implications for disease classification. Revue Neurologique 2016; 172(10) doi: 10.1016/j.neurol.2016.08.003
69
Daniel Delgado Seneor, João Paulo Barile, Patrícia Marques Mendes, Marco Orsini, Eduardo Mendonça Werneck da Silva, Igor Braga Farias, Paulo de Lima Serrano, Wladimir Bocca Vieira de Rezende Pinto, Acary Souza Bulle Oliveira, Paulo Victor Sgobbi de Souza. Arthrogryposis Multiplex Congenita: Comprehensive Review from a Neuromuscular Standpoint. Genes 2026; 17(6) doi: 10.3390/genes17060675
70
Hari Gourabathini, Mohammad Sallam, Vanessa Marthia, Omar Alibrahim. Biphasic Cuirass Noninvasive Ventilation. Noninvasive Ventilation. The Essentials 2026;  doi: 10.1007/978-3-032-20933-7_28
71
Inês Cascais, Cristina Garrido, Lurdes Morais, Rosa Amorim, Rosa Lima, Helena Ferreira Mansilha, Teresa Correia, António Oliveira, Manuela Santos. Myotonic dystrophy type 1 (Steinert disease): 29 years of experience at a tertiary pediatric hospital. European Journal of Paediatric Neurology 2024; 48 doi: 10.1016/j.ejpn.2023.12.001
72
Fang-Tzu Wu, Chih-Ping Chen. Too Much of a Good Thing: Updated Current Management and Perinatal Outcomes of Polyhydramnios. Journal of Medical Ultrasound 2024; 32(4) doi: 10.4103/jmu.jmu_83_24
73
Irene Valenzuela, Marcos Linés, Elena Martínez-Sáez, Ana Cueto-González, Félix Castillo, Eduardo Tizzano. Clinical study of a patient with congenital myotonic dystrophy reveals chylothorax as neonatal presentation of the disease. Case Reports in Perinatal Medicine 2018; 7(1) doi: 10.1515/crpm-2017-0025
74
James D. Thomas, Ruan Oliveira, Łukasz J. Sznajder, Maurice S. Swanson. Myotonic Dystrophy and Developmental Regulation of RNA Processing. Comprehensive Physiology 2018; 8(2) doi: 10.1002/j.2040-4603.2018.tb00015.x
75
Hirohisa Fujikawa, Daigo Hayashi, Minoru Saito. Myotonic dystrophy type 1 presenting with grip myotonia and functional improvement after rehabilitation. BMJ Case Reports 2021; 14(4) doi: 10.1136/bcr-2021-241552
76
Fang Kuan Chiou, Hina Rizvi, Ros Quinlivan, Girish L. Gupte. Congenital Myotonic Dystrophy with Combined Heterozygous ATP8B1/ABCB4 Mutation Leading to Progressive Cholestasis and Liver Failure. JPGN Reports 2021; 2(4) doi: 10.1097/PG9.0000000000000121
77
G. Gutiérrez Gutiérrez, J. Díaz-Manera, M. Almendrote, S. Azriel, J. Eulalio Bárcena, P. Cabezudo García, A. Camacho Salas, C. Casanova Rodríguez, A.M. Cobo, P. Díaz Guardiola, R. Fernández-Torrón, M.P. Gallano Petit, P. García Pavía, M. Gómez Gallego, A.J. Gutiérrez Martínez, I. Jericó, S. Kapetanovic García, A. López de Munaín Arregui, L. Martorell, G. Morís de la Tassa, R. Moreno Zabaleta, J.L. Muñoz-Blanco, J. Olivar Roldán, S.I. Pascual Pascual, R. Peinado Peinado, H. Pérez, J.J. Poza Aldea, M. Rabasa, A. Ramos, A. Rosado Bartolomé, M.Á. Rubio Pérez, J.A. Urtizberea, G. Zapata-Wainberg, E. Gutiérrez-Rivas. Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease. Neurología (English Edition) 2020; 35(3) doi: 10.1016/j.nrleng.2019.01.008
78
Yanyun Wu, Qianqian Wei, Junyu Lin, Huifang Shang, Ruwei Ou. Cognitive impairment, neuroimaging abnormalities, and their correlations in myotonic dystrophy: a comprehensive review. Frontiers in Cellular Neuroscience 2024; 18 doi: 10.3389/fncel.2024.1369332
79
Jodi S. Dashe, Eva K. Pressman, Judith U. Hibbard. SMFM Consult Series #46: Evaluation and management of polyhydramnios. American Journal of Obstetrics and Gynecology 2018; 219(4) doi: 10.1016/j.ajog.2018.07.016
80
Jean-Paul Praud, Gregory J. Redding. Kendig's Disorders of the Respiratory Tract in Children. 2019;  doi: 10.1016/B978-0-323-44887-1.00072-9
81
Adele D’Amico, Enrico Bertini. Neurology. 2019;  doi: 10.1016/B978-0-323-54392-7.00013-3
82
Federica Trucco, Andrea Lizio, Elisabetta Roma, Alessandra di Bari, Francesca Salmin, Emilio Albamonte, Jacopo Casiraghi, Susanna Pozzi, Stefano Becchiati, Laura Antonaci, Anna Salvalaggio, Michela Catteruccia, Michele Tosi, Gemma Marinella, Federica R. Danti, Fabio Bruschi, Marco Veneruso, Stefano Parravicini, Chiara Fiorillo, Angela Berardinelli, Antonella Pini, Isabella Moroni, Guja Astrea, Roberta Battini, Adele D’Amico, Federica Ricci, Marika Pane, Eugenio M. Mercuri, Nicholas E. Johnson, Valeria A. Sansone. Association between Reported Sleep Disorders and Behavioral Issues in Children with Myotonic Dystrophy Type 1—Results from a Retrospective Analysis in Italy. Journal of Clinical Medicine 2024; 13(18) doi: 10.3390/jcm13185459
83
Y. Chaix. Enfants DYS. 2018;  doi: 10.1016/B978-2-294-74877-6.00006-9
84
Marinee Chuah, Yoke Chin Chai, Sumitava Dastidar, Thierry VandenDriessche. Muscle Gene Therapy. 2019;  doi: 10.1007/978-3-030-03095-7_30
85
James D. Thomas, Ruan Oliveira, Łukasz J. Sznajder, Maurice S. Swanson. Comprehensive Physiology. 2018;  doi: 10.1002/cphy.c170002
86
Giuseppa Maresca, Simona Portaro, Antonino Naro, Ileana Scarcella, Placido Bramanti, David Militi, Maria Accorinti, Rosaria De Luca, Rocco Salvatore Calabrò. Look at the cognitive deficits in patients with myotonic dystrophy type 1: an exploratory research on the effects of virtual reality. International Journal of Rehabilitation Research 2020; 43(1) doi: 10.1097/MRR.0000000000000384
87
Qian Zhao, Shupeng Wang, Yang Wang, Shenggang Ding. Neonatal congenital myotonic dystrophy with DMPK gene expansion: clinical features and short-term outcomes. Frontiers in Pediatrics 2026; 13 doi: 10.3389/fped.2025.1648611
88
Meryl T Thomas, Swapnil Shah, Himanshu Popat, Bernadette Hanna, Pranav Jani. Hypoglycaemia and myotonic dystrophy. Journal of Paediatrics and Child Health 2022; 58(4) doi: 10.1111/jpc.15633
89
Milena Rizzo, Pascale Beffy, Renata Del Carratore, Alessandra Falleni, Virginia Pretini, Romina D’Aurizio, Annalisa Botta, Monica Evangelista, Andrea Stoccoro, Fabio Coppedè, Denis Furling, Marcella Simili. Activation of the interferon type I response rather than autophagy contributes to myogenesis inhibition in congenital DM1 myoblasts. Cell Death & Disease 2018; 9(11) doi: 10.1038/s41419-018-1080-1
90
Siham Ait Benichou, Dominic Jauvin, Thiéry De Serres-Bérard, Marion Pierre, Karen K. Ling, C. Frank Bennett, Frank Rigo, Genevieve Gourdon, Mohamed Chahine, Jack Puymirat. Antisense oligonucleotides as a potential treatment for brain deficits observed in myotonic dystrophy type 1. Gene Therapy 2022; 29(12) doi: 10.1038/s41434-022-00316-7
91
Michio Kobayashi. Complications of Myotonic Dystrophy. The Japanese Journal of Rehabilitation Medicine 2022; 59(2) doi: 10.2490/jjrmc.59.175
92
Deysi Licourt Otero, Melissa Toledo Licourt, Belkys Candelaria Gómez, Ilena Aurora Díaz Hernández. Congenital Myotonic Dystrophy type 1: prenatal manifestations regarding a case. SCT Proceedings in Interdisciplinary Insights and Innovations 2024; 1 doi: 10.56294/piii2023102
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