Research graph
References from Congenital Clubfoot as an Early Manifestation of Duchenne Muscular Dystrophy?. Local targets link to admitted publications; unresolved targets remain external evidence.
Analysis of data from the registry of children with idiopathic congenital clubfoot in Saint Petersburg from 2020 to 2024
10.17816/ptors701316 · 2026 · External reference
Comparison of Ponseti versus surgical treatment for idiopathic clubfoot: A short-term preliminary report
10.1007/s11999-009-0819-5 · 2009 · External reference
Modern concepts of conservative treatment methods of clubfoot
10.17816/ptors2420-31 · 2014 · External reference
The etiology of idiopathic congenital talipes equinovarus: A systematic review
10.1186/s13018-018-0913-z · 2018 · External reference
Functional Assessment of Clubfoot Associated HOXA9, TPM1, and TPM2 Variants Suggests a Potential Gene Regulation Mechanism
10.1007/s11999-016-4788-1 · 2016 · External reference
Prenatal Diagnosis and Functional Analysis of Two Compound Heterozygous Variants in the KLHL40 Gene Causing Nemaline Myopathy 8
10.1002/mgg3.70270 · 2026 · External reference
Genetic Role in Recurrence of Idiopathic CTEV: A Systematic Review
2023 · External reference
The genetics of isolated and syndromic clubfoot
10.1302/1863-2548.13.190063 · 2019 · External reference
Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion
10.1097/corr.0000000000001957 · 2022 · External reference
Diagnosis and management of Duchenne muscular dystrophy, part 1: Diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management
10.1016/s1474-4422(18)30024-3 · 2018 · External reference
Orthopedic management in Duchenne muscular dystrophy
10.1016/s0929-693x(25)00251-9 · 2025 · External reference
Current Concepts in the Orthopedic Management of Duchenne Muscular Dystrophy
2024 · External reference
Downstream Pathways of Dystrophin Deficiency in Duchenne Muscular Dystrophy: Implications for Muscle Degeneration and Regeneration
10.1002/jcsm.70333 · 2026 · External reference
Intrinsic dysfunction in muscle stem cells lacking dystrophin begins during secondary myogenesis
10.1038/s41467-025-64999-3 · 2025 · External reference
Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation
10.1242/dmm.001008 · 2009 · External reference
The evolving genetic landscape of neuromuscular fetal akinesias
10.1177/22143602251339357 · 2025 · External reference
Is webbing (pterygia) a constant feature in patients with Escobar syndrome?
10.1111/os.12064 · 2013 · External reference
Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum
10.1002/acn3.70088 · 2025 · External reference
Dystrophin and utrophin: Genetic analyzes of their role in skeletal muscle
10.1002/(sici)1097-0029(20000201/15)48:3/4<155::aid-jemt4>3.0.co;2-0 · 2000 · External reference
10.3389/fgene.2025.1664424
10.3389/fgene.2025.1664424 · External reference
Role of genetic determinants in the development of congenital scoliosis: A review
10.17816/ptors636350 · 2025 · External reference
Genetics of clubfoot
10.1097/bpb.0b013e328349927c · 2012 · External reference
Usefulness and accessibility of information on the treatment of children with congenital clubfoot: Results of a survey of parents
10.17816/ptors634027 · 2024 · External reference
Clinical and radiological variants of the nail–patella syndrome: Why is it important to make a correct diagnosis?
10.17816/ptors630082 · 2024 · External reference
Assessment of the frequency of fibrodysplasia ossificans progressiva (FOP) in Russia
2025 · External reference
Fibrodysplasia ossificans progressiva: Clinical and genetic aspects
10.1186/1750-1172-6-80 · 2011 · External reference
A Review of Muscle Relaxants in Anesthesia in Patients with Neuromuscular Disorders Including Guillain-Barré Syndrome, Myasthenia Gravis, Duchenne Muscular Dystrophy, Charcot-Marie-Tooth Disease, and Inflammatory Myopathies
10.12659/msm.945675 · 2024 · External reference
Reação atípica à anestesia em dystrophia muscular de Duchenne/Becker [Atypical reaction to anesthesia in Duchenne/Becker muscular dystrophy]
10.1016/j.bjan.2017.04.015 · 2018 · External reference
Neuromuscular conditions associated with malignant hyperthermia in pediatric patients: A 25-year retrospective study
10.1016/j.nmd.2016.02.007 · 2016 · External reference
Anesthesia and Duchenne or Becker muscular dystrophy: Review of 117 anesthetic exposures
10.1111/pan.12248 · 2013 · External reference
Treatment of the Lower Extremity Contracture/Deformities
10.1097/bpo.0000000000001005 · 2017 · External reference
10.3390/genes17050533
10.3390/genes17050533 · External reference
Rewriting Duchenne muscular dystrophy therapy
10.1016/j.cell.2026.06.011 · 2026 · External reference
Gene-based therapies for neuromuscular disorders
2024 · External reference
10.1136/jnnp-2026-339071
10.1136/jnnp-2026-339071 · External reference
Change in respiratory outcomes in adults with Duchenne muscular dystrophy in the era of corticosteroids
10.1177/22143602251386096 · 2026 · External reference
10.1371/journal.pone.0345550
10.1371/journal.pone.0345550 · External reference
Delayed diagnosis and genetic testing in spinal muscular atrophy: A case series
10.1080/07853890.2026.2728198 · 2026 · External reference
Treating neuromuscular diseases: Unveiling gene therapy breakthroughs and pioneering future applications
10.1186/s12929-025-01123-z · 2025 · External reference
Gene Therapy for Neuromuscular Diseases: Health Economic Challenges and Future Perspectives
10.3233/jnd-221540 · 2022 · External reference
Selective immunosuppressant tofacitinib in a child with multiple epiphyseal dysplasia associated with osteoarthritic changes: A case report
10.17816/ptors688792 · 2025 · External reference
10.3390/ijms26083579
10.3390/ijms26083579 · External reference
10.3390/biomedicines12040912
10.3390/biomedicines12040912 · External reference
Dystrophin and utrophin: Genetic analyzes of their role in skeletal muscle
10.1002/(sici)1097-0029(20000201/15)48:3/4<155::aid-jemt4>3.0.co;2-0 · ExternalCitation · doi-reference
Fetal Akinesia/Hypokinesia and Arthrogryposis of Neuromuscular Origin: Etiologic Groups, Genetics, and Phenotypic Spectrum
10.1002/acn3.70088 · ExternalCitation · doi-reference
Downstream Pathways of Dystrophin Deficiency in Duchenne Muscular Dystrophy: Implications for Muscle Degeneration and Regeneration
10.1002/jcsm.70333 · ExternalCitation · doi-reference
Prenatal Diagnosis and Functional Analysis of Two Compound Heterozygous Variants in the KLHL40 Gene Causing Nemaline Myopathy 8
10.1002/mgg3.70270 · ExternalCitation · doi-reference
Comparison of Ponseti versus surgical treatment for idiopathic clubfoot: A short-term preliminary report
10.1007/s11999-009-0819-5 · ExternalCitation · doi-reference
Functional Assessment of Clubfoot Associated HOXA9, TPM1, and TPM2 Variants Suggests a Potential Gene Regulation Mechanism
10.1007/s11999-016-4788-1 · ExternalCitation · doi-reference
Reação atípica à anestesia em dystrophia muscular de Duchenne/Becker [Atypical reaction to anesthesia in Duchenne/Becker muscular dystrophy]
10.1016/j.bjan.2017.04.015 · ExternalCitation · doi-reference
Rewriting Duchenne muscular dystrophy therapy
10.1016/j.cell.2026.06.011 · ExternalCitation · doi-reference
Neuromuscular conditions associated with malignant hyperthermia in pediatric patients: A 25-year retrospective study
10.1016/j.nmd.2016.02.007 · ExternalCitation · doi-reference
Orthopedic management in Duchenne muscular dystrophy
10.1016/s0929-693x(25)00251-9 · ExternalCitation · doi-reference
Diagnosis and management of Duchenne muscular dystrophy, part 1: Diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management
10.1016/s1474-4422(18)30024-3 · ExternalCitation · doi-reference
Intrinsic dysfunction in muscle stem cells lacking dystrophin begins during secondary myogenesis
10.1038/s41467-025-64999-3 · ExternalCitation · doi-reference
Delayed diagnosis and genetic testing in spinal muscular atrophy: A case series
10.1080/07853890.2026.2728198 · ExternalCitation · doi-reference
Genetics of clubfoot
10.1097/bpb.0b013e328349927c · ExternalCitation · doi-reference
Treatment of the Lower Extremity Contracture/Deformities
10.1097/bpo.0000000000001005 · ExternalCitation · doi-reference
Whole Exome Sequencing in Individuals with Idiopathic Clubfoot Reveals a Recurrent Filamin B (FLNB) Deletion
10.1097/corr.0000000000001957 · ExternalCitation · doi-reference
Is webbing (pterygia) a constant feature in patients with Escobar syndrome?
10.1111/os.12064 · ExternalCitation · doi-reference
Anesthesia and Duchenne or Becker muscular dystrophy: Review of 117 anesthetic exposures
10.1111/pan.12248 · ExternalCitation · doi-reference
10.1136/jnnp-2026-339071
10.1136/jnnp-2026-339071 · ExternalCitation · doi-reference
The evolving genetic landscape of neuromuscular fetal akinesias
10.1177/22143602251339357 · ExternalCitation · doi-reference
Change in respiratory outcomes in adults with Duchenne muscular dystrophy in the era of corticosteroids
10.1177/22143602251386096 · ExternalCitation · doi-reference
Fibrodysplasia ossificans progressiva: Clinical and genetic aspects
10.1186/1750-1172-6-80 · ExternalCitation · doi-reference
Treating neuromuscular diseases: Unveiling gene therapy breakthroughs and pioneering future applications
10.1186/s12929-025-01123-z · ExternalCitation · doi-reference
The etiology of idiopathic congenital talipes equinovarus: A systematic review
10.1186/s13018-018-0913-z · ExternalCitation · doi-reference
Muscular dystrophy begins early in embryonic development deriving from stem cell loss and disrupted skeletal muscle formation
10.1242/dmm.001008 · ExternalCitation · doi-reference
A Review of Muscle Relaxants in Anesthesia in Patients with Neuromuscular Disorders Including Guillain-Barré Syndrome, Myasthenia Gravis, Duchenne Muscular Dystrophy, Charcot-Marie-Tooth Disease, and Inflammatory Myopathies
10.12659/msm.945675 · ExternalCitation · doi-reference
The genetics of isolated and syndromic clubfoot
10.1302/1863-2548.13.190063 · ExternalCitation · doi-reference
10.1371/journal.pone.0345550
10.1371/journal.pone.0345550 · ExternalCitation · doi-reference
Modern concepts of conservative treatment methods of clubfoot
10.17816/ptors2420-31 · ExternalCitation · doi-reference
Clinical and radiological variants of the nail–patella syndrome: Why is it important to make a correct diagnosis?
10.17816/ptors630082 · ExternalCitation · doi-reference
Usefulness and accessibility of information on the treatment of children with congenital clubfoot: Results of a survey of parents
10.17816/ptors634027 · ExternalCitation · doi-reference
Role of genetic determinants in the development of congenital scoliosis: A review
10.17816/ptors636350 · ExternalCitation · doi-reference
Selective immunosuppressant tofacitinib in a child with multiple epiphyseal dysplasia associated with osteoarthritic changes: A case report
10.17816/ptors688792 · ExternalCitation · doi-reference
Analysis of data from the registry of children with idiopathic congenital clubfoot in Saint Petersburg from 2020 to 2024
10.17816/ptors701316 · ExternalCitation · doi-reference
Gene Therapy for Neuromuscular Diseases: Health Economic Challenges and Future Perspectives
10.3233/jnd-221540 · ExternalCitation · doi-reference
10.3389/fgene.2025.1664424
10.3389/fgene.2025.1664424 · ExternalCitation · doi-reference
10.3390/biomedicines12040912
10.3390/biomedicines12040912 · ExternalCitation · doi-reference
10.3390/genes17050533
10.3390/genes17050533 · ExternalCitation · doi-reference
10.3390/ijms26083579
10.3390/ijms26083579 · ExternalCitation · doi-reference
