Found: 33
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Increased Upper Extremity Muscle Mass in Ambulatory Children with Cerebral Palsy.
- Published in:
- Life (2075-1729), 2024, v. 14, n. 3, p. 303, doi. 10.3390/life14030303
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- Publication type:
- Article
Phenotype of a Patient With a 1p36.11-p35.3 Interstitial Deletion Encompassing the AHDC1.
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- Annals of Laboratory Medicine, 2017, v. 37, n. 6, p. 563, doi. 10.3343/alm.2017.37.6.563
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- Publication type:
- Article
Novel Mutation (c.8725T>C) in Two Siblings With Late-Onset LAMA2-Related Muscular Dystrophy.
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- Annals of Laboratory Medicine, 2017, v. 37, n. 4, p. 359, doi. 10.3343/alm.2017.37.4.359
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- Publication type:
- Article
Autistic and Rett-like features associated with 2q33.3-q34 interstitial deletion.
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- American Journal of Medical Genetics. Part A, 2015, v. 167A, n. 9, p. 2213, doi. 10.1002/ajmg.a.37119
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- Publication type:
- Article
Anti-inflammatory and lymphangiogenetic effects of low-level laser therapy on lymphedema in an experimental mouse tail model.
- Published in:
- 2016
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- Publication type:
- journal article
Relationship between starting age of cranial-remolding-orthosis therapy and effectiveness of treatment in children with deformational plagiocephaly.
- Published in:
- Child's Nervous System, 2017, v. 33, n. 8, p. 1349, doi. 10.1007/s00381-017-3427-9
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- Publication type:
- Article
Correlation Between Vanishing White Matter Disease and Novel Heterozygous EIF2B3 Variants Using Next-Generation Sequencing: A Case Report.
- Published in:
- Annals of Rehabilitation Medicine, 2019, v. 43, n. 2, p. 234, doi. 10.5535/arm.2019.43.2.234
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- Publication type:
- Article
A Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3.
- Published in:
- Annals of Rehabilitation Medicine, 2017, v. 41, n. 5, p. 881, doi. 10.5535/arm.2017.41.5.881
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- Publication type:
- Article
Relationship Between Mobility and Self-Care Activity in Children With Cerebral Palsy.
- Published in:
- Annals of Rehabilitation Medicine, 2017, v. 41, n. 2, p. 266, doi. 10.5535/arm.2017.41.2.266
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- Publication type:
- Article
Sonographic Findings of Polyneuropathy Associated With Cerebrotendinous Xanthomatosis: A Case Report.
- Published in:
- Annals of Rehabilitation Medicine, 2017, v. 41, n. 2, p. 313, doi. 10.5535/arm.2017.41.2.313
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- Publication type:
- Article
Identification of a Heterozygous SPG11 Mutation by Clinical Exome Sequencing in a Patient With Hereditary Spastic Paraplegia: A Case Report.
- Published in:
- 2016
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- Publication type:
- Case Study
Clinical Findings of Asymptomatic Carpal Tunnel Syndrome in Patients With Diabetes Mellitus.
- Published in:
- Annals of Rehabilitation Medicine, 2016, v. 40, n. 3, p. 489, doi. 10.5535/arm.2016.40.3.489
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- Publication type:
- Article
The Influence of Arm Swelling Duration on Shoulder Pathology in Breast Cancer Patients with Lymphedema.
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- PLoS ONE, 2015, v. 10, n. 11, p. 1, doi. 10.1371/journal.pone.0142950
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- Publication type:
- Article
Dysphagia and Hoarseness Associated with Painless Aortic Dissection: A Rare Case of Cardiovocal Syndrome.
- Published in:
- Dysphagia (0179051X), 2006, v. 21, n. 2, p. 129, doi. 10.1007/s00455-006-9015-x
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- Publication type:
- Article
Hereditary Sensory and Autonomic Neuropathy 2B Caused by a Novel RETREG1 Mutation (c.765dupT) and Paternal Uniparental Isodisomy of Chromosome 5.
- Published in:
- Frontiers in Genetics, 2019, v. 10, p. 1, doi. 10.3389/fgene.2019.01085
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- Publication type:
- Article
The Effect of the ‘Touch Screen-Based Cognitive Training’ for Children with Severe Cognitive Impairment in Special Education.
- Published in:
- Children, 2021, v. 8, n. 12, p. 1, doi. 10.3390/children8121205
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- Publication type:
- Article
Congenital Osseous Torticollis that Mimics Congenital Muscular Torticollis: A Retrospective Observational Study.
- Published in:
- Children, 2020, v. 7, n. 11, p. 1, doi. 10.3390/children7110227
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- Publication type:
- Article
Changes in Muscle Mass after Botulinum Toxin Injection in Children with Spastic Hemiplegic Cerebral Palsy.
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- Toxins, 2021, v. 13, n. 4, p. 278, doi. 10.3390/toxins13040278
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- Publication type:
- Article
Botulinum Toxin Injection in Children with Hemiplegic Cerebral Palsy: Correction of Growth through Comparison of Treated and Unaffected Limbs.
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- Toxins, 2019, v. 11, n. 12, p. 688, doi. 10.3390/toxins11120688
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- Publication type:
- Article
Comparison between the radionuclide salivagram and videofluoroscopic swallowing study methods for evaluating patients with aspiration pneumonia.
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- Annals of Nuclear Medicine, 2013, v. 27, n. 3, p. 247, doi. 10.1007/s12149-012-0680-6
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- Publication type:
- Article
Usefulness of comprehensive targeted multigene panel sequencing for neuromuscular disorders in Korean patients.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 10, p. N.PAG, doi. 10.1002/mgg3.947
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- Publication type:
- Article
Two novel mutations in TTN of a patient with congenital myopathy: A case report.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 8, p. N.PAG, doi. 10.1002/mgg3.866
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- Publication type:
- Article
Compound heterozygous variants including a novel copy number variation in a child with atypical ataxia-telangiectasia: a case report.
- Published in:
- BMC Medical Genomics, 2021, v. 14, n. 1, p. 1, doi. 10.1186/s12920-021-01053-3
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- Publication type:
- Article
Diagnostic Yield of Trio Whole-Genome Sequencing in Children with Undiagnosed Developmental Delay or Congenital Anomaly: A Prospective Cohort Study.
- Published in:
- Diagnostics (2075-4418), 2024, v. 14, n. 15, p. 1680, doi. 10.3390/diagnostics14151680
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- Publication type:
- Article
Prominent Asymmetric Muscle Weakness and Atrophy in Seronegative Immune-Mediated Necrotizing Myopathy.
- Published in:
- 2021
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- Publication type:
- Case Study
Incidental Severe Fatty Degeneration of the Erector Spinae in a Patient with L5–S1 Disc Extrusion Diagnosed with Limb-Girdle Muscular Dystrophy R2 Dysferin-Related.
- Published in:
- Diagnostics (2075-4418), 2020, v. 10, n. 8, p. 530, doi. 10.3390/diagnostics10080530
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- Publication type:
- Article
Case Report: The success of face analysis technology in extremely rare genetic diseases in Korea: Tatton-Brown-Rahman syndrome and Say-Barber -Biesecker-Young-Simpson variant of ohdo syndrome.
- Published in:
- Frontiers in Genetics, 2022, v. 13, p. 01, doi. 10.3389/fgene.2022.903199
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- Publication type:
- Article
Hypoxic conditioned medium from mesenchymal stem cells promotes lymphangiogenesis by regulation of mitochondrial-related proteins.
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- Stem Cell Research & Therapy, 2016, v. 7, p. 1, doi. 10.1186/s13287-016-0296-1
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- Publication type:
- Article
Lateral Spread Responses on Facial Motor Nucleus Suppression Using Intravenous Diazepam in Hemifacial Spasm.
- Published in:
- PM & R: Journal of Injury, Function & Rehabilitation, 2013, v. 5, n. 9, p. S152, doi. 10.1016/j.pmrj.2013.08.065
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- Publication type:
- Article
Lateral Spread Responses on Facial Motor Nucleus Suppression Using Intravenous Diazepam in Hemifacial Spasm.
- Published in:
- 2013
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- Publication type:
- Abstract
Usefulness of the Tendon Reflex for Assessing Spasticity After Botulinum Toxin-A Injection in Children With Cerebral Palsy.
- Published in:
- Journal of Child Neurology, 2013, v. 28, n. 1, p. 21, doi. 10.1177/0883073812450615
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- Publication type:
- Article
Peripheral Nerve Involvement in Fukuyama Congenital Muscular Dystrophy: A Case Report.
- Published in:
- 2013
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- Publication type:
- Case Study
Neurodevelopmental Outcomes in Very Low-Birth-Weight Infants in Korea: 1998-2007 vs 1989-1997.
- Published in:
- Journal of Child Neurology, 2011, v. 26, n. 11, p. 1405, doi. 10.1177/0883073811408606
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- Publication type:
- Article