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Telerehabilitation, Core Stability Exercises and Hereditary Ataxia (TRCore-ataxia) (TRCore-ataxia)

• Authors : Universitat Internacional de Catalunya; Hospital Clinic of Barcelona; Maria Masbernat-Almenara, Principal Investigator

• Source: Effects of a Telerehabilitation Program of Central Stability Exercises to Improve Balance and Gait in Hereditary Ataxia. A Randomized

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Hereditary Ataxia: A Focus on Heme Metabolism and Fe-S Cluster Biogenesis.

• Authors : Chiabrando D; Molecular Biotechnology Center (MBC), Department of Molecular Biotechnology and Health Sciences, University of Torino, 10126 Torino, Italy.; Bertino F

Subjects: Anemia, Sideroblastic/Anemia, Sideroblastic/Anemia, Sideroblastic/*metabolism ; Ataxia/Ataxia/Ataxia/*metabolism ; Friedreich Ataxia/Friedreich Ataxia/Friedreich Ataxia/*metabolism Anemia, sideroblastic spinocerebellar ataxia; Posterior column ataxia with retinitis pigmentosa

• Source: International journal of molecular sciences [Int J Mol Sci] 2020 May 26; Vol. 21 (11). Date of Electronic Publication: 2020 May 26.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Core Stability Exercises and Hereditary Ataxia (Core-ataxia)

• Authors : Universitat de Lleida; Rosa Cabanas Valdés, PhD

• Source: The Effectiveness of Core Stability Exercises to Improve Balance and Gait in Hereditary Ataxias. Pilot StudyChen DH, Latimer C, Yagi M, Ndugga-Kabuye MK, Heigham

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Autosomal dominant hereditary ataxia in Sri Lanka.

• Authors : Sumathipala DS; Human Genetics Unit, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.; Abeysekera GS

Subjects: Nerve Tissue Proteins/Nerve Tissue Proteins/Nerve Tissue Proteins/*genetics ; Nuclear Proteins/Nuclear Proteins/Nuclear Proteins/*genetics ; Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*epidemiology

• Source: BMC neurology [BMC Neurol] 2013 May 01; Vol. 13, pp. 39. Date of Electronic Publication: 2013 May 01.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Hereditary ataxia. An unfolded protein.

• Authors : Orr HT; Institute of Human Genetics, Department of Laboratory Medicine and Pathology, Department of Genetics, Cell Biology and Development, University of Minnesota, Mayo Mail Code 206, Minneapolis, MN 55455, USA.

Subjects: Spinocerebellar Ataxias/Spinocerebellar Ataxias/Spinocerebellar Ataxias/*genetics; Animals ; Ataxin-1

• Source: Lancet (London, England) [Lancet] 2001 Dec; Vol. 358 Suppl, pp. S35.Publisher: Elsevier Country of Publication: England NLM ID: 2985213R Publication Model: Print Cited Medium: Print ISSN: 0140-6736 (Print)

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Hereditary Ataxia: A Focus on Heme Metabolism and Fe-S Cluster Biogenesis

• Authors : Deborah Chiabrando; Emanuela Tolosano; Francesca Bertino

Subjects: Iron-Sulfur Proteins; congenital, hereditary, and neonatal diseases and abnormalities; Ataxia

• Source: International Journal of Molecular SciencesInternational Journal of Molecular Sciences, Vol 21, Iss 3760, p 3760 (2020)

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Genetic origin of patients having spastic paraplegia with or without other neurologic manifestations.

• Authors : Chen J; Department of Neuromuscular Disease, The Third Affiliated Hospital of Hebei Medical University, 139 Ziqiang Road, Shijiazhuang, Hebei, 050000, PR China.; Zhao Z

Subjects: Charcot-Marie-Tooth Disease* ; Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/diagnostic imaging ; Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/Spastic Paraplegia, Hereditary*/genetics

• Source: BMC neurology [BMC Neurol] 2022 May 16; Vol. 22 (1), pp. 180. Date of Electronic Publication: 2022 May 16.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia.

• Authors : Sytsma TM; Neuropathology Division, Department of Laboratory Medicine and Pathology, University of Washington School of Medicine, Seattle, Washington, USA.; Chen DH

Subjects: Optic Atrophy* ; Spinocerebellar Ataxias*; Aged Spastic Ataxia

• Source: Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2022 Feb; Vol. 42 (1), pp. 58-65. Date of Electronic Publication: 2021 Nov 09.Publisher: Blackwell Science Asia Country of Publication: Australia NLM ID: 9606526 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Generalized myokymia, or neuromyotonia, or both in dogs with or without spinocerebellar ataxia.

• Authors : Vanhaesebrouck, An; Van Poucke, Mario; Stee, Kimberley

Subjects: EAST syndrome; canine; hereditary ataxia

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Spinocerebellar ataxia 27B: A novel, frequent and potentially treatable ataxia.

• Authors : Pellerin D; Department of Neurology and Neurosurgery, Montreal Neurological Hospital and Institute, McGill University, Montreal, Quebec, Canada.; Department of Neuromuscular Diseases, UCL Queen Square Institute of Neurology and The National Hospital for Neurology and Neurosurgery, University College London, London, UK.

Subjects: Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/diagnosis ; Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/drug therapy ; Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/Spinocerebellar Ataxias*/genetics

• Source: Clinical and translational medicine [Clin Transl Med] 2024 Jan; Vol. 14 (1), pp. e1504.Publisher: Wiley Country of Publication: United States NLM ID: 101597971 Publication Model: Print Cited Medium: Internet ISSN: 2001-1326

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