| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Luca Leonardi, Maria Gabriella Aceto, Christian Marcotulli, Giuseppe Arcuria, Mariano Serrao, Francesco Pierelli, Paolo Paone, Alessandro Filla, Alessandro Roca, Carlo Casal. A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 38. issue 3. 2017-03-15. PMID:28039539. |
the aim of this pilot study is to test the feasibility and effectiveness of a wearable proprioceptive stabilizer that emits focal mechanical vibrations in patients affected by hereditary cerebellar ataxias. |
2017-03-15 |
2023-08-13 |
Not clear |
| Luca Leonardi, Maria Gabriella Aceto, Christian Marcotulli, Giuseppe Arcuria, Mariano Serrao, Francesco Pierelli, Paolo Paone, Alessandro Filla, Alessandro Roca, Carlo Casal. A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 38. issue 3. 2017-03-15. PMID:28039539. |
this small open-labeled study shows preliminary evidence that focal mechanical vibration exerted by a wearable proprioceptive stabilizer might improve limb and gait ataxia in patients affected by hereditary cerebellar ataxias. |
2017-03-15 |
2023-08-13 |
Not clear |
| Giulia Perucca, Nicolas Leboucq, Agathe Roubertie, François Rivier, Nicolas Menjot, Consuelo Valentini, Alain Bonaf. Role of neuroimaging in the diagnosis of hereditary cerebellar ataxias in childhood. Journal of neuroradiology = Journal de neuroradiologie. vol 43. issue 3. 2017-03-08. PMID:27126632. |
role of neuroimaging in the diagnosis of hereditary cerebellar ataxias in childhood. |
2017-03-08 |
2023-08-13 |
Not clear |
| Gerson da Silva Carvalho, Jonas Alex Morales Saute, Clarissa Branco Haas, Vitor Rocco Torrez, Andressa Wigner Brochier, Gabriele Nunes Souza, Gabriel Vasata Furtado, Tailise Gheno, Aline Russo, Thais Lampert Monte, Artur Schumacher-Schuh, Rui D'Avila, Karina Carvalho Donis, Raphael Machado Castilhos, Diogo Onofre Souza, Maria Luiza Saraiva-Pereira, Vanessa Leotti Torman, Suzi Camey, Luis Valmor Portela, Laura Bannach Jardi. Cytokines in Machado Joseph Disease/Spinocerebellar Ataxia 3. Cerebellum (London, England). vol 15. issue 4. 2017-03-06. PMID:26395908. |
age at onset, disease duration, and clinical scales scale for the assessment and rating of ataxia (sara), neurological examination score for spinocerebellar ataxias (nessca), sca functional index (scafi), and composite cerebellar functional score (ccfs) were obtained from the symptomatic carriers. |
2017-03-06 |
2023-08-13 |
Not clear |
| Joaquín Martí, María C Santa-Cruz, José P Hervás, Shirley A Bayer, Sandra Villega. Cerebellar cortex development in the weaver condition presents regional and age-dependent abnormalities without differences in Purkinje cells neurogenesis. Acta neurobiologiae experimentalis. vol 76. issue 1. 2017-03-03. PMID:27102918. |
the extrapolation of our results to patients affected with cerebellar ataxias suggests that all cerebellar cortex lobes are affected with several age-dependent alterations in cytoarchitectonics. |
2017-03-03 |
2023-08-13 |
mouse |
| Michael Dayan, G Olivito, M Molinari, Mara Cercignani, Marco Bozzali, M Leggi. Impact of cerebellar atrophy on cortical gray matter and cerebellar peduncles as assessed by voxel-based morphometry and high angular resolution diffusion imaging. Functional neurology. vol 31. issue 4. 2017-03-02. PMID:28072384. |
the significant difference in the mcp and scp dmri metrics between patients and controls as well as the significant correlation with ataxia total score and subscores support the use of dmri metrics as an imaging biomarker for cerebellar degeneration and ataxia. |
2017-03-02 |
2023-08-13 |
Not clear |
| Sung Ho Jang, Chul Hoon Chang, Young Jin Jung, Hyeok Gyu Kwo. Severe ataxia due to injuries of neural tract detected by diffusion tensor tractography in a patient with pontine hemorrhage: A case report. Medicine. vol 95. issue 50. 2017-02-17. PMID:27977594. |
we examined injuries of the dentato-rubro-thalamic tract (drtt), cortico-ponto-cerebellar tract (cpct), dorsal spinocerebellar tract (sct), and inferior cerebellar peduncle (icp) in a patient with severe ataxia following bilateral tegmental pontine hemorrhage (ph), using diffusion tensor tractography (dtt). |
2017-02-17 |
2023-08-13 |
Not clear |
| Peter Heder. Hereditary and metabolic myelopathies. Handbook of clinical neurology. vol 136. 2017-02-13. PMID:27430441. |
spastic weakness, limb ataxia without additional cerebellar signs, impaired vibration, and positional sensation are hallmark phenotypic features of these disorders. |
2017-02-13 |
2023-08-13 |
Not clear |
| Mario Manto, Christophe Haba. Cerebellar disorders: clinical/radiologic findings and modern imaging tools. Handbook of clinical neurology. vol 135. 2017-02-10. PMID:27432679. |
sporadic ataxias include stroke, toxic causes, immune ataxias, infectious/parainfectious ataxias, traumatic causes, neoplasias and paraneoplastic syndromes, endocrine disorders affecting the cerebellum, and the so-called "degenerative ataxias" (multiple system atrophy, and sporadic adult-onset ataxias). |
2017-02-10 |
2023-08-13 |
Not clear |
| Mario Manto, Christophe Haba. Cerebellar disorders: clinical/radiologic findings and modern imaging tools. Handbook of clinical neurology. vol 135. 2017-02-10. PMID:27432679. |
genetic ataxias include mainly four groups of disorders: autosomal-recessive cerebellar ataxias, autosomal-dominant ataxias (spinocerebellar ataxias and episodic ataxias), mitochondrial disorders, and x-linked ataxias. |
2017-02-10 |
2023-08-13 |
Not clear |
| Mario Manto, Christophe Haba. Cerebellar disorders: clinical/radiologic findings and modern imaging tools. Handbook of clinical neurology. vol 135. 2017-02-10. PMID:27432679. |
in addition to biochemical studies and genetic tests, brain imaging techniques are a cornerstone for the diagnosis, clinicoanatomic correlations, and follow-up of cerebellar ataxias. |
2017-02-10 |
2023-08-13 |
Not clear |
| Mario Manto, Christophe Haba. Cerebellar disorders: clinical/radiologic findings and modern imaging tools. Handbook of clinical neurology. vol 135. 2017-02-10. PMID:27432679. |
modern radiologic tools to assess cerebellar ataxias include: functional imaging studies, magnetic resonance spectroscopy, volumetric studies, and tractography. |
2017-02-10 |
2023-08-13 |
Not clear |
| Maiko Hayashida, Sadayuki Hashioka, Hiroyuki Miki, Michiharu Nagahama, Rei Wake, Tsuyoshi Miyaoka, Jun Horiguch. Aceruloplasminemia With Psychomotor Excitement and Neurological Sign Was Improved by Minocycline (Case Report). Medicine. vol 95. issue 19. 2017-02-08. PMID:27175663. |
ataxia and a wide-based gate reflected iron deposition in the dentate nuclei of the cerebellum. |
2017-02-08 |
2023-08-13 |
Not clear |
| Hélio A G Teive, Adriana Moro, Mariana Moscovich, Walter O Arruda, Renato Puppi Munho. Statin-associated cerebellar ataxia. A Brazilian case series. Parkinsonism & related disorders. vol 25. 2017-02-06. PMID:26897092. |
drug-induced cerebellar ataxias (dica) represent an important group of secondary cerebellar ataxias. |
2017-02-06 |
2023-08-13 |
Not clear |
| Pedro Braga Neto, José Luiz Pedroso, Sheng-Han Kuo, C França Marcondes Junior, Hélio Afonso Ghizoni Teive, Orlando Graziani Povoas Barsottin. Current concepts in the treatment of hereditary ataxias. Arquivos de neuro-psiquiatria. vol 74. issue 3. 2017-01-10. PMID:27050855. |
in this review, we will focus on the symptomatic treatment of the main autosomal recessive ataxias, autosomal dominant ataxias, x-linked cerebellar ataxias and mitochondrial ataxias. |
2017-01-10 |
2023-08-13 |
Not clear |
| Motonori Takahashi, Takeshi Kondo, Mai Morichika, Azumi Kuse, Kanako Nakagawa, Migiwa Asano, Yasuhiro Uen. Autopsy case of undiagnosed gangliocytoma in the medulla oblongata complicated with cerebral palsy. Legal medicine (Tokyo, Japan). vol 19. 2017-01-06. PMID:26210504. |
although gangliocytoma is a well-differentiated benign tumor, the almost total replacement of the medulla oblongata by the tumor cells was assumed to result in ataxia via the olivocerebellar tract and secondary cerebellar atrophy, followed by central hypoventilation and death of the patient. |
2017-01-06 |
2023-08-13 |
Not clear |
| Roger Kalla, Julian Teufel, Katharina Feil, Caroline Muth, Michael Strup. Update on the pharmacotherapy of cerebellar and central vestibular disorders. Journal of neurology. vol 263 Suppl 1. 2017-01-06. PMID:27083881. |
the ongoing randomized controlled trials on episodic ataxia type 2 (sustained-release form of 4-aminopyridine vs. acetazolamide vs. placebo; eat2treat), vestibular migraine with metoprolol (provemig-trial), cerebellar gait disorders (sustained-release form of 4-aminopyridine vs. placebo; faceg) and cerebellar ataxia (acetyl-dl-leucine vs. placebo; alcat) will provide new insights into the pharmacotherapy of cerebellar and central vestibular disorders. |
2017-01-06 |
2023-08-13 |
mouse |
| Irene Paradisi, Vassiliki Ikonomu, Sergio Aria. Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent. Journal of human genetics. vol 61. issue 3. 2016-12-30. PMID:26538302. |
dominantly inherited ataxias (spinocerebellar ataxias, scas) are a genetically heterogeneous group of neurologic diseases characterized by progressive cerebellar and spinal tract degeneration with ataxia and other signs, common to all known subtypes. |
2016-12-30 |
2023-08-13 |
Not clear |
| Cong Lu, Yi-Cen Zheng, Yi Dong, Hong-Fu L. Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing. BMC neurology. vol 16. issue 1. 2016-12-19. PMID:27644330. |
identification of novel senataxin mutations in chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing. |
2016-12-19 |
2023-08-13 |
Not clear |
| Cong Lu, Yi-Cen Zheng, Yi Dong, Hong-Fu L. Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing. BMC neurology. vol 16. issue 1. 2016-12-19. PMID:27644330. |
autosomal recessive cerebellar ataxias (arca) are a group of neurodegenerative disorders characterized by early onset of gait impairment, disturbed limb coordination, dysarthria, and eye movement abnormalities, most likely due to the degeneration of cerebellum, brainstem, and spinal cord. |
2016-12-19 |
2023-08-13 |
Not clear |