| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Anna Duarri, Meng-Chin A Lin, Michiel R Fokkens, Michel Meijer, Cleo J L M Smeets, Esther A R Nibbeling, Erik Boddeke, Richard J Sinke, Harm H Kampinga, Diane M Papazian, Dineke S Verbee. Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner. Cellular and molecular life sciences : CMLS. vol 72. issue 17. 2015-10-29. PMID:25854634. |
the dominantly inherited cerebellar ataxias are a heterogeneous group of neurodegenerative disorders caused by purkinje cell loss in the cerebellum. |
2015-10-29 |
2023-08-13 |
Not clear |
| E Gregianin, G Vazza, E Scaramel, F Boaretto, A Vettori, E Leonardi, S C E Tosatto, R Manara, E Pegoraro, M L Mostacciuol. A novel SACS mutation results in non-ataxic spastic paraplegia and peripheral neuropathy. European journal of neurology. vol 20. issue 11. 2015-10-22. PMID:23800155. |
mutations in the sacs gene are commonly associated with autosomal recessive spastic ataxia of charlevoix-saguenay (arsacs), a complex neurodegenerative disorder characterized by progressive degeneration of the cerebellum and spinal cord tracts. |
2015-10-22 |
2023-08-12 |
Not clear |
| Hiroshi Doi, Masao Ushiyama, Takashi Baba, Katsuko Tani, Masaaki Shiina, Kazuhiro Ogata, Satoko Miyatake, Yoko Fukuda-Yuzawa, Shoji Tsuji, Mitsuko Nakashima, Yoshinori Tsurusaki, Noriko Miyake, Hirotomo Saitsu, Shu-ichi Ikeda, Fumiaki Tanaka, Naomichi Matsumoto, Kunihiro Yoshid. Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation. Scientific reports. vol 4. 2015-10-15. PMID:25417924. |
autosomal recessive cerebellar ataxias and autosomal recessive hereditary spastic paraplegias (arhsps) are clinically and genetically heterogeneous neurological disorders. |
2015-10-15 |
2023-08-13 |
Not clear |
| Masayoshi Tada, Masatoyo Nishizawa, Osamu Onoder. Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems. Journal of neurology, neurosurgery, and psychiatry. vol 86. issue 8. 2015-09-30. PMID:25637456. |
redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems. |
2015-09-30 |
2023-08-13 |
Not clear |
| Masayoshi Tada, Masatoyo Nishizawa, Osamu Onoder. Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems. Journal of neurology, neurosurgery, and psychiatry. vol 86. issue 8. 2015-09-30. PMID:25637456. |
recent advances in our understanding of neurophysiological functions in the cerebellar system have revealed that each region involved in degenerative ataxias contributes differently. |
2015-09-30 |
2023-08-13 |
Not clear |
| Masayoshi Tada, Masatoyo Nishizawa, Osamu Onoder. Redefining cerebellar ataxia in degenerative ataxias: lessons from recent research on cerebellar systems. Journal of neurology, neurosurgery, and psychiatry. vol 86. issue 8. 2015-09-30. PMID:25637456. |
considering the neurophysiological properties of the cerebellar system, we have classified degenerative ataxias into four types depending on which system is involved: purkinje cells, the corticopontocerebellar system, the spinocerebellar system and the cerebellar deep nuclei. |
2015-09-30 |
2023-08-13 |
Not clear |
| Sun-Uk Lee, Hee-Joon Bae, Ji-Soo Ki. Ipsilesional limb ataxia and truncal ipsipulsion in isolated infarction of the superior cerebellar peduncle. Journal of the neurological sciences. vol 349. issue 1-2. 2015-09-28. PMID:25592415. |
ipsilesional limb ataxia and truncal ipsipulsion in isolated infarction of the superior cerebellar peduncle. |
2015-09-28 |
2023-08-13 |
human |
| Sunil Kumar, Mukesh Sharma, Trilochan Srivastava, Virendra Deo Sinh. Infratentorial hemorrhagic cerebral proliferative angiopathy: A rare presentation of a rare disease. Asian journal of neurosurgery. vol 10. issue 3. 2015-09-23. PMID:26396618. |
cerebellar signs in the form of scanning speech, nystagmus, impaired finger-to-nose incoordination test, dysdiadochokinesia, and limb ataxia on the left side were present. |
2015-09-23 |
2023-08-13 |
Not clear |
| Carlo Bruttini, Roberto Esposti, Francesco Bolzoni, Alessandra Vanotti, Caterina Mariotti, Paolo Cavallar. Temporal disruption of upper-limb anticipatory postural adjustments in cerebellar ataxic patients. Experimental brain research. vol 233. issue 1. 2015-09-10. PMID:25245658. |
thus, apas that stabilize the arm when the index finger is briskly flexed were recorded in 13 ataxic subjects (seven sporadic cases, four dominant ataxia type iii and two autosomal recessive), presenting a slowly progressive cerebellar syndrome with four-limb dysmetria, and compared with those obtained in 13 healthy subjects. |
2015-09-10 |
2023-08-13 |
human |
| Mario Mant. The cornerstones of Cerebellum and Ataxias: from peer review to rapid visibility in a rising discipline. Cerebellum & ataxias. vol 1. 2015-09-02. PMID:26331025. |
the cornerstones of cerebellum and ataxias: from peer review to rapid visibility in a rising discipline. |
2015-09-02 |
2023-08-13 |
Not clear |
| Emmet M Power, Ruth M Empso. Functional contributions of glutamate transporters at the parallel fibre to Purkinje neuron synapse-relevance for the progression of cerebellar ataxia. Cerebellum & ataxias. vol 1. 2015-09-02. PMID:26331027. |
two of these transporters, eaat4 in purkinje neurons (pn) and eaat1 in bergmann glia are both enriched within the cerebellum and altered in a variety of human ataxias. |
2015-09-02 |
2023-08-13 |
human |
| Ludovico Ciolli, Florian Krismer, Ferdinando Nicoletti, Gregor K Wennin. An update on the cerebellar subtype of multiple system atrophy. Cerebellum & ataxias. vol 1. 2015-09-02. PMID:26331038. |
the cerebellar variant of msa (msa-c) denotes a distinctive motor subtype characterized by progressive adult onset sporadic gait ataxia, scanning dysarthria, limb ataxia and cerebellar oculomotor dysfunction. |
2015-09-02 |
2023-08-13 |
Not clear |
| Ludovico Ciolli, Florian Krismer, Ferdinando Nicoletti, Gregor K Wennin. An update on the cerebellar subtype of multiple system atrophy. Cerebellum & ataxias. vol 1. 2015-09-02. PMID:26331038. |
here we review key aspects of msa-c including pathology, pathogenesis, diagnosis, clinical features and treatment, paying special attention to differential diagnosis in late onset sporadic cerebellar ataxias. |
2015-09-02 |
2023-08-13 |
Not clear |
| Robert D Sandler, Nigel Hoggard, Marios Hadjivassilio. Miller-Fisher Syndrome: Is the ataxia central or peripheral? Cerebellum & ataxias. vol 2. 2015-09-02. PMID:26331046. |
there has long been a debate as to whether the ataxia in mfs originates in the cerebellum or it is more peripheral. |
2015-09-02 |
2023-08-13 |
Not clear |
| William Huynh, Matthew C Kierna. Peripheral nerve axonal excitability studies: expanding the neurophysiologist's armamentarium. Cerebellum & ataxias. vol 2. 2015-09-02. PMID:26331047. |
in more recent years, the use of nerve excitability studies have additionally provided insights into the pathophysiological mechanisms underlying cerebellar disorders that include stroke and familial cerebellar ataxias such as episodic ataxia types 1 and 2. |
2015-09-02 |
2023-08-13 |
Not clear |
| William Huynh, Matthew C Kierna. Peripheral nerve axonal excitability studies: expanding the neurophysiologist's armamentarium. Cerebellum & ataxias. vol 2. 2015-09-02. PMID:26331047. |
moreover, this technique may have diagnostic and therapeutic implications that may encompass a broader range of neurodegenerative cerebellar ataxias in years to come. |
2015-09-02 |
2023-08-13 |
Not clear |
| Maryam Rahimi-Balaei, Pegah Afsharinezhad, Karen Bailey, Matthew Buchok, Behzad Yeganeh, Hassan Marzba. Embryonic stages in cerebellar afferent development. Cerebellum & ataxias. vol 2. 2015-09-02. PMID:26331050. |
afferent and efferent fibers are major components of cerebellar circuitry and impairment of these circuits causes severe cerebellar malfunction, such as ataxia. |
2015-09-02 |
2023-08-13 |
Not clear |
| Yong-Chul Kwon, Jun-Hyun Kim, Tae-Beom Ah. Ataxia of cortical origin via crossed cerebellar diaschisis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. vol 36. issue 1. 2015-09-01. PMID:24899224. |
ataxia of cortical origin via crossed cerebellar diaschisis. |
2015-09-01 |
2023-08-13 |
Not clear |
| Chaitali Mukherjee, Anna Holubowska, Nicola Schwedhelm-Domeyer, Miso Mitkovski, Shih-Ju Lee, Madhuvanthi Kannan, Annika Matz, Mayur Vadhvani, Judith Stegmülle. Loss of the neuron-specific F-box protein FBXO41 models an ataxia-like phenotype in mice with neuronal migration defects and degeneration in the cerebellum. The Journal of neuroscience : the official journal of the Society for Neuroscience. vol 35. issue 23. 2015-08-19. PMID:26063905. |
developmental defects such as impaired neuronal migration or neurodegeneration are thus detrimental to the cerebellum and can result in movement disorders including ataxias. |
2015-08-19 |
2023-08-13 |
mouse |
| M Saeed Da. Functional interaction and cross-tolerance between ethanol and Δ9-THC: possible modulation by mouse cerebellar adenosinergic A1/GABAergic-A receptors. Behavioural brain research. vol 270. 2015-08-14. PMID:24875771. |
finally, tolerance in chronic ethanol/Δ(9)-thc/-treated animals developed not only to ethanol/Δ(9)-thc-induced ataxia, respectively, but also to the ataxia potentiating effect of cha and muscimol, indicating modulation by cerebellar adenosinergic a1 and gabaa receptors. |
2015-08-14 |
2023-08-13 |
mouse |