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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1976 2
1981 2
1985 1
1989 1
1990 1
1996 1
1997 2
1998 4
1999 4
2000 1
2001 2
2002 1
2003 1
2004 1
2005 2
2006 1
2007 1
2009 2
2010 4
2011 3
2012 6
2013 5
2014 10
2015 5
2016 6
2017 4
2018 10
2019 13
2020 12
2021 9
2022 11
2023 9
2024 5

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128 results

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Page 1
Acute cerebellar ataxia: differential diagnosis and clinical approach.
Pedroso JL, Vale TC, Braga-Neto P, Dutra LA, França MC Jr, Teive HAG, Barsottini OGP. Pedroso JL, et al. Arq Neuropsiquiatr. 2019 Mar;77(3):184-193. doi: 10.1590/0004-282X20190020. Arq Neuropsiquiatr. 2019. PMID: 30970132 Free article. Review.
Cerebellar ataxia is a common finding in neurological practice and has a wide variety of causes, ranging from the chronic and slowly-progressive cerebellar degenerations to the acute cerebellar lesions due to infarction, edema and hemorrhage, configuri …
Cerebellar ataxia is a common finding in neurological practice and has a wide variety of causes, ranging from the chronic and …
The Differential Diagnosis and Treatment of Atypical Parkinsonism.
Levin J, Kurz A, Arzberger T, Giese A, Höglinger GU. Levin J, et al. Dtsch Arztebl Int. 2016 Feb 5;113(5):61-9. doi: 10.3238/arztebl.2016.0061. Dtsch Arztebl Int. 2016. PMID: 26900156 Free PMC article. Review.
In MSA, synuclein is deposited in oligodendrocytes, mainly in the cerebellum but also in the brain stem; the main clinical feature is autonomic dysfunction combined with parkinsonism or cerebellar ataxia. Synucleinopathies often impair REM (rapid eye movement) sleep …
In MSA, synuclein is deposited in oligodendrocytes, mainly in the cerebellum but also in the brain stem; the main clinical feature is autono …
Cerebellar Dizziness and Vertigo: Etiologies, Diagnostic Assessment, and Treatment.
Zwergal A, Feil K, Schniepp R, Strupp M. Zwergal A, et al. Semin Neurol. 2020 Feb;40(1):87-96. doi: 10.1055/s-0039-3400315. Epub 2019 Dec 30. Semin Neurol. 2020. PMID: 31887755 Review.
Cerebellar dizziness and vertigo account for approximately 10% of diagnoses in a tertiary dizziness center. ...Overlap syndromes with peripheral vestibular disorders, such as cerebellar ataxia, neuropathy, and vestibular areflexia, exist rarely. ...
Cerebellar dizziness and vertigo account for approximately 10% of diagnoses in a tertiary dizziness center. ...Overlap syndromes with …
The assessment and treatment of postural disorders in cerebellar ataxia: a systematic review.
Marquer A, Barbieri G, Pérennou D. Marquer A, et al. Ann Phys Rehabil Med. 2014 Mar;57(2):67-78. doi: 10.1016/j.rehab.2014.01.002. Epub 2014 Feb 6. Ann Phys Rehabil Med. 2014. PMID: 24582474 Free article. Review.
Gait and balance disorders are often major causes of handicap in patients with cerebellar ataxia. Although it was thought that postural and balance disorders in cerebellar ataxia were not treatable, recent studies have demonstrated the beneficial effec …
Gait and balance disorders are often major causes of handicap in patients with cerebellar ataxia. Although it was thought that …
Immune-mediated Cerebellar Ataxias: Practical Guidelines and Therapeutic Challenges.
Mitoma H, Manto M, Hampe CS. Mitoma H, et al. Curr Neuropharmacol. 2019;17(1):33-58. doi: 10.2174/1570159X16666180917105033. Curr Neuropharmacol. 2019. PMID: 30221603 Free PMC article. Review.
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia (GA), paraneoplastic cerebellar degenerations (PCDs), antiglutamate decarboxylase 65 (GAD) antibody-associated cerebellar a …
Immune-mediated cerebellar ataxias (IMCAs), a clinical entity reported for the first time in the 1980s, include gluten ataxia …
Ataxia-telangiectasia: recommendations for multidisciplinary treatment.
van Os NJH, Haaxma CA, van der Flier M, Merkus PJFM, van Deuren M, de Groot IJM, Loeffen J, van de Warrenburg BPC, Willemsen MAAP; A-T Study Group. van Os NJH, et al. Dev Med Child Neurol. 2017 Jul;59(7):680-689. doi: 10.1111/dmcn.13424. Epub 2017 Mar 20. Dev Med Child Neurol. 2017. PMID: 28318010 Free article. Review.
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculocutaneous telangiectasia, immunodeficiency, progressive respiratory failure, and an increased risk of malignancies. It demands specialized …
Ataxia-telangiectasia is a rare, neurodegenerative, and multisystem disease, characterized by cerebellar ataxia, oculoc …
Ataxia-telangiectasia: epidemiology, pathogenesis, clinical phenotype, diagnosis, prognosis and management.
Amirifar P, Ranjouri MR, Lavin M, Abolhassani H, Yazdani R, Aghamohammadi A. Amirifar P, et al. Expert Rev Clin Immunol. 2020 Sep;16(9):859-871. doi: 10.1080/1744666X.2020.1810570. Epub 2020 Oct 15. Expert Rev Clin Immunol. 2020. PMID: 32791865 Review.
INTRODUCTION: Ataxia-telangiectasia (A-T) is a rare autosomal recessive syndrome characterized by progressive cerebellar ataxia, oculocutaneous telangiectasia, variable immunodeficiency, radiosensitivity, and cancer predisposition. Mutations cause A-T in the …
INTRODUCTION: Ataxia-telangiectasia (A-T) is a rare autosomal recessive syndrome characterized by progressive cerebellar at …
CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.
Indelicato E, Boesch S. Indelicato E, et al. Handb Exp Pharmacol. 2023;279:227-248. doi: 10.1007/164_2022_625. Handb Exp Pharmacol. 2023. PMID: 36592223 Review.
In the last decade, variants in the Ca(2+) channel gene CACNA1A emerged as a frequent aetiology of rare neurological phenotypes sharing a common denominator of variable paroxysmal manifestations and chronic cerebellar dysfunction. The spectrum of paroxysmal manifestations …
In the last decade, variants in the Ca(2+) channel gene CACNA1A emerged as a frequent aetiology of rare neurological phenotypes sharing a co …
Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism.
Stamou MI, Georgopoulos NA. Stamou MI, et al. Metabolism. 2018 Sep;86:124-134. doi: 10.1016/j.metabol.2017.10.012. Epub 2017 Nov 3. Metabolism. 2018. PMID: 29108899 Free PMC article. Review.
IGD is also characterized by a wide variety of non-reproductive features, including midline facial defects such as cleft lip and/or palate, renal agenesis, short metacarpals and other bone abnormalities, hearing loss, synkinesia, eye movement abnormalities, poor balance due to …
IGD is also characterized by a wide variety of non-reproductive features, including midline facial defects such as cleft lip and/or palate, …
The treatment and natural course of peripheral and central vertigo.
Strupp M, Dieterich M, Brandt T. Strupp M, et al. Dtsch Arztebl Int. 2013 Jul;110(29-30):505-15; quiz 515-6. doi: 10.3238/arztebl.2013.0505. Epub 2013 Jul 22. Dtsch Arztebl Int. 2013. PMID: 24000301 Free PMC article. Review.
A newly identified subtype of bilateral vestibulopathy, termed cerebellar ataxia, neuropathy, and vestibular areflexia syndrome (CANVAS), shows no essential improvement in the long term. ...Aminopyridine, chlorzoxazone, and acetyl-DL-leucine are new treatment option …
A newly identified subtype of bilateral vestibulopathy, termed cerebellar ataxia, neuropathy, and vestibular areflexia syndrom …
128 results