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

Year Number of Results
1997 2
1998 1
1999 1
2000 3
2001 5
2003 1
2005 2
2007 2
2008 3
2009 1
2011 1
2012 2
2013 1
2014 1
2016 1
2018 1
2020 2
2023 1
2024 0

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30 results

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Page 1
Acetazolamide-responsive ataxia.
Kotagal V. Kotagal V. Semin Neurol. 2012 Nov;32(5):533-7. doi: 10.1055/s-0033-1334475. Epub 2013 May 15. Semin Neurol. 2012. PMID: 23677664 Review.
Among all of the subtypes of episodic ataxia, types 2 (EA2), 3 (EA3), and 5 (EA5) are thought be the most medication responsive. Some patients with episodic ataxia type 1 (EA1) will also describe improvement with acetazolamide. ...
Among all of the subtypes of episodic ataxia, types 2 (EA2), 3 (EA3), and 5 (EA5) are thought be the most medication responsive. Some patien …
Episodic ataxia and channelopathies.
Gordon N. Gordon N. Brain Dev. 1998 Jan;20(1):9-13. doi: 10.1016/s0387-7604(97)00086-7. Brain Dev. 1998. PMID: 9533553 Review.
Clinical details are given of different types of episodic ataxia: type 1, with myokymia, and attacks which usually last a few minutes, and may occur several times a day, and treatment with acetazolamide can reduce the number of attacks; type 2, with in …
Clinical details are given of different types of episodic ataxia: type 1, with myokymia, and attacks which usual …
Episodic ataxias 1 and 2.
Baloh RW. Baloh RW. Handb Clin Neurol. 2012;103:595-602. doi: 10.1016/B978-0-444-51892-7.00042-5. Handb Clin Neurol. 2012. PMID: 21827920 Review.
The episodic ataxias are autosomal dominant disorders usually beginning in the first two decades of life. Episodic ataxia type 1 (EA1) is characterized by brief episodes of ataxia, typically lasting seconds, and interictal myokymia, while episodic atax …
The episodic ataxias are autosomal dominant disorders usually beginning in the first two decades of life. Episodic ataxia t …
Pathophysiology of epilepsy.
Engelborghs S, D'Hooge R, De Deyn PP. Engelborghs S, et al. Acta Neurol Belg. 2000 Dec;100(4):201-13. Acta Neurol Belg. 2000. PMID: 11233674 Review.
Recently, gene defects underlying four monogenic epilepsies (generalized epilepsy with febrile seizures, autosomal dominant nocturnal frontal lobe epilepsy, benign familial neonatal convulsions and episodic ataxia type 1 with partial seizures) have bee …
Recently, gene defects underlying four monogenic epilepsies (generalized epilepsy with febrile seizures, autosomal dominant nocturnal fronta …
Episodic ataxia type 1: a neuronal potassium channelopathy.
Rajakulendran S, Schorge S, Kullmann DM, Hanna MG. Rajakulendran S, et al. Neurotherapeutics. 2007 Apr;4(2):258-66. doi: 10.1016/j.nurt.2007.01.010. Neurotherapeutics. 2007. PMID: 17395136 Free article. Review.
Episodic ataxia type 1 is a paroxysmal neurological disorder characterized by short-lived attacks of recurrent midline cerebellar dysfunction and continuous motor activity. ...Although rare, the syndrome highlights the fundamental features of genetic i …
Episodic ataxia type 1 is a paroxysmal neurological disorder characterized by short-lived attacks of recurrent m …
[Hereditary episodic ataxia].
Riant F, Vahedi K, Tournier-Lasserve E. Riant F, et al. Rev Neurol (Paris). 2011 May;167(5):401-7. doi: 10.1016/j.neurol.2010.10.016. Epub 2011 Apr 13. Rev Neurol (Paris). 2011. PMID: 21492892 Review. French.
Seven types of EA have been reported so far but the majority of clinical cases result from two recognized entities. STATE OF ART: Episodic ataxia type 1 (EA1) is characterized by brief episodes of ataxia and dysarthria, and interictal myokymia. ...PERS …
Seven types of EA have been reported so far but the majority of clinical cases result from two recognized entities. STATE OF ART: Episodi …
Episodic ataxia type 1 and 2 (familial periodic ataxia/vertigo).
Brandt T, Strupp M. Brandt T, et al. Audiol Neurootol. 1997 Nov-Dec;2(6):373-83. doi: 10.1159/000259262. Audiol Neurootol. 1997. PMID: 9390841 Review.
At least two groups of disorders have been separated clinically: (1) episodic ataxia type 1 (EA-1), which manifests without vertigo and is associated with 'interictal' myokymia, and (2) episodic ataxia type 2 (EA-2), which often manifests with vertigo …
At least two groups of disorders have been separated clinically: (1) episodic ataxia type 1 (EA-1), which manife …
Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches.
D'Adamo MC, Liantonio A, Rolland JF, Pessia M, Imbrici P. D'Adamo MC, et al. Int J Mol Sci. 2020 Apr 22;21(8):2935. doi: 10.3390/ijms21082935. Int J Mol Sci. 2020. PMID: 32331416 Free PMC article. Review.
Kv1.1 belongs to the Shaker subfamily of voltage-gated potassium channels and acts as a critical regulator of neuronal excitability in the central and peripheral nervous systems. KCNA1 is the only gene that has been associated with episodic ataxia type 1 …
Kv1.1 belongs to the Shaker subfamily of voltage-gated potassium channels and acts as a critical regulator of neuronal excitability in the c …
Neurological potassium channelopathies.
Benatar M. Benatar M. QJM. 2000 Dec;93(12):787-97. doi: 10.1093/qjmed/93.12.787. QJM. 2000. PMID: 11110585 Review.
Potassium channel dysfunction has been implicated in a variety of genetic and acquired neurological disorders that are collectively referred to as the potassium channelopathies. These include acquired neuromyotonia, episodic ataxia type-1, hereditary d …
Potassium channel dysfunction has been implicated in a variety of genetic and acquired neurological disorders that are collectively referred …
[Channelopathies in neurology].
Grippo J, Grippo T. Grippo J, et al. Rev Neurol. 2001 Oct 1-15;33(7):643-7. Rev Neurol. 2001. PMID: 11784953 Free article. Review. Spanish.
Cl and Na channels alterations produce myotonic diseases: Thomsen, Becker and paramyothonies, potassium sensible paralysis, fluctuant congenital myotonic, Andersen s syndrome. Channelopathies also produce various episodic ataxia type 1, type 2, spinoce …
Cl and Na channels alterations produce myotonic diseases: Thomsen, Becker and paramyothonies, potassium sensible paralysis, fluctuant congen …
30 results