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About 471 results

ALLMedicine™ Pes Cavus Center

Research & Reviews  235 results

A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular ...
https://doi.org/10.1111/jns.12425
Journal of the Peripheral Nervous System : JPNS REFERENCES; Fionda L, Turon-Sans J et. al.

Dec 15th, 2020 - We report the case of a patient with a clinical phenotype characterized by distal lower limb weakness and pes cavus. The electrophysiological study showed slightly reduced or normal amplitude of motor potentials, a decremental response to repetiti...

Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study.
https://doi.org/10.1212/WNL.0000000000010794
Neurology Balestrini S, Mikati MA et. al.

Sep 11th, 2020 - To define the risks and consequences of cardiac abnormalities in ATP1A3-related syndromes. Patients meeting clinical diagnostic criteria for Rapid-onset Dystonia-Parkinsonism (RDP), Alternating Hemiplegia of Childhood (AHC), and Cerebellar ataxia,...

Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-pa...
https://doi.org/10.1016/j.nbd.2020.105012
Neurobiology of Disease; Lazarov E, Hillebrand M et. al.

Jul 12th, 2020 - Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase, are the primary genetic cause for rapid-onset dystonia-parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). Recently, cerebellar ata...

Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
https://doi.org/10.1016/j.gene.2020.144709
Gene Boonsimma P, Michael Gasser M et. al.

Apr 27th, 2020 - Mutations in the ATP1A3 gene are known to be the cause of three distinct neurological syndromes including alternating hemiplegia of childhood (AHC), rapid-onset dystonia parkinsonism (RDP) and cerebellar ataxia, arefexia, pes cavus, optic atrophy ...

ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatme...
https://doi.org/10.1016/j.jocn.2020.01.041
Journal of Clinical Neuroscience : Official Journal of Th... Gasser M, Boonsimma P et. al.

Jan 21st, 2020 - ATP1A3 related disease is a clinically heterogeneous condition currently classified as alternating hemiplegia of childhood, rapid-onset dystonia-parkinsonism and cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing los...

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Clinicaltrials.gov  235 results

A new de novo SYT2 mutation presenting as distal weakness. Neuropathy or neuromuscular ...
https://doi.org/10.1111/jns.12425
Journal of the Peripheral Nervous System : JPNS REFERENCES; Fionda L, Turon-Sans J et. al.

Dec 15th, 2020 - We report the case of a patient with a clinical phenotype characterized by distal lower limb weakness and pes cavus. The electrophysiological study showed slightly reduced or normal amplitude of motor potentials, a decremental response to repetiti...

Cardiac phenotype in ATP1A3-related syndromes: A multicentre cohort study.
https://doi.org/10.1212/WNL.0000000000010794
Neurology Balestrini S, Mikati MA et. al.

Sep 11th, 2020 - To define the risks and consequences of cardiac abnormalities in ATP1A3-related syndromes. Patients meeting clinical diagnostic criteria for Rapid-onset Dystonia-Parkinsonism (RDP), Alternating Hemiplegia of Childhood (AHC), and Cerebellar ataxia,...

Comparative analysis of alternating hemiplegia of childhood and rapid-onset dystonia-pa...
https://doi.org/10.1016/j.nbd.2020.105012
Neurobiology of Disease; Lazarov E, Hillebrand M et. al.

Jul 12th, 2020 - Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase, are the primary genetic cause for rapid-onset dystonia-parkinsonism (RDP) and alternating hemiplegia of childhood (AHC). Recently, cerebellar ata...

Mutational and phenotypic expansion of ATP1A3-related disorders: Report of nine cases.
https://doi.org/10.1016/j.gene.2020.144709
Gene Boonsimma P, Michael Gasser M et. al.

Apr 27th, 2020 - Mutations in the ATP1A3 gene are known to be the cause of three distinct neurological syndromes including alternating hemiplegia of childhood (AHC), rapid-onset dystonia parkinsonism (RDP) and cerebellar ataxia, arefexia, pes cavus, optic atrophy ...

ATP1A3-related epilepsy: Report of seven cases and literature-based analysis of treatme...
https://doi.org/10.1016/j.jocn.2020.01.041
Journal of Clinical Neuroscience : Official Journal of Th... Gasser M, Boonsimma P et. al.

Jan 21st, 2020 - ATP1A3 related disease is a clinically heterogeneous condition currently classified as alternating hemiplegia of childhood, rapid-onset dystonia-parkinsonism and cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing los...

see more →

News  1 results

Custom-Made Foot Orthotics May Ease Some Types of Arthritis Pain
https://www.mdedge.com/familymedicine/article/30495/rheumatology/custom-made-foot-orthotics-may-ease-some-types-arthritis
Family Practice News; Jonathan Gardner

Custom-made foot orthotics can reduce foot pain caused by rheumatoid arthritis, pes cavus, and hallus vagus, according to a Cochrane Collaboration meta-analysis. The authors stressed, however, that there are very few high-quality studies evaluatin.

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