eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | tremor |
| Comorbidity | C0014544|epilepsy |
| Sentences | 9 |
| PubMedID- 25947986 | Genetic analysis of a chinese family provides further evidence for linkage of familial cortical myoclonic tremor with epilepsy to 5p15.31-p15. |
| PubMedID- 25863107 | [familial cortical myoclonic tremor with epilepsy in a pedigree]. |
| PubMedID- 20548044 | Conclusions: we report the clinical and genetic characteristics of a large familial cortical myoclonic tremor with epilepsy family. |
| PubMedID- 23656451 | Sodium valproate induced tremor in a patient with epilepsy and down's syndrome. |
| PubMedID- 26519379 | Familial cortical myoclonic tremor with epilepsy (fcmte), with evident purkinje cell degeneration, can be an et mimic. |
| PubMedID- 23439993 | In this study, we report the neuropathology findings in a new dutch familial cortical myoclonic tremor with epilepsy case and review the literature on this syndrome. |
| PubMedID- 26130016 | Familial cortical myoclonic tremor with epilepsy (fcmte) is an autosomal dominant epilepsy syndrome. |
| PubMedID- 23955123 | In this study, we describe the identification of two disease-segregating mutations in a large family featuring cortical myoclonic tremor with epilepsy and parkinsonism. |
| PubMedID- 22736081 | The aim of this work is to study the cognition, progressive gait impairment, and neuroimaging findings in two patients over 65 years old of the previously described type 3 familial cortical myoclonic tremor with epilepsy (fcmte3). |
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