Literature DB >> 632821

Progressive myoclonus and epilepsy with dentatorubral degeneration: a clinicopathological study of the Ramsay Hunt syndrome.

T D Bird, C M Shaw.   

Abstract

Ramsay Hunt's progressive myoclonus and epilepsy associated with dentatorubral degeneration is a rare disorder. We report a 19 year old woman with this clinical syndrome who also has a more mildly affected brother. Neuropathological in addition to dentatorubal involvement. The evidence suggests that this is a distinctive hereditary disorder producing neuromal degeneration at several levels in the central nervous system.

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Year:  1978        PMID: 632821      PMCID: PMC492982          DOI: 10.1136/jnnp.41.2.140

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  17 in total

1.  Myoclonus--a report of 67 cases and review of the literature.

Authors:  P D SWANSON; C N LUTTRELL; J W MAGLADERY
Journal:  Medicine (Baltimore)       Date:  1962-12       Impact factor: 1.889

2.  Familial myoclonic epilepsy and its association with cerebellar disturbance.

Authors:  K B NOAD; J W LANCE
Journal:  Brain       Date:  1960-12       Impact factor: 13.501

3.  Clinical and electroencephalographic investigations in myoclonic cerebellar dyssynergia.

Authors:  A KREINDLER; E CRIGHEL; I POILICI
Journal:  J Neurol Neurosurg Psychiatry       Date:  1959-08       Impact factor: 10.154

4.  [Dys-synergia cerebellaris myoclonica of Ramsay Hunt; anatomical study of a case].

Authors:  J CHRISTOPHE; J GRUNER
Journal:  Rev Neurol (Paris)       Date:  1956-10       Impact factor: 2.607

5.  Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis.

Authors:  D G HARRIMAN; J H MILLAR; A C STEVENSON
Journal:  Brain       Date:  1955-09       Impact factor: 13.501

6.  Myoclonus epilepsy as a symptom of diffuse neuronal disease.

Authors:  C W WATSON; D DENNY-BROWN
Journal:  AMA Arch Neurol Psychiatry       Date:  1953-08

7.  The graphic study of ballism and related hyperkinesia.

Authors:  J R WHITTIER
Journal:  J Neuropathol Exp Neurol       Date:  1952-07       Impact factor: 3.685

8.  Hereditary ataxia with optic atrophy of the retrobulbar neuritis type, and latent pallido-luysian degeneration.

Authors:  M ANDRE-VAN LEEUWEN; L VAN BOGAERT
Journal:  Brain       Date:  1949-09       Impact factor: 13.501

9.  [Dyssynergia cerebellaris myoclonica progressiva (Ramsay-Hunt) of predominant heredity in a Bern family].

Authors:  A FRANCESCHETTI; D KLEIN; H WILLENER
Journal:  Schweiz Arch Neurol Psychiatr       Date:  1954

10.  Dyssynergia cerebellaris progressiva.

Authors:  M CRITCHLEY
Journal:  Trans Am Neurol Assoc       Date:  1962
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  9 in total

1.  PRICKLE2 Mutations Might Not Be Involved in Epilepsy.

Authors:  Erin Sandford; Thomas D Bird; Jun Z Li; Margit Burmeister
Journal:  Am J Hum Genet       Date:  2016-03-03       Impact factor: 11.025

2.  Response to Sandford et al.: PRICKLE2 Variants in Epilepsy: A Call for Precision Medicine.

Authors:  Vinit B Mahajan; Alexander G Bassuk
Journal:  Am J Hum Genet       Date:  2016-03-03       Impact factor: 11.025

3.  Autosomal dominant late onset cerebellar ataxia with myoclonus, peripheral neuropathy and sensorineural deafness: a clinicopathological report.

Authors:  M Baraitser; W Gooddy; A M Halliday; A E Harding; P Rudge; F Scaravilli
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-01       Impact factor: 10.154

4.  Crystalloid inclusions reminiscent of Hirano bodies in autolyzed peripheral nerve of normal wistar rats.

Authors:  S Yagishita; Y Itoh; T Nakano; Y Ono; N Amano
Journal:  Acta Neuropathol       Date:  1979-08       Impact factor: 17.088

5.  Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): a condition unrelated to mitochondrial encephalomyopathies.

Authors:  C A Tassinari; R Michelucci; P Genton; J F Pellissier; J Roger
Journal:  J Neurol Neurosurg Psychiatry       Date:  1989-02       Impact factor: 10.154

6.  Region-specific disturbed iron distribution in early idiopathic Parkinson's disease measured by quantitative susceptibility mapping.

Authors:  Naying He; Huawei Ling; Bei Ding; Juan Huang; Yong Zhang; Zhongping Zhang; Chunlei Liu; Kemin Chen; Fuhua Yan
Journal:  Hum Brain Mapp       Date:  2015-08-07       Impact factor: 5.038

7.  Higher iron in the red nucleus marks Parkinson's dyskinesia.

Authors:  Mechelle M Lewis; Guangwei Du; Michal Kidacki; Nisargkumar Patel; Michele L Shaffer; Richard B Mailman; Xuemei Huang
Journal:  Neurobiol Aging       Date:  2012-11-21       Impact factor: 4.673

8.  Mutations in prickle orthologs cause seizures in flies, mice, and humans.

Authors:  Hirotaka Tao; J Robert Manak; Levi Sowers; Xue Mei; Hiroshi Kiyonari; Takaya Abe; Nader S Dahdaleh; Tian Yang; Shu Wu; Shan Chen; Mark H Fox; Christina Gurnett; Thomas Montine; Thomas Bird; Lisa G Shaffer; Jill A Rosenfeld; Juliann McConnell; Suneeta Madan-Khetarpal; Elizabeth Berry-Kravis; Hilary Griesbach; Russell P Saneto; Matthew P Scott; Dragana Antic; Jordan Reed; Riley Boland; Salleh N Ehaideb; Hatem El-Shanti; Vinit B Mahajan; Polly J Ferguson; Jeffrey D Axelrod; Anna-Elina Lehesjoki; Bernd Fritzsch; Diane C Slusarski; John Wemmie; Naoto Ueno; Alexander G Bassuk
Journal:  Am J Hum Genet       Date:  2011-02-03       Impact factor: 11.025

9.  Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm.

Authors:  Wei Guo; Dong-Mei Shang; Jing-Hui Cao; Kaiyan Feng; Yi-Chun He; Yang Jiang; ShaoPeng Wang; Yu-Fei Gao
Journal:  Biomed Res Int       Date:  2017-02-01       Impact factor: 3.411

  9 in total

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