نتایج جستجو برای: cerebellar ataxia

تعداد نتایج: 40653  

Journal: :Archives of neurology 2005
Katrin Bürk Udo Bühring Jörg Bernhard Schulz Christine Zühlke Yorck Hellenbroich Johannes Dichgans

BACKGROUND It is unknown whether multiple system atrophy of the cerebellar type (MSA-C) and idiopathic cerebellar ataxia with extracerebellar presentation (IDCA-P) represent distinct entities. OBJECTIVE To investigate the discriminative validity of magnetic resonance imaging in sporadic cerebellar ataxia. DESIGN Basal ganglia and infratentorial structures were screened for signal abnormalit...

2017
Sung Ho Jang Hyeok Gyu Kwon

RATIONALE Several studies using diffusion tensor tractography (DTT) have reported on injury in the dentato-rubro-thalamic tract (DRTT) in patients with brain injury. However, there is no study of injury in the DRTT following cerebellar infarct. We report on patients with injury in the DRTT following cerebellar infarct, demonstrated on DTT. PATIENT CONCERNS Three patients with cerebellar infar...

2017
Hye-Jin Moon Beomseok Jeon

Phenytoin (PHT) is a first line antiepileptic drug (AED) used to treat many epilepsy syndromes. As with other AEDs, there are various adverse effects associated with PHT. For this brief review, we searched for evidence of cerebellar ataxia as a chronic adverse effect of therapeutic-range PHT treatment. Many previous studies appeared related to this issue, but many of those studies were designed...

Journal: :Journal of Neurology, Neurosurgery & Psychiatry 1985

Journal: :Archives of Neurology 2006

Journal: :Proceedings of the Royal Society of Medicine 1911

2016
Sung Ho Jang Chul Hoon Chang Young Jin Jung Hyeok Gyu Kwon

RATIONALE We examined injuries of the dentato-rubro-thalamic tract (DRTT), cortico-ponto-cerebellar tract (CPCT), dorsal spinocerebellar tract (SCT), and inferior cerebellar peduncle (ICP) in a patient with severe ataxia following bilateral tegmental pontine hemorrhage (PH), using diffusion tensor tractography (DTT). PATIENT CONCERNS A 75-year-old female patient underwent conservative managem...

Journal: :Archives of neurology 2003
Ghada El Euch-Fayache Irfan Lalani Rim Amouri Ilhem Turki Karim Ouahchi Wu-Yen Hung Samir Belal Teepu Siddique Faycal Hentati

BACKGROUND Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a clinically homogenous disorder reported in Quebec caused by mutations in the SACS gene (chromosome 13q12). Recently, we identified a Tunisian kindred demonstrating linkage to the ARSACS locus. OBJECTIVE To report clinical, neurophysiological, and nerve biopsy findings in patients with autosomal recessive cerebe...

Journal: :Neurology - Neuroimmunology Neuroinflammation 2018

Journal: :Journal of Neurophysiology 2014

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