ataxia

Conclusion: The point mutation in this area of mitochondrial DNA might not be related hereditary ataxia.

Crazy The chicks show an ataxia not unlike the ataxia of vitamin E deficiency known as encephalomalacia or crazy chick disease.

Objective To explore the clinical characteristics and pathogenic mechanism of sensory ataxia form of GBS.

Objective: To investigate the clinical features of an autosomal recessive inherited ataxia pedigree and exclude known causal genes.

Neurologic symptoms of hypermagnesemia are muscular weakness, paralysis, ataxia, drowsiness, and confusion.

Physical examination revealed a lethargic patient with ophthalmoplegia, ataxia, and hyporeflexia.

and endolymphatic sac tumors. Cerebellar hemangioblastomas may be associated with headache, vomiting, and gait disturbances or ataxia.

We suggest that cerebellar ataxia may be characterized by defective feedforward control.

abstract: Objective: To investigate the therapeutic effect of scalp-plus body-acupuncture on cerebellar ataxia.

Normally involved in the response to stress and repair of DNA, ATM is mutated in the rare genetic disorder ataxia-telangiectasia (AT).

Conclusion Short-term treatment with buspirone can improve the ataxia symptoms after stroke.

When they arise in the cerebellum, ataxia and headaches secondary to compression of the fourth ventricle and hydrocephalus are common [3].

The results indicate that the two sides of welding joint is ataxia, and the dehiscence occurs.

Knuckling at fetlocks, ataxia, tail deviation and tail may be flaccid.

Methods To Summarize clinical data of 16 cases with sensory ataxia form of GBS.

Conclusion: Scalp-plus body acupuncture has a marked therapeutic effect on cerebellar ataxia.

Results Virus infection is the main cause resulted in acute ataxia in infant.

Results The buspirone can significantly improve the ataxia of patients with stroke compared with the controls(P01).

Objective To summarize the common types and medical reasons for acute infant ataxia.

It results in progressive ataxia beginning at a young age.

The patient improved rapidly although the ataxia persisted.

Conclusion Avermectine may cause ataxia by disturbing the activity of nerve metabolism enzyme in rats.

Objective To explore SCA3 gene mutation in the patients with inherited spinocerebellar ataxia.

Objective To explore the clinical and molecular biological characteristics of spinocerebellar ataxia type 3 (SCA3).

also muscle Array twin, hyperreflexia, sweating, shivering, tremor, diarrhea, ataxia, fever and so on, life-threatening.

Objective To observe the effect of buspirone on ataxia symptom after stroke.

difficult to hand pick up small objects, the lack of thumb to index finger pinch action athetosic, ataxia, mixed with action and so on.

Objective: To study the possible relationship between mitochondrial DNA point mutations and hereditary ataxia.

Objective: To study the possible relationship between mitochondrial DNA (mtDNA) and hereditary ataxia (HA).

A study of clinical analysis and genetic polymorphism in hereditary spinocerebellar ataxia with psychiatric symptoms

clinical observation on point - through - point acupuncture for treatment of cerebellar ataxia after apoplexy

Aberrance analysis of mitochondrial DNA in a family with hereditary ataxia in Guangxi province

Research on clinical characteristics and ATM gene mutations in Chinese patients with ataxia-telangiectasia

Establishment of germplasm repository of spinocerebellar ataxia

Rehabilitative evaluation and treatment for patient with cerebellar ataxia

The clinical characteristics and nursing measures of children with acute cerebellar ataxia

Observation on Therapeutic Effect of Point-through-Point Therapy on Cerebellar Ataxia After Stroke

The Treatment of Cerebellar Ataxia with Buspirone Hydrochloride

Mitochondrial DNA point mutations studies in hereditary ataxia

Molecular genetic diagnosis and clinical characteristics of spinocerebellar ataxia type 6

The clinical features and gene mutation analysis in a pedigree of spinocerebellar ataxia type 7

Intermittent cerebellar ataxia of childhood

Diagnosis and treatment of child acute cerebellar ataxia: a study of 11 cases

Distribution of different genotypes of hereditary ataxia in south China

Clinical Study on the Treatment of Apoplectic Ataxia with Scalp and Neck Acupuncture

ATM gene mutations in Chinese patients with ataxia-telangiectasia

Frequency of different subtype of spinocerebellar ataxia in Hans of South China

Cerebellar ataxia associated with optic atrophy

The applicable values of posturography on diagnosis of ataxia

Clinical and electrophysiological examination of 3 cases with sensory ataxia form Guillain-Barre Syndrome

Cerebellar ataxia plus retinitis pigmentosa

Cerebellar ataxia and crossed third-nerve palsy

Progression in the study of spinocerebellar ataxia

Hepatic lesion and ataxia due to the use of phenytoin sodium

Spinocerebellar ataxia type II gene SCA

Report a family tree of hereditary ataxia

Frequency of different subtypes of spinocerebellar ataxia in the Han nationality of Hunan province in China

Clinical analysis of 36 infant cases with acute ataxia

Survey on the causes of ataxia of calves

Severe Ataxia Caused by Amiodarone