WordNet

showing little if any change; "a static population" (同)stable, unchanging
a crackling or hissing noise caused by electrical interference (同)atmospherics, atmospheric static
angry criticism; "they will probably give you a lot of static about your editorial"
inability to coordinate voluntary muscle movements; unsteady movements and staggering gait (同)ataxy, dyssynergia, motor_ataxia
the branch of mechanics concerned with forces in equilibrium

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PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia.

Jobling RK1, Assoum M2, Gakh O3, Blaser S4, Raiman JA1, Mignot C5, Roze E6, Dürr A7, Brice A7, Lévy N8, Prasad C9, Paton T10, Paterson AD10, Roslin NM10, Marshall CR10, Desvignes JP2, Roëckel-Trevisiol N2, Scherer SW11, Rouleau GA12, Mégarbané A13, Isaya G3, Delague V14, Yoon G15.
Brain : a journal of neurology.Brain.2015 Jun;138(Pt 6):1505-17. doi: 10.1093/brain/awv057. Epub 2015 Mar 25.
Non-progressive cerebellar ataxias are a rare group of disorders that comprise approximately 10% of static infantile encephalopathies. We report the identification of mutations in PMPCA in 17 patients from four families affected with cerebellar ataxia, including the large Lebanese family previously
PMID 25808372

Treatment of detrusor external sphincter dyssynergia using ultrasound-guided trocar catheter transurethral botulinum toxin a injection in men with spinal cord injury.

Yang WX1, Zhu HJ2, Chen WG3, Zhang da W2, Su M2, Feng JF2, Liu CD2, Cai P4.
Archives of physical medicine and rehabilitation.Arch Phys Med Rehabil.2015 Apr;96(4):614-9. doi: 10.1016/j.apmr.2014.10.003. Epub 2014 Oct 24.
OBJECTIVE: To evaluate the effects of transrectal ultrasound-guided trocar catheter transurethral botulinum toxin A (BTX-A) injection into the external urethral sphincter (EUS) for treating detrusor external sphincter dyssynergia (DESD) in men with spinal cord injury (SCI).DESIGN: Descriptive study.
PMID 25450132

Santos de Oliveira LA1, Martins CP2, Horsczaruk CH2, Lima da Silva DC2, Martins JV3, Vasconcelos LF3, Rodrigues Ede C1.
Journal of physical therapy science.J Phys Ther Sci.2015 Apr;27(4):1223-5. doi: 10.1589/jpts.27.1223. Epub 2015 Apr 30.
[Purpose] Spinocerebellar ataxia consists of a group of autosomal dominant disorders that cause progressive degeneration, mainly in the cerebellum and its connections. Falls, which are a significant concern of this condition, reduce patients' mobility, deteriorate their health and have physical and
PMID 25995594

Santos de Oliveira Laura Alice,Martins Camilla Polonini,Horsczaruk Carlos Henrique Ramos,Lima da Silva Débora Cristina,Martins José Vicente Pereira,Vasconcelos Luiz Felipe Rocha,Rodrigues Erika de Carvalho
Journal of Physical Therapy Science 27(4), 1223-1225, 2015
… [Purpose] Spinocerebellar ataxia consists of a group of autosomal dominant disorders that cause progressive degeneration, mainly in the cerebellum and its connections. … The aim of this study was to test the effectiveness of a modified protocol for improving balance and diminishing the fall risk of spinocerebellar ataxia patients exclusively. …
NAID 130005067463

坂田英明,遠藤まゆみ,加我君孝
Equilibrium research 71(4), 253-263, 2012-08-01
… Concerning balancing dysfunction, as the central nervous system is under development, the peripheral static-sense system, myelination/maturation of the central nervous system, process of functional integration, and learning/acquisition of gross and fine motor skills at each age must be considered.During early childhood, brain tumors, especially cerebellar/brainstem tumors, cerebellitis, and acute cerebellar ataxia should be considered. …
NAID 10031026794

石川欽也,石黒太郎,高橋真 [他],佐藤望,網野猛志,新美祐介,水澤英洋
臨床神経学 49(11), 907-909, 2009-11-01
… Spinocerebellar ataxia (SCA) is a group of degenerative ataxias with autosomal dominant inheritance. … In addition to these dynamic mutations, static mutations, such as missense mutations and deletions, have been identified to cause SCA5, SCA11, SCA13, SCA14, SCA15 and SCA27. … Since 1992, authors have been involved in identifying the mutation (s) of autosomal dominant cerebellar ataxia with rather pure cerebellar syndrome (ADCAIII). …
NAID 10026291086