SCCMS

AcronymDefinition
SCCMSSlow-Channel Congenital Myasthenic Syndrome
SCCMSSanta Cruz County Medical Society (Santa Cruz, CA)
SCCMSSt. Clair County Medical Society (Port Huron, MI)
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TABLE A2 Simplified Sample Cross-Correlation Matrices (SCCMs) for the Standardized Residuals of the Estimated Restricted VETAR Process Lag 1 Simplified SCCM [mathematical expression not reproducible] Lag 2 Simplified SCCM [mathematical expression not reproducible] Lag 3 Simplified SCCM [mathematical expression not reproducible] Lag 4 Simplified SCCM [mathematical expression not reproducible] Lag 5 Simplified SCCM [mathematical expression not reproducible] REFERENCES
SEMICOHERENT MULTIPOPULATION MORTALITY MODELING: THE IMPACT ON LONGEVITY RISK SECURITIZATION
In patients with slow-channel CMS (SCCMS), electrophysiological examination has revealed that prolonged opening activity of the AChR channel causes depolarization block, which contributes to muscle weakness and fatigability.[sup][1] SCCMS is usually inherited in an autosomal dominant pattern.
Patients with CMS have been reported worldwide, including in East Asia,[sup][7],[8] but there have been only a few published cases of CMS in China.[sup][9] Herein, we identified three patients with SCCMS from a Chinese family who presented with muscle weakness during early or late childhood.
SCCMS is a progressive disorder and may present with ophthalmoplegia, ptosis, facial paralysis, weakness, fatigue of trunk and limb muscles, and spinal deformity such as scoliosis.
A Missense Mutation in Epsilon-subunit of Acetylcholine Receptor Causing Autosomal Dominant Slow-channel Congenital Myasthenic Syndrome in a Chinese Family
The purpose of this paper is to propose and analyse a new AB class CCI structure based on self-cascode mirrors (SCCM).
A new CMOS first generation current conveyor CCI
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