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  2. SMA connector - Wikipedia

    en.wikipedia.org/wiki/SMA_connector

    SMA connectors must not be confused with the standard household 75-ohm type F coax connector (diameters: male 7 ⁄ 16 inch (11 mm) circular or hex; female 3 ⁄ 8 inch (9.5 mm) external threads), as there is only about a 2 mm difference overall in the specifications. Type F cannot be mated with SMA connectors without the use of an adapter.

  3. Spinal muscular atrophy - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophy

    Spinal muscular atrophy (SMA) is a rare neuromuscular disorder that results in the loss of motor neurons and progressive muscle wasting. [3] [4] [5] It is usually diagnosed in infancy or early childhood and if left untreated it is the most common genetic cause of infant death. [6]

  4. Nusinersen - Wikipedia

    en.wikipedia.org/wiki/Nusinersen

    Children with SMA type 1 were treated in the UK under a Biogen-funded expanded access programme; after enrolling 80 children, the scheme closed to new people in November 2018. [36] In May 2019, however, NICE reversed its stance and announced its decision to recommend nusinersen for use across a wide spectrum of SMA for a 5-year period. [37] [38]

  5. Newborn screening for spinal muscular atrophy ‘results in ...

    www.aol.com/newborn-screening-spinal-muscular...

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  6. Onasemnogene abeparvovec - Wikipedia

    en.wikipedia.org/wiki/Onasemnogene_abeparvovec

    SMA is a neuromuscular disorder caused by a mutation in the SMN1 gene, which leads to a decrease in SMN protein, a protein necessary for survival of motor neurons. Onasemnogene abeparvovec is a biologic drug consisting of AAV9 virus capsids that contains a SMN1 transgene along with synthetic promoters . [ 5 ]

  7. Risdiplam - Wikipedia

    en.wikipedia.org/wiki/Risdiplam

    The study of later-onset SMA was a randomised controlled trial that enrolled 180 participants, aged between 2 and 25 years, with less severe forms of the disease. Participants treated with risdiplam for 12 months showed improvements in motor function compared to participants given a placebo.

  8. Spinal muscular atrophies - Wikipedia

    en.wikipedia.org/wiki/Spinal_muscular_atrophies

    SMA: Spinal muscular atrophy (SMA) 5q spinal muscular atrophy; Autosomal recessive proximal spinal muscular atrophy; Werdnig–Hoffmann disease / Kugelberg–Welander disease; 253300 253550 253400 271150: SMN1: 5q13.2: Autosomal recessive: Affects primarily proximal muscles in people of all ages, progressive, relatively common XLSMA

  9. The Complete Guide to Trend-Following Indicators

    www.aol.com/news/complete-guide-trend-following...

    The SMA is less effective for prediction in sideways and rangebound markets. The calculation simply sums up prices over the chosen period and divides by that period. Each data point adds to a line ...