You need to convert the QuickTime file made by MovingPicture to a DV Movie, using the Export option in QuickTime Pro into the DV Stream format (available from Apple for $29).

You can import DVD-Video that you have authored with DVD authoring tools like Apple's iDVD, Microsoft's Windows DVD Maker, Pinnacle Studio 11, Nero Vision, Ulead DVD MovieFactory, Roxio Easy Media Creator 9 Suite, DVDit Pro, or DVD-Video that you have received from VHS-conversion services like YesDVD, or DVD-Video that you have created using a set-top DVD Recorder. Any Movie Player or Music Player can import content in DVD-Video format from DVD, DVD-R, DVD-RW, DVD+R, and DVD+RW discs.

No. Editing in MacVCD X for basics (removing commercials or making a favorite scenes reference movie) is all that this feature is intended to accomplish. Its not designed to let you do general purpose editing of VCD content.

Your footage won't be cataloged, broken down into scenes, nor easily searchable. Plus when newer versions of FootTrack come out you won't be able to take advantage of them

The duration of the QT-interval is a measure of the time required for depolarization and repolarization to occur. In long QT syndrome, the duration of repolarization is longer than normal. Thus, the QT-interval is prolonged. An interval above 440 milliseconds (msec) is considered prolonged. QT-prolongation in is due to overload of myocardial cells with positively charged ions during ventricular repolarization.

to 470 milliseconds is considered borderline. The average QTc for someone who has long-QT syndrome is 490 milliseconds. A QTc at or above 480 milliseconds in females or 470 milliseconds in males, is probably a sign for long-QT syndrome, in the absence of drugs, electrolyte disturbance, or other conditions that might independently lengthen the QT-interval.

The latest version of Qt can be downloaded from http://www.troll.no or from ftp.troll.no, and a whole range of ftp mirror sites around the world. Look for a mirror near you on the list available under http://www.troll.no/dl/

The long QT syndrome (LQTS) is causing an abnormality of the heart's electrical system. The mechanical function of the heart is entirely normal. The electrical problem is due to defects in heart muscle cell structures called ion channels. These electrical defects predispose affected persons to a very fast heart rhythm (arrhythmia) called "Torsade de Pointes" (TdP) which leads to sudden loss of consciousness (syncope) and may cause sudden cardiac death.

The term "corrected" QT-interval may be misunderstood. It does not mean the measured QT-interval is incorrect, but adjusted for heart rate. The reason is that the QT interval is affected by the heart rate. QTc in concept is best compared to the Body Mass Index (BMI).

The diagnosis is commonly suspected or made from the electrocardiogram (ECG). All children and young adults should have an ECG as part of their evaluation for an unexplained loss of consciousness episode. On the other hand, there is the possibility to check blood samples for known gene mutations that cause LQTS.

For Windows users, you can import movies directly form your digital video cameras using USB connection or IEEE1394 connection. For Macintosh users, you can import movies directly form your digital video cameras using USB connection only. Please connect your camera to your PC using a USB cable to its USB port. Explanation on how to connect your camera to your PC can be found in the explanation book that came with your camera.

There are several programs you can use to stream movies in the Archive. Because we allow users to upload video files in any format, the same player will not always work for every single file, so it's a good idea to have a couple of programs available that you can try. Also, some files simply can't be streamed. Usually, this happens when the program that created the video file uses a codec that our software doesn't understand.

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The name of the long QT syndrome refers to the QT-interval measured on the electrocardiogram (ECG or EKG for the German term "Elektrokardiogramm"). Your specialist may refer to long QT syndrome as Romano-Ward syndrome or Jervell, Lange-Nielsen syndrome (see point 3).

INHERITED: Inherited long QT syndrome was first clearly described in 1957. There are two variants, the autosomal dominant Romano-Ward (named by the doctors who first described the disease, O. Connor Ward and C. Romano) type and the autosomal recessive Jervell, Lange-Nielsen (Doctors A. Jervell, F. Lange-Nielsen) type. Inherited long QT syndrome is caused by mutations of at least 9 genes, and possibly more. Five different genes have so far been found.

The frequency is unknown but it appears to be a common cause of sudden and unexplained death in children and young adults. It is certainly much more common than previously thought. It may be as frequent as 1 in 5000 to 7000. This means, one of 5000 to 7000 newborns have the disease. The Jervell, Lange-Nielsen form is rare, but the Romano-Ward variant is being recognized with increasing frequency. In the USA, the presence of long QT syndrome is estimated to affect about 50.

It is generally estimated that approximately 10% to 12% of all patients with long QT syndrome show a normal QT-interval on their ECG. However, this does not mean that these patients are not affected by long QT syndrome. In such cases, a more profound evaluation is needed.

It has been noticed that several cardiac arrests occur during summer time. But it is not sure if it this may be an excess in statistical terms. It is however hard to define if these cardiac arrests are related to a specific "risk" due to heat or sweating or if it is mainly a reflection of increased physical activity, excitement and playing during the summer.