Eds Sentence Examples

Denoting the cross-section a of a filament by dS and its mass by dm, the quantity wdS/dm is called the vorticity; this is the same at all points of a filament, and it does not change during the motion; and the vorticity is given by w cos edS/dm, if dS is the oblique section of which the normal makes an angle e with the filament, while the aggregate vorticity of a mass M inside a surface S is M - l fw cos edS.

Hence if dS and dS' are the areas of the ends, and +E and - E' the oppositely directed electric forces at the ends of the tube, the surface integral of normal force on the flux over the tube is EdS - E'dS' (20), and this by the theorem already given is equal to zero, since the tube includes no electricity.

A tube so chosen that EdS for one section has a value unity, is called a unit tube, since the product of force and section is then everywhere unity for the same tube.

Every tube of electric force must therefore begin and end on electrified surfaces of opposite sign, and the quantities of positive and negative electricity on its two ends are equal, since the force E just outside an electrified surface is normal to it and equal to a/41r, where a is the surface density; and since we have just proved that for the ends of a tube of force EdS = E 1 dS', it follows that adS = a'dS', or Q = Q', where Q and Q' are the quantities of electricity on the ends of the tube of force.

Turrianus - one of the papal theologians at the Council of Justificatione, 1 557), the title was used in 1659 by the Lutheran Lukas Friedrich Reinhard (1623-1688), professor of theology at Altdorf (Synopsis theologiae dogmaticae, eds.

Then these three geezers turn up, looking proper bling, wiv crowns on their ' eds.

Thales, along with EDS, were the principal sponsors of the " Digital Identity " conference held in November 2004.

Extract reprinted in Vallentyne P., and H. Steiner (eds.) 2000a.

Beck, Peggy, Nia Francisco, and Anna Lee Walters, eds.

Excessive daytime sleepiness (EDS) is a condition that causes a person to be sleepy during the day even after getting a normal amount of sleep the night before.

Siberry, George K., and Robert Iannone, eds.

The Ehlers-Danlos syndrome (EDS) refers to a group of inherited disorders that affect collagen structure and function.

Classification of EDS types was revised in 1997.

The major symptoms associated with EDS classical type involve the skin and joints.

There is no definitive test for the diagnosis of classical EDS.

Unfortunately, these tests are not sensitive enough to identify all individuals with classical EDS.

Excessively loose joints are the hallmark of this EDS type, formerly known as EDS type III.

There are two major clinical diagnostic criteria for EDS hypermobility type.

Formerly called EDS type IV, EDS vascular type is the most severe form.

There is a classic facial appearance associated with EDS vascular type.

Due to the severe complications associated with EDS type IV, death usually occurs before the fifth decade.

A study of 419 individuals with EDS vascular type, completed in 2000, found that the median survival rate was 48 years, with a range of six to 73 years.

There are four major clinical diagnostic criteria for EDS vascular type.

Laboratory testing is available for this form of EDS.

The major symptoms of kyphoscoliosis type, formerly called EDS type VI, are general joint looseness.

Also, infants with this type of EDS have an abnormal curvature of the spine (scoliosis).

There are four major clinical diagnostic criteria for EDS kyphoscoliosis type.

This form of EDS is caused by a change in the PLOD gene on chromosome 1, which encodes the enzyme lysyl hydroxylase.

This test, performed on urine, is extremely sensitive and specific for EDS kyphoscolios type.

Dislocation of the hip joint typically accompanies arthrochalasia type EDS, formerly called EDS type VIIB.

Individuals with this type of EDS may experience mildly diminished bone mass, scoliosis, and poor muscle tone.

There are two major clinical diagnostic criteria for EDS arthrochalasia type.

Individuals with this type of EDS, once called type VIIC, have extremely fragile skin that bruises easily but does not scar excessively.

There are two major clinical diagnostic criteria for EDS dematosparaxis type.

This form of EDS is caused by a change in the enzyme called procollagen I N-terminal peptidase.

There are several other forms of EDS that have not been as clearly defined as the aforementioned types.

Symptoms of EDS within this category may include soft, mildly stretchable skin, shortened bones, chronic diarrhea, joint hypermobility and dislocation, bladder rupture, or poor wound healing.

According to the Ehlers-Danlos National Foundation, one in 5,000 to one in 10,000 people are affected by some form of EDS.

There are numerous types of EDS, all caused by changes in one of several genes.

The manner in which EDS is inherited depends on the specific gene involved.

Changes or mutations in genes can cause genetic diseases in several different ways, many of which are represented within the spectrum of EDS.

In autosomal dominant EDS, only one copy of a specific gene must be changed for a person to have EDS.

In autosomal recessive EDS, both copies of a specific gene must be changed for a person to have EDS.

In X-linked EDS, a specific gene on the X chromosome must be changed.

However, because males only have one X-chromosome, they are affected if an X-linked recessive EDS gene is changed on their single X-chromosome.

Although there is much information regarding the changes in genes that cause EDS and their various inheritance patterns, the exact gene mutation for all types of EDS is not known.

Clinical symptoms such as extreme joint looseness and unusual skin qualities, along with family history, can lead to a diagnosis of EDS.

Specific tests, such as skin biopsies, are available for diagnosis of certain types of EDS, including vascular, arthrochalasia, and dermatosparaxis types.

Constitutional homeopathic treatment may be helpful in maintaining optimal health in persons with a diagnosis of EDS.

Before beginning these types of therapies, an individual with EDS should discuss them with his or her doctor.

The outlook for individuals with EDS depends on the type of EDS with which they have been diagnosed.

However, those with blood vessel involvement, particularly persons with EDS vascular type, have an increased risk of fatal complications.

Some people with EDS are not diagnosed until well into adulthood and, in the case of EDS vascular type, occasionally not until after death due to complications of the disorder.

Although children with EDS face significant challenges, it is important to remember that each child is unique with his or her own distinguished qualities and potential.

Persons with EDS go on to have families and careers, and to be respected citizens, surmounting the challenges of their disease.

If a couple has had a child diagnosed with EDS, the chance that they will have another child with the same disorder depends on the form of EDS the child has and if either parent is affected by the same disease.

In classical autosomal dominant EDS, the risk for recurrence in the parents' other children is one in four.

X-linked recessive EDS is accompanied by a slightly more complicated pattern of inheritance.

If a father with an X-linked recessive form of EDS passes a copy of his X chromosome to his children, the sons will be unaffected and the daughters will be carriers.

If a mother is a carrier for an X-linked recessive form of EDS, she may have affected or unaffected sons, or carrier or unaffected daughters, depending on the second sex chromosome inherited from the father.

Prenatal diagnosis is available for specific forms of EDS, including kyphosocliosis type and vascular type.

Prior to diagnosis, parents of children with EDS have found themselves under suspicion of child abuse.

Management of all types of EDS may include genetic counseling to help the affected individual and his or her family understand the disorder and its impact on other family members and future children.

Siberry, George, and Robert Iannone, eds.

Bellugi, Ursula, and Marie St. George, eds.

Atkinson, William, and Charles (Skip) Wolfe, eds.

Kessler, Daniel B. and Peter Dawson, eds.

Brand names include Pure Basics, Pure Comfort, Pure Essentials, Dickies EDS, Koi, Medline, and Medi-Threads.