- Best iPad App Developers 0 Comments December 19, 2011 By: Vicki Windman Dec 18 Written by: 12/18/2011 5:09 PM ShareThis As the search for the best education apps continues, certain developers are working diligently to expand from a single app to an entire line of apps. Jungle Education has three colorful apps that are multi-lingual, multiple levels and tracks student progress. eskillslearning has apps in reading comprehension, language arts, and math. Has nearly 30 apps for speech therapy, including apps for autism, apraxia, articulation, caseload management, dysphagia, fluency/stuttering, language skills, oral motor, Spanish and screening and testing. Has over 14 apps from Course Assistant Apps: Pre algebra, calculus, multivariable calculus, statistics, astronomy, music theory, physics, chemistry to reference apps: US Presidents, Words, to US States. Has grades one through three full-version math apps.
30 Useful iPad Apps for Business & Presentation Apple sold more than 1 million copies of iPads in the first 3 months. This gadget is definitely more than just a larger version of iPhone or iPod touch. With 4x the screen of an iPhone, the iPad’s display is ideal for reading and for presentations. In today’s post, we’d like to highlight some really useful iPad applications that might replace the things you do daily with your laptop or netbook. With a piece of iPad and these applications, you probably don’t need to carry a laptop around. Here are 30 useful iPad applications for Business and Presentation you might find handy on your next project pitch or business trip. Full list after jump. Presentations KeynoteKeynote is the most powerful presentation app ever designed for a mobile device. CorkulousCorkulous is incredible idea board for iPad to collect, organize, and share your ideas that feel completely natural. Power Presenter This application is used for Presentation. Graph, Charts, Diagram & Statistic Planning Page & Documents Meetings
iPad, iPhone, iPod, Android Apps for Speech Therapists The Must-Have App Review Rubric Added by Jeff Dunn on 2011-11-22 So you just downloaded a few educational apps that you think might be useful in your classroom. How do you accurately compare and contrast them? Thanks to a new app review rubric from by eMobilize , it’s easier than ever to understand just how useful an app may be in the classroom. On a related note, the Edudemic Directory features many educational apps and lets you quickly compare them to see how they stack up. I’ve rewritten the original rubric from eMobilize and tailored it to fit all school districts. Download The Rubric Here (PDF) Overview of the App App Title: App Publisher/Developer: Version: Link to App Store: Curriculum Compliance Yes/ No – Is it relevant to the curriculum framework? Operational Yes/ No – Is navigation easy? Pedagogy Yes/ No – Does the material accommodate diverse ways in which students learn? Comments are closed.
Apps in Education Positive Technology Journal bloomsapps Using Blooms Taxonomy in education is a highly effective way to scaffold learning for the students. With the recent popularity and pervasive nature of iOS devices in school districts it is essential for educators to understand how to implement Blooms in the classroom using the apps that are available. While this list is by no means fully comprehensive, it will assist educators in getting started when implementing iOS devices in the classroom. This site will change almost daily as it will be updated with new and exciting apps! If you find any that you have worked with in your classroom please email dmileham@e1b.org or tweet @bloomsapps or @dmileham75 with your suggestions. Two Links to some iTunesU courses relating to iOS Integration: 1 iPad by Erie 1 Boards of Cooperative Educational Services ( Movie Making\Digital Storytelling Camera to PDF Free - cool little app that turns your device into a scanner. LiveBinders: I would be remiss if I didn't post this.
Methadone Methadone (also known as Symoron, Dolophine, Amidone, Methadose, Physeptone, Heptadon and many other names) is a synthetic opioid. It is used medically as an analgesic and a maintenance anti-addictive and reductive preparation for use by patients with opioid dependency. It was developed in Germany in 1937, mainly because Germany required a reliable internal source of opiates. Because it is an acyclic analog of morphine or heroin, methadone acts on the same opioid receptors as these drugs, and thus has many of the same effects. Methadone is also used in managing severe chronic pain, owing to its long duration of action, extremely powerful effects, and very low cost. Methadone was introduced into the United States in 1947 by Eli Lilly and Company. Methadone is mainly used in the treatment of opioid dependence. A number of pharmaceutical companies produce and distribute methadone. Medical uses[edit] Methadone maintenance[edit] In Russia, methadone treatment is illegal. Analgesic[edit]
Cocaine Cocaine (INN) (benzoylmethylecgonine, an ecgonine derivative) is a crystalline tropane alkaloid that is obtained from the leaves of the coca plant.[5] The name comes from "coca" and the alkaloid suffix "-ine", forming "cocaine". It is a stimulant, an appetite suppressant, and a nonspecific voltage gated sodium channel blocker, which in turn causes it to produce anaesthesia at low doses. Biologically, cocaine acts as a serotonin–norepinephrine–dopamine reuptake inhibitor, also known as a triple reuptake inhibitor (TRI). It is addictive due to its effect on the mesolimbic reward pathway.[6] It is markedly more dangerous than other CNS stimulants, including the entire amphetamine drug class,[7] at high doses due to its effect on sodium channels, as blockade of Nav1.5 can cause sudden cardiac death. Unlike most molecules, cocaine has pockets[clarification needed] with both high hydrophilic and lipophilic efficiency, violating the rule of hydrophilic-lipophilic balance. Medical effects Acute
Crack - Crack cocaine Crack cocaine ‘rocks’. Appearance and characteristics In purer forms, crack rocks appear as off-white nuggets with jagged edges,[3] with a slightly higher density than candle wax. Purer forms of crack resemble a hard brittle plastic, in crystalline form[3] (snaps when broken). A crack rock acts as a local anesthetic (see: cocaine), numbing the tongue or mouth only where directly placed. Purer forms of crack will sink in water or melt at the edges when near a flame (crack vaporizes at 90 °C, 194 °F).[2] Crack cocaine as sold on the streets may be adulterated or "cut" with other substances mimicking the appearance of crack cocaine to increase bulk. Chemistry In order for cocaine (in plastic bag at bottom) to be converted to crack, several supplies are needed. A close up of the "cooking" process that creates crack. Sodium bicarbonate (NaHCO3, common baking soda) is a base used in preparation of crack, although other weak bases may substitute for it. Coc-H+Cl− + NaHCO3 → Coc + H2O + CO2 + NaCl
Ecstasy - MDMA MDMA (3,4-methylenedioxy-N-methylamphetamine) is an empathogenic drug of the phenethylamine and amphetamine classes of drugs. MDMA has become widely known as "ecstasy" (shortened to "E", "X", or "XTC"), usually referring to its street form, although this term may also include the presence of possible adulterants. The UK term "Mandy" and the US term "Molly" colloquially refer to MDMA that is relatively free of adulterants.[3] MDMA can induce euphoria, a sense of intimacy with others, diminished anxiety, and mild psychedelia. Many studies, particularly in the fields of psychology and cognitive therapy, have suggested MDMA has therapeutic benefits and facilitates therapy sessions in certain individuals, a practice for which it had been formally used in the past. Regulatory authorities in several locations around the world have approved scientific studies administering MDMA to humans to examine its therapeutic potential and its effects.[9] Medical use[edit] Recreational use[edit]
Heroin Heroin /ˈhɛroʊɪn/ (diacetylmorphine or morphine diacetate, also known as diamorphine (BAN, INN[4]) and commonly known by its street names of H, smack, boy, horse, brown, black, tar, and others[5] is an opioid analgesic originally synthesized by C.R. Alder Wright in 1874 by adding two acetyl groups to the molecule morphine, which is found naturally in the opium poppy. It is the 3,6-diacetyl ester of morphine. Illicit heroin is sometimes available in freebase form, dulling the sheen and consistency to a matte-white powder.[7] Because of its lower boiling point, the freebase form of heroin is also smokable. As with other opioids, diacetylmorphine is used as both a legal, medically prescribed drug (e.g., as an analgesic, cough suppressant and as an anti-diarrhea drug) and a recreational drug, in which case the user is seeking euphoria. Usage Short-term effects of usage[12] Medical use Recreational use Prescription for addicts Detection in biological fluids Adverse effects Withdrawal Pharmacology
Sativa - Cannabis sativa Common uses[edit] A sack made from hemp fiber Its seeds are chiefly used to make hempseed oil which can be used for cooking, lamps, lacquers, or paints. They can also used as caged-bird feed, as they provide a moderate source of nutrients for most birds. The flowers (and to a lesser extent the leaves, stems, and seeds) contain psychoactive chemical compounds known as cannabinoids that are consumed for recreational, medicinal, and spiritual purposes. Plant physiology[edit] The flowers of the female plant are arranged in racemes and can produce hundreds of seeds. A Cannabis plant in the vegetative growth phase of its life requires more than 12–13 hours of light per day to stay vegetative. In soil, the optimum pH for the plant is 6.3 to 6.8. Cultivars[edit] Broadly, there are three main Cultivar Groups of cannabis that are cultivated today: Pharmacology[edit] The flower of a hybrid Cannabis indica plant Cannabis sativa, scientific drawing from c1900 Chemical constituents[edit] References[edit]
Alcohol Ball-and-stick model of the hydroxyl (-OH) functional group in an alcohol molecule (R3COH). The three "R's" stand for carbon substituents or hydrogen atoms.[1] The hydroxyl (-OH) functional group with bond angle. An important class of alcohols are the simple acyclic alcohols, the general formula for which is CnH2n+1OH. Of these ethanol (C2H5OH) is the alcohol found in alcoholic beverages; in common speech the word alcohol refers to ethanol. Other alcohols are usually described with a clarifying adjective, as in isopropyl alcohol (propan-2-ol) or wood alcohol (methyl alcohol, or methanol). In everyday life "alcohol" without qualification usually refers to ethanol, or a beverage based on ethanol (as in the term "alcohol abuse"). Toxicity Ball-and-stick model of tert-Amyl alcohol, which is 20 times more intoxicating than ethanol and like all tertiary alcohols, cannot be metabolised to toxic aldehydes.[3][4][5] Treatment Nomenclature Systematic names Common names Alkyl chain variations in alcohols