Category Archives: Phenylketonuria

Phenylketonuria (PKU) is an autosomal recessive metabolic genetic disorder characterized by a deficiency in the hepatic enzyme phenylalanine hydroxylase (PAH). This enzyme is necessary to metabolize the amino acid phenylalanine (‘Phe’) to the amino acid tyrosine. When PAH is deficient, phenylalanine accumulates and is converted into phenylpyruvate (also known as phenylketone), which is detected in the urine. – Wikipedia

Phenylketonuria ¦ Treatment and Symptoms

Posted on April 20, 2013 by admin

XXXXXX ◅ Phenylketonuria treatment — Finding the right information about Phenylketonuria treatment & symptoms, is crucial to managing Phenylketonuria. Learn … Video Rating: 0 / 5

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Brief Introduction for Phenylketonuria (PKU)

Posted on March 16, 2013 by admin

MF011 General Biology II (Group Assignment) Topic: Phenylketonuria (PKU) Work of Group 9 members: Lee Shu Jiun (1001231699) Lim Yi Leng (1001231581) Pei Qian… Video Rating: 4 / 5

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Artificial Sweeteners: A Closer Look At Aspartame — Part 2

Posted on September 11, 2012 by admin

Let’s finish reading the article we started in Part 1 and then get down to uncovering insights. In anecdotal reports, aspartame has been linked to various neuropsychiatric disorders, including panic attacks, mood changes, visual hallucinations, manic episodes, and isolated dizziness. … Continue reading →

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BioMarin to Present at the Goldman Sachs Global Healthcare Conference – Marketwatch

Posted on May 30, 2012 by admin

for phenylketonuria (PKU), developed in partnership with Merck Serono, a division of Merck KGaA of Darmstadt, Germany; and Firdapse(TM) (amifampridine), which has been approved by the European Commission for the treatment of Lambert Eaton … Bing News – Full Story … Continue reading →

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How to Choose Best Baby Formula

Posted on May 15, 2011 by admin

If you’ve decided on formula as the choice for feeding your baby, you might be a bit confused about all the choices. What types of adapted milk are there? In the market there are various types and varieties of artificial … Continue reading →

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E280K Mutation – Phenylketonuria

Posted on March 23, 2011 by admin

For Group Tyrosine, Inquiry 2E03. Phenylketonuria mutations. Video Rating: 5 / 5

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Discovery of Phenylketonuria (PKU) by Dr. Asbjørn Følling

Posted on December 4, 2010 by admin

An interview with Dr. Asbjørn Følling, a Norwegian physician and biochemist, who discovered phenylketonuria (PKU) in 1934, while treating two children at Oslo, Norway’s Rikshospitalet. The interview was filmed in the 1970s in Oslo, and was conducted by Dr. Victoria … Continue reading →

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Toxicity Of Artificial Sweeteners

Posted on November 14, 2010 by admin

There are presently four artificial, or synthetic, sweeteners that have been approved by the U.S. Food and Drug Administration (FDA): saccharin, aspartame, acesulfame-K, and sucralose. People use artificial sweeteners because they suffer from diseases such as diabetes mellitus, because they … Continue reading →

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Phenylketonuria and Maple Syrup Urine Disease – USMLE Review

Posted on November 13, 2010 by admin

www.studywithsubstancep.com Video Rating: 5 / 5

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Purchase Generic Amoxil without a prescription

Posted on November 3, 2010 by admin

Purchase Generic Amoxil without a prescription Amoxil Generic Name: penicillin (Oral route, Injection route, Intravenous route, Intramuscular route) Commonly used brand name(s): In the U.S.AmoxilBactocillBicillin L-ACloxapenCrysticillinDynapenGeocillinNafcilPfizerpenPipracilPrincipenStaphcillinTicarVeetids In CanadaAmoxil PediatricAmpicillin SodiumApo-AmoxiApo-Amoxi Sugar-FreeApo-CloxiApo-Pen-VkGen-AmoxicillinMed AmoxicillinNadopen V 200Nadopen V 400Novamoxin Available Dosage Forms:TabletPowder for … Continue reading →

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