PALABRAS DEL INGLÉS RELACIONADAS CON «PHENYLKETONURIA»
phenylketonuria
test
adults
pronunciation
treatment
facts
diet
caused
symptoms
phenylketonuria
autosomal
recessive
metabolic
genetic
disorder
characterized
homozygous
compound
heterozygous
mutations
gene
hepatic
enzyme
diseases
conditions
mayo
clinic
birth
defect
causes
called
build
your
body
genetics
home
reference
commonly
known
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increases
levels
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blood
medlineplus
process
part
protein
almost
foods
choices
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condition
present
from
unable
break
down
builds
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healthline
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essential
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channel
occurs
food
medscape
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inborn
error
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deficiency
baby
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read
10 LIBROS DEL INGLÉS RELACIONADOS CON «PHENYLKETONURIA»
Descubre el uso de
phenylketonuria en la siguiente selección bibliográfica. Libros relacionados con
phenylketonuria y pequeños extractos de los mismos para contextualizar su uso en la literatura.
1
Low Protein Cookery for
Phenylketonuria
The nutrient calculations in this edition of the cookbook are based on the updated 1995 Low Protein Food List for PKU compiled by the author, which is the most widely used food list for the PKU diet in the United States.
Virginia E. Schuett, 1997
2
Carbohydrate and Glycoprotein Metabolism; Maternal ...
394 finding by Dr C. Jakobs, Amsterdam, was elevated plasma galactitol and/or sorbitol levels in some cataract patients with quite normal activities of the galactose-degrading enzymes and sorbitol dehydrogenase in RBC.
R. Angus Harkness, R.J. Pollitt, G.M. Addison, 1991
3
Anesthesia for Genetic, Metabolic, and Dysmorphic Syndromes ...
These patients may have only moderately elevated levels of phenylala- nine, not
high enough to warrant treatment. Approximately 1 % to 2% of patients with
phenylketonuria do not have a defect in phenylalanine hydroxylase, but instead
have ...
Victor C. Baum, Jennifer E. O'Flaherty, 2007
4
Encyclopedia of Family Health
Phenylketonuria Questions and Answers I am pregnant and worried about my
baby. Is phenylketonuria a common problem? Phenylketonuria is a rare disease,
affecting about one in every 15,000 babies born in the United States. It is
detected ...
David B. Jacoby, R. M. Youngson, 2004
5
Molecular Biology and Biotechnology: A Comprehensive Desk ...
Phenylketonuria (PKU) An inherited metabolic disorder caused by a deficiency of
phenylalanine hydroxylase (PAH). Phenylketonuria (PKU), one of the most
common inborn errors of ami im acid metabolism, is an autosomal recessive
genetic ...
Neuropsychological functioning in children with early-treated phenylketonuria:
impact of white matter abnormalities. Dev Med Child Neurol. 2004;46(4):230–238
. Baumeister AA, Baumeister AA. Dietary treatment of destructive behavior ...
Lewis P. Rowland, Timothy A. Pedley, 2010
7
Inborn Metabolic Diseases: Diagnosis and Treatment
Mol Genet Metab 81:3-8 Sarkissian CN, Shao Z, Blain F et al (1999) A different
approach to treatment of phenylketonuria: phenylalanine degradation with
recombinant phenylalanine ammonia lyase. Proc Natl Acad Sci U S A 96:2339-
2344 Liu ...
John Fernandes, Jean-Marie Saudubray, Georges van den Berghe, 2006
8
Pediatric Nutrition in Chronic Diseases and Developmental ...
Chapter. 39. Phenylketonuria. and. Maternal. Phenylketonuria. Melanie. Hunt,.
Susan. Berry,. Helen. Berry,. and. Nancy. Leslie. I remember when she was only
3 months old she lay in her basket on the sun deck of a ship. I had taken her
there ...
Shirley Ekvall, Valli K. Ekvall, 2005
9
Clinical Biochemistry: An Illustrated Colour Text
N-aspartylphenylalanine methyl ester (aspartame) is a commonly used artificial
sweetener. It is broken down in the gut to phenylalanine. Patients with
phenylketonuria must avoid any food containing this additive. It is particularly
important that ...
10
Genetic Screening: Programs, Principles, and Research
RETARDATION. AND. PHENYLKETONURIA. An Apparent Association The
association of phenylketonuria with mental retardation was discovered by Foiling
in 1934.1 Shortly thereafter, Jervis surveyed 20,300 institutionalized retardates in
the ...
10 NOTICIAS EN LAS QUE SE INCLUYE EL TÉRMINO «PHENYLKETONURIA»
Conoce de qué se habla en los medios de comunicación nacionales e internacionales y cómo se emplea el término
phenylketonuria en el contexto de las siguientes noticias.
Company Shares of BioMarin Pharmaceutical Inc. Drops by -2.75%
... Morquio Syndrome Type A (MPS IV A), PEG-PAL, an enzyme substitution therapy for the treatment of phenylketonuria (PKU), and BMN-701, ... «Insider Trading Report, Jul 15»
Friday's Trade Stocks Roundup: MGIC Investment (NYSE:MTG …
... proprietary synthetic oral form of 6R-BH4 used to treat patients with phenylketonuria (PKU), an inherited metabolic disease; Aldurazyme used ... «wsnewspublishers, Jul 15»
Pre-Market News Alert on: BioMarin Pharmaceutical (NASDAQ …
... proprietary synthetic oral form of 6R-BH4 used to treat patients with phenylketonuria (PKU), an inherited metabolic disease; Aldurazyme used ... «wsnewspublishers, Jul 15»
Explore phenylketonuria global clinical trials review for 2014
Clinical trial report, “Phenylketonuria (PKU) Global Clinical Trials Review, H1, 2014″ provides data on the Phenylketonuria (PKU) clinical trial ... «WhaTech, Jul 15»
Biomarin Pharmaceutical Inc (BMRN) Files Form 4 Insider Selling …
... Morquio Syndrome Type A (MPS IV A), PEG-PAL, an enzyme substitution therapy for the treatment of phenylketonuria (PKU), and BMN-701, ... «Insider Trading Report, Jul 15»
BioMarin Pharmaceutical Inc. (NASDAQ:BMRN) Stock Rating Update
... Morquio Syndrome Type A (MPS IV A), PEG-PAL, an enzyme substitution therapy for the treatment of phenylketonuria (PKU), and BMN-701, ... «Investor Newswire, Jul 15»
European Stocks Seen Flat To Higher
... European marketing authorization for its product Kuvan (sapropterin dihydrochloride) to allow its use in children with phenylketonuria below ... «London South East, Jul 15»
Merck Marks 30-Year Milestone in Commitment to Innovation and …
ISENTRESS chewable tablets contain phenylalanine, a component of aspartame, which may be harmful to patients with phenylketonuria. «PharmiWeb.com, Jul 15»
Large Inflow of Money Witnessed in BioMarin Pharmaceutical Inc.
... Morquio Syndrome Type A (MPS IV A), PEG-PAL, an enzyme substitution therapy for the treatment of phenylketonuria (PKU), and BMN-701, ... «OTC Outlook, Jul 15»
Active Stocks in the Spotlight: HMS Holdings Corp (NASDAQ:HMSY …
... proprietary synthetic oral form of 6R-BH4 used to treat patients with phenylketonuria (PKU), an inherited metabolic disease; Aldurazyme used ... «wsnewspublishers, Jul 15»
