与 «ACIDEMIA»相关的英语书籍
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acidemia的用法。与
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1
Inherited Metabolic Diseases: A Clinical Approach
ALGORITHMIC WORK UP OF PATIENT WITH LACTIC ACIDMIA Document
elevated Lactic Acid and/or Pyruvic Acid and/or Alanine in Blood and/or CSF and
Urine Diagnose or Exclude Organic Acidemia Passes Fast Oxidation Defect With
...
Georg F. Hoffmann, Johannes Zschocke, William L. Nyhan,
2009
2
Atlas of Metabolic Diseases Second edition
Our approach to the treatment of organic acidemia is to provide whole protein
containing the offending amino acid required for growth and little more. Our
experience with isovaleric acidemia is that the provision of protein can be
somewhat ...
William L Nyhan, Bruce A Barshop, Pinar T. Ozand,
2005
3
Nutritional Management of Renal Disease
This direct effect of acidemia on bone demin- eralization appears to occur by
different mechanisms than those induced by cortisol, PTH, or IGF-I and are
additive to those effects. For example, parathyroidec- tomy does not block the
effects of ...
Joel D. Kopple, Shaul G Massry, Kamyar Kalantar-Zadeh,
2012
4
Pediatric Nutrition in Chronic Diseases and Developmental ...
Glutaric acidemia type I (GAI), first described in 1975 by Goodman et al.,' is one of
several rare autosomal recessive organic acidemias caused by a defect in the
pathways of amino acid ca- tabolism. It was designated "type I" to distinguish it ...
Shirley Ekvall, Valli K. Ekvall,
2005
First decide whether the acidemia is a respiratory acidemia (i.e., caused by
hypoventilation) or a metabolic acidemia (i.e., caused by acid gain or bicarbonate
[HCO3] loss). Respiratory Acidemia • pH ≤ 7.35 • Partial pressure of carbon
dioxide ...
Shane A. Marshall, John Ruedy,
2011
6
Genetic Disorders and the Fetus: Diagnosis, Prevention and ...
Improved prenatal diagnosis of methylmalonic acidemia: mas fragmentography
of methylmalonic acid in amniotic fluid and maternal urine. Eur J Pediatr 1981;
137:261. 383. Zinn AB, Hine DG, Mahoney MJ, et al. The stable isotope dilution ...
Aubrey Milunsky, Jeff Milunsky,
2011
7
Nutrition Management of Patients with Inherited Metabolic ...
Vockley J, Parimoo B, Tanaka K. Molecular characterization of four different
classes of mutations in the isovaleryl-CoA dehydrogenase gene responsible for
isovaleric acidemia. Am J Hum Genet. 1991;49:147–157. Vockley J, Ensenauer
R.
8
Journal of the Medical Association of Thailand
1 5) was used to define fetal acidemia. Moreover, Piazze etal (2000)(8) also used
a modified-BPP in predictive of fetal acidemia and even though they used
different criteria for fetal acidemia {i.e. an umbilical artery pH < 7.2), they
observed a ...
9
Mosby's Pocket Guide to Fetal Monitoring: A ...
An umbilical artery pH less than 7.20 usually is considered to define acidemia.
Note that a much lower pH (7.0) is defined as the threshold of potential injury.
Acidemia is categorized as respiratory, metabolic, or mixed. Isolated respiratory ...
Lisa A. Miller, David Miller, Susan Martin Tucker,
2012
10
Textbook of Clinical Pediatrics
. Table 38.6 Diseases that are screened in a neonate by tandem mass
spectrometry Isovaleric acidemia 3-Hydroxy-3-methylglutaric acidemia Propionic
acidemia Methylmalonic acidemia Cobalamin mutations with low methionine ...
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Would I adopt this baby in five days, knowing the blood results? I'm …
Methylmalonic or propionic acidemia, orotic aciduria, severe combined immunodeficiency, pyruvic dehydrogenase deficiency, familial ... «The Express Tribune, 六月 15»
New Nightmare For Scott Baio As Wife Fights Brain Tumor
... was heartbroken when his 7-year-old daughter, Bailey DeLuca, once tested positive for a rare metabolic disorder known as glutaric acidemia ... «The National Enquirer, 六月 15»
Scott Baio's Wife Diagnosed With Brain Tumor; Scott Posts Intimate …
... Bailey's birth in November 2007, they were informed that she tested positive for a rare metabolic disorder known as glutaric acidemia type 1, ... «iSchoolGuide, 六月 15»
Scott Baio's Wife Diagnosed with Brain Tumor
In 2008, Baio opened up about his daughter possibly having a rare metabolic disorder called glutaric acidemia type 1. After over three months ... «People Magazine, 六月 15»
Children with rare metabolic disorders struggle to get right diet
An HR manager in the city lost three of her children to a rare metabolic disorder called propionic acidemia. Damayanthi K U, 40, had her first ... «Bangalore Mirror, 五月 15»
Too much protein can prove fatal for boy with rare condition
According to the National Institutes of Health, people with glutaric acidemia type 1 have inadequate levels of an enzyme that helps break down ... «Fox News, 五月 15»
Milk Or A Cheeseburger Can Kill People With A Rare Disorder
Unfortunately, Alfie has a rare disorder called Glutaric Acidemia. This disorder makes eating more than 19 grams of protein in one day ... «The Inquisitr, 五月 15»
Alfie Smith: Meet boy who could be killed by drinking a glass of milk
Little Alfie Smith is banned from drinking the liquid or munching on a McDonalds thanks to Glutaric Acidemia - which means if he eats more ... «Mirror.co.uk, 五月 15»
Amish, public schools join to serve special-needs kids
... as well as lesser-known diseases like Maple Syrup Urine Disease, which can kill babies who are not diagnosed early, and glutaric acidemia, ... «Kansas City Star, 五月 15»
Insular Amish Schools Find Ways To Serve Special Needs Kids
... as lesser-known diseases like Maple Syrup Urine Disease (which can kill babies who are not properly diagnosed early) to Glutaric acidemia, ... «Huffington Post, 五月 15»