Ketogenic amino acids

Results: 100



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21Microsoft Word - E12-p-a Sapropterin

Microsoft Word - E12-p-a Sapropterin

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Source URL: www.england.nhs.uk

Language: English - Date: 2013-08-13 12:09:53
22European Journal of Clinical Nutrition[removed], 451–462  & 2008 Nature Publishing Group All rights reserved[removed] $30.00 www.nature.com/ejcn  REVIEW

European Journal of Clinical Nutrition[removed], 451–462 & 2008 Nature Publishing Group All rights reserved[removed] $30.00 www.nature.com/ejcn REVIEW

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Source URL: www.nature.com

Language: English - Date: 2010-01-13 11:58:53
23Christos S. Katsanos, Hisamine Kobayashi, Melinda Sheffield-Moore, Asle Aarsland and Robert R. Wolfe Am J Physiol Endocrinol Metab 291:[removed], 2006. First published Feb 28, 2006; doi:[removed]ajpendo[removed]You might

Christos S. Katsanos, Hisamine Kobayashi, Melinda Sheffield-Moore, Asle Aarsland and Robert R. Wolfe Am J Physiol Endocrinol Metab 291:[removed], 2006. First published Feb 28, 2006; doi:[removed]ajpendo[removed]You might

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Source URL: www.eatrightnc.org

Language: English - Date: 2015-01-14 16:04:03
24Essential amino acids are primarily responsible for the amino acid stimulation of muscle protein anabolism in healthy elderly adults1–3 Elena Volpi, Hisamine Kobayashi, Melinda Sheffield-Moore, Bettina Mittendorfer, an

Essential amino acids are primarily responsible for the amino acid stimulation of muscle protein anabolism in healthy elderly adults1–3 Elena Volpi, Hisamine Kobayashi, Melinda Sheffield-Moore, Bettina Mittendorfer, an

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Source URL: www.eatrightnc.org

Language: English - Date: 2015-01-14 16:02:54
25doi:[removed]j.exger[removed]

doi:[removed]j.exger[removed]

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Source URL: www.eatrightnc.org

Language: English - Date: 2015-01-14 16:03:43
26Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase

Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase

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Source URL: www.sde.idaho.gov

Language: English - Date: 2009-03-18 18:56:23
27Plant proteins in relation to human and amino acid nutrition1’2 Vernon

Plant proteins in relation to human and amino acid nutrition1’2 Vernon

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Source URL: ajcn.nutrition.org

Language: English
28Phenylketonuria (PKU) Jewell C. Ward, MD, Ph D, Chief, Division of Medical Genetics Department of Pediatrics University of Tennessee-Memphis 711 Jefferson, CDD, Room 522

Phenylketonuria (PKU) Jewell C. Ward, MD, Ph D, Chief, Division of Medical Genetics Department of Pediatrics University of Tennessee-Memphis 711 Jefferson, CDD, Room 522

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Source URL: health.state.tn.us

Language: English - Date: 2006-10-30 12:01:41
29Study of Some Physicochemical and Functional Properties of Quinoa (Chenopodium Quinoa Willd) Protein Isolates

Study of Some Physicochemical and Functional Properties of Quinoa (Chenopodium Quinoa Willd) Protein Isolates

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Source URL: quinua.pe

Language: English - Date: 2013-02-15 20:04:35
30Women with PKU Second Edition California Department of Health Services Maternal PKU Program

Women with PKU Second Edition California Department of Health Services Maternal PKU Program

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Source URL: www.cdph.ca.gov

Language: English - Date: 2014-08-13 12:31:32