Ornithine transcarbamylase deficiency

Results: 14



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1Development of a novel adeno-associated viral vector in combination with tolerogenic nanoparticles for the treatment of Ornithine Transcarbamylase Deficiency Giulia De Sabbata1, Florence Boisgerault2,3, Fanny Collaud2,3,

Development of a novel adeno-associated viral vector in combination with tolerogenic nanoparticles for the treatment of Ornithine Transcarbamylase Deficiency Giulia De Sabbata1, Florence Boisgerault2,3, Fanny Collaud2,3,

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Source URL: selectabio.com

Language: English - Date: 2017-12-21 11:46:10
    2Orphanet Journal of Rare Diseases This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon. Long-term outcomes in Ornit

    Orphanet Journal of Rare Diseases This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon. Long-term outcomes in Ornit

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    Source URL: www.ojrd.com

    Language: English
    3Microsoft Word - PAR - UK-W-050-pdWSdoc

    Microsoft Word - PAR - UK-W-050-pdWSdoc

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    Source URL: www.hma.eu

    Language: English - Date: 2015-01-30 06:25:11
    4UCDC Newsletter_4.22.13_Final.pub

    UCDC Newsletter_4.22.13_Final.pub

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    Source URL: www.rarediseasesnetwork.org

    Language: English - Date: 2013-04-23 17:35:32
    5UREA CYCLE DISORDER GLOSSARY © National Urea Cycle Disorders Foundation 2013 A Allele: One of a pair of genes, situated on the same site on paired chromosomes, containing specific inheritable characteristics.

    UREA CYCLE DISORDER GLOSSARY © National Urea Cycle Disorders Foundation 2013 A Allele: One of a pair of genes, situated on the same site on paired chromosomes, containing specific inheritable characteristics.

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    Source URL: www.nucdf.org

    Language: English - Date: 2013-06-25 20:36:12
    6Urea cycle disorders A guide for patients, parents and families Contents Introduction ...................................................................................................3 Metabolic function..............

    Urea cycle disorders A guide for patients, parents and families Contents Introduction ...................................................................................................3 Metabolic function..............

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    Source URL: www.nucdf.org

    Language: English - Date: 2013-06-28 19:21:06
    7CLASSIC CITRULLINEMIA (ASS) REFERENCES (CITRULLINEMIA, TYPE I; CTLN1; ARGININOSUCCINATE SYNTHETASE DEFICIENCY; ASS DEFICIENCY) 1. 2.

    CLASSIC CITRULLINEMIA (ASS) REFERENCES (CITRULLINEMIA, TYPE I; CTLN1; ARGININOSUCCINATE SYNTHETASE DEFICIENCY; ASS DEFICIENCY) 1. 2.

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    Source URL: www.idph.state.ia.us

    Language: English - Date: 2007-06-25 16:35:49
    8PARENT FACT SHEET DISORDER Argininosuccinic Acidemia (ASA) CAUSE ASA occurs when an enzyme called argininosuccinic acid lyase is either missing or not working

    PARENT FACT SHEET DISORDER Argininosuccinic Acidemia (ASA) CAUSE ASA occurs when an enzyme called argininosuccinic acid lyase is either missing or not working

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    Source URL: www.chfs.ky.gov

    Language: English - Date: 2014-09-11 03:13:19
    9PARENT FACT SHEET DISORDER Argininosuccinic Acidemia (ASA) CAUSE ASA occurs when an enzyme called argininosuccinic acid lyase is either missing or not working

    PARENT FACT SHEET DISORDER Argininosuccinic Acidemia (ASA) CAUSE ASA occurs when an enzyme called argininosuccinic acid lyase is either missing or not working

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    Source URL: chfs.ky.gov

    Language: English - Date: 2014-08-09 11:26:15
    10Biochemical Genetics, Vol.25, Nos. 3/4, 1987  Chicken Ornithine Transacarbamylase: Its Unexpected Expression S o i e h i Tsuji 1 and S e i k i K a n a z a w a 1

    Biochemical Genetics, Vol.25, Nos. 3/4, 1987 Chicken Ornithine Transacarbamylase: Its Unexpected Expression S o i e h i Tsuji 1 and S e i k i K a n a z a w a 1

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    Source URL: www.2ndchance.info

    Language: English - Date: 2014-02-04 17:56:48