نتائج البحث - "du Moulin, Marcel"

المصدر: Santer, René; du Moulin, Marcel; Shahinyan, Tatevik; Vater, Inga; Maier, Esther; Muntau, Ania C; Steinmann, Beat (2016). A summary of molecular genetic findings in fructose-1,6-bisphosphatase deficiency with a focus on a common long-range deletion and the role of MLPA analysis. Orphanet Journal of Rare Diseases, 11:40-50.

مصطلحات موضوعية: Medical Clinic, 610 Medicine & health

وصف الملف: application/pdf

العلاقة: https://www.zora.uzh.ch/id/eprint/132337/8/ZORA132337.pdfTest; info:pmid/27101822; urn:issn:1750-1172

الإتاحة: https://doi.org/10.5167/uzh-13233710.1186/s13023-016-0415-1Test
https://www.zora.uzh.ch/id/eprint/132337Test/
https://www.zora.uzh.ch/id/eprint/132337/8/ZORA132337.pdfTest

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النص الكامل

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Häusliches Gehtraining als Nachsorge für mittelgradige COPD-Patienten nach einer ambulanten Rehabilitation :eine randomisierte, kontrollierte, beobachterblinde Studie

المؤلفون: Du Moulin, Marcel

الوصول الحر: https://www.europeana.eu/item/2048441/item_44U2I5ACC7L4VHIAZY4F36LYOZ6CJ2XZ?utm_source=api&utm_medium=api&utm_campaign=YuvuWBeCaTest

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7

Häusliches Gehtraining als Nachsorge für mittelgradige COPD-Patienten nach einer ambulanten Rehabilitation eine randomisierte, kontrollierte, beobachterblinde Studie

المؤلفون: Du Moulin, Marcel

المصدر: kostenfrei.

الإتاحة: http://d-nb.info/993735541/34Test
http://www.sub.uni-hamburg.de/opus/volltexte/2009/4037/pdf/du_Moulin_Med_Diss_2008.pdfTest
http://www.sub.uni-hamburg.de/opus/volltexte/2009/4037/index.htmlTest

8

دورية أكاديمية

Mutations in ABCD4 cause a new inborn error of vitamin B(12) metabolism

المصدر: Coelho, David; Kim, Jaeseung C; Miousse, Isabelle R; Fung, Stephen; du Moulin, Marcel; Buers, Insa; Suormala, Terttu; Burda, Patricie; Frapolli, Michele; Stucki, Martin; Nürnberg, Peter; Thiele, Holger; Robenek, Horst; Höhne, Wolfgang; Longo, Nicola; Pasquali, Marzia; Mengel, Eugen; Watkins, David; Shoubridge, Eric A; Majewski, Jacek; Rosenblatt, David S; Fowler, Brian; Rutsch, Frank; Baumgartner, Matthias R (2012). Mutations in ABCD4 cause a new inborn error of vitamin B(12) metabolism. Nature Genetics, 44(10):1152-1155.

مصطلحات موضوعية: Medical Clinic, Zurich Center for Integrative Human Physiology (ZIHP), 570 Life sciences, biology, 610 Medicine & health

وصف الملف: application/pdf

العلاقة: https://www.zora.uzh.ch/id/eprint/65573/1/aMCoelho_Nat_Genet_-S1_2012.pdfTest; https://www.zora.uzh.ch/id/eprint/65573/2/Coelho_Nat_Genet_2012.pdfTest; info:pmid/22922874; urn:issn:1061-4036

الإتاحة: https://doi.org/10.5167/uzh-65573Test
https://doi.org/10.1038/ng.2386Test
https://www.zora.uzh.ch/id/eprint/65573Test/
https://www.zora.uzh.ch/id/eprint/65573/1/aMCoelho_Nat_Genet_-S1_2012.pdfTest
https://www.zora.uzh.ch/id/eprint/65573/2/Coelho_Nat_Genet_2012.pdfTest

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9

دورية أكاديمية

Generalized Arterial Calcification of Infancy and Pseudoxanthoma Elasticum Can Be Caused by Mutations in Either ENPP1 or ABCC6

المصدر: Nitschke , Y , Baujat , G , Botschen , U , Wittkampf , T , du Moulin , M , Stella , J , Le Merrer , M , Guest , G , Lambot , K , Tazarourte-Pinturier , M-F , Chassaing , N , Roche , O , Feenstra , I , Loechner , K , Deshpande , C , Garber , S J , Chikarmane , R , Steinmann , B , Shahinyan , T , Martorell , L , Davies , J , Smith , W E , Kahler , S G , McCulloch , ....

مصطلحات موضوعية: VITAMIN-K, MOUSE MODEL, MOLECULAR-GENETICS, MINERALIZATION, DEFICIENCY, PHENOTYPE, SPECTRUM, CARBOXYLATION, TRANSPORTER, COUNTERACT

الإتاحة: https://doi.org/10.1016/j.ajhg.2011.11.020Test
https://kclpure.kcl.ac.uk/portal/en/publications/8f2b2c33-6c31-447c-998e-b2f06186545bTest

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10

دورية أكاديمية

Cerebral Arterial Stenoses and Stroke: Novel Features of Aicardi-Goutières Syndrome Caused by the Arg164X Mutation in SAMHD1 Are Associated with Altered Cytokine Expression

المؤلفون: Thiele, Holger, Du Moulin, Marcel, Barczyk, Katarzyna, George, Christel, Schwindt, Wolfram, Nürnberg, Gudrun, Frosch, Michael, Kurlemann, Gerd, Roth, Johannes, Nürnberg, Peter, Rutsch, Frank

المساهمون: Cologne Center for Genomics (CCG), University of Cologne, General Pediatrics, Muenster University Children's Hospital, Immunology, Muenster University Hospital, Clinical Radiology

المصدر: ISSN: 1059-7794.

مصطلحات موضوعية: Life Sciences

العلاقة: hal-00576253; https://hal.archives-ouvertes.fr/hal-00576253Test; https://hal.archives-ouvertes.fr/hal-00576253/documentTest; https://hal.archives-ouvertes.fr/hal-00576253/file/PEER_stage2_10.1002%252Fhumu.21357.pdfTest

الإتاحة: https://doi.org/10.1002/humu.21357Test
https://hal.archives-ouvertes.fr/hal-00576253Test
https://hal.archives-ouvertes.fr/hal-00576253/documentTest
https://hal.archives-ouvertes.fr/hal-00576253/file/PEER_stage2_10.1002%252Fhumu.21357.pdfTest

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