المؤلفون: Stabler, Sally P.^Aff13, Freehauf, Cynthia^Aff14, Allen, Robert H.^Aff13, Thomas, Janet^Aff14, Gallagher, Renata^Aff15

المساهمون: Baumgartner, Matthias, Series editor^{Aff1, Aff8}, Patterson, Marc, Series editor^{Aff2, Aff9}, Rahman, Shamima, Series editor^{Aff3, Aff10}, Peters, Verena, Series editor^{Aff4, Aff12}, Morava, Eva, Editor-in-chief^{Aff5, Aff7}, Zschocke, Johannes, Series editor^{Aff6, Aff11}

المصدر: JIMD Reports, Volume 37. 37:55-61

المؤلفون: Freehauf, Cynthia^Aff4

المساهمون: Bernstein, Laurie E., editor^Aff1, Rohr, Fran, editor^Aff2, Helm, Joanna R., editor^Aff3

المصدر: Nutrition Management of Inherited Metabolic Diseases : Lessons from Metabolic University. :3-14

Degree: RN, CGC

المؤلفون: Chien, Yin-Hsiu, Abdenur, Jose E., Baronio, Federico, Bannick, Allison Anne, Corrales, Fernando, Couce, Maria, Donner, Markus G., Ficicioglu, Can, Freehauf, Cynthia, Frithiof, Deborah, Gotway, Garrett, Hirabayashi, Koichi, Hofstede, Floris, Hoganson, George, Hwu, Wuh-Liang, James, Philip, Kim, Sook, Korman, Stanley H., Lachmann, Robin, Levy, Harvey, Lindner, Martin, Lykopoulou, Lilia, Mayatepek, Ertan, Muntau, Ania, Okano, Yoshiyuki, Raymond, Kimiyo, Rubio-Gozalbo, Estela, Scholl-Buergi, Sabine, Schulze, Andreas, Singh, Rani, Stabler, Sally, Stuy, Mary, Thomas, Janet, Wagner, Conrad, Wilson, William G., Wortmann, Saskia, Yamamoto, Shigenori, Pao, Maryland, Blom, Henk J.

المصدر: Orphanet Journal of Rare Diseases. 10

وصف الملف: electronic

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-108133
https://doi.org/10.1186/s13023-015-0321-y
https://umu.diva-portal.org/smash/get/diva2:855515/FULLTEXT01.pdf

المؤلفون: Van Hove, Johan L. K., Freehauf, Cynthia, Miyamoto, Shelley, Vladutiu, Georgirene D., Pancrudo, Jacklyn, Bonilla, Eduardo, Lovell, Mark A., Mierau, Gary W., Thomas, Janet A., Shanske, Sara

المصدر: European Journal of Pediatrics. July 2008 167(7):771-776

المؤلفون: Mierau, Gary W., Tyson, R. Weslie, Freehauf, Cynthia L.

المصدر: Pediatric and Developmental Pathology. December 2004 7(6):637-640

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المؤلفون: Van Hove, Johan L. K., Freehauf, Cynthia L., Ficicioglu, Can, Pena, Loren D. M., Moreau, Kerrie L., Henthorn, Thomas K., Christians, Uwe, Jiang, Hua, Cowan, Tina M., Young, Sarah P., Hite, Michelle, Friederich, Marisa W., Stabler, Sally P., Spector, Elaine B., Kronquist, Kathryn E., Thomas, Janet A., Emmett, Peggy, Harrington, Mary J., Pyle, Laura, Creadon‐Swindell, Geralyn

المصدر: Journal of Inherited Metabolic Disease; May2019, Vol. 42 Issue 3, p424-437, 14p

المؤلفون: MDL patientenzorg, Child Health, Chien, Yin-Hsiu, Abdenur, Jose E., Baronio, Federico, Bannick, Allison Anne, Corrales, Fernando, Couce, Maria, Donner, Markus G., Ficicioglu, Can, Freehauf, Cynthia, Frithiof, Deborah, Gotway, Garrett, Hirabayashi, Koichi, Hofstede, FC, Hoganson, George, Hwu, Wuh-Liang, James, Philip, Kim, Sook, Korman, Stanley H., Lachmann, Robin, Levy, Harvey, Lindner, Martin, Lykopoulou, Lilia, Mayatepek, Ertan, Muntau, Ania, Okano, Yoshiyuki, Raymond, Kimiyo, Rubio-Gozalbo, Estela, Scholl-Buergi, Sabine, Schulze, Andreas, Singh, Rani, Stabler, Sally, Stuy, Mary, Thomas, Janet, Wagner, Conrad, Wilson, William G., Wortmann, Saskia, Yamamoto, Shigenori, Pao, Maryland, Blom, Henk J.

URL: https://doi.org/10.1186/s13023-015-0321-y
http://hdl.handle.net/1874/332879
https://dspace.library.uu.nl/handle/1874/332879
1750-1172
Orphanet Journal of Rare Diseases
10
10:99

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