Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry): Orphanet Journal of Rare Diseases

T. Pinós; A.L. Andreu; C. Bruno; G.M. Hadjigeorgiou; R. Haller; P. Laforêt; A. Lucía; M.A. Martín; A. Martinuzzi; C. Navarro; P. Oflazer; J. Pouget; R. Quinlivan; S. Sacconi; R.S. Scalco; A. Toscano; J. Vissing; M. Vorgerd; A. Wakelin; R. Martí; N. Baruch; F.J. Ortega; B. San-Millán; I. Vieitez; M. Vavla; O. Musumeci; R. Scalco; G. Hadjgeorgiou; E. Zintzaras; E. Zülow; R. Haller; H. Durmus; A. Santalla; EUROMAC Consortium

doi:10.1186/s13023-020-01455-z

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry): Orphanet Journal of Rare Diseases

T. Pinós, A.L. Andreu, C. Bruno, G.M. Hadjigeorgiou, R. Haller, P. Laforêt, A. Lucía, M.A. Martín, A. Martinuzzi, C. Navarro, P. Oflazer, J. Pouget, R. Quinlivan, S. Sacconi, R.S. Scalco, A. Toscano, J. Vissing, M. Vorgerd, A. Wakelin, R. MartíN. Baruch, F.J. Ortega, B. San-Millán, I. Vieitez, M. Vavla, O. Musumeci, R. Scalco, G. Hadjgeorgiou, E. Zintzaras, E. Zülow, R. Haller, H. Durmus, A. Santalla, EUROMAC Consortium

Research output: Contribution to journal › Article › peer-review

Original language	English
Journal	Orphanet J. Rare Dis.
Volume	15
Issue number	1
DOIs	https://doi.org/10.1186/s13023-020-01455-z
Publication status	Published - 2020

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10.1186/s13023-020-01455-z

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Pinós, T., Andreu, A. L., Bruno, C., Hadjigeorgiou, G. M., Haller, R., Laforêt, P., Lucía, A., Martín, M. A., Martinuzzi, A., Navarro, C., Oflazer, P., Pouget, J., Quinlivan, R., Sacconi, S., Scalco, R. S., Toscano, A., Vissing, J., Vorgerd, M., Wakelin, A., ... Consortium, EUROMAC. (2020). Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry): Orphanet Journal of Rare Diseases. Orphanet J. Rare Dis., 15(1). https://doi.org/10.1186/s13023-020-01455-z

Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry) : Orphanet Journal of Rare Diseases. / Pinós, T.; Andreu, A.L.; Bruno, C.; Hadjigeorgiou, G.M.; Haller, R.; Laforêt, P.; Lucía, A.; Martín, M.A.; Martinuzzi, A.; Navarro, C.; Oflazer, P.; Pouget, J.; Quinlivan, R.; Sacconi, S.; Scalco, R.S.; Toscano, A.; Vissing, J.; Vorgerd, M.; Wakelin, A.; Martí, R.; Baruch, N.; Ortega, F.J.; San-Millán, B.; Vieitez, I.; Vavla, M.; Musumeci, O.; Scalco, R.; Hadjgeorgiou, G.; Zintzaras, E.; Zülow, E.; Haller, R.; Durmus, H.; Santalla, A.; Consortium, EUROMAC.

In: Orphanet J. Rare Dis., Vol. 15, No. 1, 2020.

Research output: Contribution to journal › Article › peer-review

Pinós, T, Andreu, AL, Bruno, C, Hadjigeorgiou, GM, Haller, R, Laforêt, P, Lucía, A, Martín, MA , Martinuzzi, A, Navarro, C, Oflazer, P, Pouget, J, Quinlivan, R, Sacconi, S, Scalco, RS, Toscano, A, Vissing, J, Vorgerd, M, Wakelin, A, Martí, R, Baruch, N, Ortega, FJ, San-Millán, B, Vieitez, I, Vavla, M, Musumeci, O, Scalco, R, Hadjgeorgiou, G, Zintzaras, E, Zülow, E, Haller, R, Durmus, H, Santalla, A & Consortium, EUROMAC 2020, 'Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry): Orphanet Journal of Rare Diseases', Orphanet J. Rare Dis., vol. 15, no. 1. https://doi.org/10.1186/s13023-020-01455-z

Pinós, T. ; Andreu, A.L. ; Bruno, C. ; Hadjigeorgiou, G.M. ; Haller, R. ; Laforêt, P. ; Lucía, A. ; Martín, M.A. ; Martinuzzi, A. ; Navarro, C. ; Oflazer, P. ; Pouget, J. ; Quinlivan, R. ; Sacconi, S. ; Scalco, R.S. ; Toscano, A. ; Vissing, J. ; Vorgerd, M. ; Wakelin, A. ; Martí, R. ; Baruch, N. ; Ortega, F.J. ; San-Millán, B. ; Vieitez, I. ; Vavla, M. ; Musumeci, O. ; Scalco, R. ; Hadjgeorgiou, G. ; Zintzaras, E. ; Zülow, E. ; Haller, R. ; Durmus, H. ; Santalla, A. ; Consortium, EUROMAC. / Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry) : Orphanet Journal of Rare Diseases. In: Orphanet J. Rare Dis. 2020 ; Vol. 15, No. 1.

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author = "T. Pin{\'o}s and A.L. Andreu and C. Bruno and G.M. Hadjigeorgiou and R. Haller and P. Lafor{\^e}t and A. Luc{\'i}a and M.A. Mart{\'i}n and A. Martinuzzi and C. Navarro and P. Oflazer and J. Pouget and R. Quinlivan and S. Sacconi and R.S. Scalco and A. Toscano and J. Vissing and M. Vorgerd and A. Wakelin and R. Mart{\'i} and N. Baruch and F.J. Ortega and B. San-Mill{\'a}n and I. Vieitez and M. Vavla and O. Musumeci and R. Scalco and G. Hadjgeorgiou and E. Zintzaras and E. Z{\"u}low and R. Haller and H. Durmus and A. Santalla and EUROMAC Consortium",

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AU - Hadjigeorgiou, G.M.

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AU - Lucía, A.

AU - Martín, M.A.

AU - Martinuzzi, A.

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AU - Oflazer, P.

AU - Pouget, J.

AU - Quinlivan, R.

AU - Sacconi, S.

AU - Scalco, R.S.

AU - Toscano, A.

AU - Vissing, J.

AU - Vorgerd, M.

AU - Wakelin, A.

AU - Martí, R.

AU - Baruch, N.

AU - Ortega, F.J.

AU - San-Millán, B.

AU - Vieitez, I.

AU - Vavla, M.

AU - Musumeci, O.

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AU - Hadjgeorgiou, G.

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AU - Durmus, H.

AU - Santalla, A.

AU - Consortium, EUROMAC

N1 - Cited By :1 Export Date: 26 March 2021 Correspondence Address: Martí, R.; Biomedical Network Research Centre on Rare Diseases (CIBERER), Pg. Vall d’Hebron 119, Spain; email: ramon.marti@vhir.org

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