Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms

D. Cheillan; M.J. Curt; G. Briand; G.S. Salomons; K. Mention-Mulliez; D. Dobbelaere; J.M. Cuisset; L. Lion-Francois; V.D. Portes; A. Chabli; V. Valayannopoulos; J.F. Benoist; J.M. Pinard; G. Simard; O. Douay; K. Deiva; A. Afenjar; D. Heron; F. Rivier; B. Chabrol; F. Prieur; F. Cartault; G. Pitelet; A. Goldenberg; S. Bekri; M. Gerard; R. Delorme; M. Tardieu; N. Porchet; C. Vianey-Saban; J. Vamecq

doi:https://doi.org/10.1186/1750-1172-7-96

Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms

D. Cheillan, M.J. Curt, G. Briand, G.S. Salomons, K. Mention-Mulliez, D. Dobbelaere, J.M. Cuisset, L. Lion-Francois, V.D. Portes, A. Chabli, V. Valayannopoulos, J.F. Benoist, J.M. Pinard, G. Simard, O. Douay, K. Deiva, A. Afenjar, D. Heron, F. Rivier, B. ChabrolF. Prieur, F. Cartault, G. Pitelet, A. Goldenberg, S. Bekri, M. Gerard, R. Delorme, M. Tardieu, N. Porchet, C. Vianey-Saban, J. Vamecq

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

29 Citations (Scopus)

Original language	English
Article number	96
Journal	Orphanet Journal of Rare Diseases
Volume	7
DOIs	https://doi.org/10.1186/1750-1172-7-96
Publication status	Published - 2012

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Cheillan, D., Curt, M. J., Briand, G., Salomons, G. S., Mention-Mulliez, K., Dobbelaere, D., Cuisset, J. M., Lion-Francois, L., Portes, V. D., Chabli, A., Valayannopoulos, V., Benoist, J. F., Pinard, J. M., Simard, G., Douay, O., Deiva, K., Afenjar, A., Heron, D., Rivier, F., ... Vamecq, J. (2012). Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms. Orphanet Journal of Rare Diseases, 7, Article 96. https://doi.org/10.1186/1750-1172-7-96

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title = "Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms",

author = "D. Cheillan and M.J. Curt and G. Briand and G.S. Salomons and K. Mention-Mulliez and D. Dobbelaere and J.M. Cuisset and L. Lion-Francois and V.D. Portes and A. Chabli and V. Valayannopoulos and J.F. Benoist and J.M. Pinard and G. Simard and O. Douay and K. Deiva and A. Afenjar and D. Heron and F. Rivier and B. Chabrol and F. Prieur and F. Cartault and G. Pitelet and A. Goldenberg and S. Bekri and M. Gerard and R. Delorme and M. Tardieu and N. Porchet and C. Vianey-Saban and J. Vamecq",

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Cheillan, D, Curt, MJ, Briand, G, Salomons, GS, Mention-Mulliez, K, Dobbelaere, D, Cuisset, JM, Lion-Francois, L, Portes, VD, Chabli, A, Valayannopoulos, V, Benoist, JF, Pinard, JM, Simard, G, Douay, O, Deiva, K, Afenjar, A, Heron, D, Rivier, F, Chabrol, B, Prieur, F, Cartault, F, Pitelet, G, Goldenberg, A, Bekri, S, Gerard, M, Delorme, R, Tardieu, M, Porchet, N, Vianey-Saban, C & Vamecq, J 2012, 'Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms', Orphanet Journal of Rare Diseases, vol. 7, 96. https://doi.org/10.1186/1750-1172-7-96

TY - JOUR

T1 - Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms

AU - Cheillan, D.

AU - Curt, M.J.

AU - Briand, G.

AU - Salomons, G.S.

AU - Mention-Mulliez, K.

AU - Dobbelaere, D.

AU - Cuisset, J.M.

AU - Lion-Francois, L.

AU - Portes, V.D.

AU - Chabli, A.

AU - Valayannopoulos, V.

AU - Benoist, J.F.

AU - Pinard, J.M.

AU - Simard, G.

AU - Douay, O.

AU - Deiva, K.

AU - Afenjar, A.

AU - Heron, D.

AU - Rivier, F.

AU - Chabrol, B.

AU - Prieur, F.

AU - Cartault, F.

AU - Pitelet, G.

AU - Goldenberg, A.

AU - Bekri, S.

AU - Gerard, M.

AU - Delorme, R.

AU - Tardieu, M.

AU - Porchet, N.

AU - Vianey-Saban, C.

AU - Vamecq, J.

PY - 2012

Y1 - 2012

U2 - https://doi.org/10.1186/1750-1172-7-96

DO - https://doi.org/10.1186/1750-1172-7-96

M3 - Article

C2 - 23234264

SN - 1750-1172

VL - 7

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

M1 - 96

ER -