Clinical pathways for inborn errors of metabolism: warranted and feasible

S. Demirdas; I.N. van Kessel; M.J. Korndewal; C.E. Hollak; H. Meutgeert; A. Klaren; M. van Rijn; F.J. van Spronsen; F.W. Asselbergs; A.C. Blank; E.F. Diekman; P.M. van Hasselt; Th.A.M. van den Hurk; C. Timmer; G. Visser; H.W. de Valk; x. Dutch Working group; A.M. Bosch

Clinical pathways for inborn errors of metabolism: warranted and feasible

Translated title of the contribution: Clinical pathways for inborn errors of metabolism: warranted and feasible

S. Demirdas
, I.N. van Kessel
, M.J. Korndewal
, C.E. Hollak
, H. Meutgeert
, A. Klaren
, M. van Rijn
, F.J. van Spronsen
, F.W. Asselbergs
, A.C. Blank
, E.F. Diekman
, P.M. van Hasselt
, Th.A.M. van den Hurk
, C. Timmer
, G. Visser
, H.W. de Valk
, x. Dutch Working group
, A.M. Bosch

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

Translated title of the contribution	Clinical pathways for inborn errors of metabolism: warranted and feasible
Original language	Undefined/Unknown
Article number	37
Pages (from-to)	37
Number of pages	1
Journal	Orphanet Journal of Rare Diseases
Volume	25
Issue number	8
Publication status	Published - 2013

Access to Document

http://www.ncbi.nlm.nih.gov/pubmed/23442887

Cite this

Demirdas, S., van Kessel, I. N., Korndewal, M. J., Hollak, C. E., Meutgeert, H., Klaren, A., van Rijn, M., van Spronsen, F. J., Asselbergs, F. W., Blank, A. C., Diekman, E. F., van Hasselt, P. M., van den Hurk, T. A. M., Timmer, C., Visser, G., de Valk, H. W., Dutch Working group, X., & Bosch, A. M. (2013). Clinical pathways for inborn errors of metabolism: warranted and feasible. Orphanet Journal of Rare Diseases, 25(8), 37. Article 37. http://www.ncbi.nlm.nih.gov/pubmed/23442887

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title = "Clinical pathways for inborn errors of metabolism: warranted and feasible",

author = "S. Demirdas and \{van Kessel\}, I.N. and M.J. Korndewal and C.E. Hollak and H. Meutgeert and A. Klaren and \{van Rijn\}, M. and \{van Spronsen\}, F.J. and F.W. Asselbergs and A.C. Blank and E.F. Diekman and \{van Hasselt\}, P.M. and \{van den Hurk\}, Th.A.M. and C. Timmer and G. Visser and \{de Valk\}, H.W. and \{Dutch Working group\}, x. and A.M. Bosch",

year = "2013",

language = "Undefined/Unknown",

volume = "25",

pages = "37",

journal = "Orphanet Journal of Rare Diseases",

issn = "1750-1172",

publisher = "BioMed Central Ltd.",

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}

Demirdas, S, van Kessel, IN, Korndewal, MJ, Hollak, CE, Meutgeert, H, Klaren, A, van Rijn, M, van Spronsen, FJ, Asselbergs, FW, Blank, AC, Diekman, EF, van Hasselt, PM, van den Hurk, TAM, Timmer, C, Visser, G, de Valk, HW, Dutch Working group, X & Bosch, AM 2013, 'Clinical pathways for inborn errors of metabolism: warranted and feasible', Orphanet Journal of Rare Diseases, vol. 25, no. 8, 37, pp. 37. <http://www.ncbi.nlm.nih.gov/pubmed/23442887>

TY - JOUR

T1 - Clinical pathways for inborn errors of metabolism: warranted and feasible

AU - Demirdas, S.

AU - van Kessel, I.N.

AU - Korndewal, M.J.

AU - Hollak, C.E.

AU - Meutgeert, H.

AU - Klaren, A.

AU - van Rijn, M.

AU - van Spronsen, F.J.

AU - Asselbergs, F.W.

AU - Blank, A.C.

AU - Diekman, E.F.

AU - van Hasselt, P.M.

AU - van den Hurk, Th.A.M.

AU - Timmer, C.

AU - Visser, G.

AU - de Valk, H.W.

AU - Dutch Working group, x.

AU - Bosch, A.M.

PY - 2013

Y1 - 2013

M3 - Article

SN - 1750-1172

VL - 25

SP - 37

JO - Orphanet Journal of Rare Diseases

JF - Orphanet Journal of Rare Diseases

IS - 8

M1 - 37

ER -