Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

Philippe Moulin; Robert Dufour; Maurizio Averna; Marcello Arca; Angelo B. Cefalù; Davide Noto; Laura D'Erasmo; Alessia di Costanzo; Christophe Marçais; Luis Antonio Alvarez-Sala Walther; Maciej Banach; Jan Borén; Robert Cramb; Ioanna Gouni-Berthold; Elizabeth Hughes; Colin Johnson; Xavier Pintó; Željko Reiner; Jeanine Roeters van Lennep; Handrean Soran; Claudia Stefanutti; Erik Stroes; Eric Bruckert

doi:https://doi.org/10.1016/j.dib.2018.10.125

Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

Philippe Moulin, Robert Dufour, Maurizio Averna, Marcello Arca, Angelo B. Cefalù, Davide Noto, Laura D'Erasmo, Alessia di Costanzo, Christophe Marçais, Luis Antonio Alvarez-Sala Walther, Maciej Banach, Jan Borén, Robert Cramb, Ioanna Gouni-Berthold, Elizabeth Hughes, Colin Johnson, Xavier Pintó, Željko Reiner, Jeanine Roeters van Lennep, Handrean SoranClaudia Stefanutti, Erik Stroes, Eric Bruckert

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

3 Citations (Scopus)

Abstract

Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts.

Original language	English
Pages (from-to)	1334-1336
Journal	Data in brief
Volume	21
DOIs	https://doi.org/10.1016/j.dib.2018.10.125
Publication status	Published - 2018

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Moulin, P., Dufour, R., Averna, M., Arca, M., Cefalù, A. B., Noto, D., D'Erasmo, L., di Costanzo, A., Marçais, C., Walther, L. A. A.-S., Banach, M., Borén, J., Cramb, R., Gouni-Berthold, I., Hughes, E., Johnson, C., Pintó, X., Reiner, Ž., van Lennep, J. R., ... Bruckert, E. (2018). Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score. Data in brief, 21, 1334-1336. https://doi.org/10.1016/j.dib.2018.10.125

@article{a73fd3bd10ea4042b30afee906a1a90f,

title = "Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score",

abstract = "Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts.",

author = "Philippe Moulin and Robert Dufour and Maurizio Averna and Marcello Arca and Cefal{\`u}, {Angelo B.} and Davide Noto and Laura D'Erasmo and {di Costanzo}, Alessia and Christophe Mar{\c c}ais and Walther, {Luis Antonio Alvarez-Sala} and Maciej Banach and Jan Bor{\'e}n and Robert Cramb and Ioanna Gouni-Berthold and Elizabeth Hughes and Colin Johnson and Xavier Pint{\'o} and {\v Z}eljko Reiner and {van Lennep}, {Jeanine Roeters} and Handrean Soran and Claudia Stefanutti and Erik Stroes and Eric Bruckert",

year = "2018",

doi = "https://doi.org/10.1016/j.dib.2018.10.125",

language = "English",

volume = "21",

pages = "1334--1336",

journal = "Data in brief",

issn = "2352-3409",

publisher = "Elsevier BV",

}

Moulin, P, Dufour, R, Averna, M, Arca, M, Cefalù, AB, Noto, D, D'Erasmo, L, di Costanzo, A, Marçais, C, Walther, LAA-S, Banach, M, Borén, J, Cramb, R, Gouni-Berthold, I, Hughes, E, Johnson, C, Pintó, X, Reiner, Ž, van Lennep, JR, Soran, H, Stefanutti, C, Stroes, E & Bruckert, E 2018, 'Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score', Data in brief, vol. 21, pp. 1334-1336. https://doi.org/10.1016/j.dib.2018.10.125

TY - JOUR

T1 - Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

AU - Moulin, Philippe

AU - Dufour, Robert

AU - Averna, Maurizio

AU - Arca, Marcello

AU - Cefalù, Angelo B.

AU - Noto, Davide

AU - D'Erasmo, Laura

AU - di Costanzo, Alessia

AU - Marçais, Christophe

AU - Walther, Luis Antonio Alvarez-Sala

AU - Banach, Maciej

AU - Borén, Jan

AU - Cramb, Robert

AU - Gouni-Berthold, Ioanna

AU - Hughes, Elizabeth

AU - Johnson, Colin

AU - Pintó, Xavier

AU - Reiner, Željko

AU - van Lennep, Jeanine Roeters

AU - Soran, Handrean

AU - Stefanutti, Claudia

AU - Stroes, Erik

AU - Bruckert, Eric

PY - 2018

Y1 - 2018

N2 - Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts.

AB - Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts.

UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85056230161&origin=inward

UR - https://www.ncbi.nlm.nih.gov/pubmed/30456254

U2 - https://doi.org/10.1016/j.dib.2018.10.125

DO - https://doi.org/10.1016/j.dib.2018.10.125

M3 - Article

C2 - 30456254

SN - 2352-3409

VL - 21

SP - 1334

EP - 1336

JO - Data in brief

JF - Data in brief

ER -

Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

Abstract

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