Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.

J Sykut-Cegielska; W Gradowska; D Piekutowska-Abramczuk; Brage Storstein Andresen; RKJ Olsen; M Ołtarzewski; M Pronicki; M Pajdowska; A Bogdańska; E Jabłonska; B Radomyska; K Kusmierska; M Krajewska-Walasek; N Gregersen; E Pronicka

doi:10.1007/s10545-010-9244-x

Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.

J Sykut-Cegielska, W Gradowska, D Piekutowska-Abramczuk , Brage Storstein Andresen, RKJ Olsen, M Ołtarzewski, M Pronicki, M Pajdowska, A Bogdańska, E Jabłonska, B Radomyska, K Kusmierska, M Krajewska-Walasek, N Gregersen, E Pronicka

Research output: Contribution to journal › Journal article › Research › peer-review

Original language	English
Journal	Journal of Inherited Metabolic Disease
Volume	34
Issue number	1
Pages (from-to)	185-195
ISSN	0141-8955
DOIs	https://doi.org/10.1007/s10545-010-9244-x
Publication status	Published - 2011

Documents & Links

10.1007/s10545-010-9244-x

Cite this

Sykut-Cegielska, J., Gradowska, W., Piekutowska-Abramczuk , D., Andresen, B. S., Olsen, RKJ., Ołtarzewski, M., Pronicki, M., Pajdowska, M., Bogdańska, A., Jabłonska, E., Radomyska, B., Kusmierska, K., Krajewska-Walasek, M., Gregersen, N., & Pronicka, E. (2011). Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. Journal of Inherited Metabolic Disease, 34(1), 185-195. https://doi.org/10.1007/s10545-010-9244-x

Sykut-Cegielska, J ; Gradowska, W ; Piekutowska-Abramczuk , D ; Andresen, Brage Storstein ; Olsen, RKJ ; Ołtarzewski, M ; Pronicki, M ; Pajdowska, M ; Bogdańska, A ; Jabłonska, E ; Radomyska, B ; Kusmierska, K ; Krajewska-Walasek, M ; Gregersen, N ; Pronicka, E. / Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. In: Journal of Inherited Metabolic Disease. 2011 ; Vol. 34, No. 1. pp. 185-195.

@article{0baf3f94633c422f89feb4390efc88f6,

title = "Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.",

author = "J Sykut-Cegielska and W Gradowska and D Piekutowska-Abramczuk and Andresen, {Brage Storstein} and RKJ Olsen and M O{\l}tarzewski and M Pronicki and M Pajdowska and A Bogda{\'n}ska and E Jab{\l}onska and B Radomyska and K Kusmierska and M Krajewska-Walasek and N Gregersen and E Pronicka",

year = "2011",

doi = "10.1007/s10545-010-9244-x",

language = "English",

volume = "34",

pages = "185--195",

journal = "Journal of Inherited Metabolic Disease",

issn = "0141-8955",

publisher = "Springer",

number = "1",

}

Sykut-Cegielska, J, Gradowska, W, Piekutowska-Abramczuk , D, Andresen, BS, Olsen, RKJ, Ołtarzewski, M, Pronicki, M, Pajdowska, M, Bogdańska, A, Jabłonska, E, Radomyska, B, Kusmierska, K, Krajewska-Walasek, M, Gregersen, N & Pronicka, E 2011, 'Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.', Journal of Inherited Metabolic Disease, vol. 34, no. 1, pp. 185-195. https://doi.org/10.1007/s10545-010-9244-x

Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. / Sykut-Cegielska, J; Gradowska, W; Piekutowska-Abramczuk , D; Andresen, Brage Storstein; Olsen, RKJ; Ołtarzewski, M; Pronicki, M; Pajdowska, M; Bogdańska, A; Jabłonska, E; Radomyska, B; Kusmierska, K; Krajewska-Walasek, M; Gregersen, N; Pronicka, E.

In: Journal of Inherited Metabolic Disease, Vol. 34, No. 1, 2011, p. 185-195.

Research output: Contribution to journal › Journal article › Research › peer-review

TY - JOUR

T1 - Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening.

AU - Sykut-Cegielska, J

AU - Gradowska, W

AU - Piekutowska-Abramczuk , D

AU - Andresen, Brage Storstein

AU - Olsen, RKJ

AU - Ołtarzewski, M

AU - Pronicki, M

AU - Pajdowska, M

AU - Bogdańska, A

AU - Jabłonska, E

AU - Radomyska, B

AU - Kusmierska, K

AU - Krajewska-Walasek, M

AU - Gregersen, N

AU - Pronicka, E

PY - 2011

Y1 - 2011

U2 - 10.1007/s10545-010-9244-x

DO - 10.1007/s10545-010-9244-x

M3 - Journal article

VL - 34

SP - 185

EP - 195

JO - Journal of Inherited Metabolic Disease

JF - Journal of Inherited Metabolic Disease

SN - 0141-8955

IS - 1

ER -

Sykut-Cegielska J, Gradowska W, Piekutowska-Abramczuk D, Andresen BS, Olsen RKJ, Ołtarzewski M et al. Urgent metabolic service improves survival in long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) deficiency detected by symptomatic identification and pilot newborn screening. Journal of Inherited Metabolic Disease. 2011;34(1):185-195. https://doi.org/10.1007/s10545-010-9244-x