Works matching IS 01418955 AND DT 2013 AND VI 36 AND IP 4

Results: 12

Erratum to: Enzyme replacement therapy for mucopolysaccharidosis VI-experience in Taiwan.

Published in:

2013

By:

Lin, Hsiang-Yu;
Chen, Ming-Ren;
Chuang, Chih-Kuang;
Chen, Chih-Ping;
Lin, Dar-Shong;
Chien, Yin-Hsiu;
Ke, Yu-Yuan;
Tsai, Fuu-Jen;
Pan, Hui-Ping;
Lin, Shio-Jean;
Hwu, Wuh-Liang;
Niu, Dau-Ming;
Lee, Ni-Chung;
Lin, Shuan-Pei

Publication type:

Correction Notice

Pathophysiology of fatty acid oxidation disorders and resultant phenotypic variability.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 645, doi. 10.1007/s10545-013-9611-5

By:

Olpin, Simon

Publication type:

Article

Liver transplantation and cell therapies for inborn errors of metabolism.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 675, doi. 10.1007/s10545-012-9581-z

By:

McKiernan, Patrick

Publication type:

Article

Impact of new screening technologies: should we screen and does phenotype influence this decision?

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 681, doi. 10.1007/s10545-013-9598-y

By:

Bonham, James

Publication type:

Article

Current concepts in organic acidurias: understanding intra- and extracerebral disease manifestation.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 635, doi. 10.1007/s10545-013-9600-8

By:

Kölker, Stefan;
Burgard, Peter;
Sauer, Sven;
Okun, Jürgen

Publication type:

Article

Ammonia toxicity to the brain.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 595, doi. 10.1007/s10545-012-9546-2

By:

Braissant, Olivier;
McLin, Valérie;
Cudalbu, Cristina

Publication type:

Article

Erratum to: Expanded newborn screening in Greece: 30 months of experience.

Published in:

2013

By:

Loukas, Yannis;
Soumelas, Georgios-Stefanos;
Dotsikas, Yannis;
Georgiou, Vassiliki;
Molou, Elina;
Thodi, Georgia;
Boutsini, Maria;
Biti, Sofia;
Papadopoulos, Konstantinos

Publication type:

Correction Notice

The neuropsychiatry of inborn errors of metabolism.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 687, doi. 10.1007/s10545-013-9618-y

By:

Walterfang, Mark;
Bonnot, Olivier;
Mocellin, Ramon;
Velakoulis, Dennis

Publication type:

Article

Gastrointestinal and hepatic manifestations of mitochondrial disorders.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 659, doi. 10.1007/s10545-013-9614-2

By:

Rahman, Shamima

Publication type:

Article

Erratum to: Simultaneous LC-MS/MS determination of phenylbutyrate, phenylacetate, benzoate and their corresponding metabolites phenylacetylglutamine and hippurate in blood and urine.

Published in:

2013

By:

Laryea, Maurice;
Herebian, Diran;
Meissner, Thomas;
Mayatepek, Ertan

Publication type:

Correction Notice

Effects of hypoglycaemia on neuronal metabolism in the adult brain: role of alternative substrates to glucose.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 621, doi. 10.1007/s10545-012-9553-3

By:

Amaral, Ana

Publication type:

Article

An update on serine deficiency disorders.

Published in:

Journal of Inherited Metabolic Disease, 2013, v. 36, n. 4, p. 613, doi. 10.1007/s10545-013-9592-4

By:

Crabben, S.;
Verhoeven-Duif, N.;
Brilstra, E.;
Maldergem, L.;
Coskun, T.;
Rubio-Gozalbo, E.;
Berger, R.;
Koning, T.

Publication type:

Article