Publications by authors named "Berit Woldseth"

Claim this Profile
A
A monoallelic UXS1 variant associated with short-limbed short stature.
Cecilie F Rustad, Paul Hoff Backe, Chunsheng Jin, Else Merckoll, Kristian Tveten, Berit Woldseth

Mol Genet Genomic Med· June 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The effects of transitioning from immediate release to extended release cysteamine therapy in Norwegian patients with nephropathic cystinosis: a retrospective study.
Anna Bjerre, Sonja Amdal Aase, Maria Radtke, Christian Siva, Helga Gudmundsdottir, Berit Woldseth

Pediatr Nephrol· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Performance of Expanded Newborn Screening in Norway Supported by Post-Analytical Bioinformatics Tools and Rapid Second-Tier DNA Analyses.
Trine Tangeraas, Ingjerd Sæves, Claus Klingenberg, Jens Jørgensen, Erle Kristensen, Berit Woldseth

Int J Neonatal Screen· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
Normal Neurological Development During Infancy Despite Massive Hyperammonemia in Early Treated NAGS Deficiency.
Hallvard Reigstad, Berit Woldseth, Johannes Häberle

JIMD Rep· March 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients.
Rosalba Carrozzo, Daniela Verrigni, Magnhild Rasmussen, Rene de Coo, Hernan Amartino, Berit Woldseth

J Inherit Metab Dis· March 2016

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform.
Tuva Barøy, Janet Koster, Petter Strømme, Merel S Ebberink, Doriana Misceo, Berit Woldseth

Hum Mol Genet· October 2015

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genome instability in Maple Syrup Urine Disease correlates with impaired mitochondrial biogenesis.
Janne M Strand, Ragnhild Skinnes, Katja Scheffler, Terje Rootvelt, Berit Woldseth

Metabolism· August 2014

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
No effect of combined coenzyme Q10 and selenium supplementation on atorvastatin-induced myopathy.
Martin Prøven Bogsrud, Gisle Langslet, Leiv Ose, Kjell-Erik Arnesen, Milada Cvancarova Sm Stuen, Berit Woldseth

Scand Cardiovasc J· April 2013

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Metabolic acidosis mimicking diabetic ketoacidosis after use of calorie-free mineral water.
Gry T Dahl, Berit Woldseth, Rolf Lindemann

Eur J Pediatr· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Hereditary tyrosinaemia type I in Norway: incidence and three novel small deletions in the fumarylacetoacetase gene.
Yngve T Bliksrud, Else Brodtkorb, Paul H Backe, Berit Woldseth, Helge Rootwelt

Scand J Clin Lab Invest· September 2012

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A novel mucopolysaccharidosis type I associated splice site mutation and IDUA splice variants.
Sara Bremer, Annika Ohlsson, Else Brodtkorb, Helge Rootwelt, Terje Rootwelt, Berit Woldseth

Mol Genet Metab· November 2011

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Four novel mutations identified in Norwegian patients result in intermittent maple syrup urine disease when combined with the R301C mutation.
Else Brodtkorb, Janne Strand, Paul Hoff Backe, Anne Marie Lund, Magnar Bjørås, Berit Woldseth

Mol Genet Metab· August 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Plasma oxalate following kidney transplantation in patients without primary hyperoxaluria.
Katja B P Elgstoen, Linda Flaa Johnsen, Berit Woldseth, Lars Morkrid, Anders Hartmann

Nephrol Dial Transplant· July 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Liquid chromatography-tandem mass spectrometry determination of oxalate in spot urine.
Katja B P Elgstoen, Berit Woldseth, Kari Hoie, Lars Morkrid

Scand J Clin Lab Invest· April 2010

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[A newborn infant with hyperventilation].
Rolf Lindemann, Mia C Myhre, Mari Bakken, Drude Fugelseth, Cecilie F Rustad, Berit Woldseth

Tidsskr Nor Laegeforen· June 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mortality in childhood progressive encephalopathy from 1985 to 2004 in Oslo, Norway: a population-based study.
Petter Strømme, Per Magnus, Øivind Juris Kanavin, Terje Rootwelt, Berit Woldseth

Acta Paediatr· January 2008

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
2
2-methylbutyryl-CoA dehydrogenase deficiency associated with autism and mental retardation: a case report.
Oivind J Kanavin, Berit Woldseth, Egil Jellum, Bjorn Tvedt, Brage S Andresen

J Med Case Rep· September 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Incidence rates of progressive childhood encephalopathy in Oslo, Norway: a population based study.
Petter Stromme, Oivind Juris Kanavin, Michael Abdelnoor, Berit Woldseth, Terje Rootwelt

BMC Pediatr· June 2007

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
[
[Mitochondrial beta-oxidation defects].
Berit Woldseth, Terje Rootwelt

Tidsskr Nor Laegeforen· March 2006

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis