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Niklas Darin

Professor/ chief physician

Niklas Darin
Professor/ chief physician
niklas.darin@gu.se

Postal Address: Drottning silvias barn o ungdomsjukh, 41685 Göteborg
Visiting Address: Drottning silvias barn o ungdomsjukh , 41685 Göteborg


Department of Pediatrics at Institute of Clinical Sciences (More Information)
Drottning Silvias Barn O ungdomsjukh
416 85 Göteborg
Visiting Address: Drottning Silvias Barn O ungdomsjukh , 416 85 Göteborg

Latest publications

Structural anomaly in the reticular formation in narcolepsy type 1, suggesting lower levels of neuromelanin
N. M. Drissi, M. Warntjes, A. Wessén, Attila Szakacs, Niklas Darin et al.
NeuroImage: Clinical, Journal article 2019
Journal article

Unexpected Fat Distribution in Adolescents With Narcolepsy
N. M. Drissi, T. Romu, A. M. Landtblom, A. Szakacs, Tove Hallböök et al.
Frontiers in Endocrinology, Journal article 2018
Journal article

Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications.
Omar Hikmat, Karin Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen et al.
Epilepsia, Journal article 2018
Journal article

γ-glutamyl transpeptidase deficiency caused by a large homozygous intragenic deletion in GGT1.
Niklas Darin, Karin Leckström, Per Sikora, Julia Lindgren, Gabriella Almén et al.
European journal of human genetics : EJHG, Journal article 2018
Journal article

Oxygen consumption in platelets as an adjunct diagnostic method for pediatric mitochondrial disease.
Emil Westerlund, Sigurður E Marelsson, Johannes K Ehinger, Fredrik Sjövall, Saori Morota et al.
Pediatric research, Journal article 2018
Journal article

Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients.
Kalliopi Sofou, Irenaeus F M de Coo, Elsebet Ostergaard, Pirjo Isohanni, Karin Naess et al.
Journal of medical genetics, Journal article 2018
Journal article

Showing 51 - 60 of 97

2013

2012

Phenotypic and genotypic variability in Alpers syndrome.
Kalliopi Sofou, Ali-Reza Moslemi, Gittan Kollberg, Ingibjörg Bjarnadottir, Anders Oldfors et al.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society, Journal article 2012
Journal article

Fortskridande hjärnsjukdomar
Niklas Darin, Jan-Eric Månsson
Barnmedicin, (red) K.Hanseus, H.Lagercrantz, T. Lindberg., Lund, Studentlitteratur, Chapter in book 2012
Chapter in book

2011

FGF-21 as a biomarker for muscle-manifesting mitochondrial respiratory chain deficiencies: a diagnostic study.
Anu Suomalainen, Jenni M Elo, Kirsi H Pietiläinen, Anna H Hakonen, Ksenia Sevastianova et al.
Lancet neurology, Journal article 2011
Journal article

Corneal thickness in children and adolescents with mitochondrial disorders
Antovan Seyedi Honarvar , Niklas Darin, Mar Tulinius, E. Rudholm, Marita Andersson Grönlund
Nordiska barnögonläkarmöte (NPOG), Selfors, Island, 28-29 sept, 2011. Föredrag., Conference contribution 2011
Conference contribution

Muscular dystrophies and congenital myopathies in childhood
Brynja Kristin Thorarinsdottir, Mar Tulinius, Niklas Darin
Neuromuscular Disorders, Poster 2011
Poster

Systemic administration of PRO051 in Duchenne's muscular dystrophy.
Nathalie M Goemans, Mar Tulinius, Johanna T van den Akker, Brigitte E Burm, Peter F Ekhart et al.
The New England journal of medicine, Magazine article 2011
Magazine article

2010

Showing 51 - 60 of 97

Page Manager: Katarina Olinder Eriksson|Last update: 10/1/2013
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