Staffan Lundberg
Overview
Explore the profile of Staffan Lundberg including associated specialties, affiliations and a list of published articles.
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13
Citations
288
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Recent Articles
1.
Tornhage M, Sandberg E, Lundberg S
Eur J Paediatr Neurol
. 2019 Dec;
25:139-144.
PMID: 31866100
Aims: Results from a previous study indicated that children with Rolandic epilepsy (RE) exhibit abnormalities of oromotor and dichotic listening performance. The current study aimed to investigate whether the same...
2.
Stattin E, Johansson J, Gudmundsson S, Ameur A, Lundberg S, Bondeson M, et al.
Am J Med Genet A
. 2018 Apr;
176(6):1405-1410.
PMID: 29663639
Arthrogryposis multiplex congenita (AMC) is a heterogeneous disorder characterized by multiple joint contractures often in association with other congenital abnormalities. Pretibial linear vertical creases are a rare finding associated with...
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Lourenco Dos Santos S, Baraibar M, Lundberg S, Eeg-Olofsson O, Larsson L, Friguet B
Redox Biol
. 2015 Jun;
5:267-274.
PMID: 26073261
Sarcopenia corresponds to the degenerative loss of skeletal muscle mass, quality, and strength associated with ageing and leads to a progressive impairment of mobility and quality of life. However, the...
6.
Livingston J, Mayer J, Jenkinson E, Kasher P, Stivaros S, Berger A, et al.
Neuropediatrics
. 2014 Jan;
45(3):175-82.
PMID: 24407470
Objective: With the identification of mutations in the conserved telomere maintenance component 1 (CTC1) gene as the cause of Coats plus (CP) disease, it has become evident that leukoencephalopathy with...
7.
Anderson B, Kasher P, Mayer J, Szynkiewicz M, Jenkinson E, Bhaskar S, et al.
Nat Genet
. 2012 Jan;
44(3):338-42.
PMID: 22267198
Coats plus is a highly pleiotropic disorder particularly affecting the eye, brain, bone and gastrointestinal tract. Here, we show that Coats plus results from mutations in CTC1, encoding conserved telomere...
8.
Bajic D, Kumlien E, Mattsson P, Lundberg S, Wang C, Raininko R
Eur Radiol
. 2009 May;
19(10):2544-50.
PMID: 19440714
Incomplete hippocampal inversion (IHI) has been described in patients with epilepsy or severe midline malformations but also in nonepileptic subjects without obvious developmental anomalies. We studied the frequency of IHI...
9.
Bajic D, Wang C, Kumlien E, Mattsson P, Lundberg S, Eeg-Olofsson O, et al.
Eur Radiol
. 2007 Sep;
18(1):138-42.
PMID: 17828540
Incomplete inversion of the hippocampus, an imperfect fetal development, has been described in patients with epilepsy or severe midline malformations. We studied this condition in a nonepileptic population without obvious...
10.
Lundberg S, Frylmark A, Eeg-Olofsson O
Dev Med Child Neurol
. 2005 Sep;
47(9):603-8.
PMID: 16138667
Twenty children (11 females; age range 8y 2mo to 14y 7mo, mean 10y 6mo, SD 1y 8mo) with electroclinically typical rolandic epilepsy (RE), were investigated to demonstrate possible occurrence of...