I Harting
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Explore the profile of I Harting including associated specialties, affiliations and a list of published articles.
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25
Citations
252
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Recent Articles
1.
Harting I, Karch S, Moog U, Seitz A, Pouwels P, Wolf N
AJNR Am J Neuroradiol
. 2019 May;
40(5):903-907.
PMID: 31048294
Oculodentodigital dysplasia, a rare genetic disorder caused by mutations in the gene encoding gap junction protein 1, classically presents with typical facial features, dental and ocular anomalies, and syndactyly. Oligosymptomatic...
2.
Staufner C, Blom H, Dionisi-Vici C, Freisinger P, Makhseed N, Ballhausen D, et al.
Neuroradiology
. 2016 Mar;
58(7):697-703.
PMID: 26993811
Introduction: Adenosine kinase deficiency (ADK deficiency) is a recently described disorder of methionine and adenosine metabolism resulting in a neurological phenotype with developmental delay, muscular hypotonia, and epilepsy as well...
3.
Harting I, Kotzaeridou U, Poretti A, Seitz A, Pietz J, Bendszus M, et al.
AJNR Am J Neuroradiol
. 2011 Jun;
32(7):1286-9.
PMID: 21636654
The so-called molar tooth sign is the radiologic hallmark of JSRD. Joubert syndrome is a rare, most often autosomal-recessive disorder with a characteristic malformation of the midhindbrain. We describe 3...
4.
Briggs T, Wolf N, DArrigo S, Ebinger F, Harting I, Dobyns W, et al.
Am J Med Genet A
. 2008 Nov;
146A(24):3173-80.
PMID: 19012351
The combination of intracranial calcification and polymicrogyria is usually seen in the context of intrauterine infection, most frequently due to cytomegalovirus. Rare familial occurrences have been reported. We describe five...
5.
Harting I, Seitz A, Geb S, Zwickler T, Porto L, Lindner M, et al.
J Inherit Metab Dis
. 2008 May;
31(3):368-78.
PMID: 18470632
We report imaging abnormalities from 5 brain MR examinations in 4 children with methylmalonic acidaemia between the ages of 20 days and 31 months. In addition to bilateral basal ganglia...
6.
Lettau M, Harting I, Schenk J, Sartor K
Radiologe
. 2008 Apr;
48(11):1055-7.
PMID: 18408908
No abstract available.
7.
Wolf N, Harting I, Innes A, Patzer S, Zeitler P, Schneider A, et al.
Neuropediatrics
. 2007 Aug;
38(2):64-70.
PMID: 17712733
We present four children, three of them boys, affected with an identical clinical pattern consisting of early-onset ataxia, delayed dentition, hypomyelination and cerebellar atrophy. Dental radiographs showed variable absence of...
8.
Bast T, Wright T, Boor R, Harting I, Feneberg R, Rupp A, et al.
Clin Neurophysiol
. 2007 Jun;
118(8):1721-35.
PMID: 17572142
Objective: The study aimed to evaluate differences between EEG and MEG analysis of early somatosensory evoked activity in patients with focal epilepsies in localizing eloquent areas of the somatosensory cortex....
9.
Sakowitz O, Harting I, Kohlhof P, Unterberg A, Steiner H
Br J Neurosurg
. 2006 Feb;
19(3):260-4.
PMID: 16455530
Low-grade (WHO level I) meningiomas are slow-growing, benign tumours typically presenting with unspecific symptoms (e.g. headache), seizures, cranial nerve compression and neuropsychological symptoms determined by location and size of the...
10.
Kulkens S, Harting I, Sauer S, Zschocke J, Hoffmann G, Gruber S, et al.
Neurology
. 2005 Jun;
64(12):2142-4.
PMID: 15985591
Neurologic disease in glutaryl-CoA dehydrogenase (GCDH) deficiency usually presents with acute encephalopathic crises before 2 years of age. The authors report two previously asymptomatic patients with macrocephaly presenting with progressive...