Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 1 to 50 of 257

1.

Prof. Fukuyama Yukio (1928-2014).

Hanefeld F.

Neuropediatrics. 2015 Apr;46(2):149-50. doi: 10.1055/s-0035-1548674. Epub 2015 Mar 22. No abstract available.

PMID:
25796461
2.

Intrathecal IgM synthesis in pediatric MS is not a negative prognostic marker of disease progression: quantitative versus qualitative IgM analysis.

Stauch C, Reiber H, Rauchenzauner M, Strasak A, Pohl D, Hanefeld F, Gärtner J, Rostásy KM.

Mult Scler. 2011 Mar;17(3):327-34. doi: 10.1177/1352458510388543. Epub 2010 Dec 1.

PMID:
21123302
3.

Paediatric and adult multiple sclerosis: age-related differences and time course of the neuroimmunological response in cerebrospinal fluid.

Reiber H, Teut M, Pohl D, Rostasy KM, Hanefeld F.

Mult Scler. 2009 Dec;15(12):1466-80. doi: 10.1177/1352458509348418. Epub 2009 Dec 7.

PMID:
19995844
4.

Intrathecal antibody production against Epstein-Barr and other neurotropic viruses in pediatric and adult onset multiple sclerosis.

Pohl D, Rostasy K, Jacobi C, Lange P, Nau R, Krone B, Hanefeld F.

J Neurol. 2010 Feb;257(2):212-6. doi: 10.1007/s00415-009-5296-y. Epub 2009 Aug 28.

5.

Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS study.

Dreha-Kulaczewski SF, Dechent P, Finsterbusch J, Brockmann K, Gärtner J, Frahm J, Hanefeld FA.

Pediatr Res. 2008 Apr;63(4):444-9. doi: 10.1203/01.pdr.0000304934.90198.25.

PMID:
18356755
6.

Common infectious agents in multiple sclerosis: a case-control study in children.

Krone B, Pohl D, Rostasy K, Kahler E, Brunner E, Oeffner F, Grange JM, Gärtner J, Hanefeld F.

Mult Scler. 2008 Jan;14(1):136-9. Epub 2007 Oct 17.

PMID:
17942525
7.

Proton MRS of a child with Sandhoff disease reveals elevated brain hexosamine.

Wilken B, Dechent P, Hanefeld F, Frahm J.

Eur J Paediatr Neurol. 2008 Jan;12(1):56-60. Epub 2007 Jul 10.

PMID:
17625939
8.

Chronic relapsing opsoclonus-myoclonus syndrome: combination of cyclophosphamide and dexamethasone pulses.

Wilken B, Baumann M, Bien CG, Hero B, Rostasy K, Hanefeld F.

Eur J Paediatr Neurol. 2008 Jan;12(1):51-5. Epub 2007 Jul 10.

PMID:
17625938
9.

Pediatric multiple sclerosis: a short history of a long story.

Hanefeld F.

Neurology. 2007 Apr 17;68(16 Suppl 2):S3-6.

PMID:
17438236
10.

Valproic acid-induced pancreatitis: 16 new cases and a review of the literature.

Gerstner T, Büsing D, Bell N, Longin E, Kasper JM, Klostermann W, Hebing B, Hanefeld F, Eckel U, Hoffmann R, Bettendorf U, Weidner B, Wiemer-Kruel A, Brockmann K, Neumann FW, Sandrieser T, Wolff M, König S.

J Gastroenterol. 2007 Jan;42(1):39-48. Epub 2007 Feb 16. Review.

PMID:
17322992
11.

Virchow-Robin spaces on magnetic resonance images of children with adrenoleukodystrophy.

Groeschel S, Brockmann K, Hanefeld F.

Eur J Paediatr Neurol. 2007 May;11(3):142-5. Epub 2007 Jan 24.

PMID:
17254818
12.

Paediatric multiple sclerosis and acute disseminated encephalomyelitis in Germany: results of a nationwide survey.

Pohl D, Hennemuth I, von Kries R, Hanefeld F.

Eur J Pediatr. 2007 May;166(5):405-12. Epub 2007 Jan 12.

PMID:
17219129
13.

Quantitative proton MRS of cerebral metabolites in laminin alpha2 chain deficiency.

Brockmann K, Dechent P, Bönnemann C, Schreiber G, Frahm J, Hanefeld F.

Brain Dev. 2007 Jul;29(6):357-64. Epub 2006 Dec 15.

PMID:
17174499
14.

High seroprevalence of Epstein-Barr virus in children with multiple sclerosis.

Pohl D, Krone B, Rostasy K, Kahler E, Brunner E, Lehnert M, Wagner HJ, Gärtner J, Hanefeld F.

Neurology. 2006 Dec 12;67(11):2063-5.

PMID:
17159123
15.

Patient with actin aggregate myopathy and not formerly identified ACTA1 mutation is heterozygous for the Gly15Arg mutation of ACTA1, which has previously been associated with actinopathy.

Goebel HH, Brockman K, Bönnemann CG, Warlo IA, Hanefeld F, Labeit S, Durling HJ, Laing NG.

J Child Neurol. 2006 Jun;21(6):545. No abstract available.

PMID:
16948949
16.

Recurrent optic neuritis associated with Chlamydia pneumoniae infection of the central nervous system.

Pohl D, Rostasy K, Gieffers J, Maass M, Hanefeld F.

Dev Med Child Neurol. 2006 Sep;48(9):770-2.

17.

Virchow-Robin spaces on magnetic resonance images: normative data, their dilatation, and a review of the literature.

Groeschel S, Chong WK, Surtees R, Hanefeld F.

Neuroradiology. 2006 Oct;48(10):745-54. Epub 2006 Aug 5. Review.

PMID:
16896908
18.

Pediatric multiple sclerosis: detection of clinically silent lesions by multimodal evoked potentials.

Pohl D, Rostasy K, Treiber-Held S, Brockmann K, Gärtner J, Hanefeld F.

J Pediatr. 2006 Jul;149(1):125-7.

PMID:
16860140
19.

Magnetic resonance imaging and proton magnetic resonance spectroscopy of megalencephaly and dilated Virchow-Robin spaces.

Groeschel S, Brockmann K, Dechent P, Wilichowski E, Frahm J, Hanefeld F.

Pediatr Neurol. 2006 Jan;34(1):35-40.

PMID:
16376276
20.

Baló's concentric sclerosis associated with primary human herpesvirus 6 infection.

Pohl D, Rostasy K, Krone B, Hanefeld F.

J Neurol Neurosurg Psychiatry. 2005 Dec;76(12):1723-5.

21.

Quantitative proton MRS of Pelizaeus-Merzbacher disease: evidence of dys- and hypomyelination.

Hanefeld FA, Brockmann K, Pouwels PJ, Wilken B, Frahm J, Dechent P.

Neurology. 2005 Sep 13;65(5):701-6.

PMID:
16157902
22.

X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene.

Brockmann K, Dumitrescu AM, Best TT, Hanefeld F, Refetoff S.

J Neurol. 2005 Jun;252(6):663-6. Epub 2005 Apr 18.

PMID:
15834651
23.

Identification of ten novel mutations in patients with eIF2B-related disorders.

Ohlenbusch A, Henneke M, Brockmann K, Goerg M, Hanefeld F, Kohlschütter A, Gärtner J.

Hum Mutat. 2005 Apr;25(4):411.

PMID:
15776425
24.

Treatment of early onset multiple sclerosis with subcutaneous interferon beta-1a.

Pohl D, Rostasy K, Gärtner J, Hanefeld F.

Neurology. 2005 Mar 8;64(5):888-90.

PMID:
15753430
25.

Ullrich congenital muscular dystrophy: connective tissue abnormalities in the skin support overlap with Ehlers-Danlos syndromes.

Kirschner J, Hausser I, Zou Y, Schreiber G, Christen HJ, Brown SC, Anton-Lamprecht I, Muntoni F, Hanefeld F, Bönnemann CG.

Am J Med Genet A. 2005 Jan 30;132A(3):296-301.

PMID:
15690374
26.

Escalating immunotherapy of multiple sclerosis--new aspects and practical application.

Rieckmann P, Toyka KV, Bassetti C, Beer K, Beer S, Buettner U, Chofflon M, Götschi-Fuchs M, Hess K, Kappos L, Kesselring J, Goebels N, Ludin HP, Mattle H, Schluep M, Vaney C, Baumhackl U, Berger T, Deisenhammer F, Fazekas F, Freimüller M, Kollegger H, Kristoferitsch W, Lassmann H, Markut H, Strasser-Fuchs S, Vass K, Altenkirch H, Bamborschke S, Baum K, Benecke R, Brück W, Dommasch D, Elias WG, Gass A, Gehlen W, Haas J, Haferkamp G, Hanefeld F, Hartung HP, Heesen C, Heidenreich F, Heitmann R, Hemmer B, Hense T, Hohlfeld R, Janzen RW, Japp G, Jung S, Jügelt E, Koehler J, Kölmel W, König N, Lowitzsch K, Manegold U, Melms A, Mertin J, Oschmann P, Petereit HF, Pette M, Pöhlau D, Pohl D, Poser S, Sailer M, Schmidt S, Schock G, Schulz M, Schwarz S, Seidel D, Sommer N, Stangel M, Stark E, Steinbrecher A, Tumani H, Voltz R, Weber F, Weinrich W, Weissert R, Wiendl H, Wiethölter H, Wildemann U, Zettl UK, Zipp F, Zschenderlein R, Izquierdo G, Kirjazovas A, Packauskas L, Miller D, Koncan Vracko B, Millers A, Orologas A, Panellus M, Sindic CJ, Bratic M, Svraka A, Vella NR, Stelmasiak Z, Selmaj K, Bartosik-Psujik H, Mitosek-Szewczyk K, Belniak E, Mochecka A, Bayas A, Chan A, Flachenecker P, Gold R, Kallmann B, Leussink V, Mäurer M, Ruprecht K, Stoll G, Weilbach FX; Multiple Sclerosis Therapy Consensus Group.

J Neurol. 2004 Nov;251(11):1329-39. Review.

PMID:
15592728
27.

CSF characteristics in early-onset multiple sclerosis.

Pohl D, Rostasy K, Reiber H, Hanefeld F.

Neurology. 2004 Nov 23;63(10):1966-7.

PMID:
15557527
28.

Alexander disease: past and present.

Hanefeld FA.

Cell Mol Life Sci. 2004 Nov;61(21):2750-2. No abstract available.

PMID:
15549177
29.

Monocyte/macrophage differentiation in dermatomyositis and polymyositis.

Rostasy KM, Piepkorn M, Goebel HH, Menck S, Hanefeld F, Schulz-Schaeffer WJ.

Muscle Nerve. 2004 Aug;30(2):225-30.

PMID:
15266639
30.

Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene.

Ferreiro A, Ceuterick-de Groote C, Marks JJ, Goemans N, Schreiber G, Hanefeld F, Fardeau M, Martin JJ, Goebel HH, Richard P, Guicheney P, Bönnemann CG.

Ann Neurol. 2004 May;55(5):676-86.

PMID:
15122708
31.

Actin-related myopathy without any missense mutation in the ACTA1 gene.

Goebel HH, Brockmann K, Bönnemann CG, Warlo IA, Hanefeld F, Labeit S, Durling HJ, Laing NG.

J Child Neurol. 2004 Feb;19(2):149-53.

PMID:
15072110
32.

Stroke-like pattern in DTI and MRS of childhood mitochondrial leukoencephalopathy.

Brockmann K, Finsterbusch J, Schara U, Wilichowski E, Frahm J, Hanefeld F.

Neuroradiology. 2004 Apr;46(4):267-71. Epub 2004 Mar 18.

PMID:
15034698
33.

CNS disease as the main manifestation of hemophagocytic lymphohistiocytosis in two children.

Rostasy K, Kolb R, Pohl D, Mueller H, Fels C, Moers AV, Bergmann M, Hanefeld F, Pekrun A, Schulz-Schaeffer W.

Neuropediatrics. 2004 Feb;35(1):45-9.

PMID:
15002052
34.

Severe encephalopathy with epilepsy in an infant caused by subclinical maternal pernicious anaemia: case report and review of the literature.

Korenke GC, Hunneman DH, Eber S, Hanefeld F.

Eur J Pediatr. 2004 Apr;163(4-5):196-201. Epub 2004 Feb 5. Review.

PMID:
14762712
35.

Evaluation of the preventive effect of glyceryl trioleate-trierucate ("Lorenzo's oil") therapy in X-linked adrenoleukodystrophy: results of two concurrent trials.

Moser HW, Raymond GV, Koehler W, Sokolowski P, Hanefeld F, Korenke GC, Green A, Loes DJ, Hunneman DH, Jones RO, Lu SE, Uziel G, Giros ML, Roels F.

Adv Exp Med Biol. 2003;544:369-87. No abstract available.

PMID:
14713253
36.

Muscle ultrasound in Bethlem myopathy.

Bönnemann CG, Brockmann K, Hanefeld F.

Neuropediatrics. 2003 Dec;34(6):335-6. No abstract available.

PMID:
14681763
37.

Progressive muscle weakness after high-dose steroids in two children with CIDP.

Rostasy KM, Diepold K, Buckard J, Brockmann K, Wilken B, Hanefeld F.

Pediatr Neurol. 2003 Sep;29(3):236-8.

PMID:
14629908
38.

Tarsal tunnel syndrome in a 7-year-old boy.

Brockmann K, Schneider-Sickert F, Kolenda H, Aden I, Hanefeld F.

Eur J Pediatr. 2004 Jan;163(1):46-7. Epub 2003 Nov 12. No abstract available.

PMID:
14614624
39.

Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantation.

Wilken B, Dechent P, Brockmann K, Finsterbusch J, Baumann M, Ebell W, Korenke GC, Pouwels PJ, Hanefeld FA, Frahm J.

Neuropediatrics. 2003 Jun;34(5):237-46.

PMID:
14598229
40.

Role of leukotrienes as indicators of the inflammatory demyelinating reaction in x-linked cerebral adrenoleukodystrophy.

Mayatepek E, Baumann M, Meissner T, Hanefeld F, Korenke GC.

J Neurol. 2003 Oct;250(10):1259-60. No abstract available.

PMID:
14586618
41.

Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC).

Blattner R, Von Moers A, Leegwater PA, Hanefeld FA, Van Der Knaap MS, Köhler W.

Neuropediatrics. 2003 Aug;34(4):215-8. Review.

PMID:
12973664
42.

A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?

Brockmann K, Meins M, Taubert A, Trappe R, Grond M, Hanefeld F.

Eur Neurol. 2003;50(2):100-5.

PMID:
12944715
43.

[The Levy-Hollister syndrome: a syndrome of dysplasias with ENT-manifestations].

Fierek O, Laskawi R, Bönnemann C, Hanefeld F.

HNO. 2003 Aug;51(8):654-7. Epub 2003 Apr 16. German.

PMID:
12942181
44.
45.

The spectrum of phenotypes in females with Rett Syndrome.

Huppke P, Held M, Laccone F, Hanefeld F.

Brain Dev. 2003 Aug;25(5):346-51.

PMID:
12850514
46.

Chlamydia pneumoniae in children with MS: frequency and quantity of intrathecal antibodies.

Rostasy K, Reiber H, Pohl D, Lange P, Ohlenbusch A, Eiffert H, Maass M, Hanefeld F.

Neurology. 2003 Jul 8;61(1):125-8.

PMID:
12847174
47.

Two brothers with findings resembling congenital intrauterine infection-like syndrome (pseudo-TORCH syndrome).

Knoblauch H, Tennstedt C, Brueck W, Hammer H, Vulliamy T, Dokal I, Lehmann R, Hanefeld F, Tinschert S.

Am J Med Genet A. 2003 Jul 15;120A(2):261-5.

PMID:
12833411
48.

Mutation analysis in the MECP2 gene and genetic counselling for Rett syndrome.

Gill H, Cheadle JP, Maynard J, Fleming N, Whatley S, Cranston T, Thompson EM, Leonard H, Davis M, Christodoulou J, Skjeldal O, Hanefeld F, Kerr A, Tandy A, Ravine D, Clarke A.

J Med Genet. 2003 May;40(5):380-4. No abstract available.

49.

Megalencephalic leukoencephalopathy with subcortical cysts in an adult: quantitative proton MR spectroscopy and diffusion tensor MRI.

Brockmann K, Finsterbusch J, Terwey B, Frahm J, Hanefeld F.

Neuroradiology. 2003 Mar;45(3):137-42. Epub 2003 Feb 14.

PMID:
12684714
50.

Unusual localization of a choroid plexus papilloma in a 4-year-old female.

Rostasy KM, Sponholz S, Bahn E, Ludwig HC, Hanefeld F.

Pediatr Neurol. 2003 Jan;28(1):66-8.

PMID:
12657424

Supplemental Content

Loading ...
Support Center