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Items: 1 to 50 of 100

1.

Health-related quality of life in pre-school age children with single-ventricle CHD.

Heye KN, Knirsch W, Scheer I, Beck I, Wetterling K, Hahn A, Hofmann K, Latal B, Reich B, Landolt MA.

Cardiol Young. 2019 Feb;29(2):162-168. doi: 10.1017/S1047951118001993. Epub 2019 Jan 2.

PMID:
30599815
2.

Comparison of DTI analysis methods for clinical research: influence of pre-processing and tract selection methods.

Ressel V, van Hedel HJA, Scheer I, O'Gorman Tuura R.

Eur Radiol Exp. 2018 Nov 14;2(1):33. doi: 10.1186/s41747-018-0066-1.

3.

Inclusion Cysts after Fetal Spina Bifida Repair: A Third Hit?

Heye P, Moehrlen U, Mazzone L, Weil R, Altermatt S, Wille DA, Scheer I, Meuli M, Horst M.

Fetal Diagn Ther. 2018 Sep 10:1-7. doi: 10.1159/000491877. [Epub ahead of print]

PMID:
30199879
4.

Torcular Pseudomass.

Boltshauser E, Toelle SP, Scheer I, Hackenberg A.

Neuropediatrics. 2018 Jun;49(3):225-226. doi: 10.1055/s-0038-1635076. Epub 2018 Feb 27. No abstract available.

PMID:
29486503
5.

Sedation for magnetic resonance imaging using propofol with or without ketamine at induction in pediatrics-A prospective randomized double-blinded study.

Schmitz A, Weiss M, Kellenberger C, O'Gorman Tuura R, Klaghofer R, Scheer I, Makki M, Sabandal C, Buehler PK.

Paediatr Anaesth. 2018 Mar;28(3):264-274. doi: 10.1111/pan.13315. Epub 2018 Jan 27.

PMID:
29377404
6.

Microvascular perfusion of the placenta, developing fetal liver, and lungs assessed with intravoxel incoherent motion imaging.

Jakab A, Tuura RL, Kottke R, Ochsenbein-Kölble N, Natalucci G, Nguyen TD, Kellenberger C, Scheer I.

J Magn Reson Imaging. 2018 Jul;48(1):214-225. doi: 10.1002/jmri.25933. Epub 2017 Dec 27.

PMID:
29281153
7.

Reduction of brain volumes after neonatal cardiopulmonary bypass surgery in single-ventricle congenital heart disease before Fontan completion.

Heye KN, Knirsch W, Latal B, Scheer I, Wetterling K, Hahn A, Akintürk H, Schranz D, Beck I, O´Gorman Tuura R, Reich B.

Pediatr Res. 2018 Jan;83(1-1):63-70. doi: 10.1038/pr.2017.203. Epub 2017 Sep 27.

8.

In utero diffusion tensor imaging of the fetal brain: A reproducibility study.

Jakab A, Tuura R, Kellenberger C, Scheer I.

Neuroimage Clin. 2017 Jun 9;15:601-612. doi: 10.1016/j.nicl.2017.06.013. eCollection 2017.

9.

Corrigendum: SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 May 26;49(6):969. doi: 10.1038/ng0617-969c. No abstract available.

PMID:
28546579
10.

Elevated APOBEC3B expression drives a kataegic-like mutation signature and replication stress-related therapeutic vulnerabilities in p53-defective cells.

Nikkilä J, Kumar R, Campbell J, Brandsma I, Pemberton HN, Wallberg F, Nagy K, Scheer I, Vertessy BG, Serebrenik AA, Monni V, Harris RS, Pettitt SJ, Ashworth A, Lord CJ.

Br J Cancer. 2017 Jun 27;117(1):113-123. doi: 10.1038/bjc.2017.133. Epub 2017 May 23.

11.

Evolution of posterior fossa and brain morphology after in utero repair of open neural tube defects assessed by MRI.

Rethmann C, Scheer I, Meuli M, Mazzone L, Moehrlen U, Kellenberger CJ.

Eur Radiol. 2017 Nov;27(11):4571-4580. doi: 10.1007/s00330-017-4807-y. Epub 2017 May 12.

PMID:
28500367
12.

SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome.

Shaw ND, Brand H, Kupchinsky ZA, Bengani H, Plummer L, Jones TI, Erdin S, Williamson KA, Rainger J, Stortchevoi A, Samocha K, Currall BB, Dunican DS, Collins RL, Willer JR, Lek A, Lek M, Nassan M, Pereira S, Kammin T, Lucente D, Silva A, Seabra CM, Chiang C, An Y, Ansari M, Rainger JK, Joss S, Smith JC, Lippincott MF, Singh SS, Patel N, Jing JW, Law JR, Ferraro N, Verloes A, Rauch A, Steindl K, Zweier M, Scheer I, Sato D, Okamoto N, Jacobsen C, Tryggestad J, Chernausek S, Schimmenti LA, Brasseur B, Cesaretti C, García-Ortiz JE, Buitrago TP, Silva OP, Hoffman JD, Mühlbauer W, Ruprecht KW, Loeys BL, Shino M, Kaindl AM, Cho CH, Morton CC, Meehan RR, van Heyningen V, Liao EC, Balasubramanian R, Hall JE, Seminara SB, Macarthur D, Moore SA, Yoshiura KI, Gusella JF, Marsh JA, Graham JM Jr, Lin AE, Katsanis N, Jones PL, Crowley WF Jr, Davis EE, FitzPatrick DR, Talkowski ME.

Nat Genet. 2017 Feb;49(2):238-248. doi: 10.1038/ng.3743. Epub 2017 Jan 9. Erratum in: Nat Genet. 2017 May 26;49(6):969.

13.

Intra-voxel incoherent motion MRI of the living human foetus: technique and test-retest repeatability.

Jakab A, Tuura R, Kottke R, Kellenberger CJ, Scheer I.

Eur Radiol Exp. 2017;1(1):26. doi: 10.1186/s41747-017-0031-4. Epub 2017 Dec 22.

14.

Structural cerebral abnormalities and neurodevelopmental status in single ventricle congenital heart disease before Fontan procedure.

Knirsch W, Mayer KN, Scheer I, Tuura R, Schranz D, Hahn A, Wetterling K, Beck I, Latal B, Reich B.

Eur J Cardiothorac Surg. 2017 Apr 1;51(4):740-746. doi: 10.1093/ejcts/ezw399.

PMID:
28013288
15.

Ommaya reservoir "off-duty" causing major late-onset complications in a child with medulloblastoma.

Walker JH, Hackenberg A, Bozinov O, Berger C, Scheer I, Grotzer MA, Gerber NU.

Pediatr Blood Cancer. 2017 Jun;64(6). doi: 10.1002/pbc.26384. Epub 2016 Dec 1. No abstract available.

PMID:
27905687
16.

Delayed cortical gray matter development in neonates with severe congenital heart disease.

Claessens NH, Moeskops P, Buchmann A, Latal B, Knirsch W, Scheer I, Išgum I, de Vries LS, Benders MJ, von Rhein M.

Pediatr Res. 2016 Nov;80(5):668-674. doi: 10.1038/pr.2016.145. Epub 2016 Jul 19.

PMID:
27434120
17.

Diffusion tensor imaging predicts motor outcome in children with acquired brain injury.

Ressel V, O'Gorman Tuura R, Scheer I, van Hedel HJA.

Brain Imaging Behav. 2017 Oct;11(5):1373-1384. doi: 10.1007/s11682-016-9637-z.

PMID:
27734299
18.

Comparison of automated brain volumetry methods with stereology in children aged 2 to 3 years.

Mayer KN, Latal B, Knirsch W, Scheer I, von Rhein M, Reich B, Bauer J, Gummel K, Roberts N, Tuura RO.

Neuroradiology. 2016 Sep;58(9):901-10. doi: 10.1007/s00234-016-1714-x. Epub 2016 Jul 5.

PMID:
27380040
19.

Cerebellar Bottom-of-Fissure Dysplasia-a Novel Cerebellar Gray Matter Neuroimaging Pattern.

Poretti A, Capone A, Hackenberg A, Kraegeloh-Mann I, Kurlemann G, Laube G, Pietz J, Schimmel M, Schwindt W, Scheer I, Boltshauser E.

Cerebellum. 2016 Dec;15(6):705-709.

PMID:
26525217
20.

Detection of uracil within DNA using a sensitive labeling method for in vitro and cellular applications.

Róna G, Scheer I, Nagy K, Pálinkás HL, Tihanyi G, Borsos M, Békési A, Vértessy BG.

Nucleic Acids Res. 2016 Feb 18;44(3):e28. doi: 10.1093/nar/gkv977. Epub 2015 Oct 1.

21.

Severe Congenital Heart Defects Are Associated with Global Reduction of Neonatal Brain Volumes.

von Rhein M, Buchmann A, Hagmann C, Dave H, Bernet V, Scheer I, Knirsch W, Latal B; Heart and Brain Research Group.

J Pediatr. 2015 Dec;167(6):1259-63.e1. doi: 10.1016/j.jpeds.2015.07.006. Epub 2015 Jul 29.

PMID:
26233604
22.

Cerebellar Hypoplasia and Dysmorphia in Neurofibromatosis Type 1.

Toelle SP, Poretti A, Weber P, Seute T, Bromberg JE, Scheer I, Boltshauser E.

Cerebellum. 2015 Dec;14(6):642-9. doi: 10.1007/s12311-015-0658-8.

PMID:
25728839
23.

Cerebellar cysts in children: a pattern recognition approach.

Boltshauser E, Scheer I, Huisman TA, Poretti A.

Cerebellum. 2015 Jun;14(3):308-16. doi: 10.1007/s12311-014-0633-9. Review.

24.

NLS copy-number variation governs efficiency of nuclear import--case study on dUTPases.

Róna G, Pálinkás HL, Borsos M, Horváth A, Scheer I, Benedek A, Nagy GN, Zagyva I, Vértessy BG.

FEBS J. 2014 Dec;281(24):5463-78. doi: 10.1111/febs.13086. Epub 2014 Oct 25.

25.

Does amplitude-integrated electroencephalogram background pattern correlate with cerebral injury in neonates with hypoxic-ischaemic encephalopathy?

Padden B, Scheer I, Brotschi B, Wohlrab G, Latal B, Bernet V.

J Paediatr Child Health. 2015 Feb;51(2):180-5. doi: 10.1111/jpc.12697. Epub 2014 Aug 15.

PMID:
25123158
26.

The metagenomic telescope.

Szalkai B, Scheer I, Nagy K, Vértessy BG, Grolmusz V.

PLoS One. 2014 Jul 23;9(7):e101605. doi: 10.1371/journal.pone.0101605. eCollection 2014.

27.

Sensory stimulus-sensitive drop attacks and basal ganglia calcification: new findings in a patient with FOLR1 deficiency.

Toelle SP, Wille D, Schmitt B, Scheer I, Thöny B, Plecko B.

Epileptic Disord. 2014 Mar;16(1):88-92. doi: 10.1684/epd.2014.0629.

28.

Mucopolysaccharidoses type I and II: new neuroimaging findings in the cerebellum.

Alqahtani E, Huisman TA, Boltshauser E, Scheer I, Güngör T, Tekes A, Maegawa GH, Poretti A.

Eur J Paediatr Neurol. 2014 Mar;18(2):211-7. doi: 10.1016/j.ejpn.2013.11.014. Epub 2013 Dec 31.

PMID:
24423630
29.

Quantitative cerebral perfusion imaging in children and young adults with Moyamoya disease: comparison of arterial spin-labeling-MRI and H(2)[(15)O]-PET.

Goetti R, Warnock G, Kuhn FP, Guggenberger R, O'Gorman R, Buck A, Khan N, Scheer I.

AJNR Am J Neuroradiol. 2014 May;35(5):1022-8. doi: 10.3174/ajnr.A3799. Epub 2013 Dec 12.

30.

Phosphorylation adjacent to the nuclear localization signal of human dUTPase abolishes nuclear import: structural and mechanistic insights.

Róna G, Marfori M, Borsos M, Scheer I, Takács E, Tóth J, Babos F, Magyar A, Erdei A, Bozóky Z, Buday L, Kobe B, Vértessy BG.

Acta Crystallogr D Biol Crystallogr. 2013 Dec;69(Pt 12):2495-505. doi: 10.1107/S0907444913023354. Epub 2013 Nov 19.

PMID:
24311590
31.

Unrecognized pediatric adult-type tuberculosis puts school contacts at risk.

Steppacher A, Scheer I, Relly C, Začek B, Turk A, Altpeter E, Berger C, Nadal D.

Pediatr Infect Dis J. 2014 Mar;33(3):325-8. doi: 10.1097/INF.0000000000000091.

32.

Fatal outcome of rhino-orbital-cerebral mucormycosis due to bilateral internal carotid occlusion in a child after hematopoietic stem cell transplantation.

Abela L, Toelle SP, Hackenberg A, Scheer I, Güngör T, Plecko B.

Pediatr Infect Dis J. 2013 Oct;32(10):1149-50. doi: 10.1097/INF.0b013e31829e69e7.

PMID:
24067555
33.

Premiere use of Integra™ artificial skin to close an extensive fetal skin defect during open in utero repair of myelomeningocele.

Meuli M, Meuli-Simmen C, Flake AW, Zimmermann R, Ochsenbein N, Scheer I, Mazzone L, Moehrlen U.

Pediatr Surg Int. 2013 Dec;29(12):1321-6. doi: 10.1007/s00383-013-3412-7. Epub 2013 Sep 22.

PMID:
24057923
34.

Cerebral lesions on magnetic resonance imaging correlate with preoperative neurological status in neonates undergoing cardiopulmonary bypass surgery.

Bertholdt S, Latal B, Liamlahi R, Prêtre R, Scheer I, Goetti R, Dave H, Bernet V, Schmitz A, von Rhein M, Knirsch W; Research Group Heart and Brain.

Eur J Cardiothorac Surg. 2014 Apr;45(4):625-32. doi: 10.1093/ejcts/ezt422. Epub 2013 Sep 12.

35.

Natural history of a medulloblastoma: 30 months of wait and see in a child with a cerebellar incidentaloma.

Zeilhofer UB, Scheer I, Warmuth-Metz M, Rushing EJ, Pietsch T, Boltshauser E, Grotzer MA, Gerber NU.

Childs Nerv Syst. 2013 Jul;29(7):1207-10. doi: 10.1007/s00381-013-2077-9. Epub 2013 Mar 16.

36.

Arterial spin labelling MRI for assessment of cerebral perfusion in children with moyamoya disease: comparison with dynamic susceptibility contrast MRI.

Goetti R, O'Gorman R, Khan N, Kellenberger CJ, Scheer I.

Neuroradiology. 2013 May;55(5):639-47. doi: 10.1007/s00234-013-1155-8. Epub 2013 Feb 13.

37.

Isolated intraspinal juvenile xanthogranuloma in an infant presenting as acute paraplegia.

Wille DA, Bozinov O, Scheer I, Grotzer MA, Boltshauser E.

Neuropediatrics. 2013 Jun;44(3):171-3. doi: 10.1055/s-0032-1329908. Epub 2012 Dec 19.

38.

Fetal surgery in Zurich: key features of our first open in utero repair of myelomeningocele.

Meuli M, Moehrlen U, Flake A, Ochsenbein N, Huesler M, Biro P, Scheer I, Tharakan S, Dürig P, Zimmermann R.

Eur J Pediatr Surg. 2013 Dec;23(6):494-8. doi: 10.1055/s-0032-1329700. Epub 2012 Nov 19. No abstract available.

PMID:
23165510
39.

Idiopathic spinal cord herniation: first reported case in a child.

Goetti R, Wille D, Kretzschmar U, Klein A, Scheer I.

JAMA Neurol. 2013 Jan;70(1):125-6. doi: 10.1001/jamaneurol.2013.586. No abstract available.

PMID:
23070462
40.

Pediatric papillary tumors of the pineal region: to observe or to treat following gross total resection?

Abela L, Rushing EJ, Ares C, Scheer I, Bozinov O, Boltshauser E, Grotzer MA.

Childs Nerv Syst. 2013 Feb;29(2):307-10. doi: 10.1007/s00381-012-1935-1. Epub 2012 Oct 6. Review.

41.

Abnormal interhemispheric connectivity in neonates with D-transposition of the great arteries undergoing cardiopulmonary bypass surgery.

Makki M, Scheer I, Hagmann C, Liamlahi R, Knirsch W, Dave H, Bernet V, Batinic K, Latal B.

AJNR Am J Neuroradiol. 2013 Mar;34(3):634-40. doi: 10.3174/ajnr.A3256. Epub 2012 Oct 4.

42.

Pelvic organ support, symptoms and quality of life during pregnancy: a prospective study.

Elenskaia K, Thakar R, Sultan AH, Scheer I, Onwude J.

Int Urogynecol J. 2013 Jul;24(7):1085-90. doi: 10.1007/s00192-012-1935-4. Epub 2012 Sep 22.

PMID:
23001047
43.

Effect of childbirth on pelvic organ support and quality of life: a longitudinal cohort study.

Elenskaia K, Thakar R, Sultan AH, Scheer I, Onwude J.

Int Urogynecol J. 2013 Jun;24(6):927-37. doi: 10.1007/s00192-012-1932-7. Epub 2012 Sep 7.

PMID:
22955252
44.

Bannayan-Riley-Ruvalcaba syndrome with progressive spinal epidural lipomatosis.

Toelle S, Poretti A, Scheer I, Huisman T, Boltshauser E.

Neuropediatrics. 2012 Aug;43(4):221-4. doi: 10.1055/s-0032-1324402. Epub 2012 Aug 21.

PMID:
22911484
45.

Glutamine supplementation in a child with inherited GS deficiency improves the clinical status and partially corrects the peripheral and central amino acid imbalance.

Häberle J, Shahbeck N, Ibrahim K, Schmitt B, Scheer I, O'Gorman R, Chaudhry FA, Ben-Omran T.

Orphanet J Rare Dis. 2012 Jul 25;7:48. doi: 10.1186/1750-1172-7-48.

46.

Non-invasive diagnosis of lung tuberculosis in children by single voxel ¹H-magnetic resonance spectroscopy.

Santy K, Nan P, Chantana Y, Laurent D, Scheer I, Steinmann B, Nadal D, Richner B.

Eur J Pediatr. 2012 Aug;171(8):1257-63. doi: 10.1007/s00431-012-1768-7. Epub 2012 Jul 7.

PMID:
22772834
47.

Chudley-McCullough syndrome: case report and review of the neuroimaging spectrum.

Kau T, Veraguth D, Schiegl H, Scheer I, Boltshauser E.

Neuropediatrics. 2012 Feb;43(1):44-7. doi: 10.1055/s-0032-1307451. Epub 2012 Mar 19. Review.

PMID:
22430160
48.

Acid-base parameters for predicting magnetic resonance imaging measures of neurologic outcome after perinatal hypoxia-ischemia: is the strong ion gap superior to base excess and lactate?

Mann C, Latal B, Padden B, Scheer I, Goebel G, Bernet V.

Am J Perinatol. 2012 May;29(5):361-8. doi: 10.1055/s-0031-1300969. Epub 2012 Feb 3.

PMID:
22307844
49.

Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI.

Poretti A, Vitiello G, Hennekam RC, Arrigoni F, Bertini E, Borgatti R, Brancati F, D'Arrigo S, Faravelli F, Giordano L, Huisman TA, Iannicelli M, Kluger G, Kyllerman M, Landgren M, Lees MM, Pinelli L, Romaniello R, Scheer I, Schwarz CE, Spiegel R, Tibussek D, Valente EM, Boltshauser E.

Orphanet J Rare Dis. 2012 Jan 11;7:4. doi: 10.1186/1750-1172-7-4.

50.

Incidental findings of mass lesions on neuroimages in children.

Perret C, Boltshauser E, Scheer I, Kellenberger CJ, Grotzer MA.

Neurosurg Focus. 2011 Dec;31(6):E20. doi: 10.3171/2011.9.FOCUS11121.

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