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    Results: 1 to 50 of 344

    1.

    Diagnosis of childhood cancer.

    Raab CP, Gartner JC Jr.

    Prim Care. 2009 Dec;36(4):671-84.PMID: 19913181 [PubMed - in process]Related articles

    2.

    Novel CLN8 mutations confirm the clinical and ethnic diversity of late infantile neuronal ceroid lipofuscinosis.

    Reinhardt K, Grapp M, Schlachter K, Brück W, Gärtner J, Steinfeld R.

    Clin Genet. 2009 Oct 6. [Epub ahead of print]PMID: 19807737 [PubMed - as supplied by publisher]Related articles

    3.

    Polymicrogyria in fetal alcohol syndrome.

    Reinhardt K, Mohr A, Gärtner J, Spohr HL, Brockmann K.

    Birth Defects Res A Clin Mol Teratol. 2009 Sep 17. [Epub ahead of print]PMID: 19764076 [PubMed - as supplied by publisher]Related articles

    4.

    Folate receptor alpha defect causes cerebral folate transport deficiency: a treatable neurodegenerative disorder associated with disturbed myelin metabolism.

    Steinfeld R, Grapp M, Kraetzner R, Dreha-Kulaczewski S, Helms G, Dechent P, Wevers R, Grosso S, Gärtner J.

    Am J Hum Genet. 2009 Sep;85(3):354-63.PMID: 19732866 [PubMed - indexed for MEDLINE]Related articles

    5.

    Immunoglobulin therapy in idiopathic hypothalamic dysfunction.

    Huppke P, Heise A, Rostasy K, Huppke B, Gärtner J.

    Pediatr Neurol. 2009 Sep;41(3):232-4.PMID: 19664546 [PubMed - indexed for MEDLINE]Related articles

    6.

    To score or not to score? Tripling insights for participatory design.

    Smuc M, Mayr E, Lammarsch T, Aigner W, Miksch S, Gärtner J.

    IEEE Comput Graph Appl. 2009 May-Jun;29(3):29-38. No abstract available. PMID: 19642613 [PubMed - indexed for MEDLINE]Related articles

    7.

    Organelle interplay in peroxisomal disorders.

    Thoms S, Grønborg S, Gärtner J.

    Trends Mol Med. 2009 Jul;15(7):293-302. Epub 2009 Jun 26. Review.PMID: 19560974 [PubMed - indexed for MEDLINE]Related articles

    8.

    RNASET2-deficient cystic leukoencephalopathy resembles congenital cytomegalovirus brain infection.

    Henneke M, Diekmann S, Ohlenbusch A, Kaiser J, Engelbrecht V, Kohlschütter A, Krätzner R, Madruga-Garrido M, Mayer M, Opitz L, Rodriguez D, Rüschendorf F, Schumacher J, Thiele H, Thoms S, Steinfeld R, Nürnberg P, Gärtner J.

    Nat Genet. 2009 Jul;41(7):773-5. Epub 2009 Jun 14.PMID: 19525954 [PubMed - indexed for MEDLINE]Related articles

    9.

    Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adults.

    Kohlschütter A, Bley A, Brockmann K, Gärtner J, Krägeloh-Mann I, Rolfs A, Schöls L.

    Brain Dev. 2009 May 6. [Epub ahead of print]PMID: 19427149 [PubMed - as supplied by publisher]Related articles

    10.

    Paediatric multiple sclerosis: the experience of the German Centre for Multiple Sclerosis in Childhood and Adolescence.

    Stark W, Huppke P, Gärtner J.

    J Neurol. 2008 Dec;255 Suppl 6:119-22.PMID: 19300972 [PubMed - indexed for MEDLINE]Related articles

    11.

    Suppression of nonsense mutations in Rett syndrome by aminoglycoside antibiotics.

    Brendel C, Klahold E, Gärtner J, Huppke P.

    Pediatr Res. 2009 May;65(5):520-3.PMID: 19190538 [PubMed - indexed for MEDLINE]Related articles

    12.

    Rational diagnostic strategy for Zellweger syndrome spectrum patients.

    Krause C, Rosewich H, Gärtner J.

    Eur J Hum Genet. 2009 Jun;17(6):741-8. Epub 2009 Jan 14.PMID: 19142205 [PubMed - indexed for MEDLINE]Related articles

    13.

    Natalizumab use in pediatric multiple sclerosis.

    Huppke P, Stark W, Zürcher C, Huppke B, Brück W, Gärtner J.

    Arch Neurol. 2008 Dec;65(12):1655-8.PMID: 19064754 [PubMed - indexed for MEDLINE]Related articles

    14.

    Structure of tripeptidyl-peptidase I provides insight into the molecular basis of late infantile neuronal ceroid lipofuscinosis.

    Pal A, Kraetzner R, Gruene T, Grapp M, Schreiber K, Grønborg M, Urlaub H, Becker S, Asif AR, Gärtner J, Sheldrick GM, Steinfeld R.

    J Biol Chem. 2009 Feb 6;284(6):3976-84. Epub 2008 Nov 26.PMID: 19038966 [PubMed - indexed for MEDLINE]Related articles

    15.

    Serial proton MR spectroscopy and diffusion tensor imaging in infantile Balo's concentric sclerosis.

    Dreha-Kulaczewski SF, Helms G, Dechent P, Hofer S, Gärtner J, Frahm J.

    Neuroradiology. 2009 Feb;51(2):113-21. Epub 2008 Oct 29.PMID: 18958461 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Broadened and elevated humoral immune response to EBNA1 in pediatric multiple sclerosis.

    Lünemann JD, Huppke P, Roberts S, Brück W, Gärtner J, Münz C.

    Neurology. 2008 Sep 23;71(13):1033-5. No abstract available. PMID: 18809840 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Axonal neuropathy with unusual pattern of amyotrophy and alacrima associated with a novel AAAS mutation p.Leu430Phe.

    Koehler K, Brockmann K, Krumbholz M, Kind B, Bönnemann C, Gärtner J, Huebner A.

    Eur J Hum Genet. 2008 Dec;16(12):1499-506. Epub 2008 Jul 16.PMID: 18628786 [PubMed - indexed for MEDLINE]Related articles

    18.

    Palifermin mediates immunoregulatory effects in addition to its cytoprotective effects in mice with acute graft-versus-host disease.

    Ellison CA, Makar BM, Wiseman JM, Gheorghiu I, Taniguchi M, Gartner JG.

    J Clin Immunol. 2008 Sep;28(5):600-15. Epub 2008 Jul 1.PMID: 18592360 [PubMed - indexed for MEDLINE]Related articles

    19.

    Cerebral involvement in axonal Charcot-Marie-Tooth neuropathy caused by mitofusin2 mutations.

    Brockmann K, Dreha-Kulaczewski S, Dechent P, Bönnemann C, Helms G, Kyllerman M, Brück W, Frahm J, Huehne K, Gärtner J, Rautenstrauss B.

    J Neurol. 2008 Jul;255(7):1049-58. Epub 2008 Apr 21.PMID: 18425620 [PubMed - indexed for MEDLINE]Related articles

    20.

    Cerebral MRI as a valuable diagnostic tool in Zellweger spectrum patients.

    Weller S, Rosewich H, Gärtner J.

    J Inherit Metab Dis. 2008 Apr 14. [Epub ahead of print]PMID: 18415699 [PubMed - as supplied by publisher]Related articles

    21.

    CACNA1A R1347Q: a frequent recurrent mutation in hemiplegic migraine.

    Stam AH, Vanmolkot KR, Kremer HP, Gärtner J, Brown J, Leshinsky-Silver E, Gilad R, Kors EE, Frankhuizen WS, Ginjaar HB, Haan J, Frants RR, Ferrari MD, van den Maagdenberg AM, Terwindt GM.

    Clin Genet. 2008 Nov;74(5):481-5. Epub 2008 Apr 8.PMID: 18400034 [PubMed - indexed for MEDLINE]Related articles

    22.

    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.PMID: 18356755 [PubMed - indexed for MEDLINE]Related articles

    23.

    Anti-apoptotic function of a microRNA encoded by the HSV-1 latency-associated transcript.

    Gartner JJ, Sethupathy P, Hatzigeorgiou AG, Fraser NW.

    Nature. 2008 Jan 31;451(7178):600. No abstract available. PMID: 18235505 [PubMed - indexed for MEDLINE]Related articles

    24.

    Molecular analysis of SUMF1 mutations: stability and residual activity of mutant formylglycine-generating enzyme determine disease severity in multiple sulfatase deficiency.

    Schlotawa L, Steinfeld R, von Figura K, Dierks T, Gärtner J.

    Hum Mutat. 2008 Jan;29(1):205.PMID: 18157819 [PubMed - indexed for MEDLINE]Related articles

    25.

    GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like disease.

    Henneke M, Combes P, Diekmann S, Bertini E, Brockmann K, Burlina AP, Kaiser J, Ohlenbusch A, Plecko B, Rodriguez D, Boespflug-Tanguy O, Gärtner J.

    Neurology. 2008 Mar 4;70(10):748-54. Epub 2007 Dec 19.PMID: 18094336 [PubMed - indexed for MEDLINE]Related articles

    26.

    Disturbances of breathing in Rett syndrome: results from patients and animal models.

    Stettner GM, Huppke P, Gärtner J, Richter DW, Dutschmann M.

    Adv Exp Med Biol. 2008;605:503-7. No abstract available. PMID: 18085325 [PubMed - indexed for MEDLINE]Related articles

    27.

    [Leukodystrophies: diseases of white matter of the nervous system]

    Gärtner J, Kohlschütter A, Gieselmann V.

    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2007 Dec;50(12):1531-40. Review. German. PMID: 18026884 [PubMed - indexed for MEDLINE]Related articles

    28.

    Acute onset of fatal vegetative symptoms: unusual presentation of adult Alexander disease.

    Huttner HB, Richter G, Hildebrandt M, Blümcke I, Fritscher T, Brück W, Gärtner J, Seifert F, Staykov D, Hilz MJ, Schwab S, Bardutzky J.

    Eur J Neurol. 2007 Nov;14(11):1251-5.PMID: 17956445 [PubMed - indexed for MEDLINE]Related articles

    29.

    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 [PubMed - indexed for MEDLINE]Related articles

    30.

    Spontaneous central apneas occur in the C57BL/6J mouse strain.

    Stettner GM, Zanella S, Huppke P, Gärtner J, Hilaire G, Dutschmann M.

    Respir Physiol Neurobiol. 2008 Jan 1;160(1):21-7. Epub 2007 Aug 6.PMID: 17869191 [PubMed - indexed for MEDLINE]Related articles

    31.

    Overcoming the challenges of providing clinical/practice education.

    MacFarlane E, Milliken J, Ouellet LL, Thrasher C, Gartner J, Harder N, Cox K.

    Can Nurse. 2007 Jun;103(6):18-22.PMID: 17622031 [PubMed - indexed for MEDLINE]Related articles

    32.

    Live cell FRET microscopy: homo- and heterodimerization of two human peroxisomal ABC transporters, the adrenoleukodystrophy protein (ALDP, ABCD1) and PMP70 (ABCD3).

    Hillebrand M, Verrier SE, Ohlenbusch A, Schäfer A, Söling HD, Wouters FS, Gärtner J.

    J Biol Chem. 2007 Sep 14;282(37):26997-7005. Epub 2007 Jul 3.PMID: 17609205 [PubMed - indexed for MEDLINE]Related articlesFree article

    33.

    Infratentorial meningioma in an 8-year-old child as first sign of neurofibromatosis type 2.

    Stettner GM, Rostasy KM, Ludwig HC, Merkler D, Fahsold R, Gärtner J.

    Neuropediatrics. 2007 Feb;38(1):29-31.PMID: 17607601 [PubMed - indexed for MEDLINE]Related articles

    34.

    Genotype-phenotype analysis in patients with giant axonal neuropathy (GAN).

    Koop O, Schirmacher A, Nelis E, Timmerman V, De Jonghe P, Ringelstein B, Rasic VM, Evrard P, Gärtner J, Claeys KG, Appenzeller S, Rautenstrauss B, Hühne K, Ramos-Arroyo MA, Wörle H, Moilanen JS, Hammans S, Kuhlenbäumer G.

    Neuromuscul Disord. 2007 Aug;17(8):624-30. Epub 2007 Jun 22.PMID: 17587580 [PubMed - indexed for MEDLINE]Related articles

    35.

    Aspects of genome plasticity in pathogenic Escherichia coli.

    Bielaszewska M, Dobrindt U, Gärtner J, Gallitz I, Hacker J, Karch H, Müller D, Schubert S, Alexander Schmidt M, Sorsa LJ, Zdziarski J.

    Int J Med Microbiol. 2007 Nov;297(7-8):625-39. Epub 2007 Apr 25.PMID: 17462951 [PubMed - indexed for MEDLINE]Related articles

    36.

    Genotype and protein expression after bone marrow transplantation for adrenoleukodystrophy.

    Schönberger S, Roerig P, Schneider DT, Reifenberger G, Göbel U, Gärtner J.

    Arch Neurol. 2007 May;64(5):651-7. Epub 2007 Mar 12.PMID: 17353371 [PubMed - indexed for MEDLINE]Related articlesFree article

    37.

    High dose pulsatile dexamethasone therapy in children with opsoclonus-myoclonus syndrome.

    Rostásy K, Wilken B, Baumann M, Müller-Deile K, Bieber I, Gärtner J, Möller P, Angelini P, Hero B.

    Neuropediatrics. 2006 Oct;37(5):291-5.PMID: 17236108 [PubMed - indexed for MEDLINE]Related articles

    38.

    Breathing dysfunctions associated with impaired control of postinspiratory activity in Mecp2-/y knockout mice.

    Stettner GM, Huppke P, Brendel C, Richter DW, Gärtner J, Dutschmann M.

    J Physiol. 2007 Mar 15;579(Pt 3):863-76. Epub 2007 Jan 4.PMID: 17204503 [PubMed - indexed for MEDLINE]Related articlesFree article

    39.

    Treatment of epilepsy in Rett syndrome.

    Huppke P, Köhler K, Brockmann K, Stettner GM, Gärtner J.

    Eur J Paediatr Neurol. 2007 Jan;11(1):10-6. Epub 2006 Dec 18.PMID: 17178248 [PubMed - indexed for MEDLINE]Related articles

    40.

    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 [PubMed - indexed for MEDLINE]Related articles

    41.

    [Pain and symptom management in palliative care]

    Gärtner J, Voltz R, Golla H, Ostgathe C.

    Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2006 Nov;49(11):1097-103. Review. German. PMID: 17072512 [PubMed - indexed for MEDLINE]Related articles

    42.

    Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.

    Krause C, Rosewich H, Thanos M, Gärtner J.

    Hum Mutat. 2006 Nov;27(11):1157.PMID: 17041890 [PubMed - indexed for MEDLINE]Related articles

    43.

    Cerebral metabolic and structural alterations in hereditary spastic paraplegia with thin corpus callosum assessed by MRS and DTI.

    Dreha-Kulaczewski S, Dechent P, Helms G, Frahm J, Gärtner J, Brockmann K.

    Neuroradiology. 2006 Dec;48(12):893-8. Epub 2006 Sep 30.PMID: 17013586 [PubMed - indexed for MEDLINE]Related articles

    44.

    [Bilateral rupture of the Achilles tendon--an unusual occurrence]

    Schikora N, Delank KS, Gärtner J, Eysel P.

    Z Orthop Ihre Grenzgeb. 2006 Sep-Oct;144(5):507-10. German. PMID: 16991068 [PubMed - indexed for MEDLINE]Related articles

    45.

    Effect of palifermin in a murine model of graft-versus-host disease (GVHD) associated with Th2 cytokine production, autoantibody production, and glomerulonephritis.

    Ellison CA, Gibson IW, Hayglass KT, Gartner JG.

    J Clin Immunol. 2006 Sep;26(5):485-94. Epub 2006 Sep 2.PMID: 16952010 [PubMed - indexed for MEDLINE]Related articles

    46.

    X-linked adrenoleukodystrophy: clinical, biochemical and pathogenetic aspects.

    Berger J, Gärtner J.

    Biochim Biophys Acta. 2006 Dec;1763(12):1721-32. Epub 2006 Jul 26. Review.PMID: 16949688 [PubMed - indexed for MEDLINE]Related articles

    47.

    The cystathionine beta-synthase variant c.844_845ins68 protects against CNS demyelination in X-linked adrenoleukodystrophy.

    Linnebank M, Semmler A, Kleijer WJ, van der Sterre ML, Gärtner J, Fliessbach K, Sokolowski P, Köhler W, Schlegel U, Klockgether T, Wanders RJ, Schmidt S, Wüllner U, Kemp S.

    Hum Mutat. 2006 Oct;27(10):1063-4.PMID: 16941496 [PubMed - indexed for MEDLINE]Related articles

    48.

    Characterization of a spliced exon product of herpes simplex type-1 latency-associated transcript in productively infected cells.

    Kang W, Mukerjee R, Gartner JJ, Hatzigeorgiou AG, Sandri-Goldin RM, Fraser NW.

    Virology. 2006 Dec 5-20;356(1-2):106-14. Epub 2006 Aug 30.PMID: 16938324 [PubMed - indexed for MEDLINE]Related articles

    49.

    Graft-versus-host disease in recipients of grafts from natural killer T cell-deficient (Jalpha281(-/-)) donors.

    Ellison CA, Taniguchi M, Fischer JM, Hayglass KT, Gartner JG.

    Immunology. 2006 Nov;119(3):338-47. Epub 2006 Jul 26.PMID: 16879624 [PubMed - indexed for MEDLINE]Related articlesFree article

    50.

    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 [PubMed - indexed for MEDLINE]Related articles

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