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Items: 1 to 50 of 117

1.

Peroxisomal localization of the proopiomelanocortin-derived peptides beta-lipotropin and beta-endorphin.

Höftberger R, Kunze M, Voigtländer T, Unterberger U, Regelsberger G, Bauer J, Aboul-Enein F, Garzuly F, Forss-Petter S, Bernheimer H, Berger J, Budka H.

Endocrinology. 2010 Oct;151(10):4801-10. doi: 10.1210/en.2010-0249. Epub 2010 Sep 1.

PMID:
20810565
2.

Quantification of α-galactosidase activity in intact leukocytes.

Hölzl MA, Gärtner M, Kovarik JJ, Hofer J, Bernheimer H, Sunder-Plassmann G, Zlabinger GJ.

Clin Chim Acta. 2010 Nov 11;411(21-22):1666-70. doi: 10.1016/j.cca.2010.06.023. Epub 2010 Jun 25.

PMID:
20599861
3.

Danon disease: case report and detection of new mutation.

Regelsberger G, Höftberger R, Pickl WF, Zlabinger GJ, Körmöczi U, Salzer-Muhar U, Luckner D, Bodamer OA, Mayr JA, Muss WH, Budka H, Bernheimer H.

J Inherit Metab Dis. 2009 Dec;32 Suppl 1:S115-22. doi: 10.1007/s10545-009-1097-9. Epub 2009 Jul 7.

PMID:
19588270
4.

125th anniversary of the Institute of Neurology (Obersteiner Institute) in Vienna. "Germ Cell" of interdisciplinary neuroscience.

Kreft G, Kovacs GG, Voigtländer T, Haberler C, Hainfellner JA, Bernheimer H, Budka H.

Clin Neuropathol. 2008 Nov-Dec;27(6):439-43. No abstract available.

PMID:
19130743
5.

[The beginning -- and how it progresses: 125 years of the Clinical Institute for Neurology].

Bernheimer H.

Wien Klin Wochenschr. 2008;120(19-20):583-6. doi: 10.1007/s00508-008-1014-5. German. No abstract available.

PMID:
19083161
6.

Creutzfeldt-Jakob disease in Austria: an autopsy-controlled study.

Gelpi E, Heinzl H, Hoftberger R, Unterberger U, Strobel T, Voigtlander T, Drobna E, Jarius C, Lang S, Waldhor T, Bernheimer H, Budka H.

Neuroepidemiology. 2008;30(4):215-21. doi: 10.1159/000126915. Epub 2008 Apr 18.

PMID:
18424902
7.

Distribution and cellular localization of adrenoleukodystrophy protein in human tissues: implications for X-linked adrenoleukodystrophy.

Höftberger R, Kunze M, Weinhofer I, Aboul-Enein F, Voigtländer T, Oezen I, Amann G, Bernheimer H, Budka H, Berger J.

Neurobiol Dis. 2007 Nov;28(2):165-74. Epub 2007 Aug 29.

PMID:
17761426
8.

Involvement of the endosomal-lysosomal system correlates with regional pathology in Creutzfeldt-Jakob disease.

Kovács GG, Gelpi E, Ströbel T, Ricken G, Nyengaard JR, Bernheimer H, Budka H.

J Neuropathol Exp Neurol. 2007 Jul;66(7):628-36. Erratum in: J Neuropathol Exp Neurol. 2007 Sep;66(9):870-2.

PMID:
17620988
9.

Diagnosis of X-linked adrenoleukodystrophy in blood leukocytes.

Unterberger U, Regelsberger G, Sundt R, Bernheimer H, Voigtländer T.

Clin Biochem. 2007 Sep;40(13-14):1037-44. Epub 2007 May 3.

PMID:
17524384
10.

Late-onset metachromatic leukodystrophy: genotype strongly influences phenotype.

Rauschka H, Colsch B, Baumann N, Wevers R, Schmidbauer M, Krammer M, Turpin JC, Lefevre M, Olivier C, Tardieu S, Krivit W, Moser H, Moser A, Gieselmann V, Zalc B, Cox T, Reuner U, Tylki-Szymanska A, Aboul-Enein F, LeGuern E, Bernheimer H, Berger J.

Neurology. 2006 Sep 12;67(5):859-63.

PMID:
16966551
11.

Mutations c.459+1G>A and p.P426L in the ARSA gene: prevalence in metachromatic leukodystrophy patients from European countries.

Lugowska A, Amaral O, Berger J, Berna L, Bosshard NU, Chabas A, Fensom A, Gieselmann V, Gorovenko NG, Lissens W, Mansson JE, Marcao A, Michelakakis H, Bernheimer H, Ol'khovych NV, Regis S, Sinke R, Tylki-Szymanska A, Czartoryska B.

Mol Genet Metab. 2005 Nov;86(3):353-9. Epub 2005 Sep 2.

PMID:
16140556
12.

Refsum's disease in an Arabian family.

Fertl E, Földy D, Vass K, Auff E, Vass C, Molzer B, Bernheimer H.

J Neurol Neurosurg Psychiatry. 2001 Apr;70(4):564-5. No abstract available.

13.

Analysis of EEG and CSF 14-3-3 proteins as aids to the diagnosis of Creutzfeldt-Jakob disease.

Zerr I, Pocchiari M, Collins S, Brandel JP, de Pedro Cuesta J, Knight RS, Bernheimer H, Cardone F, Delasnerie-Lauprêtre N, Cuadrado Corrales N, Ladogana A, Bodemer M, Fletcher A, Awan T, Ruiz Bremón A, Budka H, Laplanche JL, Will RG, Poser S.

Neurology. 2000 Sep 26;55(6):811-5.

PMID:
10994001
14.
18.

Antiglycosphingolipid immune responses in neurology. The Vienna experience with isotypes, subclasses, and disease.

Gatterbauer B, Neisser A, Bernheimer H, Schwerer B.

Ann N Y Acad Sci. 1998 Jun 19;845:353-62.

PMID:
9668368
19.

[Cerebrospinal fluid diagnosis of Creutzfeldt-Jakob disease].

Bernheimer H, Gatterbauer B, Radbauer C, Budka H.

Wien Med Wochenschr. 1998;148(4):96-100. German.

PMID:
9611349
20.

Targeted inactivation of the X-linked adrenoleukodystrophy gene in mice.

Forss-Petter S, Werner H, Berger J, Lassmann H, Molzer B, Schwab MH, Bernheimer H, Zimmermann F, Nave KA.

J Neurosci Res. 1997 Dec 1;50(5):829-43.

PMID:
9418970
21.

False polymerase chain reaction-based diagnosis: is it avoidable?

Berger J, Bernheimer H, Forss-Petter S.

Am J Med Genet. 1997 Oct 17;72(2):241. No abstract available.

PMID:
9382151
22.

Serum antibodies against gangliosides and Campylobacter jejuni lipopolysaccharides in Miller Fisher syndrome.

Neisser A, Bernheimer H, Berger T, Moran AP, Schwerer B.

Infect Immun. 1997 Oct;65(10):4038-42.

23.

Serum antibodies to gangliosides in systemic lupus erythematosus.

Neisser A, Gatterbauer B, Graninger W, Menschik M, Bernheimer H.

Ann N Y Acad Sci. 1997 Aug 14;823:300-2. No abstract available.

PMID:
9292057
24.

Occurrence, distribution, and phenotype of arylsulfatase A mutations in patients with metachromatic leukodystrophy.

Berger J, Löschl B, Bernheimer H, Lugowska A, Tylki-Szymanska A, Gieselmann V, Molzer B.

Am J Med Genet. 1997 Mar 31;69(3):335-40.

PMID:
9096767
25.

A new polymorphism of arylsulfatase A within the coding region.

Berger J, Gmach M, Faé I, Molzer B, Bernheimer H.

Hum Genet. 1996 Sep;98(3):348-50.

PMID:
8707308
26.

T-cell-mediated ganglionitis associated with acute sensory neuronopathy.

Hainfellner JA, Kristoferitsch W, Lassmann H, Bernheimer H, Neisser A, Drlicek M, Beer F, Budka H.

Ann Neurol. 1996 Apr;39(4):543-7. Review.

PMID:
8619534
27.

Differentiation of rare leukodystrophies by post-mortem morphological and biochemical studies: female adrenoleukodystrophy-like disease and late-onset Krabbe disease.

Gullotta F, Hughes JL, Wittkowski W, Poulos A, Sträter R, Bernheimer H, Harzer K.

Neuropediatrics. 1996 Feb;27(1):37-41.

PMID:
8677024
28.

Detection of IgA anti-PGL-I specific antigen to Mycobacterium leprae in mangabey monkeys inoculated with M. leprae.

Saad MH, Gormus BJ, Cho SN, Bernheimer H, Schwerer B.

Lepr Rev. 1995 Dec;66(4):296-306.

PMID:
8637383
29.

Association of X-linked adrenoleukodystrophy with HLA DRB1 alleles.

Berger J, Bernheimer H, Faé I, Braun A, Roscher A, Molzer B, Fischer G.

Biochem Biophys Res Commun. 1995 Nov 13;216(2):447-51.

PMID:
7488132
30.

Antibodies to Campylobacter jejuni react with myelin proteins of the central nervous system.

Polt RJ, Moran AP, Bernheimer H, Schwerer B.

J Infect. 1995 Nov;31(3):249-50. No abstract available.

PMID:
8586851
31.

X-linked adrenoleukodystrophy (ALD): a novel mutation of the ALD gene in 6 members of a family presenting with 5 different phenotypes.

Berger J, Molzer B, Faé I, Bernheimer H.

Biochem Biophys Res Commun. 1994 Dec 30;205(3):1638-43.

PMID:
7811247
32.

Chronic progressive motor polyneuropathy after ganglioside treatment.

Schwerer B, Pichler S, Bernheimer H, Safoschnik G, Pötzl G.

J Neurol Neurosurg Psychiatry. 1994 Feb;57(2):238. No abstract available.

33.

GM 1 antibodies in Guillain-Barré syndrome: isotypes, course and clinical outcome.

Seiser A, Pötzl G, Safoschnik G, Pichler S, Bernheimer H, Schwerer B.

Wien Klin Wochenschr. 1994;106(6):159-63.

PMID:
8197746
34.

Simultaneous detection of the two most frequent metachromatic leukodystrophy mutations.

Berger J, Molzer B, Gieselmann V, Bernheimer H.

Hum Genet. 1993 Oct;92(4):421-3.

PMID:
7901143
35.
36.

Specific inhibition of mRNA accumulation for lymphokines in human T cell line Jurkat by mycobacterial lipoarabinomannan antigen.

Chujor CS, Kuhn B, Schwerer B, Bernheimer H, Levis WR, Bevec D.

Clin Exp Immunol. 1992 Mar;87(3):398-403.

37.

[Peroxisomal neurologic diseases and Refsum disease: very long chain fatty acids and phytanic acid as diagnostic markers].

Molzer B, Stöckler S, Bernheimer H.

Wien Klin Wochenschr. 1992;104(21):665-70. Review. German.

PMID:
1282286
38.

Serum antibodies against peripheral nervous system antigens in leprosy.

Chujor CS, Regele H, Bernheimer H, Meeker HC, Levis WR, Schwerer B.

Int J Lepr Other Mycobact Dis. 1991 Dec;59(4):590-7.

PMID:
1724981
39.

Serum IgA1 and IgM antibodies against Mycobacterium leprae-derived phenolic glycolipid-I: a comparative study in leprosy patients and their contacts.

Chujor CS, Bernheimer H, Levis WR, Schwerer B.

Int J Lepr Other Mycobact Dis. 1991 Sep;59(3):441-9.

PMID:
1890368
40.

IgA antibodies against phenolic glycolipid I from Mycobacterium leprae in serum of leprosy patients and contacts: subclass distribution and relation to disease activity.

Schwerer B, Chujor CS, Bernheimer H, Radl J, Haaijman JJ, Meeker HC, Sersen G, Levis WR.

Clin Immunol Immunopathol. 1989 Nov;53(2 Pt 1):202-11.

PMID:
2676273
41.

Phytanic acid and very long chain fatty acids in genetic peroxisomal disorders.

Molzer B, Kainz-Korschinsky M, Sundt-Heller R, Bernheimer H.

J Clin Chem Clin Biochem. 1989 May;27(5):309-14.

PMID:
2474624
42.
43.

Adrenoleukodystrophy in an adult female. A clinical, morphological, and neurochemical study.

Schlote W, Molzer B, Peiffer J, Poremba M, Schumm F, Harzer K, Schnabel R, Bernheimer H.

J Neurol. 1987 Oct;235(1):1-9.

PMID:
3430177
44.
45.

Anti-myelin antibodies in cerebrospinal fluid and serum of patients with meningopolyneuritis Garin-Bujadoux-Bannwarth and other neurological diseases.

Suchanek G, Kristoferitsch W, Stanek G, Bernheimer H.

Zentralbl Bakteriol Mikrobiol Hyg A. 1986 Dec;263(1-2):160-8.

PMID:
3577478
46.
47.

Specificity of ganglioside binding to rat macrophages.

Förster O, Boltz-Nitulescu G, Holzinger C, Wiltschke C, Riedl M, Ortel B, Fellinger A, Bernheimer H.

Mol Immunol. 1986 Nov;23(11):1267-73.

PMID:
3821740
48.

[Lipid storage diseases (lipidoses): genetic, biochemical and clinico-chemical aspects].

Bernheimer H, Molzer B.

Klin Padiatr. 1986 Mar-Apr;198(2):84-8. German.

PMID:
3702277
50.

The cerebrohepatorenal (Zellweger) syndrome: an improved method for the biochemical diagnosis and its potential value for prenatal detection.

Roscher A, Molzer B, Bernheimer H, Stöckler S, Mutz I, Paltauf F.

Pediatr Res. 1985 Sep;19(9):930-3.

PMID:
4047762

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