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Items: 1 to 50 of 209

1.

Sequestosome-1 (P62) expression reveals chaperone-assisted selective autophagy in immune mediated necrotizing myopathies.

Fischer N, Preuße C, Radke J, Pehl D, Allenbach Y, Schneider U, Feist E, von Casteleyn V, Hahn K, Ruck T, Meuth SG, Goebel HH, Graf R, Mammen A, Benveniste O, Stenzel W.

Brain Pathol. 2019 Aug 3. doi: 10.1111/bpa.12772. [Epub ahead of print]

PMID:
31376301
2.

Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy reading.

Olivier PA, De Paepe B, Aronica E, Berfelo F, Colman R, Amato A, Dimitri D, Gallardo E, Gherardi R, Goebel HH, Hilton-Jones D, Hofer M, Holton J, Daa Schrøder H, Selcen D, Stenzel W, de Visser M, De Bleecker JL.

Neurology. 2019 Jul 29. pii: 10.1212/WNL.0000000000008005. doi: 10.1212/WNL.0000000000008005. [Epub ahead of print]

PMID:
31358616
3.

Fulminant cerebral venous thrombosis associated with the m.3243A>G MELAS mutation: A new guise for an old disease.

Nikolaus M, Tietze A, Schweizer L, Kaindl AM, Stenzel W, Schuelke M, Knierim E.

Brain Dev. 2019 Jul 22. pii: S0387-7604(19)30166-4. doi: 10.1016/j.braindev.2019.07.002. [Epub ahead of print]

PMID:
31345444
4.

Inflammation-induced fibrosis in skeletal muscle of female carriers of Duchenne muscular dystrophy.

Preuße C, von Moers A, Kölbel H, Pehl D, Goebel HH, Schara U, Stenzel W.

Neuromuscul Disord. 2019 Jul;29(7):487-496. doi: 10.1016/j.nmd.2019.05.003. Epub 2019 May 10.

PMID:
31326192
5.

Biomarkers in Inflammatory Myopathies-An Expanded Definition.

Benveniste O, Goebel HH, Stenzel W.

Front Neurol. 2019 Jun 4;10:554. doi: 10.3389/fneur.2019.00554. eCollection 2019. Review.

6.

Proteomic Profiling Unravels a Key Role of Specific Macrophage Subtypes in Sporadic Inclusion Body Myositis.

Roos A, Preusse C, Hathazi D, Goebel HH, Stenzel W.

Front Immunol. 2019 May 9;10:1040. doi: 10.3389/fimmu.2019.01040. eCollection 2019.

7.

1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018.

Udd B, Stenzel W, Oldfors A, Olivé M, Romero N, Lammens M, Kusters B, Sewry C, Goebel HH, Evangelista T.

Neuromuscul Disord. 2019 Jun;29(6):483-485. doi: 10.1016/j.nmd.2019.03.002. Epub 2019 Mar 15. No abstract available.

PMID:
31101462
8.

Mass cytometry reveals an impairment of B cell homeostasis in anti-synthetase syndrome.

Dzangué-Tchoupou G, Allenbach Y, Preuße C, Stenzel W, Benveniste O.

J Neuroimmunol. 2019 Jul 15;332:212-215. doi: 10.1016/j.jneuroim.2019.04.014. Epub 2019 Apr 29.

PMID:
31082769
9.

[Infections of the central nervous system by protozoa, helminths and fungi].

Deigendesch N, Schlüter D, Siebert E, Stenzel W.

Nervenarzt. 2019 Jun;90(6):623-641. doi: 10.1007/s00115-019-0719-1. German.

PMID:
31073673
10.

Recently Identified Congenital Myopathies.

Radke J, Stenzel W, Goebel HH.

Semin Pediatr Neurol. 2019 Apr;29:83-90. doi: 10.1016/j.spen.2019.01.008. Epub 2019 Feb 10.

PMID:
31060728
11.

PD1 pathway in immune-mediated myopathies: Pathogenesis of dysfunctional T cells revisited.

Knauss S, Preusse C, Allenbach Y, Leonard-Louis S, Touat M, Fischer N, Radbruch H, Mothes R, Matyash V, Böhmerle W, Endres M, Goebel HH, Benveniste O, Stenzel W.

Neurol Neuroimmunol Neuroinflamm. 2019 Apr 10;6(3):e558. doi: 10.1212/NXI.0000000000000558. eCollection 2019 May.

12.

[Peripheral nerve involvement in rheumatic diseases].

Casteleyn V, Hahn K, Stenzel W, Siegert E.

Z Rheumatol. 2019 May;78(4):339-351. doi: 10.1007/s00393-019-0621-z. German.

PMID:
30944998
13.

Immunoglobulin (Ig)G-4 related myositis - A new entity?

Casteleyn V, Radbruch H, Diekhoff T, Rose T, Spengler L, Schneider U, Stenzel W.

Neuromuscul Disord. 2019 Jan;29(1):70-74. doi: 10.1016/j.nmd.2018.11.009. Epub 2018 Nov 24.

PMID:
30578098
14.

Distribution and prognostic impact of microglia/macrophage subpopulations in gliomas.

Zeiner PS, Preusse C, Golebiewska A, Zinke J, Iriondo A, Muller A, Kaoma T, Filipski K, Müller-Eschner M, Bernatz S, Blank AE, Baumgarten P, Ilina E, Grote A, Hansmann ML, Verhoff MA, Franz K, Feuerhake F, Steinbach JP, Wischhusen J, Stenzel W, Niclou SP, Harter PN, Mittelbronn M.

Brain Pathol. 2019 Jul;29(4):513-529. doi: 10.1111/bpa.12690. Epub 2019 Jan 15.

PMID:
30506802
15.

De novo mutation in ELOVL1 causes ichthyosis, acanthosis nigricans, hypomyelination, spastic paraplegia, high frequency deafness and optic atrophy.

Mueller N, Sassa T, Morales-Gonzalez S, Schneider J, Salchow DJ, Seelow D, Knierim E, Stenzel W, Kihara A, Schuelke M.

J Med Genet. 2019 Mar;56(3):164-175. doi: 10.1136/jmedgenet-2018-105711. Epub 2018 Nov 28.

PMID:
30487246
16.

Autophagic vacuolar myopathy is a common feature of CLN3 disease.

Radke J, Koll R, Gill E, Wiese L, Schulz A, Kohlschütter A, Schuelke M, Hagel C, Stenzel W, Goebel HH.

Ann Clin Transl Neurol. 2018 Oct 14;5(11):1385-1393. doi: 10.1002/acn3.662. eCollection 2018 Nov.

17.

Author Correction: Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia.

Latham SL, Ehmke N, Reinke PYA, Taft MH, Eicke D, Reindl T, Stenzel W, Lyons MJ, Friez MJ, Lee JA, Hecker R, Frühwald MC, Becker K, Neuhann TM, Horn D, Schrock E, Niehaus I, Sarnow K, Grützmann K, Gawehn L, Klink B, Rump A, Chaponnier C, Figueiredo C, Knöfler R, Manstein DJ, Di Donato N.

Nat Commun. 2018 Nov 19;9(1):4930. doi: 10.1038/s41467-018-07404-6.

18.

Immune Checkpoint Inhibitor-Associated Myositis.

Anquetil C, Salem JE, Lebrun-Vignes B, Johnson DB, Mammen AL, Stenzel W, Léonard-Louis S, Benveniste O, Moslehi JJ, Allenbach Y.

Circulation. 2018 Aug 14;138(7):743-745. doi: 10.1161/CIRCULATIONAHA.118.035898. No abstract available.

PMID:
30359135
19.

Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia.

Latham SL, Ehmke N, Reinke PYA, Taft MH, Eicke D, Reindl T, Stenzel W, Lyons MJ, Friez MJ, Lee JA, Hecker R, Frühwald MC, Becker K, Neuhann TM, Horn D, Schrock E, Niehaus I, Sarnow K, Grützmann K, Gawehn L, Klink B, Rump A, Chaponnier C, Figueiredo C, Knöfler R, Manstein DJ, Di Donato N.

Nat Commun. 2018 Oct 12;9(1):4250. doi: 10.1038/s41467-018-06713-0. Erratum in: Nat Commun. 2018 Nov 19;9(1):4930.

20.

Diagnostic potential of sarcoplasmic myxovirus resistance protein A expression in subsets of dermatomyositis.

Uruha A, Allenbach Y, Charuel JL, Musset L, Aussy A, Boyer O, Mariampillai K, Landon-Cardinal O, Rasmussen C, Bolko L, Maisonobe T, Leonard-Louis S, Suzuki S, Nishino I, Stenzel W, Benveniste O.

Neuropathol Appl Neurobiol. 2019 Aug;45(5):513-522. doi: 10.1111/nan.12519. Epub 2018 Nov 22.

PMID:
30267437
21.

Cytoplasmic body myopathy revisited.

Schuelke M, Schwarz M, Stenzel W, Goebel HH.

Neuromuscul Disord. 2018 Nov;28(11):969-971. doi: 10.1016/j.nmd.2018.08.006. Epub 2018 Aug 30. No abstract available.

PMID:
30253894
22.

New variant of necklace fibres display peculiar lysosomal structures and mitophagy.

Rinnenthal JL, Dittmayer C, Irlbacher K, Wacker I, Schröder R, Goebel HH, Butori C, Villa L, Sacconi S, Stenzel W.

Neuromuscul Disord. 2018 Oct;28(10):846-856. doi: 10.1016/j.nmd.2018.06.010. Epub 2018 Jul 2.

PMID:
30149909
23.

Immune checkpoint inhibitor-related myositis and myocarditis in patients with cancer.

Touat M, Maisonobe T, Knauss S, Ben Hadj Salem O, Hervier B, Auré K, Szwebel TA, Kramkimel N, Lethrosne C, Bruch JF, Laly P, Cadranel J, Weiss N, Béhin A, Allenbach Y, Benveniste O, Lenglet T, Psimaras D, Stenzel W, Léonard-Louis S.

Neurology. 2018 Sep 4;91(10):e985-e994. doi: 10.1212/WNL.0000000000006124. Epub 2018 Aug 8. Erratum in: Neurology. 2019 Aug 6;93(6):280.

PMID:
30089619
24.

Characterization of Naïve and Vitamin C-Treated Mouse Schwann Cell Line MSC80: Induction of the Antioxidative Thioredoxin Related Transmembrane Protein 1.

Phan V, Schmidt J, Matyash V, Malchow S, Thanisch M, Lorenz C, Diepolder I, Schulz JB, Stenzel W, Roos A, Gess B.

J Proteome Res. 2018 Sep 7;17(9):2925-2936. doi: 10.1021/acs.jproteome.8b00022. Epub 2018 Aug 10.

PMID:
30044099
25.

The Curse of Apneic Spells.

Radke J, Dreesmann M, Radke M, von Moers A, Abicht A, Stenzel W, Goebel HH.

Semin Pediatr Neurol. 2018 Jul;26:56-58. doi: 10.1016/j.spen.2017.03.006. Epub 2017 Apr 13.

PMID:
29961520
26.

JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis.

Ladislau L, Suárez-Calvet X, Toquet S, Landon-Cardinal O, Amelin D, Depp M, Rodero MP, Hathazi D, Duffy D, Bondet V, Preusse C, Bienvenu B, Rozenberg F, Roos A, Benjamim CF, Gallardo E, Illa I, Mouly V, Stenzel W, Butler-Browne G, Benveniste O, Allenbach Y.

Brain. 2018 Jun 1;141(6):1609-1621. doi: 10.1093/brain/awy105.

PMID:
29741608
27.

Muscle Weakness, Cardiomyopathy, and L-2-Hydroxyglutaric Aciduria Associated with a Novel Recessive SLC25A4 Mutation.

von Renesse A, Morales-Gonzalez S, Gill E, Salomons GS, Stenzel W, Schuelke M.

JIMD Rep. 2019;43:27-35. doi: 10.1007/8904_2018_93. Epub 2018 Apr 14.

28.

Architectural B-cell organization in skeletal muscle identifies subtypes of dermatomyositis.

Radke J, Koll R, Preuße C, Pehl D, Todorova K, Schönemann C, Allenbach Y, Aronica E, de Visser M, Heppner FL, Weis J, Doostkam S, Maisonobe T, Benveniste O, Goebel HH, Stenzel W.

Neurol Neuroimmunol Neuroinflamm. 2018 Mar 6;5(3):e451. doi: 10.1212/NXI.0000000000000451. eCollection 2018 May.

29.

Necrosis in anti-SRP+ and anti-HMGCR+myopathies: Role of autoantibodies and complement.

Allenbach Y, Arouche-Delaperche L, Preusse C, Radbruch H, Butler-Browne G, Champtiaux N, Mariampillai K, Rigolet A, Hufnagl P, Zerbe N, Amelin D, Maisonobe T, Louis-Leonard S, Duyckaerts C, Eymard B, Goebel HH, Bergua C, Drouot L, Boyer O, Benveniste O, Stenzel W.

Neurology. 2018 Feb 6;90(6):e507-e517. doi: 10.1212/WNL.0000000000004923. Epub 2018 Jan 12.

PMID:
29330311
30.

224th ENMC International Workshop:: Clinico-sero-pathological classification of immune-mediated necrotizing myopathies Zandvoort, The Netherlands, 14-16 October 2016.

Allenbach Y, Mammen AL, Benveniste O, Stenzel W; Immune-Mediated Necrotizing Myopathies Working Group.

Neuromuscul Disord. 2018 Jan;28(1):87-99. doi: 10.1016/j.nmd.2017.09.016. Epub 2017 Oct 23. No abstract available.

PMID:
29221629
31.

Aicardi-Goutières syndrome with muscle involvement in early infancy.

Deigendesch N, Morales-Gonzalez S, Weschke B, Goebel HH, Schuelke M, Stenzel W.

Neuropathol Appl Neurobiol. 2018 Dec;44(7):737-742. doi: 10.1111/nan.12454. No abstract available.

PMID:
29210089
32.

Parasitic and fungal infections.

Deigendesch N, Costa Nunez J, Stenzel W.

Handb Clin Neurol. 2017;145:245-262. doi: 10.1016/B978-0-12-802395-2.00018-3. Review.

PMID:
28987173
33.

Acute and chronic viral infections.

Deigendesch N, Stenzel W.

Handb Clin Neurol. 2017;145:227-243. doi: 10.1016/B978-0-12-802395-2.00017-1. Review.

PMID:
28987172
34.

Acute and chronic bacterial infections and sarcoidosis.

Deigendesch N, Stenzel W.

Handb Clin Neurol. 2017;145:217-226. doi: 10.1016/B978-0-12-802395-2.00016-X. Review.

PMID:
28987171
35.

Neurometabolic and neurodegenerative diseases in children.

Radke J, Stenzel W, Goebel HH.

Handb Clin Neurol. 2017;145:133-146. doi: 10.1016/B978-0-12-802395-2.00009-2.

PMID:
28987164
36.

Analyzing Nicotinamide Adenine Dinucleotide Phosphate Oxidase Activation in Aging and Vascular Amyloid Pathology.

Radbruch H, Mothes R, Bremer D, Seifert S, Köhler R, Pohlan J, Ostendorf L, Günther R, Leben R, Stenzel W, Niesner RA, Hauser AE.

Front Immunol. 2017 Jul 31;8:844. doi: 10.3389/fimmu.2017.00844. eCollection 2017.

37.

Recessive mutation in EXOSC3 associates with mitochondrial dysfunction and pontocerebellar hypoplasia.

Schottmann G, Picker-Minh S, Schwarz JM, Gill E, Rodenburg RJT, Stenzel W, Kaindl AM, Schuelke M.

Mitochondrion. 2017 Nov;37:46-54. doi: 10.1016/j.mito.2017.06.007. Epub 2017 Jul 4.

PMID:
28687512
38.

Musculoskeletal Disease in MDA5-Related Type I Interferonopathy: A Mendelian Mimic of Jaccoud's Arthropathy.

de Carvalho LM, Ngoumou G, Park JW, Ehmke N, Deigendesch N, Kitabayashi N, Melki I, Souza FFL, Tzschach A, Nogueira-Barbosa MH, Ferriani V, Louzada-Junior P, Marques W Jr, Lourenço CM, Horn D, Kallinich T, Stenzel W, Hur S, Rice GI, Crow YJ.

Arthritis Rheumatol. 2017 Oct;69(10):2081-2091. doi: 10.1002/art.40179. Epub 2017 Aug 22.

39.

A recessive mutation in beta-IV-spectrin (SPTBN4) associates with congenital myopathy, neuropathy, and central deafness.

Knierim E, Gill E, Seifert F, Morales-Gonzalez S, Unudurthi SD, Hund TJ, Stenzel W, Schuelke M.

Hum Genet. 2017 Jul;136(7):903-910. doi: 10.1007/s00439-017-1814-7. Epub 2017 May 24.

PMID:
28540413
40.

Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.

Schnitzler LJ, Schreckenbach T, Nadaj-Pakleza A, Stenzel W, Rushing EJ, Van Damme P, Ferbert A, Petri S, Hartmann C, Bornemann A, Meisel A, Petersen JA, Tousseyn T, Thal DR, Reimann J, De Jonghe P, Martin JJ, Van den Bergh PY, Schulz JB, Weis J, Claeys KG.

Orphanet J Rare Dis. 2017 May 11;12(1):86. doi: 10.1186/s13023-017-0640-2. Review.

41.

Inherited and Acquired Muscle Weakness: A Moving Target for Diagnostic Muscle Biopsy.

Stenzel W, Schoser B.

Neuropediatrics. 2017 Aug;48(4):226-232. doi: 10.1055/s-0037-1601859. Epub 2017 Apr 15. Review.

PMID:
28411586
42.

Recent advances in Myopathology.

Stenzel W, Goebel HH.

Neuropathol Appl Neurobiol. 2017 Feb;43(1):3-4. doi: 10.1111/nan.12389. No abstract available.

PMID:
28297097
43.

Pathogenic role of anti-signal recognition protein and anti-3-Hydroxy-3-methylglutaryl-CoA reductase antibodies in necrotizing myopathies: Myofiber atrophy and impairment of muscle regeneration in necrotizing autoimmune myopathies.

Arouche-Delaperche L, Allenbach Y, Amelin D, Preusse C, Mouly V, Mauhin W, Tchoupou GD, Drouot L, Boyer O, Stenzel W, Butler-Browne G, Benveniste O.

Ann Neurol. 2017 Apr;81(4):538-548. doi: 10.1002/ana.24902.

PMID:
28224701
44.

The Deubiquitinating Enzyme Cylindromatosis Dampens CD8+ T Cell Responses and Is a Critical Factor for Experimental Cerebral Malaria and Blood-Brain Barrier Damage.

Schmid U, Stenzel W, Koschel J, Raptaki M, Wang X, Naumann M, Matuschewski K, Schlüter D, Nishanth G.

Front Immunol. 2017 Feb 1;8:27. doi: 10.3389/fimmu.2017.00027. eCollection 2017.

45.

Sequestration of cholesterol within the host late endocytic pathway restricts liver-stage Plasmodium development.

Petersen W, Stenzel W, Silvie O, Blanz J, Saftig P, Matuschewski K, Ingmundson A.

Mol Biol Cell. 2017 Mar 15;28(6):726-735. doi: 10.1091/mbc.E16-07-0531. Epub 2017 Jan 25.

46.

Integrated classification of inflammatory myopathies.

Allenbach Y, Benveniste O, Goebel HH, Stenzel W.

Neuropathol Appl Neurobiol. 2017 Feb;43(1):62-81. doi: 10.1111/nan.12380. Review.

PMID:
28075491
47.

P2Y12 receptor is expressed on human microglia under physiological conditions throughout development and is sensitive to neuroinflammatory diseases.

Mildner A, Huang H, Radke J, Stenzel W, Priller J.

Glia. 2017 Feb;65(2):375-387. doi: 10.1002/glia.23097. Epub 2016 Nov 12.

PMID:
27862351
48.

MORC2 mutation causes severe spinal muscular atrophy-phenotype, cerebellar atrophy, and diaphragmatic paralysis.

Schottmann G, Wagner C, Seifert F, Stenzel W, Schuelke M.

Brain. 2016 Dec;139(Pt 12):e70. doi: 10.1093/brain/aww252. Epub 2016 Oct 29. No abstract available.

PMID:
27794525
49.

Advances in serological diagnostics of inflammatory myopathies.

Benveniste O, Stenzel W, Allenbach Y.

Curr Opin Neurol. 2016 Oct;29(5):662-73. doi: 10.1097/WCO.0000000000000376. Review.

PMID:
27538058
50.

The immunoproteasomes are key to regulate myokines and MHC class I expression in idiopathic inflammatory myopathies.

Bhattarai S, Ghannam K, Krause S, Benveniste O, Marg A, de Bruin G, Xin BT, Overkleeft HS, Spuler S, Stenzel W, Feist E.

J Autoimmun. 2016 Dec;75:118-129. doi: 10.1016/j.jaut.2016.08.004. Epub 2016 Aug 10.

PMID:
27522114

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