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Lebenslauf Dr. med. Jennifer Just (Mädchenname: Müller vom Hagen)

10/2003 – 05/2010

Studium der Humanmedizin an der Eberhard-Karls-Universität Tübingen

 

10/2009 – 01/2010

Praktisches Jahr im Bereich Neurologie im Robert C. Byrd Health Sciences Center der West Virginia University, Morgantown, West Virginia, USA.

 

12/2011

Dissertation. Arbeitstitel „Differenzierung von Hydromyelie und Syringomyelie auf der Basis magnetresonanztomographischer,

elektrophysiologischer und klinischer Untersuchungen“, magna cum laude

 

08/2010 – 10/2017

Assistenzärztin für Neurologie, Universitätsklinikum Tübingen

 

11/2017 – 02/2019

Fachärztin für Neurologie, Universitätsklinikum Tübingen

 

03/2019

Hospitanz in der neurologischen Facharztpraxis bei Herrn Prof. Dr. med. Wolfgang Kießling

 

seit 04/2019

Gründung und Leitung der Neuropraxis Freudenstadt, Dr. med. Jennifer Just als Nachfolgerin von Herrn Prof. Dr. med. Wolfgang Kießling

 

Zusatzqualifikationen

  • Unter anderem betreute Spezialambulanzen:
    • cerebelläre Ataxien
    • spastische Spinalparalysen
    • Motoneuronenerkrankungen
    • Leukodystrophien und Leukenzephalopathien
    • seltene neurologische Erkrankungen und Beteiligung am Aufbau des Zentrums für Seltene Erkrankungen (ZSE des Universitätsklinikums Tübingen)
  • Sonstige Qualifikationen: Einstellung und Betreuung von
    • Apomorphinpumpen
    • Duodopapumpen
    • Tiefenhirnstimulatoren (deep brain stimulation, DBS)
    • Intrathekale Baclofenpumpen

 

Publikationen

Erstautorenschaften:

 

Leukodystrophies in idiopathic adult-onset ataxia: frequency and phenotype in 105 patients.

Müller Vom Hagen J, Synofzik M, Schicks J, Krägeloh-Mann I, Schöls L.

Mov Disord. 2013 Dec;28(14):2033-5. doi: 10.1002/mds.25617. Epub 2013 Aug 7. No abstract available.

PMID: 23926051

 

Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy.

Müller Vom Hagen J, Schicks J, Bauer P, Beck-Wödl S, Biskup S, Krägeloh-Mann I, Schöls L, Synofzik M.

Neurology. 2013 Mar 19;80(12):1169-70. doi: 10.1212/WNL.0b013e31828869f9. Epub 2013 Feb 20. No abstract available.

PMID: 23427322

 

Leukodystrophies underlying cryptic spastic paraparesis: frequency and phenotype in 76 patients.

Müller vom Hagen J, Karle KN, Schüle R, Krägeloh-Mann I, Schöls L.

Eur J Neurol. 2014 Jul;21(7):983-8. doi: 10.1111/ene.12423. Epub 2014 Apr 2.

PMID: 24698313

 

Koautorenschaften:

Multifocal, hypoechogenic nerve thickening in Cerebrotendinous Xanthomatosis.

Roeben B, Just J, Hengel H, Bender F, Pöschl P, Synofzik M, et al.

Clinical Neurophysiology. 2020;131.

 

Comparative Analysis of Cerebral Magnetic Resonance Imaging Changes in Nontreated Infantile, Juvenile and Adult Patients with Niemann-Pick Disease Type C.

Gburek-Augustat J1,2,3, Groeschel S2,3, Kern J2,3, Beck-Woedl S3,4, Just J3,5, Harzer K2,3, Stampfer M3,4, Kraegeloh-Mann I2,3.

Neuropediatrics. 2020 Feb;51(1):37-44. doi: 10.1055/s-0039-1698451. Epub 2019 Oct 22.

 

Phenotypic variation between siblings with Metachromatic Leukodystrophy

Saskia Elgün, Jakob Waibel, Christiane Kehrer, Diane van Rappard, Judith Böhringer, Stefanie Beck-Wödl, Jennifer Just, Ludger Schöls, Nicole Wolf, Ingeborg Krägeloh-Mann, Samuel Groeschel

Orphanet J Rare Dis. 2019; 14: 136. Published online 2019 Jun 11. doi: 10.1186/s13023-019-1113-6

PMCID: PMC6560893

 

Pattern of Cerebellar Atrophy in Friedreich’s Ataxia-Using the SUIT Template.

Lindig T, Bender B, Kumar VJ, Hauser TK, Grodd W, Brendel B, Just J, Synofzik M, Klose U, Scheffler K, Ernemann U, Schöls L.

Cerebellum. 2019 Jun;18(3):435-447. doi: 10.1007/s12311-019-1008-z.

PMID: 30771164

 

Case series: Slowing alpha rhythm in late-stage ALS patients.

Hohmann MR, Fomina T, Jayaram V, Emde T, Just J, Synofzik M, Schölkopf B, Schöls L, Grosse-Wentrup M.

Clin Neurophysiol. 2018 Feb;129(2):406-408. doi: 10.1016/j.clinph.2017.11.013. Epub 2017 Nov 26.

PMID: 29291492

 

Nerve ultrasound characterizes AMN polyneuropathy as inhomogeneous and focal hypertrophic

Tim W. Rattay, Jennifer Just, Benjamin Röben, Holger Hengel, Rebecca Schüle, Matthis Synofzik, Anne S. Söhn, Natalie Winter, Nele Dammeier, Ludger Schöls, Alexander Grimm

Orphanet J Rare Dis. 2018; 13: 194. Published online 2018 Nov 3. doi: 10.1186/s13023-018-0939-7

PMCID: PMC6215661

 

Absence of EEG correlates of self-referential processing depth in ALS.

Fomina T, Weichwald S, Synofzik M, Just J, Schöls L, Schölkopf B, Grosse-Wentrup M.

PLoS One. 2017 Jun 29;12(6):e0180136. doi: 10.1371/journal.pone.0180136. eCollection 2017.

PMID: 28662161

 

TBK1 Mutation Spectrum in an Extended European Patient Cohort with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Julie van der Zee, Ilse Gijselinck, Sara Van Mossevelde, Federica Perrone, Lubina Dillen, Bavo Heeman, Veerle Bäumer, Sebastiaan Engelborghs, Jan De Bleecker, Jonathan Baets, Ellen Gelpi, Ricardo Rojas‐García, Jordi Clarimón, Alberto Lleó, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Robert Perneczky, Matthis Synofzik, Jennifer Just, Ludger Schöls, Caroline Graff, Håkan Thonberg, Barbara Borroni, Alessandro Padovani, Albena Jordanova, Stayko Sarafov, Ivailo Tournev, Alexandre de Mendonça, Gabriel Miltenberger‐Miltényi, Frederico Simões do Couto, Alfredo Ramirez, Frank Jessen, Michael T. Heneka, Estrella Gómez‐Tortosa, Adrian Danek, Patrick Cras, Rik Vandenberghe, Peter De Jonghe, Peter P. De Deyn, Kristel Sleegers, Marc Cruts, Christine Van Broeckhoven, Johan Goeman, Dirk Nuytten, Katrien Smets, Wim Robberecht, Philip Van Damme, Jan De Bleecker, Patrick Santens, Bart Dermaut, Jan Versijpt, Alex Michotte, Adrian Ivanoiu, Olivier Deryck, Bruno Bergmans, Jean Delbeck, Marc Bruyland, Christiana Willems, Eric Salmon, Pau Pastor, Sara Ortega‐Cubero, Luisa Benussi, Roberta Ghidoni, Giuliano Binetti, Isabel Hernández, Mercè Boada, Agustín Ruiz, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Raquel Sanchez‐Valle, Albert Llado, Isabel Santana, Maria Rosário Almeida, Giovanni B Frisoni, Walter Maetzler, Radoslav Matej, Matthew J. Fraidakis, Gabor G. Kovacs, Gian Maria Fabrizi, Silvia Testi

Hum Mutat. 2017 Mar; 38(3): 297–309. Published online 2017 Jan 19. doi: 10.1002/humu.23161

PMCID: PMC5324646

 

Friedreich and dominant ataxias: quantitative differences in cerebellar dysfunction measurements.

Tanguy Melac A, Mariotti C, Filipovic Pierucci A, Giunti P, Arpa J, Boesch S, Klopstock T, Müller Vom Hagen J, Klockgether T, Bürk K, Schulz JB, Reetz K, Pandolfo M, Durr A, Tezenas du Montcel S; EFACTS group.

J Neurol Neurosurg Psychiatry. 2018 Jun;89(6):559-565. doi: 10.1136/jnnp-2017-316964. Epub 2017 Dec 26.

PMID: 29279305

 

A cognitive brain-computer interface for patients with amyotrophic lateral sclerosis.

Hohmann MR, Fomina T, Jayaram V, Widmann N, Förster C, Just J, Synofzik M, Schölkopf B, Schöls L, Grosse-Wentrup M.

Prog Brain Res. 2016;228:221-39. doi: 10.1016/bs.pbr.2016.04.022. Epub 2016 Jun 10.

PMID: 27590971

 

Identifying Niemann-Pick type C in early-onset ataxia: two quick clinical screening tools.

Synofzik M, Fleszar Z, Schöls L, Just J, Bauer P, Torres Martin JV, Kolb S.

J Neurol. 2016 Oct;263(10):1911-8. doi: 10.1007/s00415-016-8178-0. Epub 2016 Jun 17.

PMID: 27314965

 

Serum Levels of Progranulin Do Not Reflect Cerebrospinal Fluid Levels in Neurodegenerative Disease.

Wilke C, Gillardon F, Deuschle C, Dubois E, Hobert MA, Müller vom Hagen J, Krüger S, Biskup S, Blauwendraat C, Hruscha M, Kaeser SA, Heutink P, Maetzler W, Synofzik M.

Curr Alzheimer Res. 2016;13(6):654-62.

PMID: 26971930

 

Chorein Sensitive Arrangement of Cytoskeletal Architecture.

Honisch S, Gu S, Vom Hagen JM, Alkahtani S, Al Kahtane AA, Tsapara A, Hermann A, Storch A, Schöls L, Lang F, Stournaras C.

Cell Physiol Biochem. 2015;37(1):399-408. doi: 10.1159/000430363. Epub 2015 Aug 27.

PMID: 26316086

 

Biological and clinical characteristics of the European Friedreich’s Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.

Reetz K, Dogan I, Costa AS, Dafotakis M, Fedosov K, Giunti P, Parkinson MH, Sweeney MG, Mariotti C, Panzeri M, Nanetti L, Arpa J, Sanz-Gallego I, Durr A, Charles P, Boesch S, Nachbauer W, Klopstock T, Karin I, Depondt C, vom Hagen JM, Schöls L, Giordano IA, Klockgether T, Bürk K, Pandolfo M, Schulz JB.

Lancet Neurol. 2015 Feb;14(2):174-82. doi: 10.1016/S1474-4422(14)70321-7. Epub 2015 Jan 5.

PMID: 25566998

 

Brain-computer interfacing in amyotrophic lateral sclerosis: Implications of a resting-state EEG analysis.

Jayaram V, Widmann N, Förster C, Fomina T, Hohmann M, Müller Vom Hagen J, Synofzik M, Schölkopf B, Schöls L, Grosse-Wentrup M.

Conf Proc IEEE Eng Med Biol Soc. 2015;2015:6979-82. doi: 10.1109/EMBC.2015.7319998.

PMID: 26737898

 

NPC1 is enriched in unexplained early onset ataxia: a targeted high-throughput screening.

Synofzik M, Harmuth F, Stampfer M, Müller Vom Hagen J, Schöls L, Bauer P.

J Neurol. 2015 Nov;262(11):2557-63. doi: 10.1007/s00415-015-7889-y. Epub 2015 Sep 4.

PMID: 26338816

 

High prevalence of NMDA receptor IgA/IgM antibodies in different dementia types

Sarah Doss, Klaus-Peter Wandinger, Bradley T Hyman, Jessica A Panzer, Matthis Synofzik, Bradford Dickerson, Brit Mollenhauer, Clemens R Scherzer, Adrian J Ivinson, Carsten Finke, Ludger Schöls, Jennifer Müller vom Hagen, Claudia Trenkwalder, Holger Jahn, Markus Höltje, Bharat B Biswal, Lutz Harms, Klemens Ruprecht, Ralph Buchert, Günther U Höglinger, Wolfgang H Oertel, Marcus M Unger, Peter Körtvélyessy, Daniel Bittner, Josef Priller, Eike J Spruth, Friedemann Paul, Andreas Meisel, David R Lynch, Ulrich Dirnagl, Matthias Endres, Bianca Teegen, Christian Probst, Lars Komorowski, Winfried Stöcker, Josep Dalmau, Harald Prüss

Ann Clin Transl Neurol. 2014 Oct; 1(10): 822–832. Published online 2014 Oct 18. doi: 10.1002/acn3.120

PMCID: PMC4241809

 

Safety and tolerability of carbamylated erythropoietin in Friedreich’s ataxia.

Boesch S, Nachbauer W, Mariotti C, Sacca F, Filla A, Klockgether T, Klopstock T, Schöls L, Jacobi H, Büchner B, vom Hagen JM, Nanetti L, Manicom K.

Mov Disord. 2014 Jun;29(7):935-9. doi: 10.1002/mds.25836. Epub 2014 Feb 11.

PMID: 24515352

 

Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration

Julie van der Zee, Tim Van Langenhove, Gabor G. Kovacs, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut, Katrien Smets, Philip Van Damme, Céline Merlin, Annelies Laureys, Marleen Van Den Broeck, Maria Mattheijssens, Karin Peeters, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Pau Pastor, Cristina Razquin, Sara Ortega-Cubero, Isabel Hernández, Mercè Boada, Agustín Ruiz, Alexandre de Mendonça, Gabriel Miltenberger-Miltényi, Frederico Simões do Couto, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Caroline Graff, Huei-Hsin Chiang, Håkan Thonberg, Robert Perneczky, Janine Diehl-Schmid, Panagiotis Alexopoulos, Giovanni B. Frisoni, Christian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Ludger Schöls, Tobias B. Haack, Tim M. Strom, Holger Prokisch, Oriol Dols-Icardo, Jordi Clarimón, Alberto Lleó, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Michael T. Heneka, Frank Jessen, Alfredo Ramirez, Raquel Sanchez-Valle, Albert Llado, Ellen Gelpi, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Eva Parobkova, Gian Maria Fabrizi, Silvia Testi, Eric Salmon, Thomas Ströbel, Patrick Santens, Wim Robberecht, Peter De Jonghe, Jean-Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Kristel Sleegers, Christine Van Broeckhoven

Acta Neuropathol. 2014; 128(3): 397–410. Published online 2014 Jun 5. doi: 10.1007/s00401-014-1298-7

PMCID: PMC4131163

 

X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation

Matthis Synofzik, Jennifer Müller vom Hagen, Tobias B Haack, Christian Wilhelm, Tobias Lindig, Stefanie Beck-Wödl, Sander B Nabuurs, André BP van Kuilenburg, Arjan PM de Brouwer, Ludger Schöls

Orphanet J Rare Dis. 2014; 9: 24. Published online 2014 Feb 14. doi: 10.1186/1750-1172-9-24

PMCID: PMC3931488

 

A Pan-European Study of the C9orf72 Repeat Associated with FTLD: Geographic Prevalence, Genomic Instability, and Intermediate Repeats

Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben, Veerle Bäumer, Githa Maes, Ellen Corsmit, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl-Schmid, Alexandre de Mendonça, Gabriel Miltenberger-Miltenyi, Sónia Pereira, José Pimentel, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Caroline Graff, Huei-Hsin Chiang, Marie Westerlund, Raquel Sanchez-Valle, Albert Llado, Ellen Gelpi, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Giovanni Frisoni, Orazio Zanetti, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Ludger Schöls, Michael T Heneka, Frank Jessen, Radoslav Matej, Eva Parobkova, Gabor G Kovacs, Thomas Ströbel, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Adrian Danek, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Eric Salmon, Patrick Santens, Jean-Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Christine Van Broeckhoven, on behalf of the European Early-Onset Dementia (EOD) Consortium

Hum Mutat. 2013 Feb; 34(2): 363–373. Published online 2012 Oct 30. doi: 10.1002/humu.22244

 

Chorein sensitivity of cytoskeletal organization and degranulation of platelets.

Schmidt EM, Schmid E, Münzer P, Hermann A, Eyrich AK, Russo A, Walker B, Gu S, vom Hagen JM, Faggio C, Schaller M, Föller M, Schöls L, Gawaz M, Borst O, Storch A, Stournaras C, Lang F.

FASEB J. 2013 Jul;27(7):2799-806. doi: 10.1096/fj.13-229286. Epub 2013 Apr 8.

PMID: 23568775

 

D90A-SOD1 ALS mimicking monoclonal gammopathy-associated ALS.

Synofzik M, Hagen JM, Biskup S, Schöls L.

Amyotroph Lateral Scler. 2012 May;13(3):326-7. doi: 10.3109/17482968.2012.656312. Epub 2012 Mar 13. No abstract available.

PMID: 22409356

 

Chorein-sensitive polymerization of cortical actin and suicidal cell death in chorea-acanthocytosis.

Föller M, Hermann A, Gu S, Alesutan I, Qadri SM, Borst O, Schmidt EM, Schiele F, vom Hagen JM, Saft C, Schöls L, Lerche H, Stournaras C, Storch A, Lang F.

FASEB J. 2012 Apr;26(4):1526-34. doi: 10.1096/fj.11-198317. Epub 2012 Jan 6.

PMID: 22227296

 

Screening in ALS and FTD patients reveals 3 novel UBQLN2 mutations outside the PXX domain and a pure FTD phenotype.

Synofzik M, Maetzler W, Grehl T, Prudlo J, Vom Hagen JM, Haack T, Rebassoo P, Munz M, Schöls L, Biskup S.

Neurobiol Aging. 2012 Dec;33(12):2949.e13-7. doi: 10.1016/j.neurobiolaging.2012.07.002. Epub 2012 Aug 11.

PMID: 22892309

 

Defining the line between hydromyelia and syringomyelia. A differentiation is possible based on electrophysiological and magnetic resonance imaging studies.

Roser F, Ebner FH, Sixt C, Hagen JM, Tatagiba MS.

Acta Neurochir (Wien). 2010 Feb;152(2):213-9; discussion 219. doi: 10.1007/s00701-009-0427-x. Epub 2009 Jun 16.

PMID: 19533016