Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Hans Heinrich Jung"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-7 (2024)
Abstract Introduction We present a systematic review of phenotypes of McLeod syndrome (MLS) and a case of a 73-year-old female carrier of the genetic alteration leading to MLS with the typical progressive supranuclear palsy (PSP) phenotype. Methods T
Externí odkaz:
https://doaj.org/article/e626aa902cbd4ba4816652ead92bc4e3
Autor:
Carsten Saft, Jean-Marc Burgunder, Matthias Dose, Hans Heinrich Jung, Regina Katzenschlager, Josef Priller, Huu Phuc Nguyen, Kathrin Reetz, Ralf Reilmann, Klaus Seppi, Georg Bernhard Landwehrmeyer
Publikováno v:
Neurological Research and Practice, Vol 5, Iss 1, Pp 1-11 (2023)
Abstract Introduction Choreiform movement disorders are characterized by involuntary, rapid, irregular, and unpredictable movements of the limbs, face, neck, and trunk. These movements often initially go unnoticed by the affected individuals and may
Externí odkaz:
https://doaj.org/article/d590a3c651f34c46a0ea9583802bc1bd
Autor:
Carsten Saft, Jean-Marc Burgunder, Matthias Dose, Hans Heinrich Jung, Regina Katzenschlager, Josef Priller, Huu Phuc Nguyen, Kathrin Reetz, Ralf Reilmann, Klaus Seppi, Georg Bernhard Landwehrmeyer
Publikováno v:
Neurological Research and Practice, Vol 5, Iss 1, Pp 1-10 (2023)
Abstract Introduction Ameliorating symptoms and signs of Huntington’s disease (HD) is essential to care but can be challenging and hard to achieve. The pharmacological treatment of motor signs (e.g. chorea) may favorably or unfavorably impact other
Externí odkaz:
https://doaj.org/article/82e711d767b446e48816d7f63ace04bb
Autor:
Ilijas Jelcic, Elisabeth Probst-Müller, Esther I. Schwarz, Konrad E. Bloch, Bernhard Schwizer, Andreas Lutterotti, Bettina Schreiner, Jana Werner, Hans-Heinrich Jung, Jakob Nilsson
ObjectiveTo expand the spectrum of anti-IgLON5 disease by adding 5 novel anti-IgLON5–seropositive cases with bulbar motor neuron disease-like phenotype.MethodsWe characterized the clinical course, brain MRI and laboratory findings, and therapy resp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb70797ad0772a6724285603063d499b
https://www.zora.uzh.ch/id/eprint/207749/
https://www.zora.uzh.ch/id/eprint/207749/
Autor:
Tobias Bethge, Hans-Heinrich Jung, Fabian Chablais, Roland Spiegel, Roman Guggenberger, Juliane Bremer, Elisabeth J. Rushing, Violeta Mihaylova
Publikováno v:
Journal of clinical neuromuscular disease. 22(3)
Collagen VI-related myopathies are caused by mutations of COL6A1, COL6A2, and COL6A3 and present with a wide phenotypic spectrum ranging from severe Ulrich congenital muscular dystrophy to mild Bethlem myopathy. Here, we report a consanguineous Kurdi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d96d2d747d15aa79ecf142fc0197ca46
https://pubmed.ncbi.nlm.nih.gov/33596003
https://pubmed.ncbi.nlm.nih.gov/33596003
Publikováno v:
Neurology: Genetics
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9a79ed365e63ae0881d77bfcca396c1a
https://pubmed.ncbi.nlm.nih.gov/32637634
https://pubmed.ncbi.nlm.nih.gov/32637634
Autor:
Florian Ingelfinger, Michael Kramer, Sebastian Utz, Sarah Mundt, Sinduya Krishnarajah, Edoardo Galli, Mirjam Lutz, Nicole Puertas Jurado, Corinne Widmer, Ina Camille Reichen, Luca Piccoli, Federica Sallusto, Didier Schneiter, Isabelle Opitz, Hans Heinrich Jung, Antonio Lanzavecchia, Bettina Schreiner, Burkhard Becher
Publikováno v:
The Journal of Immunology. 204:224.50-224.50
Myasthenia gravis is a rare but archetypic autoimmune disease that is characterized by the autoantibody-mediated disruption of the neuromuscular junction leading to a skeletal muscle weakness. Immunomodulatory treatment options for Myasthenia gravis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67e8008293e81ee8975b73086251daaf
https://doi.org/10.4049/jimmunol.204.supp.224.50
https://doi.org/10.4049/jimmunol.204.supp.224.50
A 55-year-old man presented with left leg weakness, incontinence, and fever. Three weeks prior, he had undergone gluteal infiltration for pain related to coxarthrosis. C-reactive protein (197 mg/L) and leukocytes (12.5 G/L) were elevated; CSF was nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daf9017886b9633015740d43676aaa55
https://doi.org/10.5167/uzh-160913
https://doi.org/10.5167/uzh-160913
Pneumocephalus is commonly associated with head and facial trauma, ear infection or surgical interventions. We describe the rare case of a spontaneous pneumocephalus arising from lateral mastoid air cells. A 48-year-old man presented with a 10-day hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0196d38a985d077052b1ae6697cdd2e
http://doc.rero.ch/record/309997/files/405_2004_Article_754.pdf
http://doc.rero.ch/record/309997/files/405_2004_Article_754.pdf
Autor:
Werner, Jana, Jelcic, Ilijas, Schwarz, Esther Irene, Probst-Muller, Elisabeth, Nilsson, Jakob, Schwizer, Bernhard, Bloch, Konrad Ernst, Lutterotti, Andreas, Hans-Heinrich Jung, Schreiner, Bettina
Publikováno v:
Neurology® Neuroimmunology & Neuroinflammation; Mar2021, Vol. 8 Issue 2, p1-7, 7p