1
0
0
(1 - 17 von 17
)
In vitro supplementation with deoxynucleoside monophosphates rescues...
www.sciencedirect.com
Affiliations. Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University of Munich, Germany. ,. Hanns Lochmüller. x. Hanns Lochmüller.
A new web-based method for automated analysis of muscle histology |...
bmcmusculoskeletdisord.biomedcentral.com
Duchenne Muscular Dystrophy is an inherited degenerative neuromuscular disease characterised by rapidly progressive muscle weakness. Currently, curative...
Verfasser Suchresultate
katalog.ub.uni-leipzig.de
Treffer von 108 für Suche: 'Hanns Lochmüller'. Sortieren. Relevanz, Erscheinungsjahr, absteigend, Erscheinungsjahr, aufsteigend, Person / Institution ...
Prof. Dr. Hanns Lochmüller
www.klinikum.uni-muenchen.de
Prof. Dr. Hanns Lochmüller Institute of Human Genetics Newcastle. Institute of Human Genetics University of Newcastle upon Tyne
The TREAT-NMD care and trial site registry: an online registry to...
ojrd.biomedcentral.com
Sunil Rodger, Hanns Lochmüller, Adrian Tassoni, Kathrin Gramsch, Kirsten König, Kate Bushby, Volker Straub, Rudolf Korinthenberg and ...
Kongenitale Myasthene Syndrome (CMS)
www.klinikum.uni-muenchen.de
International besteht eine enge Zusammenarbeit mit der CMS-Arbeitsgruppe von Prof. Dr. Hanns Lochmüller, Newcastle, UK. Weitere Kooperationspartner sind:
Orphanet Journal of Rare Diseases | 6th european conference on rare...
ojrd.biomedcentral.com
Encompassing all aspects of rare diseases and orphan drugs, Orphanet Journal of Rare Diseases features high quality reviews and original articles in ...
FreiDok plus - Lochmüller, Hanns
freidok.uni-freiburg.de
FreiDok plus · Universitätsbibliothek Freiburg. Suchen. Titel Personen Institutionen Projekte. Neuer Eintrag. Titel Projekt. Über. Über Hilfe Kontakt. myFreiDok.
Prevalence, incidence and carrier frequency of 5q–linked spinal...
ojrd.biomedcentral.com
Ingrid E. C. Verhaart,; Agata Robertson,; Ian J. Wilson,; Annemieke Aartsma-Rus,; Shona Cameron,; Cynthia C. Jones,; Suzanne F. Cook and; Hanns Lochmüller Email authorView ORCID ID profile. Orphanet Journal of Rare Diseases : https://doi.org s © The Author(s) Received: ...
Neuroscience Group: Collaborations & Training
www2.medizin.uni-greifswald.de
... [Neuroscience Group] ... During her visit at the partner institute in Newcastle in the laboratory of Prof. Hanns Lochmüller she had the opportunity to learn ...
Mitochondrial mutation linked to congenital myasthenic syndrome
www.sciencedaily.com
"While mitochondrial gene defects can cause a myriad of neurological disorders including myopathies and neuropathies, these have not been specifically implicated in defects of the neuromuscular junction," says Hanns Lochmüller, MD , Professor of Experimental Myology, Institute of Genetic Medicine, ...
Targeted therapy for sleep disorders helps patients with muscular...
www.sciencedaily.com
Sophie D. West, Hanns Lochmüller, Joan Hughes, Antonio Atalaia, Chiara Marini-Bettolo, Simon V. Baudouin, Kirstie N. Anderson. Sleepiness and Sleep-related Breathing Disorders in Myotonic Dystrophy and Responses to Treatment: A Prospective Cohort Study. Journal of Neuromuscular Diseases,
Betreute Arbeiten
www.klinikum.uni-muenchen.de
Betreuer: Prof. Dr. Hanns Lochmüller; Promotion Humanbiologie. Stefanie Bulst, – (summa cum laude) Biochemische und biophysikalische Untersuchungsmethoden bei
Neuroscience Group: WP6
www2.medizin.uni-greifswald.de
Prof. Hanns Lochmüller Institute of Human Genetics (IHG) in Newcastle up on Tyne, UK Prof. Volker Straub Institute of Human Genetics (IHG) in Newcastle up on Tyne, UK
Verwandte Suchanfragen zu Hanns Lochmüller
Volker Straub Rachel Thompson Heike Kölbel | Andreas Roos Juliane Müller Ulrike Schara | Sabine Krause Rita Horvath Angela Abicht |
Personen Vorname "Hanns" (829) Name "Lochmüller" (101) |
sortiert nach Relevanz / Datum