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1 . Academic Journal
Long-term effect of thymectomy plus prednisone versus prednisone alone in patients with non-thymomatous myasthenia gravis: 2-year extension of the MGTX randomised trial
저자
by
Cutter, Gary
;
Aban, Inmaculada
;
Minisman, Greg
;
Feese, Michelle
;
Kuo, Hui-Chien
, et al.
소스
In
The Lancet Neurology
March 2019 18(3):259-268
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7 . Academic Journal
Semi-Hybrid CO2 Laser Metal Deposition Method with Inter Substrate Buffer Zone
저자
by
Bogdan Antoszewski
;
Hubert Danielewski
;
Jan Dutkiewicz
;
Łukasz Rogal
;
Marek St. Węglowski
, et al.
소스
Materials, Vol 14, Iss 4, p 720 (2021)
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7 . Academic Journal
NMR-based Metabonomics of Cerebrospinal Fluid Applied to Amyotrophic Lateral Sclerosis
저자
by
Toczylowska, Beata
;
Jamrozik, Zygmunt
;
Liebert, Adam
;
Kwiecinski, Hubert
.
소스
In
Biocybernetics and Biomedical Engineering
2013 33(1):21-32
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6 .
Identification of genetic variants associated with Huntington's disease progression
저자
by
Davina J Hensman Moss
;
Antonio F Pardiñas
;
Douglas Langbehn
;
Kitty Lo
;
Blair R Leavitt
, et al.
소스
The Lancet Neurology, 16(9), 701-711. Lancet Publishing Group
BASE-Bielefeld Academic Search Engine
The Lancet Neurology, 16(9), 701-711
The Lancet Neurology
The Lancet Neurology, Elsevier, 2017, 16, pp.701-711
Moss, D J H, Tabrizi, S J, Mead, S, Lo, K, Pardiñas, A F, Holmans, P, Jones, L, Langbehn, D, Leavitt, B R, Roos, R, Durr, A, Durr, A, TRACK-HD investigators & REGISTRY investigators† 2017, ' Identification of genetic variants associated with Huntington's disease progression : a genome-wide association study ', The Lancet Neurology, vol. 16, no. 9, pp. 701-711 . https://doi.org/10.1016/S1474-4422(17)30161-8
The Lancet Neurology, 2017, 16 (9), pp.701-711. ⟨10.1016/S1474-4422(17)30161-8⟩
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7 . Academic Journal
Small deletions disturb desmin architecture leading to breakdown of muscle cells and development of skeletal or cardioskeletal myopathy
저자
by
Kaminska, Anna
;
Strelkov, Sergei V.
;
Goudeau, Bertrand
;
Olivé, Montse
;
Dagvadorj, Ayush
, et al.
소스
Human Genetics
. February 2004 114(3):306-313
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7 . Academic Journal
Analysis of PITX3 Gene in Patients with Multisystem Atrophy, Progressive Supranuclear Palsy and Corticobasal Degeneration
저자
by
Jamrozik, Zygmunt
;
Berdynski, Mariusz
;
Zekanowski, Cezary
;
Baranczyk-Kuzma, Anna
;
Sławek, Jarosław
, et al.
소스
Annals of Clinical & Laboratory Science
. Jan 01, 2013 43(2):151-153
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7 . Academic Journal
Mitochondrial encephalopathy in a patient with a 13042G>A de novo mutation
저자
by
Slawek, Jaroslaw
;
Kierdaszuk, Biruta
;
Tonska, Katarzyna
;
Kodron, Agata
;
Schinwelski, Michal
, et al.
소스
Journal of Clinical Pathology
. Dec 01, 2012 65(12):1147-1149
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7 . Academic Journal
Dissections after childbirth
저자
by
Gasecki, A. P.
;
Kwiecinski, Hubert
;
Lyrer, Philippe A.
;
Lynch, Thomas G.
;
Baxter, Timothy
.
소스
Journal of Neurology
. August 1999 246(8):712-715
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7 .
Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study
저자
by
Mcnulty, Paul
;
Pilcher, Richard
;
Ramesh, Raviram
;
Necuiniate, Renata
;
Hughes, Alis
, et al.
소스
Journal of Huntington's Disease, Vol. 7, no.3, p. 209-222 (2018)
Journal of huntington's disease
7 (2018): 209–222. doi:10.3233/JHD-170263
info:cnr-pdr/source/autori:McNulty P.; Pilcher R.; Ramesh R.; Necuiniate R.; Hughes A.; Farewell D.; Holmans P.; Jones L.; Bonelli R.M.; Hecht K.; Herranhof B.; Holl A.; Kapfhammer H.-P.; Koppitz M.; Lilek S.; Magnet M.; Muller N.; Otti D.; Painold A.; Reisinger K.; Scheibl M.; Schoggl H.; Ullah J.; Braunwarth E.-M.; Brugger F.; Buratti L.; Hametner E.-M.; Hepperger C.; Holas C.; Hotter A.; Hussl A.; Larcher B.; Mahlknecht P.; Muller C.; Pinter B.; Poewe W.; Reiter E.-M.; Seppi K.; Sprenger F.; Wenning G.; Ladurner G.; Lilek S.; Sinadinosa D.; Staffen W.; Walleczek A.M.; Constant E.; Gillardin A.-F.; Leonard M.-C.; Verellen-Dumoulin C.; Van De Wyngaerde F.; Dupuis M.; Minet C.; Ribai P.; Van Paemel D.; Boogaerts A.; Vandenberghe W.; Van Reijen D.; Kaiserova M.; Senkarova Z.; Klempir J.; Majerova V.; Roth J.; Madsen L.H.; Moller A.T.; Hjermind L.; Jacobsen O.; Lindquist S.; Nielsen J.; Regeur L.; Stockholm J.; Larsen I.U.; Vangsted-Hansen C.; Vinther-Jensen T.; Lolk A.; Lundsgaard M.; Wermuth L.; Andersson C.; Nyberg C.; Sundblom J.; Peippo M.; Sipponen M.; Hartikainen P.; Ollokainen M.; Aman J.; Ignatius J.; Karppa M.; Mustonen A.; Kajula O.; Jaaskalainen O.; Moilanen J.; Santala M.; Eklund P.; Hiivola H.; Hypponen H.; Martikainen K.; Tuuha K.; Allain P.; Bonneau D.; Bost M.; Gohier B.; Guerid M.-A.; Olivier A.; Prouzet J.; Prundean A.; Scherer-Gagou C.; Verny C.; Babiloni B.; Debruxelles S.; Duche C.; Goizet C.; Jameau L.; Lafoucriere D.; Spampinato U.; Couttier J.; Debilly B.; Delaigue C.; Durif F.; Legendre P.; Loiseau S.; Ulla M.; Vidal T.; Bachoud-Levi A.-C.; Badei F.; Boisse M.-F.; Boudali L.; De Langavant L.C.; Lemoine L.; Morgado G.; Youssov K.; Annic A.; Barthelemy R.; De Bruycker C.; Cabaret M.; Carette A.-S.; Carriere N.; Decorte E.; Defebvre L.; Delliaux M.; Delval A.; Depelchin A.; Destee A.; Dewulf-Pasz N.; Dondaine T.; Dugauquier F.; Dujardin K.; Hopes L.; Krystkowiak P.; Lemaire M.-H.; Manouvrier S.; Mutez E.; Peter M.; Plomhause L.; Sablonniere B.; Simonin C.; 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Thiel S.; Andrich J.; Ellrichmann G.; Herrmann L.; Hoffmann R.; Kaminski B.; Kraus P.; Saft C.; Stamm C.; Lange H.; Maiwald R.; Bosredon C.; Hunger U.; Lohle M.; Maass A.; Ossig C.; Schmidt S.; Storch A.; Wolz A.; Wolz M.; Kohl Z.; Kozay C.; Winkler J.; Bergmann U.; Boringer R.; Capetian P.; Kammel G.; Lambeck J.; Machtel M.; Meier S.; Rijntjes M.; Zucker B.; Boelmans K.; Ganos C.; Goerendt I.; Heinicke W.; Hidding U.; Lewerenz J.; Munchau A.; Orth M.; Schmalfeld J.; Stubbe L.; Zittel S.; DIercks G.; Dressler D.; Francis F.; Gayde-Stephan S.; Gorzolla H.; Kramer B.; Minschke R.; Schrader C.; Tacik P.; Ribbat M.; Longinus B.; Lusebrink A.; Muhlau M.; Peinemann A.; Stadtler M.; Weindl A.; Winkelmann J.; Ziegler C.; Bechtel N.; Beckmann H.; Bohlen S.; Gopfert N.; Holzner E.; Reilmann R.; Rohm S.; Rumpf S.; Schepers S.; Weber N.; Bachmeier M.; Dose M.; Hofstetter N.; Marquard R.; Muhlback A.; Barth K.; Buck A.; Connemann J.; Ecker D.; Geitner C.; Held C.; Kesse A.; Landwehrmeyer B.; Lezius F.; 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Agarwal V.; Anderson M.; Gunner K.; Harris K.; Hayward E.; Heywood M.; Keys L.; MacKinnon L.; Kipps C.; Smalley S.; Bethwaite P.; Edwards R.; Fuller K.; Gowers L.; Phillips M.; Powell K.; Biunno I.; Bronzova J.; Giuliano J.; Handley O.J.; Illarioshkin S.; Illmann T.; Levey J.; McLean T.; Koivisto S.P.; Paivarinta M.; Uhrova T.; Betz S.; Come A.; Capodarca S.; Charpentier S.; Da Silva W.V.; DI Renzo M.; Finisterra A.M.; Genoves C.; Gilling M.; Hvalstedt C.; Koppers K.; Lamanna C.; Laura M.; Munkel K.; Mutze L.; Oehmen M.; Padieu H.; Paterski L.; Rindal B.; Roren N.; Sasinkova P.; Seliverstov Y.; Timewell E.; Witjes-Ane M.-N.; Yudina E.; Zielonka E./titolo:Reduced Cancer Incidence in Huntington's Disease: Analysis in the Registry Study/doi:10.3233%2FJHD-170263/rivista:Journal of huntington's disease (Print)/anno:2018/pagina_da:209/pagina_a:222/intervallo_pagine:209–222/volume:7
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7 . Academic Journal
Frequency of a tau genotype in amyotrophic lateral sclerosis
저자
by
Münch, Christoph
;
Prechter, Florian
;
Xu, Renshi
;
Linke, Peter
;
Prudlo, Johannes
, et al.
소스
In
Journal of the Neurological Sciences
2005 236(1):13-16
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