Multiple study < Multiple system atrophy < Multiple system organ failure

Facettes : Author.f AffPays.f AffRegion.f AffVille.f AffOrg.f KwdFr.f Mesh.f MeshFr.f Teeft.f

List of bibliographic references indexed by Multiple system atrophy

Number of relevant bibliographic references: 21.
[0-20] [0 - 20][0 - 21][20-20][20-40]

Ident.	Authors (with country if any)	Title
001133 (2013)		Poster Presentations
001386 (2012)		Poster Session 1, Sunday 9 September
001387 (2012)		Poster Presentations
001612 (2011)		Poster Presentations
002105 (2007)		Abstracts of The Movement Disorder Society's Eleventh International Congress of Parkinson's Disease and Movement Disorders
002792 (2004)		Subject index
002951 (2004)		Author index
002A29 (2003)		Third German‐Scandinavian Meeting on Movement Disorders Gothenburg and Kiel, May 15‐19, 2003
002B70 (2002)	Alberto Bizzi [Italie] ; Marianna Bugiani [Italie] ; Gajja S. Salomons [Pays-Bas] ; Donald H. Hunneman [Allemagne] ; Isabella Moroni [Italie] ; Margherita Estienne [Italie] ; Ugo Danesi [Italie] ; Cornelis Jakobs [Pays-Bas] ; Graziella Uziel [Italie]	X‐linked creatine deficiency syndrome: A novel mutation in creatine transporter gene SLC6A8
002B72 (2002)	Philippe Gailloud [États-Unis] ; Argye Hillis [États-Unis] ; Bruce Perler [États-Unis] ; Kieran J. Murphy [États-Unis]	Vertebrobasilar stroke as a late complication of a Blalock‐Taussig shunt
002B77 (2002)		Subject index
002B82 (2002)	Claudia Sommer [Allemagne] ; Thies Lindenlaub [Allemagne] ; Detlef Zillikens [Allemagne] ; Klaus V. Toyka [Allemagne] ; Markus Naumann [Allemagne]	Selective loss of cholinergic sudomotor fibers causes anhidrosis in Ross syndrome
002B88 (2002)	Sheng-Ting Li [États-Unis] ; Raghuveer Dendi [États-Unis] ; Courtney Holmes [États-Unis] ; David S. Goldstein [États-Unis]	Progressive loss of cardiac sympathetic innervation in Parkinson's disease
002B98 (2002)	Patrick F. Chinnery [Royaume-Uni] ; Timothy J. Walls [Royaume-Uni] ; Michael G. Hanna [Royaume-Uni] ; David Bates [Royaume-Uni] ; Peter R. W. Fawcett [Royaume-Uni]	Normokalemic periodic paralysis revisited: Does it exist?
002B99 (2002)	Ennio Toscano [Italie] ; Alessandro Simonati [Italie] ; Yasuhiro Indo [Japon] ; Generoso Andria [Italie]	No mutation in the TRKA (NTRK1) gene encoding a receptor tyrosine kinase for nerve growth factor in a patient with hereditary sensory and autonomic neuropathy type V
002C15 (2002)	Richard Dodel [Allemagne, États-Unis] ; Harald Hampel [Allemagne] ; Candan Depboylu [Allemagne] ; Suizhen Lin [États-Unis] ; Feng Gao [États-Unis] ; Sabine Schock [Allemagne] ; Steffi J Ckel [Allemagne] ; Xing Wei [États-Unis] ; Katharina Buerger [Allemagne] ; Christine Höft [Allemagne] ; Bernhard Hemmer [Allemagne] ; Hans-Jürgen Möller [Allemagne] ; Martin Farlow [États-Unis] ; Wolfgang H. Oertel [Allemagne] ; Norbert Sommer [Allemagne] ; Yansheng Du [États-Unis]	Human antibodies against amyloid β peptide: A potential treatment for Alzheimer's disease
002C30 (2002)	Roland Wenzelburger [Allemagne] ; Bao-Rong Zhang [Allemagne, République populaire de Chine] ; Meike Poepping [Allemagne] ; Bettina Schrader [Allemagne] ; Dieter Müller [Allemagne] ; Florian Kopper [Allemagne] ; Urban Fietzek [Allemagne] ; Hubertus M. Mehdorn [Allemagne] ; Günther Deuschl [Allemagne] ; Paul Krack [Allemagne]	Dyskinesias and grip control in Parkinson's disease are normalized by chronic stimulation of the subthalamic nucleus
002C33 (2002)	Cristina Baldoli [Italie] ; Andrea Righini [Italie] ; Cecilia Parazzini [Italie] ; Giuseppe Scotti [Italie] ; Fabio Triulzi [Italie]	Demonstration of acute ischemic lesions in the fetal brain by diffusion magnetic resonance imaging
002C38 (2002)	Eli Hershkovitz [Israël] ; Ginat Narkis [Israël] ; Zamir Shorer [Israël] ; Ann B. Moser [États-Unis] ; Paul A. Watkins [États-Unis] ; Hugo W. Moser [États-Unis] ; Esther Manor [Israël]	Cerebral X‐linked adrenoleukodystrophy in a girl with Xq27‐Ter deletion
002C55 (2002)	Jan-Willem Taanman [Royaume-Uni] ; Ihab Kateeb [Israël] ; Ania C. Muntau [Allemagne] ; Michaela Jaksch [Allemagne] ; Nadine Cohen [Israël] ; Hanna Mandel [Israël]	A novel mutation in the deoxyguanosine kinase gene causing depletion of mitochondrial DNA
003234 (1995)	Guochuan Tsai [États-Unis] ; Joseph T. Coyle [États-Unis]	N -Acetylaspartate in neuropsychiatric disorders

---

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/StressCovidV1/Data/Main/Exploration

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/Teeft.i -k "Multiple system atrophy" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Exploration/Teeft.i  \
                -Sk "Multiple system atrophy" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Exploration/biblio.hfd 

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    StressCovidV1
   |flux=    Main
   |étape=   Exploration
   |type=    indexItem
   |index=    Teeft.i
   |clé=    Multiple system atrophy
}}

---

This area was generated with Dilib version V0.6.33. Data generation: Wed May 6 16:44:09 2020. Site generation: Sun Mar 28 08:26:57 2021