Movement Disorders (revue) - Checkpoint (PubMed)

Index « Mesh.i » - entrée « Aspartic Acid »
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List of bibliographic references

Number of relevant bibliographic references: 25.
[0-20] [0 - 20][0 - 25][20-24][20-40]
Ident.Authors (with country if any)Title
000511 (2014) Jeannie M. Padowski [États-Unis] ; Kurt E. Weaver ; Todd L. Richards ; Mercy Y. Laurino ; Ali Samii ; Elizabeth H. Aylward ; Kevin E. ConleyNeurochemical correlates of caudate atrophy in Huntington's disease.
000643 (2014) Fu-Bo Cheng [République populaire de Chine] ; Jia-Chun Feng ; Ling-Yan Ma ; Jing Miao ; Thomas Ott ; Xin-Hua Wan ; Kathrin GrundmannCombined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.
000A95 (2013) Malgorzata Marja Ska [États-Unis] ; Stéphane Lehéricy ; Romain Valabrègue ; Traian Popa ; Yulia Worbe ; Margherita Russo ; Edward J. Auerbach ; David Grabli ; Cecilia Bonnet ; Cécile Gallea ; Mathieu Coudert ; Lydia Yahia-Cherif ; Marie Vidailhet ; Sabine MeunierBrain dynamic neurochemical changes in dystonic patients: a magnetic resonance spectroscopy study.
000B66 (2012) Maya Ando [Japon] ; Manabu Funayama ; Yuanzhe Li ; Kenichi Kashihara ; Yoshitake Murakami ; Nobutaka Ishizu ; Chizuko Toyoda ; Katsuhiko Noguchi ; Takashi Hashimoto ; Naoki Nakano ; Ryogen Sasaki ; Yasumasa Kokubo ; Shigeki Kuzuhara ; Kotaro Ogaki ; Chikara Yamashita ; Hiroyo Yoshino ; Taku Hatano ; Hiroyuki Tomiyama ; Nobutaka HattoriVPS35 mutation in Japanese patients with typical Parkinson's disease.
000C37 (2012) Maddalena Ruggieri ; Claudia Serpino ; Edmondo Ceci ; Vittorio Sciruicchio ; Giovanni Franco ; Carmela Pica ; Maria Trojano ; Paolo Livrea ; Marina De TommasoSerum levels of N-acetylaspartate in Huntington's disease: preliminary results.
000F19 (2012) Paul G. Unschuld [États-Unis] ; Richard A E. Edden ; Aaron Carass ; Xinyang Liu ; Megan Shanahan ; Xin Wang ; Kenichi Oishi ; Jason Brandt ; Susan S. Bassett ; Graham W. Redgrave ; Russell L. Margolis ; Peter C M. Van Zijl ; Peter B. Barker ; Christopher A. RossBrain metabolite alterations and cognitive dysfunction in early Huntington's disease.
000F43 (2012) Simon J G. Lewis [Australie] ; James M. Shine ; Shantel Duffy ; Glenda Halliday ; Sharon L. NaismithAnterior cingulate integrity: executive and neuropsychiatric features in Parkinson's disease.
001392 (2011) Thilo Herzfeld ; Rudolf Korinthenberg ; Ulrich MüllerD216H polymorphism within TOR1A does not affect penetrance in DRD and is not a general modifier in primary dystonia.
001441 (2011) Yuhei Takado [Japon] ; Hironaka Igarashi ; Kenshi Terajima ; Takayoshi Shimohata ; Tetsutaro Ozawa ; Kouichirou Okamoto ; Masatoyo Nishizawa ; Tsutomu NakadaBrainstem metabolites in multiple system atrophy of cerebellar type: 3.0-T magnetic resonance spectroscopy study.
001757 (2010) Gülin Oz [États-Unis] ; Diane Hutter ; Ivan Tkác ; H Brent Clark ; Myron D. Gross ; Hong Jiang ; Lynn E. Eberly ; Khalaf O. Bushara ; Christopher M. GomezNeurochemical alterations in spinocerebellar ataxia type 1 and their correlations with clinical status.
001B34 (2009) Mélissa Yana Frédéric [France] ; Fabienne Clot ; Arnaud Blanchard ; Claire-Marie Dhaenens ; Gaëtan Lesca ; Laura Cif ; Alexandra Dürr ; Marie Vidailhet ; Bernard Sablonniere ; Alain Calender ; Maria Martinez ; Nicolas Molinari ; Alexis Brice ; Mireille Claustres ; Sylvie Tuffery-Giraud ; Gwenaëlle Collod-BeroudThe p.Asp216His TOR1A allele effect is not found in the French population.
001B98 (2009) Hiroshi Kataoka ; Josep Dalmau ; Toshiaki Taoka ; Satoshi UenoReduced N-acetylaspartate in the basal ganglia of a patient with anti-NMDA receptor encephalitis.
001C64 (2009) Yih-Ru Wu ; Chiung-Mei Chen ; Chih-Ying Chao ; Ron-Kuo Lyu ; Guey-Jen Lee-ChenPantothenate kinase-associated neurodegeneration in two Taiwanese siblings: identification of a novel PANK2 gene mutation.
002226 (2008) Norman C. Reynolds [États-Unis] ; Robert W. Prost ; Leighton P. Mark ; Suja A. JosephMR-spectroscopic findings in juvenile-onset Huntington's disease.
002227 (2008) Beata Tarnacka [Pologne] ; Wojciech Szeszkowski ; Marek Golebiowski ; Anna CzlonkowskaMR spectroscopy in monitoring the treatment of Wilson's disease patients.
002249 (2008) W R Wayne Martin [Canada] ; Marguerite Wieler ; Myrlene Gee ; Christopher C. Hanstock ; Richard M. CamicioliIntact presupplementary motor area function in early, untreated Parkinson's disease.
002770 (2007) Claudio Lucetti [Italie] ; Paulo Del Dotto ; Gianna Gambaccini ; Roberto Ceravolo ; Chiara Logi ; Caterina Berti ; Giuseppe Rossi ; Maria Cristina Bianchi ; Michela Tosetti ; Luigi Murri ; Ubaldo BonuccelliInfluences of dopaminergic treatment on motor cortex in Parkinson disease: a MRI/MRS study.
002825 (2007) Heloísa H. Ruocco [Brésil] ; Iscia Lopes-Cendes ; Li M. Li ; Fernando CendesEvidence of thalamic dysfunction in Huntington disease by proton magnetic resonance spectroscopy.
003008 (2005) Lorraine N. Clark [États-Unis] ; Angelique Nicolai ; Shehla Afridi ; Juliette Harris ; Helen Mejia-Santana ; Lisa Strug ; Lucien J. Cote ; Elan D. Louis ; Howard Andrews ; Cheryl Waters ; Blair Ford ; Steven Frucht ; Stanley Fahn ; Richard Mayeux ; Ruth Ottman ; K. MarderPilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicity.
003035 (2005) Yu-Hu Zhang [République populaire de Chine] ; Bei-Sha Tang ; Ai-Ling Zhao ; Kun Xia ; Zhi-Gao Long ; Ji-Feng Guo ; Shawn K. Westaway ; Susan J. HayflickNovel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase-associated neurodegeneration.
003737 (2003) Marina A J. Tijssen [Pays-Bas] ; Peter Brown ; David Macmanus ; Mary A. Mclean ; Charles DavieMagnetic resonance spectroscopy of cerebral cortex is normal in hereditary hyperekplexia due to mutations in the GLRA1 gene.

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