Nuclear Pore Complex Proteins < Nuclear Proteins < Nuclear Receptor Subfamily 4, Group A, Member 2

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 72.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000835 (2002)	Johannes Schiefer [Allemagne] ; G Bernhard Landwehrmeyer ; Hans-Gerd Lüesse ; Arne Sprünken ; Christiane Puls ; Anna Milkereit ; Eva Milkereit ; Christoph M. Kosinski	Riluzole prolongs survival time and alters nuclear inclusion formation in a transgenic mouse model of Huntington's disease.
000C07 (2003)	Yoshiki Sekijima [Japon] ; Takao Hashimoto ; Osam Onodera ; Hidetoshi Date ; Tomomi Okano ; Kosuke Naito ; Shoji Tsuji ; Shu-Ichi Ikeda	Severe generalized dystonia as a presentation of a patient with aprataxin gene mutation.
000C97 (2004)	Susan Hollán [Hongrie] ; Lászl Vécsei ; Kálmán Magyar	Adverse effects of dopamine potentiation by long-term treatment with selegiline.
000D40 (2004)	Jürgen Andrich [Allemagne] ; Carsten Saft ; Anneliese Arz ; Birgit Schneider ; Markus W. Agelink ; Peter H. Kraus ; Wilfried Kuhn ; Thomas Müller	Hyperhomocysteinaemia in treated patients with Huntington's disease homocysteine in HD.
000E19 (2004)	Patrice Péran [France] ; Jean-François Démonet ; Cyril Pernet ; Dominique Cardebat	Verb and noun generation tasks in Huntington's disease.
001149 (2005)	Carsten Saft [Allemagne] ; Jochen Zange ; Jürgen Andrich ; Klaus Müller ; Katrin Lindenberg ; Bernhard Landwehrmeyer ; Matthias Vorgerd ; Peter H. Kraus ; Horst Przuntek ; Ludger Schöls	Mitochondrial impairment in patients and asymptomatic mutation carriers of Huntington's disease.
001187 (2005)	William Freeman ; Zbigniew Wszolek	Botulinum toxin type A for treatment of spasticity in spinocerebellar ataxia type 3 (Machado-Joseph disease).
001298 (2005)	Galit Kleiner-Fisman [États-Unis] ; Noel Y. Calingasan ; Mary Putt ; June Chen ; M Flint Beal ; Anthony E. Lang	Alterations of striatal neurons in benign hereditary chorea.
001369 (2005)	John Hardy [États-Unis] ; Andrew J. Lees	Parkinson's disease: a broken nosology.
001622 (2006)	José Berciano [Espagne] ; Jon Infante ; Antonio García ; Carmen De Pablos ; Guillermo Amer ; José Miguel Polo ; Victor Volpini ; Onofre Combarros	Stiff man-like syndrome and generalized myokymia in spinocerebellar ataxia type 3.
001649 (2006)	Marcondes C. França [Brésil] ; Maria E. Calcagnotto ; Jaderson C. Da Costa ; Iscia Lopes-Cendes	Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family.
001782 (2006)	Peter Bauer [Allemagne] ; Friedmar R. Kreuz ; Katrin Bürk ; Carsten Saft ; Jürgen Andrich ; Hubert Heilemann ; Olaf Riess ; Ludger Schöls	Mutations in TITF1 are not relevant to sporadic and familial chorea of unknown cause.
001817 (2006)	Matthias Reimold [Allemagne] ; Christoph Globas ; Marc Gleichmann ; Michael Schulze ; Christian Gerloff ; Roland Bares ; H-J Machulla ; Katrin Bürk	Spinocerebellar ataxia type 1, 2, and 3 and restless legs syndrome: striatal dopamine D2 receptor status investigated by [11C]raclopride positron emission tomography.
001900 (2006)	David Devos [France] ; Isabelle Vuillaume ; Alix De Becdelievre ; Berengère De Martinville ; Claire-Marie Dhaenens ; Jean-Christophe Cuvellier ; Jean-Marie Cuisset ; Louis Vallée ; Marie-Pierre Lemaitre ; Hélène Bourteel ; Eric Hachulla ; Benoit Wallaert ; Alain Destée [France] ; Luc Defebvre [France] ; Bernard Sablonnière	New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genes.
001957 (2007)	Christopher Kenney [États-Unis] ; Suzanne Powell ; Joseph Jankovic [États-Unis]	Autopsy-proven Huntington's disease with 29 trinucleotide repeats.
001979 (2007)	Melissa J. Nirenberg [États-Unis] ; Jenny Libien ; Jean-Paul Vonsattel ; Stanley Fahn	Multiple system atrophy in a patient with the spinocerebellar ataxia 3 gene mutation.
001B64 (2007)	Elisa Alonso [Mexique] ; Leticia Martínez-Ruano ; Irene De Biase ; Christopher Mader ; Adriana Ochoa ; Petra Yescas ; Roxana Gutiérrez ; Misti White ; Luís Ruano ; Marcela Fragoso-Benítez ; Tetsuo Ashizawa ; Sanjay I. Bidichandani ; Astrid Rasmussen	Distinct distribution of autosomal dominant spinocerebellar ataxia in the Mexican population.
001C87 (2007)	Christopher Turner [Royaume-Uni] ; J Mark Cooper ; Anthony H V. Schapira	Clinical correlates of mitochondrial function in Huntington's disease muscle.
001D96 (2007)	Galit Kleiner-Fisman [Canada] ; Anthony E. Lang	Benign hereditary chorea revisited: a journey to understanding.
001D99 (2007)	Friedrich Asmus [Allemagne] ; Anita Devlin ; Marita Munz ; Alexander Zimprich ; Thomas Gasser ; Patrick F. Chinnery	Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.
001E15 (2007)	Eng-King Tan [Singapour] ; Justina Tong ; Ratnagopal Pavanni ; Meng-Cheong Wong ; Yi Zhao	Genetic analysis of SCA 2 and 3 repeat expansions in essential tremor and atypical Parkinsonism.

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