Induced Pluripotent Stem Cells < Infant < Infant, Newborn

Facettes :

List of bibliographic references

Number of relevant bibliographic references: 69.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000423 (2014)	Claudia Dufke [Allemagne] ; Marc Sturm ; Christopher Schroeder ; Susanne Moll ; Thomas Ott ; Olaf Riess ; Peter Bauer ; Kathrin Grundmann	Screening of mutations in GNAL in sporadic dystonia patients.
000512 (2014)	Yael Hacohen [Royaume-Uni] ; Kumaran Deiva ; Phillipa Pettingill ; Patrick Waters ; Ata Siddiqui ; Pascale Chretien ; Esse Menson ; Jean-Pierre Lin ; Marc Tardieu ; Angela Vincent ; Ming J. Lim	N-methyl-D-aspartate receptor antibodies in post-herpes simplex virus encephalitis neurological relapse.
000520 (2014)	Shekeeb S. Mohammad [Australie] ; Victor S C. Fung ; Padraic Grattan-Smith ; Deepak Gill ; Sekhar Pillai ; Sudarshini Ramanathan ; Fabienne Brilot ; Russell C. Dale	Movement disorders in children with anti-NMDAR encephalitis and other autoimmune encephalopathies.
000570 (2014)	Rachel Saunders-Pullman [États-Unis] ; Tania Fuchs ; Marta San Luciano ; Deborah Raymond ; Alison Brashear ; Robert Ortega ; Andres Deik ; Laurie J. Ozelius ; Susan B. Bressman	Heterogeneity in primary dystonia: lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
000571 (2014)	Shekeeb S. Mohammad [Australie] ; Kate Sinclair ; Sekhar Pillai ; Vera Merheb ; Tim D. Aumann ; Deepak Gill ; Russell C. Dale ; Fabienne Brilot	Herpes simplex encephalitis relapse with chorea is associated with autoantibodies to N-Methyl-D-aspartate receptor or dopamine-2 receptor.
000624 (2014)	Valerija Dobri I [Allemagne] ; Nikola Kresojevi ; Ana Westenberger ; Marina Svetel ; Aleksandra Tomi ; Vesna Rali ; Igor Petrovi ; Milica Je Menica Luki ; Katja Lohmann ; Ivana Novakovi ; Christine Klein ; Vladimir S. Kosti	De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient.
000862 (2013)	Hannah M. Tully [États-Unis] ; Jennifer C. Dempsey ; Gisele E. Ishak ; Margaret P. Adam ; Jonathan W. Mink ; William B. Dobyns ; Sidney M. Gospe ; Avery Weiss ; James O. Phillips ; Dan Doherty	Persistent figure-eight and side-to-side head shaking is a marker for rhombencephalosynapsis.
000913 (2013)	Yi-Chun Chen [Taïwan] ; Yun-Shien Lee ; Chen-Chang Shih ; Tony Wu ; Chiung-Mei Chen	Mutations of proline-rich transmembrane protein-2 and paroxysmal kinesigenic dyskinesia in Taiwan.
000947 (2013)	Roser Pons [Grèce] ; Dimitris Syrengelas ; Sotiris Youroukos ; Irene Orfanou ; Arqirios Dinopoulos ; Bru Cormand ; Aida Ormazabal ; Angels Garzía-Cazorla ; Mercedes Serrano ; Rafael Artuch	Levodopa-induced dyskinesias in tyrosine hydroxylase deficiency.
000B84 (2012)	Ainhi D. Ha [Australie] ; Kaitlyn L. Parratt ; Nanna D. Rendtorff ; Marianne Lodahl ; Karl Ng ; Dominic B. Rowe ; Carolyn M. Sue ; Michael W. Hayes ; Lisbeth Tranebjaerg ; Victor S C. Fung	The phenotypic spectrum of dystonia in Mohr-Tranebjaerg syndrome.
001384 (2011)	Aida Ormazabal ; Mercedes Serrano ; Angels Garcia-Cazorla ; Jaume Campistol ; Rafael Artuch ; Pedro Castro De Castro ; Estíbaliz Barredo-Valderrama ; Judith Armstrong ; Claudio Toma ; Bru Cormand	Deletion in the tyrosine hydroxylase gene in a patient with a mild phenotype.
001421 (2011)	Thomas Opladen [Allemagne] ; Georg Hoffmann ; Friederike Hörster ; Anne-B Rbel Hinz ; Katharina Neidhardt ; Christine Klein ; Nicole Wolf	Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia.
001553 (2010)	Roser Pons [Grèce] ; Abbie Collins ; Michael Rotstein ; Kristin Engelstad ; Darryl C. De Vivo	The spectrum of movement disorders in Glut-1 deficiency.
001617 (2010)	Gurusidheshwar M. Wali ; Beat Thony ; Nenad Blau	Sepiapterin reductase deficiency: two Indian siblings with unusual clinical features.
001731 (2010)	Julia Schicks [Allemagne] ; Matthis Synofzik ; Claudia Schulte ; Ludger Schöls	POLG, but not PEO1, is a frequent cause of cerebellar ataxia in Central Europe.
001768 (2010)	Jong Sam Baik [Corée du Sud] ; Myung Sik Lee	Movement disorders associated with moyamoya disease: a report of 4 new cases and a review of literatures.
001825 (2010)	Jan Linder [Suède] ; Hans Stenlund ; Lars Forsgren	Incidence of Parkinson's disease and parkinsonism in northern Sweden: a population-based study.
001869 (2010)	Xin Liu [République populaire de Chine] ; Shu-Shan Zhang ; Deng-Fu Fang ; Ming-Yi Ma ; Xiao-Yan Guo ; Yuan Yang ; Hui-Fang Shang	GCH1 mutation and clinical study of Chinese patients with dopa-responsive dystonia.
001909 (2010)	Hiroshi Sakuma [Japon] ; Yuko Shimizu ; Yoshiaki Saito ; Kenji Sugai ; Masumi Inagaki ; Makiko Kaga ; Masayuki Sasaki	Electrophysiological evidence of cerebral dysfunction in childhood opsoclonus-myoclonus syndrome.
001A30 (2010)	Michael R. Pranzatelli [États-Unis] ; Elizabeth D. Tate ; Jennifer A. Swan ; Anna L. Travelstead ; Jerry A. Colliver ; Steven J. Verhulst ; Carl J. Crosley ; William D. Graf ; Suja A. Joseph ; Howard M. Kelfer ; G Praveen Raju	B cell depletion therapy for new-onset opsoclonus-myoclonus.
001B38 (2009)	Slavko M. Jankovi ; Dragoslav V. Soki ; Nikola M. Vojvodi ; Aleksandar J. Risti ; Vladimir S. Kosti	The first cinematic presentation of a possible rhythmic movement disorder in a Disney film precedes its scientific debut by 60 years.

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