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
000079 (1999)	J M Errea [Espagne] ; J R Ara ; C. Aibar ; J. De Pedro-Cuesta	Prevalence of Parkinson's disease in lower Aragon, Spain.
000087 (1999)	S. Nagamitsu [Japon] ; T. Matsuishi ; K. Hashimoto ; Y. Yamashita ; M. Aihara ; K. Shimizu ; M. Mizuguchi ; H. Iwamoto ; S. Saitoh ; Y. Hirano ; H. Kato ; Y. Fukuyama ; M. Shimada	Multicenter study of paroxysmal dyskinesias in Japan--clinical and pedigree analysis.
000094 (1999)	S. Frucht [États-Unis] ; S. Fahn	Paroxysmal kinesigenic dyskinesia in infancy.
000280 (2000)	P E Greene [États-Unis] ; S B Bressman ; B. Ford ; K. Hyland	Parkinsonism, dystonia, and hemiatrophy.
000418 (2000)	M A Koning-Tijssen [Pays-Bas] ; O F Brouwer	Hyperekplexia in the first year of life.
000590 (2001)	E D Louis [États-Unis] ; L S Dure ; S. Pullman	Essential tremor in childhood: a series of nineteen cases.
000729 (2002)	Padraic J. Grattan-Smith [Australie] ; Ron A. Wevers ; Gerry C. Steenbergen-Spanjers ; Victor S C. Fung ; John Earl ; Bridget Wilcken	Tyrosine hydroxylase deficiency: clinical manifestations of catecholamine insufficiency in infancy.
000748 (2002)	Michele De Mari ; Angelo Zenzola ; Paolo Lamberti	Antiparkinsonian treatment in pregnancy.
000831 (2002)	Sian D. Spacey [Royaume-Uni] ; Enza-Maria Valente ; Gurusidheshwar M. Wali ; Thomas T. Warner ; Paul R. Jarman ; Anthony H V. Schapira ; Peter H. Dixon ; Mary B. Davis ; Kailash P. Bhatia ; Nicholas W. Wood	Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
000964 (2002)	Michael R. Pranzatelli [États-Unis] ; Elizabeth D. Tate ; Marcel Kinsbourne ; Verne S. Caviness ; Bibhuti Mishra	Forty-one year follow-up of childhood-onset opsoclonus-myoclonus-ataxia: cerebellar atrophy, multiphasic relapses, and response to IVIG.
000A85 (2003)	Anjan Chatterjee [États-Unis] ; Steven J. Frucht	Tetrabenazine in the treatment of severe pediatric chorea.
000C06 (2003)	Shinichi Matsumoto [Japon] ; Masataka Nishimura ; Hiroshi Shibasaki ; Ryuji Kaji	Epidemiology of primary dystonias in Japan: comparison with Western countries.
000C85 (2004)	Madhavi Thomas [États-Unis] ; Susan J. Hayflick ; Joseph Jankovic [États-Unis]	Clinical heterogeneity of neurodegeneration with brain iron accumulation (Hallervorden-Spatz syndrome) and pantothenate kinase-associated neurodegeneration.
000E66 (2004)	Michael R. Pranzatelli [États-Unis] ; Anna L. Travelstead ; Elizabeth D. Tate ; Tyler J. Allison ; Steven J. Verhulst	CSF B-cell expansion in opsoclonus-myoclonus syndrome: a biomarker of disease activity.
001023 (2005)	Nicte I. Mejia [États-Unis] ; Joseph Jankovic [États-Unis]	Metoclopramide-induced tardive dyskinesia in an infant.
001256 (2005)	Michael H. Pourfar [États-Unis] ; Renzo Guerrini ; Dominique Parain ; Steven J. Frucht	Classification conundrums in paroxysmal dyskinesias: a new subtype or variations on classic themes?
001269 (2005)	Giovanna Zorzi [Italie] ; Carlo Marras ; Nardo Nardocci ; Angelo Franzini ; Luisa Chiapparini ; Elio Maccagnano ; Lucia Angelini ; Dario Caldiroli ; Giovanni Broggi	Stimulation of the globus pallidus internus for childhood-onset dystonia.
001327 (2005)	Daniel M. Huse [États-Unis] ; Kathy Schulman ; Lucinda Orsini ; Jane Castelli-Haley ; Sean Kennedy ; Gregory Lenhart	Burden of illness in Parkinson's disease.
001438 (2006)	Emmanuel Roze [Suisse] ; Marie Vidailhet ; Nenad Blau ; Lisbeth Birk Moller ; Diane Doummar ; Thierry Billette De Villemeur ; Anne Roubergue	Long-term follow-up and adult outcome of 6-pyruvoyl-tetrahydropterin synthase deficiency.
001515 (2006)	Giacomo Della Marca [Italie] ; Marco Rubino ; Catello Vollono ; Isabella Vasta ; Emanuele Scarano ; Paolo Mariotti ; Alessandro Cianfoni ; Gioacchino Francesco Mennuni ; Pietro Tonali ; Giuseppe Zampino	Rhythmic tongue movements during sleep: a peculiar parasomnia in Costello syndrome.
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.

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