deferiprone < deficiency < deficient

Facettes :

List of bibliographic references indexed by deficiency

Number of relevant bibliographic references: 51.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000496 (2014)	Alberto J. Espay [États-Unis] ; Peter A. Lewitt ; Horacio Kaufmann	Norepinephrine deficiency in Parkinson's disease: the case for noradrenergic enhancement.
000718 (2013)	Mario Mastrangelo ; Caterina Caputi ; Serena Galosi ; Maria Teresa Giannini ; Vincenzo Leuzzi	Transdermal rotigotine in the treatment of aromatic L-amino acid decarboxylase deficiency.
000854 (2013)	Renaud Chambon [France] ; Sandrine Vuillaumier-Barrot ; Nathalie Seta ; Sabrina Wagner ; Catherine Sarret	Partial effectiveness of acetazolamide in a mild form of GLUT1 deficiency: a pediatric observation.
000899 (2013)	Michael C. Kruer [États-Unis] ; Tyler N. Jepperson ; Jill M. Weimer ; Amy Mroch ; Laura Davis-Keppen ; Patricia Crotwell ; Jillian Parboosingh	Mutations in VLDLR associated with ataxia with secondary vitamin E deficiency.
000903 (2013)	Wilhelmina G. Leen [Pays-Bas] ; Leena Mewasingh ; Marcel M. Verbeek ; Erik-Jan Kamsteeg ; Bart P. Van De Warrenburg ; Michel A. Willemsen	Movement disorders in GLUT1 deficiency syndrome respond to the modified Atkins diet.
000908 (2013)	Fadi Alkufri ; Tim Harrower ; Yusof Rahman ; Elaine Hughes ; Helen Mundy ; Jonathan A. Knibb ; John Moriarty ; Stephen Connor ; Michael Samuel	Molybdenum cofactor deficiency presenting with a parkinsonism-dystonia syndrome.
000933 (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.
000B24 (2013)	Daniela Buha [Canada] ; Geneviève Bernard ; Toshiyuki Fukao ; Jean-Claude Décarie ; Sylvain Chouinard ; Grant A. Mitchell	A treatable new cause of chorea: beta-ketothiolase deficiency.
000C34 (2012)	Mercedes Serrano [Espagne] ; M Nica Rebollo ; Christel Depienne ; Agnès Rastetter ; Emilio Fernández-Álvarez ; Jordi Muchart ; Loreto Martorell ; Rafael Artuch ; José A. Obeso ; Belén Pérez-Due As	Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency.
000C84 (2012)	Tetsutaro Ozawa [Japon]	Oligodendroglial dysfunction associated with lactate transport deficiency contributes to neurodegeneration.
000C98 (2012)	Tetsutaro Ozawa [Japon]	Neuronal iron accumulation associated with tau deficiency in parkinsonism.
000F13 (2012)	Stella Gagliardi ; Annalisa Davin ; Ivana Ricca ; Gaetano S. Grieco ; Roberta Zangaglia ; Francesco Pierelli ; Andrea Ghiroldi ; Claudio Pacchetti ; Carlo Casali ; Cristina Cereda	A new GLUT-1 mutation in a family with glucose transporter 1 deficiency syndrome.
000F98 (2012)	Mercedes Serrano [Espagne] ; Monica Rebollo [Espagne] ; Christel Depienne [France] ; Agnes Rastetter [France] ; Emilio Fernandez-Alvarez [Espagne] ; Jordi Muchart [Espagne] ; Loreto Martorell [Espagne] ; Rafael Artuch [Espagne] ; José A. Obeso [Espagne] ; Belén Perez-Duenas [Espagne]	Reversible Generalized Dystonia and Encephalopathy from Thiamine Transporter 2 Deficiency
001233 (2012)	Stella Gagliardi [Italie] ; Annalisa Davin [Italie] ; Ivana Ricca [Italie] ; Gaetano S. Grieco [Italie] ; Roberta Zangaglia [Italie] ; Francesco Pierelli [Italie] ; Andrea Ghiroldi [Italie] ; Claudio Pacchetti [Italie] ; Carlo Casali [Italie] ; Christina Cereda [Italie]	A New GLUT-1 Mutation in a Family with Glucose Transporter 1 Deficiency Syndrome
001545 (2011)	Andrea Cortese [Italie] ; Roberta Zangaglia [Italie] ; Alessando Lozza [Italie] ; Giovanni Piccolo [Italie] ; Claudio Pacchetti [Italie]	Monitoring late complications of zinc treatment in Wilson's disease. Reply to the letter: Copper deficiency in Wilson's disease: An avoidable complication of treatment
001733 (2011)	Andrea Cortese [Italie] ; Roberta Zangaglia [Italie] ; Alessandro Lozza [Italie] ; Giovanni Piccolo [Italie] ; Claudio Pacchetti [Italie]	Copper deficiency in Wilson's disease: Peripheral neuropathy and myelodysplastic syndrome complicating zinc treatment
001734 (2011)	Francisco Pereira Da Silva-Júnior [Brésil] ; Leandro Tavares Lucato [Brésil] ; Alexandre Aluizio Costa Machado [Brésil] ; Egberto Reis Barbosa [Brésil]	Copper deficiency in Wilson's disease: An avoidable complication of treatment
001752 (2011)	Thomas Opladen [Allemagne] ; Georg Hoffmann [Allemagne] ; Friederike Hörster [Allemagne] ; Anne-B Rbel Hinz [Allemagne] ; Katharina Neidhardt [Allemagne] ; Christine Klein [Allemagne] ; Nicole Wolf [Pays-Bas]	Clinical and biochemical characterization of patients with early infantile onset of autosomal recessive GTP cyclohydrolase I deficiency without hyperphenylalaninemia
001923 (2010)	Roser Pons [Grèce] ; Mercedes Serrano [Espagne] ; Aida Ormazabal [Espagne] ; Claudio Toma [Espagne] ; Angels Garcia-Cazorla [Espagne] ; Estela Area [États-Unis] ; Marta Ribasés [Espagne] ; Emmanuel Kanavakis [Grèce] ; Kaliopi Drakaki [Grèce] ; Aristotelis Giannakopoulos [Grèce] ; Irene Orfanou [Grèce] ; Sotiris Youroukos [Grèce] ; Bru Cormand [Espagne] ; Rafael Artuch [Espagne]	Tyrosine hydroxylase deficiency in three Greek patients with a common ancestral mutation
001947 (2010)	Roser Pons [Grèce] ; Abbie Collins [États-Unis] ; Michael Rotstein [États-Unis] ; Kristin Engelstad [États-Unis] ; Darryl C. De Vivo [États-Unis]	The spectrum of movement disorders in Glut‐1 deficiency
001986 (2010)	Peter P. Urban [Allemagne] ; Ingmar Wellach [Allemagne] ; Siegbert Faiss [Allemagne] ; Peter Layer [Allemagne] ; Thorsten Rosenkranz [Allemagne] ; Karl Knop [Allemagne] ; Joachim Weis [Allemagne]	Subacute axonal neuropathy in Parkinson's disease with cobalamin and vitamin B6 deficiency under duodopa therapy

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