hereditaria < hereditary < heritability

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List of bibliographic references indexed by hereditary

Number of relevant bibliographic references: 62.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000167 (2015)	Dahlia Kancheva [Belgique] ; Teodora Chamova [Bulgarie] ; Velina Guergueltcheva [Bulgarie] ; Vanio Mitev [Bulgarie] ; Dimitar N. Azmanov [Australie] ; Luba Kalaydjieva [Australie] ; Ivailo Tournev [Bulgarie] ; Albena Jordanova [Belgique]	Mosaic dominant TUBB4A mutation in an inbred family with complicated hereditary spastic paraplegia.
000339 (2015)	Kishore Raj Kumar [Australie] ; Victor S C. Fung [Australie]	ADCY5 identified as a novel cause of benign hereditary chorea.
001511 (2011)	Li Cao [République populaire de Chine] ; Qing-Zhou Fei [République populaire de Chine] ; Wei-Guo Tang ; Jian-Rong Liu [République populaire de Chine] ; Lan Zheng [République populaire de Chine] ; Qin Xiao [République populaire de Chine] ; Song-Bin He ; Yi Fu [République populaire de Chine] ; Sheng-Di Chen [République populaire de Chine]	Novel mutations in the CYP7B1 gene cause hereditary spastic paraplegia
001513 (2011)	Arianna Guidubaldi [Italie] ; Carla Piano [Italie] ; Filippo M. Santorelli [Italie] ; Gabriella Silvestri [Italie] ; Martina Petracca [Italie] ; Alessandra Tessa [Italie] ; Anna Rita Bentivoglio [Italie]	Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early‐onset levodopa‐responsive Parkinsonism
001524 (2011)	Susanne A. Schneider [Allemagne]	NBIA due to FA2H gene mutations is allelic with hereditary spastic paraplegia (SPG35) and a form of familial leukodystrophy
001668 (2011)	Melissa J. Armstrong [Canada] ; Binit B. Shah [Canada] ; Robert Chen [Canada] ; Michael J. Angel [Canada] ; Anthony E. Lang [Canada]	Expanding the phenomenology of benign hereditary chorea: Evolution from chorea to myoclonus and dystonia
001999 (2010)	Thomas Duning [Allemagne] ; Tobias Warnecke [Allemagne] ; Anja Schirmacher [Allemagne] ; Hagen Schiffbauer [Allemagne] ; Hubertus Lohmann [Allemagne] ; Siawoosh Mohammadi [Allemagne] ; Peter Young [Allemagne] ; Michael Deppe [Allemagne]	Specific pattern of early white‐matter changes in pure hereditary spastic paraplegia
001C56 (2010)	Sui H. Wong [Royaume-Uni] ; Malcolm J. Steiger [Royaume-Uni] ; Andrew J. Larner [Royaume-Uni] ; Nicholas A. Fletcher [Royaume-Uni]	Hereditary myoclonus dystonia (DYT11): A novel SGCE gene mutation with intrafamilial phenotypic heterogeneity
001D38 (2010)	Francis O. Walker [États-Unis]	Does hereditary hemochromatosis influence the age of onset of Huntington's disease?
001E32 (2010)	Elena Salvatore [Italie] ; Luigi Di Maio [Italie] ; Alessandro Filla [Italie] ; Alfonso M. Ferrara [Italie] ; Carlo Rinaldi [Italie] ; Francesco Saccà [Italie] ; Silvio Peluso [Italie] ; Paolo E. Macchia [Italie] ; Sabina Pappatà [Italie] ; Giuseppe De Michele [Italie]	Benign hereditary chorea: Clinical and neuroimaging features in an Italian family
001E63 (2010)	Gloria Maccabelli [Italie] ; Anna Pichiecchio [Italie] ; Andrea Guala [Italie] ; Michela Ponzio [Italie] ; Fulvia Palesi [Italie] ; Diego Maranzana Rt [Italie] ; Guy Umberto Poloni [Italie] ; Stefano Bastianello [Italie] ; Cesare Danesino [Italie]	Advanced magnetic resonance imaging in benign hereditary chorea: Study of two familial cases
002277 (2009)	Christine Klein [Allemagne, Canada] ; Susanne A. Schneider [Allemagne, Royaume-Uni] ; Anthony E. Lang [Canada]	Hereditary parkinsonism: Parkinson disease look‐alikes—An algorithm for clinicians to “PARK” genes and beyond
002397 (2009)	Fabienne Ory-Magne [France] ; Christine Brefel-Courbon [France] ; Pierre Payoux [France] ; Sabrina Debruxelles [France] ; Igor Sibon [France] ; Cyril Goizet [France] ; Pierre Labauge [France] ; Patrice Menegon [France] ; Emmanuelle Uro-Coste [France] ; Bernardino Ghetti [États-Unis] ; Marie Bernadetle Delisle [France] ; Ruben Vidal [États-Unis] ; Olivier Rascol [France]	Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498‐499InsTC)
002475 (2009)	Donald L. Gilbert [États-Unis] ; Elizabeth J. Leslie [États-Unis] ; Mehdi Keddache [États-Unis] ; Nancy D. Leslie [États-Unis]	A novel hereditary spastic paraplegia with dystonia linked to chromosome 2q24‐2q31
002482 (2009)	Patric Blomstedt [Suède] ; Marwan I. Hariz [Suède, Royaume-Uni] ; Stephen Tisch [Australie] ; Monica Holmberg [Suède] ; Tommy A. Bergenheim [Suède] ; Lars Forsgren [Suède]	A family with a hereditary form of torsion dystonia from Northern Sweden treated with bilateral pallidal deep brain stimulation
002527 (2009)	Fabienne Ory-Magne [France] ; Christine Brefel-Courbon [France] ; Pierre Payoux [France] ; Sabrina Debruxelles [France] ; Igor Sibon [France] ; Cyril Goizet [France] ; Pierre Labauge [France] ; Patrice Menegon [France] ; Emmanuelle Uro-Coste [France] ; Bernardino Ghetti [États-Unis] ; Marie Bernadetle Delisle [France] ; Ruben Vidal [États-Unis] ; Olivier Rascol [France]	Clinical Phenotype and Neuroimaging Findings in a French Family with Hereditary Ferritinopathy (FTL498-499InsTC)
002553 (2008)	Shu-Shan Zhang [République populaire de Chine] ; Qin Chen [République populaire de Chine] ; Xue-Ping Chen [République populaire de Chine] ; Jian-Gang Wang [République populaire de Chine] ; Jean-Marc Burgunder [République populaire de Chine] ; Hui-Fang Shang [République populaire de Chine] ; Jean-Marc Burgunder [Suisse] ; Yuan Yang [République populaire de Chine]	Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum
002664 (2008)	Amir Glik [Israël] ; Isabelle Vuillaume [France] ; David Devos [France] ; Rivka Inzelberg [Israël]	Psychosis, short stature in benign hereditary chorea: A novel thyroid transcription factor‐1 mutation
002972 (2008)	Martin J. Hecht [Allemagne] ; Henning Stolze [Allemagne] ; Matthias Auf Dem Brinke [Allemagne] ; Ralf Giess [Allemagne] ; Thoams Treig [Allemagne] ; Martin Winterholler [Allemagne] ; Jörg Wissel [Allemagne]	Botulinum neurotoxin type A injections reduce spasticity in mild to moderate hereditary spastic paraplegia— Report of 19 cases
002A12 (2008)	Catherine C. S. Delnooz [Pays-Bas] ; Jurgen H. Schelhaas [Pays-Bas] ; Bart P. C. Van De Warrenburg [Pays-Bas] ; Robert-Jan De Graaf [Pays-Bas] ; Gajja S. Salomons [Pays-Bas]	Alexander disease causing hereditary late‐onset ataxia with only minimal white matter changes: A report of two sibs
002C44 (2007)	Marcondes C. França Jr. [Brésil] ; Anelyssa D'Abreu [Brésil] ; Cláudia V. Maurer-Morelli [Brésil] ; Rodrigo Seccolin [Brésil] ; Simone Appenzeller [Brésil] ; Andréia Alessio [Brésil] ; Benito P. Damasceno [Brésil] ; Anamarli Nucci [Brésil] ; Fernando Cendes [Brésil] ; Iscia Lopes-Cendes [Brésil]	Prospective neuroimaging study in hereditary spastic paraplegia with thin corpus callosum

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