Keywords
Curation
Ncbi
Racine
Curation
Checkpoint
Ncbi
Racine
Ncbi
Exploration
Accueil
Racine
Racine

Movement Disorders (revue) - Curation (Ncbi)

Index « Keywords » - entrée « Lod Score »
Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.
Locus Coeruleus (physiopathology) < Lod Score < Logic  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 15.
Ident.Authors (with country if any)Title
000350 (2000) A. Münchau [Royaume-Uni] ; E M Valente ; M B Davis ; V. Stinton ; N W Wood ; N P Quinn ; K P BhatiaA Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.
000366 (2000) S N Illarioshkin [Russie] ; I A Ivanova-Smolenskaya ; R A Rahmonov ; E D Markova ; G. Stevanin ; A. BriceClinical and genetic study of familial essential tremor in an isolate of Northern Tajikistan.
000517 (2001) S. Bohlega [Arabie saoudite] ; A. Al-Tahan ; M. Kambouris ; M. DivakaranNeurodegenerative Huntington-like disorder.
000606 (2001) A R Bentivoglio [Italie] ; P. Cortelli ; E M Valente ; T. Ialongo ; A. Ferraris ; A. Elia ; P. Montagna ; A. AlbanesePhenotypic characterisation of autosomal recessive PARK6-linked parkinsonism in three unrelated Italian families.
000736 (2002) Francesco Brancati [Italie] ; Giovanni Defazio ; Viviana Caputo ; Enza Maria Valente ; Antonio Pizzuti ; Paolo Livrea ; Alfredo Berardelli ; Bruno DallapiccolaNovel Italian family supports clinical and genetic heterogeneity of primary adult-onset torsion dystonia.
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. WoodGenetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.
001416 (2006) Juliane Winkelmann [Allemagne] ; Peter Lichtner ; Benno Pütz ; Claudia Trenkwalder ; Stephanie Hauk ; Thomas Meitinger ; Tim Strom ; Bertram Muller-MyhsokEvidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
001445 (2006) Susanna Adel [Allemagne] ; Ana Djarmati ; Kemal Kabakci ; Irene Pichler ; Cordula Eskelson ; Thora Lohnau ; Norman Kock ; Johann Hagenah ; Katja Hedrich ; Eberhard Schwinger ; Patricia L. Kramer ; Peter P. Pramstaller ; Christine KleinCo-occurrence of restless legs syndrome and Parkin mutations in two families.
001713 (2006) Shaochun Ma [États-Unis] ; Thomas L. Davis ; Marcia A. Blair ; John Y. Fang ; Yuki Bradford ; Jonathan L. Haines ; Peter HederaFamilial essential tremor with apparent autosomal dominant inheritance: should we also consider other inheritance modes?
001F81 (2008) Amir Boukhris [Tunisie] ; Imed Feki ; Elodie Denis ; Mohamed Imed Miladi ; Alexis Brice ; Chokri Mhiri ; Giovanni StevaninSpastic paraplegia 15: linkage and clinical description of three Tunisian families.
002388 (2009) Anastasia Levchenko [Canada] ; Jacques-Yves Montplaisir ; Géraldine Asselin ; Sylvie Provost ; Simon L. Girard ; Lan Xiong ; Emmanuelle Lemyre ; Judith St-Onge ; Pascale Thibodeau ; Alex Desautels ; Gustavo Turecki ; Claudia Gaspar ; Marie-Pierre Dubé ; Guy A. RouleauAutosomal-dominant locus for Restless Legs Syndrome in French-Canadians on chromosome 16p12.1.
002C32 (2010) Anne Weissbach [Allemagne] ; Ana Djarmati ; Christine Klein ; Natasa Dragasevi ; Christine Zühlke ; Aleksandar Rakovi ; Miodrag Guzvi ; Elisabeth Butz ; Holger Tönnies ; Reiner Siebert ; Igor Petrovi ; Marina Svetel ; Vladimir S. Kosti ; Katja LohmannPossible genetic heterogeneity of spinocerebellar ataxia linked to chromosome 15.
002D12 (2010) Antonetta M G. Sas [Pays-Bas] ; Alessio Di Fonzo ; Stef L M. Bakker ; Erik J. Simons ; Ben A. Oostra ; Anneke J. Maat-Kievit ; Agnita J W. Boon ; Vincenzo BonifatiAutosomal dominant restless legs syndrome maps to chromosome 20p13 (RLS-5) in a Dutch kindred.
004970 (1993) D. Conway [Royaume-Uni] ; P G Bain ; T T Warner ; M B Davis ; L J Findley ; P D Thompson ; C D Marsden ; A E HardingLinkage analysis with chromosome 9 markers in hereditary essential tremor.
005084 (1998) J J Higgins [États-Unis] ; J M Loveless ; Joseph Jankovic [États-Unis] ; P I PatelEvidence that a gene for essential tremor maps to chromosome 2p in four families.

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Wicri/Santé/explor/MovDisordV3/Data/Ncbi/Curation

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Curation/KwdEn.i -k "Lod Score" 

HfdIndexSelect -h $EXPLOR_AREA/Data/Ncbi/Curation/KwdEn.i  \
                -Sk "Lod Score" \
         | HfdSelect -Kh $EXPLOR_AREA/Data/Ncbi/Curation/biblio.hfd

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Wicri/Santé
   |area=    MovDisordV3
   |flux=    Ncbi
   |étape=   Curation
   |type=    indexItem
   |index=    KwdEn.i
   |clé=    Lod Score
}}
Wicri

This area was generated with Dilib version V0.6.23.
Data generation: Sun Jul 3 12:29:32 2016. Site generation: Wed Feb 14 10:52:30 2024