Pénétrance génique And NotLars Olson

List of bibliographic references

Number of relevant bibliographic references: 11.

Ident.	Authors (with country if any)	Title
000550	Stefano Goldwurm [Italie] ; Sara Tunesi [Italie] ; Silvana Tesei [Italie] ; Michela Zini [Italie] ; Francesca Sironi [Italie] ; Paola Primignani [Italie] ; Corrado Magnani [Italie] ; Gianni Pezzoli [Italie]	Kin-Cohort Analysis of LRRK2-G2019S Penetrance in Parkinson's Disease
000581	Maria Sierra [Espagne] ; Isabel Gonzalez-Aramburu [Espagne] ; Pascual Sanchez-Juan [Espagne] ; Coro Sanchez-Quintana [Espagne] ; Jose Miguel Polo [Espagne] ; Jose Berciano [Espagne] ; Onofre Combarros [Espagne] ; Jon Infante [Espagne]	High Frequency and Reduced Penetrance of LRRK2 G2019S Mutation Among Parkinson's Disease Patients in Cantabria (Spain)
000647	Thilo Herzfeld [Allemagne] ; Rudolf Korinthenberg [Allemagne] ; Ulrich Müller [Allemagne]	D216H Polymorphism Within TOR1A Does Not Affect Penetrance in DRD and is Not a General Modifier in Primary Dystonia
000906	Javier Ruiz-Martinez [Espagne] ; Ana Gorostidi [Espagne] ; Berta Ibanez [Espagne] ; Ainhoa Alzualde [Espagne] ; David Otaegui [Espagne] ; Fermin Moreno [Espagne] ; Adolfo Lopez De Munain [Espagne] ; Alberto Bergareche [Espagne] ; Juan Carlos Gomez-Esteban [Espagne] ; José F. Marti Masso [Espagne]	Penetrance in Parkinson's Disease Related to the LRRK2 R1441G Mutation in the Basque Country (Spain)
000B57	Marta San Luciano [États-Unis] ; Richard B. Lipton [États-Unis] ; CUILING WANG [États-Unis] ; Mindy Katz [États-Unis] ; Molly E. Zimmerman [États-Unis] ; Amy E. Sanders [États-Unis] ; Laurie J. Ozelius [États-Unis] ; Susan B. Bressman [États-Unis] ; Rachel Saunders-Pullman [États-Unis]	Clinical Expression of LRRK2 G2019S Mutations in the Elderly
000E84	Kenya Nishioka [Japon, États-Unis] ; Owen A. Ross [États-Unis] ; Kenji Ishii [Japon] ; Jennifer M. Kachergus [États-Unis] ; Kiichi Ishiwata [Japon] ; Mayumi Kitagawa [Japon] ; Satoshi Kono [Japon] ; Tomokazu Obi [Japon] ; Koichi Mizoguchi [Japon] ; Yuichi Inoue [Japon] ; Hisamasa Imai [Japon] ; Masashi Takanashi [Japon] ; Yoshikuni Mizuno [Japon] ; Matthew J. Farrer [États-Unis] ; Nobutaka Hattori [Japon]	Expanding the Clinical Phenotype of SNCA Duplication Carriers
001C22	Mattia Gambarin [Italie] ; Enza Maria Valente [Italie] ; Paolo Liberini [Italie] ; Giuseppe Barrano [Italie] ; Alberto Bonizzato [Italie] ; Alessandro Padovani [Italie] ; Giuseppe Moretto [Italie] ; Mirta Fiorio [Italie] ; Bruno Dallapiccola [Italie] ; Nicola Smania [Italie] ; Antonio Fiaschi [Italie] ; Michele Tinazzi [Italie]	Atypical phenotypes and clinical variability in a large Italian family with DYT1-primary torsion dystonia
001F60	Antonino Uncini [Italie] ; Maria Vittoria De Angelis [Italie] ; Patrizia Di Fulvio [Italie] ; Michele Ragno [Italie] ; Grazia Annesi [Italie] ; Alessandro Filla [Italie] ; Liborio Stuppia [Italie] ; Domenico Gambi [Italie]	Wide expressivity variation and high but no gender-related penetrance in two dopa-responsive dystonia families with a novel GCH-I mutation
002491	Ruth H. Walker [États-Unis] ; P. Shashidharan [États-Unis]	Developments in the molecular biology of DYT1 dystonia
002B02	Alain Destée [France] ; Isabelle Delalande [France] ; Isabelle Vuillaume [France] ; Susanna Schraen-Maschke [France] ; Luc Defebvre [France] ; Bernard Sablonniere [France]	The first identified French family with dentatorubral-pallidoluysian atrophy
002D12	A. Lazzarini [États-Unis] ; A. S. Walters [États-Unis] ; K. Hickey [États-Unis] ; G. Coccagna [Italie] ; E. Lugaresi [Italie] ; B. L. Ehrenberg [États-Unis] ; D. L. Picchietti [États-Unis] ; M. F. Brin [États-Unis] ; E. S. Stenroos [États-Unis] ; T. Verrico [États-Unis] ; W. G. Johnson [États-Unis]	Studies of penetrance and anticipation in five autosomal-dominant restless legs syndrome pedigrees

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