Family Characteristics < Family Health < Family Leave

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List of bibliographic references

Number of relevant bibliographic references: 135.
[0-20] [0 - 20][0 - 50][20-40]

Ident.	Authors (with country if any)	Title
000004 (1999)	N. Sabbagh [France] ; A. Brice ; D. Marez ; A. Dürr ; M. Legrand ; J M Lo Guidice ; A. Destée ; Yves Agid [France] ; F. Broly	CYP2D6 polymorphism and Parkinson's disease susceptibility.
000017 (1999)	N. Georgiou [Australie] ; J L Bradshaw ; E. Chiu ; A. Tudor ; L. O'Gorman ; J G Phillips	Differential clinical and motor control function in a pair of monozygotic twins with Huntington's disease.
000021 (1999)	M. Fukuda [Japon] ; O. Hashimoto ; S. Nagakubo ; A. Hata	A family with an atonic variant of paroxysmal kinesigenic choreoathetosis and hypercalcitoninemia.
000078 (1999)	O. Joost [États-Unis] ; C A Taylor ; C A Thomas ; L A Cupples ; M H Saint-Hilaire ; R G Feldman ; C T Baldwin ; R H Myers	Absence of effect of seven functional mutations in the CYP2D6 gene in Parkinson's disease.
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.
000091 (1999)	C. Kamm [Allemagne] ; E. Castelon-Konkiewitz ; M. Naumann ; F. Heinen ; M. Brack ; A. Nebe ; A. Ceballos-Baumann ; T. Gasser	GAG deletion in the DYT1 gene in early limb-onset idiopathic torsion dystonia in Germany.
000C08 (2003)	Takao Hashimoto [Japon] ; Osamu Sasaki ; Kunihiro Yoshida ; Yo-Ichi Takei ; Shu-Ichi Ikeda	Periodic alternating nystagmus and rebound nystagmus in spinocerebellar ataxia type 6.
000F10 (2004)	Giovanni Abbruzzese [Italie] ; Simona Pigullo ; Angelo Schenone ; Emilia Bellone ; Roberta Marchese ; Emilio Di Maria ; Luana Benedetti ; Paola Ciotti ; Lucilla Nobbio ; Vincenzo Bonifati ; Franco Ajmar ; Paola Mandich	Does parkin play a role in the peripheral nervous system? A family report.
000F54 (2005)	Nicola Vanacore [Italie] ; Vincenzo Bonifati ; Giovanni Fabbrini ; Carlo Colosimo ; Giuseppe De Michele ; Roberto Marconi ; Fabrizio Stocchi ; David Nicholl ; Ubaldo Bonuccelli ; Michele De Mari ; Peter Vieregge ; Giuseppe Meco	Case-control study of multiple system atrophy.
001017 (2005)	Giovanni Fabbrini [Italie] ; Francesco Brancati ; Laura Vacca ; Enza Maria Valente ; Andrea Nemeth ; Angela Meesaq ; Nuala Sykes ; Bruno Dallapiccola ; Alfredo Berardelli	A novel family with an unusual early-onset generalized dystonia.
001049 (2005)	Paolo Moretti [États-Unis] ; Peter Hedera ; John Wald ; John Fink	Autosomal recessive primary generalized dystonia in two siblings from a consanguineous family.
001075 (2005)	Aideen Mcinerney-Leo [États-Unis] ; Donald W. Hadley ; Katrina Gwinn-Hardy ; John Hardy	Genetic testing in Parkinson's disease.
001182 (2005)	Anne-Fleur Van Rootselaar [Pays-Bas] ; Ivo N. Van Schaik ; Arn M J M. Van Den Maagdenberg ; Johannes H T M. Koelman ; Petra M C. Callenbach ; Marina A J. Tijssen	Familial cortical myoclonic tremor with epilepsy: a single syndromic classification for a group of pedigrees bearing common features.
001258 (2005)	Antonio Orlacchio [Italie] ; Toshitaka Kawarai ; Fabrizio Gaudiello ; Antonio Totaro ; Orazio Schillaci ; Alessandro Stefani ; Roberto Floris ; Peter H. St George-Hyslop ; Sandro Sorbi ; Giorgio Bernardi	Clinical and genetic study of a large SPG4 Italian family.
001303 (2005)	Akio Ikeda ; Saiko Kurihara ; Hiroshi Shibasaki	Possible anticipation in BAFME: three generations examined in a Japanese family.
001311 (2005)	Denise M. Kay ; Patricia Kramer ; Don Higgins ; Cyrus P. Zabetian ; Haydeh Payami	Escaping Parkinson's disease: a neurologically healthy octogenarian with the LRRK2 G2019S mutation.
001351 (2005)	Matthias Maschke [Allemagne] ; Gary Oehlert ; Ting-Dong Xie ; Susan Perlman ; Sub H. Subramony ; Neeraj Kumar ; Louis J. Ptacek ; Christopher M. Gomez	Clinical feature profile of spinocerebellar ataxia type 1-8 predicts genetically defined subtypes.
001354 (2005)	Eliecer Coto [Espagne] ; Daniel Armenta ; Raúl Espinosa ; Joaquín Argente ; M Nica G. Castro ; Victoria Alvarez	Recessive hyperekplexia due to a new mutation (R100H) in the GLRA1 gene.
001428 (2005)	Jose Miguel Bras [Portugal] ; Rita Joao Guerreiro ; Maria Helena Ribeiro ; Cristina Januario ; Ana Morgadinho ; Catarina Resende Oliveira ; Luis Cunha ; John Hardy ; Andrew Singleton	G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort.
001508 (2006)	William G. Ondo [États-Unis] ; Dejian Lai	Association between restless legs syndrome and essential tremor.
001516 (2006)	Denise M. Kay [États-Unis] ; Cyrus P. Zabetian ; Stewart A. Factor ; John G. Nutt ; Ali Samii ; Alida Griffith ; Tom D. Bird ; Patricia Kramer ; Donald S. Higgins ; Haydeh Payami	Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.

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