phenomenon < phenotype < phenotypes

Facettes :

List of bibliographic references indexed by phenotype

Number of relevant bibliographic references: 14.

Ident.	Authors (with country if any)	Title
000680 (2010)	Shona Pfeiffer [Irlande (pays)] ; David Mclaughlin [Irlande (pays)]	In vitro differentiation of human amniotic fluid‐derived cells: Augmentation towards a neuronal dopaminergic phenotype
000945 (2009)	Simon P. Brooks [Royaume-Uni] ; Stephen B. Dunnett [Royaume-Uni]	Tests to assess motor phenotype in mice: a user's guide
000A29 (2009)	Anna Członkowska [Pologne] ; Gra Yna Gromadzka [Pologne] ; Grzegorz Chabik [Pologne]	Monozygotic female twins discordant for phenotype of Wilson's disease
000A76 (2009)	Ming-Jen Lee [Taïwan] ; Ignacio F. Mata [États-Unis] ; Chin-Hsien Lin [Taïwan] ; Kai-Yuan Tzen [Taïwan] ; Sarah J. Lincoln [États-Unis] ; Rebecca Bounds [États-Unis] ; Paul J. Lockhart [Australie] ; Mary M. Hulihan [États-Unis] ; Matthew J. Farrer [États-Unis] ; Ruey-Meei Wu [Taïwan]	Genotype–phenotype correlates in Taiwanese patients with early‐onset recessive parkinsonism
000A91 (2009)	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
000C56 (2008)	Renato P. Munhoz [Brésil] ; Yosuke Wakutani [Canada] ; Connie Marras [Canada] ; Helio A. Teive [Brésil] ; Salmo Raskin [Brésil] ; Lineu C. Werneck [Brésil] ; Danielle Moreno [Canada] ; Christine Sato [Canada] ; Anthony E. Lang [Canada] ; Ekaterina Rogaeva [Canada]	The G2019S LRRK2 mutation in Brazilian patients with Parkinson's disease: Phenotype in monozygotic twins
000C78 (2008)	Carola Schiesling ; Nicole Kieper ; Kay Seidel [Allemagne] ; Rejko Krüger	Review: Familial Parkinson's disease – genetics, clinical phenotype and neuropathology in relation to the common sporadic form of the disease
000D07 (2008)	J-P Taylor [Royaume-Uni] ; E N Rowan [Royaume-Uni] ; D. Lett [Royaume-Uni] ; J T O Rien [Royaume-Uni] ; I G Mckeith [Royaume-Uni] ; D J Burn [Royaume-Uni]	Poor attentional function predicts cognitive decline in patients with non-demented Parkinson’s disease independent of motor phenotype
001123 (2007)	B. G. H. Schoser ; J. Müller-Höcker ; R. Horvath ; K. Gempel [Allemagne] ; D. Pongratz ; H. Lochmüller ; W. Müller-Felber	Adult‐onset glycogen storage disease type 2: clinico‐pathological phenotype revisited
001337 (2006)	Liesl M. Allcock [Royaume-Uni] ; Rose Anne Kenny [Royaume-Uni] ; David J. Burn [Royaume-Uni]	Clinical phenotype of subjects with Parkinson's disease and orthostatic hypotension: Autonomic symptom and demographic comparison
001528 (2005)	S. Papapetropoulos [États-Unis] ; A. Lieberman [États-Unis] ; J. Gonzalez [États-Unis] ; D. C. Mash [États-Unis]	Can Alzheimer's type pathology influence the clinical phenotype of Parkinson's disease?
001761 (2003)	Hideo Mori [Japon] ; Nobutaka Hattori [Japon] ; Yoshikuni Mizuno [Japon]	Genotype–phenotype correlation: Familial Parkinson disease
001A94 (2001)	S. Papapetropoulos ; C. Paschalis ; A. Athanassiadou ; A. Papadimitriou ; J. Ellul ; M H Polymeropoulos ; Th Papapetropoulos	Clinical phenotype in patients with α-synuclein Parkinson's disease living in Greece in comparison with patients with sporadic Parkinson's disease
001B91 (2000)	Christine Klein [États-Unis, Allemagne] ; Peter P. Pramstaller [Italie] ; Bernhard Kis [Allemagne, Italie] ; Curtis C. Page [États-Unis] ; Martin Kann [États-Unis] ; Joanne Leung [États-Unis] ; Heather Woodward [États-Unis] ; Claudio C. Castellan [Italie] ; Monika Scherer [Italie] ; Peter Vieregge [Allemagne] ; Xandra O. Breakefield [États-Unis] ; Patricia L. Kramer [États-Unis] ; Laurie J. Ozelius [États-Unis]	Parkin deletions in a family with adult‐onset, tremor‐dominant parkinsonism: Expanding the phenotype

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