المؤلفون: Saad M; INSERM U563, CPTP, CHU Purpan, 31024 Toulouse, France., Lesage S, Saint-Pierre A, Corvol JC, Zelenika D, Lambert JC, Vidailhet M, Mellick GD, Lohmann E, Durif F, Pollak P, Damier P, Tison F, Silburn PA, Tzourio C, Forlani S, Loriot MA, Giroud M, Helmer C, Portet F, Amouyel P, Lathrop M, Elbaz A, Durr A, Martinez M, Brice A

مؤلفون مشاركون: French Parkinson's Disease Genetics Study Group

المصدر: Human molecular genetics [Hum Mol Genet] 2011 Feb 01; Vol. 20 (3), pp. 615-27. Date of Electronic Publication: 2010 Nov 17.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE

مواضيع طبية MeSH: ADP-ribosyl Cyclase/*genetics , Antigens, CD/*genetics , Parkinson Disease/*epidemiology , Parkinson Disease/*genetics, Adult ; Aged ; Brain ; Case-Control Studies ; Chromosomes, Human, Pair 12 ; Chromosomes, Human, Pair 4 ; Europe/epidemiology ; Female ; GPI-Linked Proteins/genetics ; Genetic Loci ; Genetic Predisposition to Disease ; Genetic Variation ; Genome-Wide Association Study ; Genotype ; Humans ; Male ; Middle Aged ; Polymorphism, Single Nucleotide ; Risk Factors ; Transcription Factors

المؤلفون: Hariz MI; Department of Neurosurgery, University Hospital of Northern Sweden, Umeå, Sweden. m.hariz@ion.ucl.ac.uk, Krack P, Alesch F, Augustinsson LE, Bosch A, Ekberg R, Johansson F, Johnels B, Meyerson BA, N'Guyen JP, Pinter M, Pollak P, von Raison F, Rehncrona S, Speelman JD, Sydow O, Benabid AL

المصدر: Journal of neurology, neurosurgery, and psychiatry [J Neurol Neurosurg Psychiatry] 2008 Jun; Vol. 79 (6), pp. 694-9. Date of Electronic Publication: 2007 Sep 26.

نوع المنشور: Journal Article; Multicenter Study; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: BMJ Publishing Group Country of Publication: England NLM ID: 2985191R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-330X (Electronic) Linking ISSN: 00223050 NLM ISO Abbreviation: J Neurol Neurosurg Psychiatry Subsets: MEDLINE

مواضيع طبية MeSH: Deep Brain Stimulation*, Parkinsonian Disorders/*therapy , Tremor/*therapy , Ventral Thalamic Nuclei/*physiopathology, Activities of Daily Living/classification ; Adult ; Aged ; Antiparkinson Agents/administration & dosage ; Combined Modality Therapy ; Disability Evaluation ; Disease Progression ; Europe ; Female ; Follow-Up Studies ; Humans ; Male ; Middle Aged ; Neurologic Examination ; Parkinsonian Disorders/physiopathology ; Treatment Outcome ; Tremor/physiopathology

المؤلفون: Lesage S; Institut National de la Santé et de la Recherche Médicale Unité 679, Neurology and Experimental Therapeutics, and Faculté de Médecine, Université Pierre et Marie Curie, 75651 Paris CEDEX 13, France., Janin S, Lohmann E, Leutenegger AL, Leclere L, Viallet F, Pollak P, Durif F, Thobois S, Layet V, Vidailhet M, Agid Y, Dürr A, Brice A, Bonnet AM, Borg M, Broussolle E, Damier P, Destée A, Martinez M, Penet C, Rasco O, Tison F, Tranchan C, Vérin M

مؤلفون مشاركون: French Parkinson's Disease Genetics Study Group

المصدر: Archives of neurology [Arch Neurol] 2007 Mar; Vol. 64 (3), pp. 425-30.

نوع المنشور: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: American Medical Assn Country of Publication: United States NLM ID: 0372436 Publication Model: Print Cited Medium: Print ISSN: 0003-9942 (Print) Linking ISSN: 00039942 NLM ISO Abbreviation: Arch Neurol Subsets: MEDLINE

مواضيع طبية MeSH: Mutation*, Exons/*genetics , Parkinson Disease/*genetics , Protein Serine-Threonine Kinases/*genetics, Adolescent ; Adult ; Aged ; Aged, 80 and over ; DNA Mutational Analysis/methods ; Europe ; Female ; Histidine/genetics ; Humans ; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 ; Male ; Middle Aged ; Serine/genetics ; Threonine/genetics ; Tyrosine/genetics

المؤلفون: Ibáñez P; INSERM U289, Neurologie et thérapeutique expérimentale, Hôpital de la Salpêtrière, Paris, France., Lohmann E, Pollak P, Durif F, Tranchant C, Agid Y, Dürr A, Brice A

مؤلفون مشاركون: French Parkinson's Disease Genetics Study Group

المصدر: Neurology [Neurology] 2004 Jun 08; Vol. 62 (11), pp. 2133-4.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.

بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print Cited Medium: Internet ISSN: 1526-632X (Electronic) Linking ISSN: 00283878 NLM ISO Abbreviation: Neurology Subsets: MEDLINE

مواضيع طبية MeSH: DNA-Binding Proteins/*genetics , Parkinson Disease/*genetics , Transcription Factors/*genetics, Adult ; Age of Onset ; Aged ; Aged, 80 and over ; DNA Mutational Analysis ; Europe/ethnology ; Exons/genetics ; Female ; France/epidemiology ; Genes, Dominant ; Humans ; Male ; Middle Aged ; Nuclear Receptor Subfamily 4, Group A, Member 2 ; Parkinson Disease/epidemiology

المؤلفون: Periquet M; INSERM U289, Hôpital de la Salpêtrière, 75651 Paris, Cedex 13, France., Lücking C, Vaughan J, Bonifati V, Dürr A, De Michele G, Horstink M, Farrer M, Illarioshkin SN, Pollak P, Borg M, Brefel-Courbon C, Denefle P, Meco G, Gasser T, Breteler MM, Wood N, Agid Y, Brice A

مؤلفون مشاركون: French Parkinson's Disease Genetics Study Group. The European Consortium on Genetic Susceptibility in Parkinson's Disease

المصدر: American journal of human genetics [Am J Hum Genet] 2001 Mar; Vol. 68 (3), pp. 617-26. Date of Electronic Publication: 2001 Feb 14.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Print ISSN: 0002-9297 (Print) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE

مواضيع طبية MeSH: Chromosomes, Human, Pair 6* , Exons* , Founder Effect* , Gene Rearrangement* , Mutation*, Ligases/*genetics , Parkinson Disease/*genetics , Parkinsonian Disorders/*genetics , White People/*genetics, Age of Onset ; Chromosome Mapping ; Europe ; Family ; Genes, Recessive ; Genetic Markers ; Humans ; Linkage Disequilibrium ; Microsatellite Repeats/genetics ; Nuclear Family ; Point Mutation ; Sequence Deletion ; Ubiquitin-Protein Ligases