Molecular imaging in hereditary forms of parkinsonism
暂无分享,去创建一个
R. Bressan | A. Felício | M. Shih | H. B. Ferraz | L. D. de Andrade | C. Godeiro-Junior | C. de Oliveira Godeiro-Junior | P. de Carvalho Aguiar | L. A. F. D. Andrade | H. Ferraz | P. Aguiar
[1] Houeto Jean-Luc. [Parkinson's disease]. , 2022, La Revue du praticien.
[2] E. Amaro,et al. Higher nigrostriatal dopamine neuron loss in early than late onset Parkinson's disease?—A [99mTc]‐TRODAT‐1 SPECT study , 2007, Movement disorders : official journal of the Movement Disorder Society.
[3] S. Tufik,et al. Neuroimagem do transportador de dopamina na doença de Parkinson: primeiro estudo com [99mTc]-TRODAT-1 e SPECT no Brasil , 2006 .
[4] A. Antonini,et al. Striatal dopamine transporter binding in Parkinson's disease associated with the LRRK2 Gly2019Ser mutation , 2006, Movement disorders : official journal of the Movement Disorder Society.
[5] N. Quinn,et al. Upregulation of dopamine D2 receptors in dopaminergic drug‐naive patients with parkin gene mutations , 2006, Movement disorders : official journal of the Movement Disorder Society.
[6] M. Toft,et al. Parkinson's disease: the genetics of a heterogeneous disorder , 2006, European journal of neurology.
[7] R. Bressan,et al. Parkinson's disease and dopamine transporter neuroimaging: a critical review. , 2006, Sao Paulo medical journal = Revista paulista de medicina.
[8] Anette Schrag,et al. Epidemiological, clinical, and genetic characteristics of early-onset parkinsonism , 2006, The Lancet Neurology.
[9] Michele T. M. Hu,et al. Nigral degeneration and striatal dopaminergic dysfunction in idiopathic and parkin‐linked Parkinson's disease , 2006, Movement disorders : official journal of the Movement Disorder Society.
[10] Andrew B West,et al. Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[11] Vesna Sossi,et al. PET in LRRK2 mutations: comparison to sporadic Parkinson's disease and evidence for presymptomatic compensation. , 2005, Brain : a journal of neurology.
[12] A. Singleton,et al. Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data. , 2005, Brain : a journal of neurology.
[13] D. Grosset,et al. The role of radiotracer imaging in Parkinson disease , 2005, Neurology.
[14] N. Wood,et al. Molecular genetic pathways in Parkinson's disease: a review. , 2005, Clinical science.
[15] P. Tienari,et al. How useful is [123I]β-CIT SPECT in clinical practice? , 2005, Journal of Neurology, Neurosurgery & Psychiatry.
[16] Andrew B West,et al. Molecular pathophysiology of Parkinson's disease. , 2005, Annual review of neuroscience.
[17] C. Klein,et al. Early-onset parkinsonism associated with PINK1 mutations: Frequency, genotypes, and phenotypes , 2005, Neurology.
[18] Juha O. Rinne,et al. Cortical 6-[18F]fluoro-l-dopa uptake and frontal cognitive functions in early Parkinson's disease , 2005, Neurobiology of Aging.
[19] S. Przedborski. Pathogenesis of nigral cell death in Parkinson's disease. , 2005, Parkinsonism & related disorders.
[20] Y. Hsin,et al. Early-onset Parkinson's disease in a Chinese population: 99mTc-TRODAT-1 SPECT, Parkin gene analysis and clinical study. , 2005, Parkinsonism & related disorders.
[21] K. Kessler,et al. Dopaminergic function in a family with the PARK6 form of autosomal recessive Parkinson’s syndrome , 2005, Journal of Neural Transmission.
[22] Janel O. Johnson,et al. Clinical and positron emission tomography of Parkinson's disease caused by LRRK2 , 2005, Annals of neurology.
[23] Deborah B. Goldberg. Somatoform Disorders: A Medicolegal Guide , 2005 .
[24] Nicholas W Wood,et al. A common LRRK2 mutation in idiopathic Parkinson's disease , 2005, The Lancet.
[25] D. Brooks,et al. Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation , 2005, Neurology.
[26] Andrew Lees,et al. Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease , 2004, Neuron.
[27] Thomas Meitinger,et al. Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology , 2004, Neuron.
[28] N. Hattori,et al. PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations , 2004, Neurology.
[29] R. Krüger,et al. Novel homozygous p.E64D mutation in DJ1 in early onset Parkinson disease (PARK7) , 2004, Human mutation.
[30] A. Bentivoglio,et al. PINK1 mutations are associated with sporadic early‐onset parkinsonism , 2004, Annals of neurology.
[31] Richard S. Frackowiak,et al. PET and SPECT functional imaging studies in Parkinsonian syndromes: from the lesion to its consequences , 2004, NeuroImage.
[32] P. Piccini. Neurodegenerative movement disorders: the contribution of functional imaging , 2004, Current opinion in neurology.
[33] Mark A. Wilson,et al. The Parkinson's disease protein DJ-1 is neuroprotective due to cysteine-sulfinic acid-driven mitochondrial localization , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[34] Nicola Pavese,et al. Striatal and cortical pre- and postsynaptic dopaminergic dysfunction in sporadic parkin-linked parkinsonism. , 2004, Brain : a journal of neurology.
[35] R. Nussbaum,et al. Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1 , 2004, Science.
[36] A. Antonini,et al. PET and SPECT functional imaging in Parkinson's disease. , 2004, Sleep medicine.
[37] J. Hoenicka,et al. The new mutation, E46K, of α‐synuclein causes parkinson and Lewy body dementia , 2004, Annals of neurology.
[38] W. Oertel,et al. Role of dopamine transporter SPECT for the practitioner and the general neurologist , 2003, Movement disorders : official journal of the Movement Disorder Society.
[39] Vladimir N Uversky,et al. A Protein-Chameleon: Conformational Plasticity of α-Synuclein, a Disordered Protein Involved in Neurodegenerative Disorders , 2003, Journal of biomolecular structure & dynamics.
[40] K. Leenders. Significance of non‐presynaptic SPECT tracer methods in Parkinson's disease , 2003, Movement disorders : official journal of the Movement Disorder Society.
[41] Alexandra Durr,et al. How much phenotypic variation can be attributed to parkin genotype? , 2003, Annals of neurology.
[42] C. V. van Duijn,et al. Parkinson's disease: piecing together a genetic jigsaw. , 2003, Brain : a journal of neurology.
[43] Vincenzo Bonifati,et al. Clinical features and neuroimaging of PARK7‐linked parkinsonism , 2003, Movement disorders : official journal of the Movement Disorder Society.
[44] Nicolas Costes,et al. Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography study. , 2003, Archives of neurology.
[45] Paola Piccini,et al. Clinical and subclinical dopaminergic dysfunction in PARK6‐linked parkinsonism: An 18F‐dopa PET study , 2002, Annals of neurology.
[46] C. Nahmias. Molecular imaging: the next frontier. , 2002, Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes.
[47] Patrizia Rizzu,et al. Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism , 2002, Science.
[48] Nicola Pavese,et al. Progression of nigrostriatal dysfunction in a parkin kindred: an [18F]dopa PET and clinical study. , 2002, Brain : a journal of neurology.
[49] F. Fazio,et al. Striatal dopaminergic denervation in early and late onset Parkinson's disease assessed by PET and the tracer [11C]FECIT: preliminary findings in one patient with autosomal recessive parkinsonism (Park2) , 2002, Neurological Sciences.
[50] R. Marconi,et al. Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7 , 2002, Neurological Sciences.
[51] Karl Herholz,et al. The striatal dopaminergic deficit is dependent on the number of mutant alleles in a family with mutations in the parkin gene: evidence for enzymatic parkin function in humans , 2002, Neuroscience Letters.
[52] C. Goetz,et al. Parkin mutations in a patient with hemiparkinsonism–hemiatrophy: A clinical–genetic and PET study , 2002, Neurology.
[53] J. Seibyl,et al. [123I]β-CIT SPECT imaging assessment of the rate of Parkinson’s disease progression , 2001, Neurology.
[54] J. Houwing-Duistermaat,et al. Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36. , 2001, American journal of human genetics.
[55] D. Dickson,et al. Alpha-synuclein and the Lewy body disorders. , 2001, Current opinion in neurology.
[56] Merja Haaparanta,et al. Rate of progression in Parkinson's disease: A 6‐[18F]fluoro‐L‐dopa PET study , 2001, Movement disorders : official journal of the Movement Disorder Society.
[57] K L Leenders,et al. The nigrostriatal dopaminergic system in familial early onset parkinsonism with parkin mutations , 2001, Neurology.
[58] N. Hattori,et al. An apparently sporadic case with parkin gene mutation in a Korean woman. , 2001, Archives of neurology.
[59] R. P. Maguire,et al. Familial parkinsonism with synuclein pathology: Clinical and PET studies of A30P mutation carriers , 2001 .
[60] W D Heiss,et al. Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial Parkinsonism associated with mutations in the Parkin gene , 2001, Annals of neurology.
[61] A Dürr,et al. [18F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations , 2000, Neurology.
[62] N. Hattori,et al. Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification , 2000, Brain and Development.
[63] Shinsei Minoshima,et al. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase , 2000, Nature Genetics.
[64] Bonifati,et al. Association between early-onset Parkinson's disease and mutations in the parkin gene. , 2000, The New England journal of medicine.
[65] Heidi Phillips,et al. Mice Lacking α-Synuclein Display Functional Deficits in the Nigrostriatal Dopamine System , 2000, Neuron.
[66] Vesna Sossi,et al. Prevalence of epilepsy in rural Bolivia , 1999, Neurology.
[67] T. Hosoya,et al. Evaluation of the substantia nigra in patients with Parkinsonian syndrome accomplished using multishot diffusion-weighted MR imaging. , 1999, AJNR. American journal of neuroradiology.
[68] S. Minoshima,et al. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism , 1998, Nature.
[69] Robert L. Nussbaum,et al. Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease , 1997 .
[70] M. Polymeropoulos,et al. Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23 , 1996, Science.
[71] J. Hughes,et al. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. , 1992, Journal of neurology, neurosurgery, and psychiatry.
[72] B. Snow. Positron Emission Tomography in Parkinson’s Disease , 1992, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.
[73] S. Kish,et al. Uneven pattern of dopamine loss in the striatum of patients with idiopathic Parkinson's disease. Pathophysiologic and clinical implications. , 1988, The New England journal of medicine.
[74] C Nahmias,et al. Cerebral Metabolism of 6–[18F]Fluoro‐l‐3,4‐Dihydroxyphenylalanine in the Primate , 1987, Journal of neurochemistry.
[75] J. Degroot,et al. Magnetic resonance imaging of the midbrain in Parkinson's disease , 1986, Annals of neurology.
[76] E. Amaro,et al. [Neuroimaging of the dopamine transporter in Parkinsons disease: first study using [99mTc]-TRODAT-1 and SPECT in Brazil]. , 2006, Arquivos de neuro-psiquiatria.
[77] R A Koeppe,et al. Imaging the vesicular monoamine transporter. , 2001, Advances in neurology.
[78] V Sossi,et al. PET studies of parkinsonism associated with mutation in the alpha-synuclein gene. , 1999, Neurology.
[79] R. Krüger,et al. Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease. , 1998, Nature genetics.