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Abbreviation : FPD
Long Form : familial PD
No. Year Title Co-occurring Abbreviation
2020 Rapid Alpha-Synuclein Toxicity in a Neural Cell Model and Its Rescue by a Stearoyl-CoA Desaturase Inhibitor. alphaS, PD, SCD, YFP
2016 Analysis of the genetic variability in Parkinson's disease from Southern Spain. EOPD, LOPD, PD
2016 Discovery of a frameshift mutation in podocalyxin-like (PODXL) gene, coding for a neural adhesion molecule, as causal for autosomal-recessive juvenile Parkinsonism. AR-JP, PD, PODXL
2016 Is age-related failure of metabolic reprogramming a principal mediator in idiopathic Parkinson's disease? Implications for treatment and inverse cancer risk. IPD, OXPHOS, SNc
2015 Alpha-synuclein A53T mutation is not frequent on a sample of Brazilian Parkinson's disease patients. PD, SNCA, sPD
2014 Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease. ADPD, DLB, GBA, PD
2010 Biochemical and molecular features of LRRK2 and its pathophysiological roles in Parkinson's disease. LRR, LRRK2, PD
2010 New insights into the role of mitochondrial dysfunction and protein aggregation in Parkinson's disease. PD
2009 Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings. PD, PET
10  2009 LRRK2 gene G2019S mutation and SNPs [haplotypes] in subtypes of Parkinson's disease. LRRK2, PD, sPD
11  2007 Animal models of Parkinson's disease: similarities and differences between the disease and models. PD
12  2007 Association of alpha-synuclein gene haplotypes with Parkinson's disease. LD, PD, SNCA, SNPs, sPD
13  2007 [Clinical molecular genetics for PARK8 (LRRK2)]. ADPD, PD
14  2007 [The pathogenesis of Parkinson's disease: a hint from insights of familial Parkinson's disease]. PD
15  2006 Cellular and molecular mechanisms of Parkinson's disease: neurotoxins, causative genes, and inflammatory cytokines. CA, DA, PD, sPD, UPS
16  2004 Axonal transport of human alpha-synuclein slows with aging but is not affected by familial Parkinson's disease-linked mutations. alpha-Syn, hu, LBs, LNs, PD, SC, Tg
17  2004 [The gene products for familial Parkinson's disease provide us hints to elucidate the mechanisms of nigral degeneration]. PD
18  2003 Familial Parkinson's disease: a hint to elucidate the mechanisms of nigral degeneration. PD, UCHL1
19  2002 Association of homozygous 7048G7049 variant in the intron six of Nurr1 gene with Parkinson's disease. MPTP, sPD
20  2000 Clinical and genetic study of familial Parkinson's disease in Tunisia. AD, AR, LD, MG, SG, SR
21  1997 "Familial Parkinson's disease"--a case-control study of families. nfPD, PD