128
Views
15
CrossRef citations to date
0
Altmetric
Case Report

Late-onset Pompe disease with complicated intracranial aneurysm: a Chinese case report

, , , , , & show all
Pages 713-717 | Published online: 29 Mar 2016

References

  • Di RoccoMBuzziDTaroMGlycogen storage disease type II: clinical overviewActa Myol2007261424417915568
  • FukudaTRobertsAPlotzPHRabenNAcid alpha-glucosidase deficiency (Pompe disease)Curr Neurol Neurosci Rep200771717717217857
  • KishnaniPSSteinerRDBaliDPompe disease diagnosis and management guidelineGenet Med20068526728816702877
  • HirschornRReuserAGlycogen storage disease type II: acid alpha glucosidase (acid maltase) deficiencyScriverThe Metabolic and Molecular Bases of Inherited DiseaseNew YorkMcGraw-Hill200133893420
  • SchullerAWenningerSStrigl-PillNSchoserBToward deconstructing the phenotype of late-onset Pompe diseaseAm J Med Genet C Semin Med Genet2012160C1808822253010
  • PericSFumicKBilicKReuserARakocevic StojanovicVRupture of the middle cerebral artery aneurysm as a presenting symptom of late-onset Pompe disease in an adult with a novel GAA gene mutationActa Neurol Belg2014114216516624338761
  • RefaiDLevRCrossDTShimonyJSLeonardJRThrombotic complications of a basilar artery aneurysm in a young adult with Pompe diseaseSurg Neurol200870551852018207222
  • SacconiSBocquetJDChanaletSTanantVSalviatiLDesnuelleCAbnormalities of cerebral arteries are frequent in patients with late-onset Pompe diseaseJ Neurol2010257101730173320559845
  • MatsuokaYSendaYHirayamaMMatsuiTTakahashiALate-onset acid maltase deficiency associated with intracranial aneurysmJ Neurol198823563713733139844
  • KretzschmarHAWagnerHHubnerGDanekAWittTNMehraeinPAneurysms and vacuolar degeneration of cerebral arteries in late-onset acid maltase deficiencyJ Neurol Sci1990982–31691832243227
  • MiyamotoYEtohYJohRNodaKOhyaIMorimatsuMAdult-onset acid maltase deficiency in siblingsActa Pathol Jpn1985356153315423937437
  • MakosMMMcCombRDHartMNBennettDRAlpha-glucosidase deficiency and basilar artery aneurysm: report of a sibshipAnn Neurol19872256296333322184
  • BijvoetAGVan HirtumHVermeyMPathological features of glycogen storage disease type II highlighted in the knockout mouse modelJ Pathol1999189341642410547605
  • RabenNTakikitaSPittisMGDeconstructing Pompe disease by analyzing single muscle fibers: to see a world in a grain of sandAutophagy20073654655217592248
  • NascimbeniACFaninMMasieroEAngeliniCSandriMThe role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)Cell Death Differ201219101698170822595755
  • BraunsdorfWEFusiform aneurysm of basilar artery and ectatic internal carotid arteries associated with glycogenosis type2 (Pompe’s disease)Neurosurgery19872157487493480453
  • LaforetPPetiotPNicolinoMDilative arteriopathy and basilar artery dolichoectasia complicating late-onset Pompe diseaseNeurology200870222063206618505979