Related references
Note: Only part of the references are listed.Pilot trial on the efficacy and safety of pantethine in children with pantothenate kinase-associated neurodegeneration: a single-arm, open-label study
Xuting Chang et al.
ORPHANET JOURNAL OF RARE DISEASES (2020)
Novel PANK2 mutation in a Chinese boy with PANK2-associated neurodegeneration A case report and review of Chinese cases
Yingying Zhang et al.
MEDICINE (2019)
Novel PANK2 mutation discovered among South East Asian children living in Thailand affected with pantothenate kinase associated neurodegeneration
Kullasate Sakpichaisakul et al.
JOURNAL OF CLINICAL NEUROSCIENCE (2019)
Incidence of PKAN determined by bioinformatic and population-based analysis of ∼140,000 humans
Daniel Brezavar et al.
MOLECULAR GENETICS AND METABOLISM (2019)
Continuous Positive Airway Pressure Therapy in a Patient with Pantothenate-Kinase-Associated Neurodegeneration
Hyung Seok Guk et al.
JOURNAL OF CLINICAL NEUROLOGY (2019)
A variation in PANK2 gene is causing Pantothenate kinase-associated Neurodegeneration in a family from Jammu and Kashmir - India
Arshia Angural et al.
SCIENTIFIC REPORTS (2017)
Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports
Hassan Dastsooz et al.
BMC MEDICAL GENETICS (2017)
Clinical Heterogeneity of Atypical Pantothenate Kinase-Associated Neurodegeneration in Koreans
Jae-Hyeok Lee et al.
JOURNAL OF MOVEMENT DISORDERS (2016)
Novel gene mutations and clinical features in patients with pantothenate kinase-associated neurodegeneration
L. -Y. Ma et al.
CLINICAL GENETICS (2015)
Metabolism and energy requirements in pantothenate kinase-associated neurodegeneration
Sarah Williams et al.
MOLECULAR GENETICS AND METABOLISM (2013)
PANK2 and C19orf12 mutations are common causes of neurodegeneration with brain iron accumulation
Mitra Ansari Dezfouli et al.
MOVEMENT DISORDERS (2013)
Pantothenate kinase-associated neurodegeneration is not a synucleinopathy
A. Li et al.
NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY (2013)
Compartmentalization of Mammalian Pantothenate Kinases
Adolfo Alfonso-Pecchio et al.
PLOS ONE (2012)
Young-Onset Parkinsonism in a Hong Kong Chinese Man With Adult-Onset Hallervorden-Spatz Syndrome
Chloe Miu Mak et al.
INTERNATIONAL JOURNAL OF NEUROSCIENCE (2011)
Low prevalence of PANK2 mutations in Brazilian patients with early onset generalised dystonia and basal ganglia abnormalities on MRI
S. T. Camargos et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)
Pantothenate Kinase-Associated Neurodegeneration: Novel Mutations in the PANK2 Gene in an Argentinean Young Woman
Emilia Gatto
MOVEMENT DISORDERS (2010)
A Novel PANK2 Mutation in a Patient with Atypical Pantothenate-Kinase-Associated Neurodegeneration Presenting with Adult-Onset Parkinsonism
Joo-Hyun Seo et al.
JOURNAL OF CLINICAL NEUROLOGY (2009)
Pantothenate Kinase-Associated Neurodegeneration in Two Taiwanese Siblings: Identification of a Novel PANK2 Gene Mutation
Yih-Ru Wu et al.
MOVEMENT DISORDERS (2009)
Clinical and genetic delineation of neurodegeneration with brain iron accumulation
A. Gregory et al.
JOURNAL OF MEDICAL GENETICS (2009)
The diverse phenotype and genotype of pantothenate kinase-associated neurodegeneration
MT Pellecchia et al.
NEUROLOGY (2005)
Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
SJ Hayflick et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)
A novel pantothenate kinase gene (PANK2) is defective in Hallervorden-Spatz syndrome
B Zhou et al.
NATURE GENETICS (2001)
Share Paper
