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郭弘周 醫師

神經肌肉疾病、感染性神經疾病、粒腺體疾病、紫質症

教職 : 副教授

醫師網路掛號

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語言

  • 國語,英語

現職

  • 林口長庚紀念醫院神經肌肉疾病科主任
  • 林口長庚紀念醫院神經內科副教授級主治醫師

學歷

  • 高雄醫學院醫學系學士

經歷

  • 林口長庚紀念醫院神經內科主治醫師
  • 林口長庚紀念醫院神經內科住院醫師

論文及期刊發表

  • Reappraisal of the incidence, various types and risk factors of malignancies in patients with dermatomyositis and polymyositis in Taiwan.
  • Differences in Clinical Presentation of Behavioral and Psychological Symptoms of Dementia in Alzheimer's Disease According to Sex and Education Level.
  • Serum levels of cell adhesion molecules in patients with neuromyelitis optica spectrum disorder.
  • Granulocyte Colony Stimulating Factor (GCSF) Can Attenuate Neuropathic Pain by Suppressing Monocyte Chemoattractant Protein-1 (MCP-1) Expression, through Upregulating the Early MicroRNA-122 Expression in the Dorsal Root Ganglia.
  • Diabetic Distal Symmetrical Polyneuropathy: Correlation of Clinical, Laboratory, and Electrophysiologic Studies in Patients with Type 2 Diabetes Mellitus.
  • Clinical Presentations and Outcome Studies of Cranial Nerve Involvement in Herpes Zoster Infection: A Retrospective Single-Center Analysis.
  • A Hybrid Fuzzy Clustering Approach for the Recognition and Visualization of MRI Images of Parkinson's Disease.
  • Sensor-based detection of abnormal events for elderly people using deep belief networks.
  • Clinical, neuroimaging, and nerve conduction characteristics of spontaneous Conus Medullaris infarction.
  • A Fuzzy Approach to Determining Critical Factors of Diabetic Retinopathy and Enhancing Data Classification Accuracy.
  • Correlation between visual association memory test and structural changes in patients with Alzheimer's disease and amnestic mild cognitive impairment.
  • A comparison between spinal cord infarction and neuromyelitis optica spectrum disorders: Clinical and MRI studies.
  • A metabolomic approach to identifying biomarkers in blood of Alzheimer's disease.
  • Predictive Factors for Early Initiation of Artificial Feeding in Patients With Sporadic Creutzfeldt-Jakob Disease.
  • Genetic and functional characters of GRN p.T487I mutation in Taiwanese patients with atypical parkinsonian disorders.
  • Validation and evaluation of two porphobilinogen deaminase activity assays for diagnosis of acute intermittent porphyria.
  • Elevated serum levels of endothelin-1 in patients with chronic inflammatory demyelinating polyneuropathy.
  • Health Symptom Checking System for Elderly People Using Fuzzy Analytic Hierarchy Process.
  • A prospective, observational study of patients with uncommon distal symmetric painful small-fiber neuropathy.
  • Dual-phase 18F-florbetapir positron emission tomography in patients with primary progressive aphasia, Alzheimer's disease, and healthy controls: A preliminary study.
  • Phenotypic expressions of hereditary Transthyretin Ala97Ser related Amyloidosis (ATTR) in Taiwanese.
  • Disturbance of Plasma Lipid Metabolic Profile in Guillain-Barre Syndrome.
  • Non-alcoholic Wernicke's encephalopathy with cortical involvement and polyneuropathy following gastrectomy
  • Peripheral neuropathy in limbic encephalitis with anti-glutamate receptor antibodies
  • Dual-phase 18F-florbetapir positron emission tomography in patients with primary progressive aphasia, Alzheimer's disease, and healthy controls: A preliminary study
  • Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease
  • Correlations between biophysical dysfunctions and clinical phenotypes of GJB1 mutations
  • Clinical and Electrodiagnostic Characteristics of nitrous oxide-induced neuropathy in Taiwan
  • Porphyric neuropathies in an acute intermittent porphyria family
  • Reply to "Demyelinating Neuropathy in Genetically-Confirmed Acute Intermittent Porphyria" comment to The Clinical Presentation and Electrophysiological Findings of Porphyric Neuropathies"
  • Wegener's granulomatosis with nervous system involvement: a hospital-based study
  • Family caregivers’ role implementation at different stages of dementia
  • High frequency of SPG4 in Taiwanese families with autosomal dominant hereditary spastic paraplegia
  • Effect of coexistent carpal tunnel abnormality on sensory conduction findings in polyneuropathy
  • Cerebrospinal fluid biomarkers for neuropsychological symptoms in early stage of late-onset Alzheimer's disease
  • The clinical presentation and electrophysiological findings of porphyric neuropathies: a follow-up study
  • Clinical and Genetic Analysis of Taiwanese Patients with Hereditary Spastic Paraplegia Type 5
  • Motor Conduction Findings in Fisher Syndrome
  • Distinct features between longitudinally extensive transverse myelitis presenting with and without anti-aquaporin 4 antibodies
  • Rapid progression and brain atrophy in anti-AMPA receptor encephalitis
  • Regional Amyloid Deposition in Amnestic Mild Cognitive Impairment and Alzheimer's Disease Evaluated by [18F]AV-45 Positron Emission Tomography in Chinese Population
  • Sensory Conduction Study in Fisher Syndrome: Patterns of Abnormalities and Their Clinical Correlation
  • Brain fluorodeoxyglucose positron emission tomography( 18 FDG PET) in patients with acute thallium intoxication
  • Use of a Modified Spatial-Context Memory Test to Detect Amnestic Mild Cognitive Impairment
  • Analyses of haptoglobin level in the cerebrospinal fluid and serum of patients with neuromyelitis optica and multiple sclerosis
  • Association between GRN rs5848 polymorphism and Parkinson's disease in Taiwanese population
  • Long-term follow-up of spinal and bulbar muscular atrophy in Taiwan
  • Screening for C9orf72 repeat expansions in parkinsonism syndrome
  • Long-term neurotoxic effects of dimethylamine borane intoxication
  • Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
  • Features of varicella zoster virus myelitis and dependence on immune status