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羅榮昇 醫師

神經遺傳性疾病、多發性硬化症、病態性神經疼痛、頭痛、肌肉病變、重症肌無力症、一般神經疾病

教職 : 教授

醫師網路掛號

※直接點選進入醫師網路掛號畫面※

語言

  • 國語,英語,閩南語

現職

  • 林口長庚紀念醫院神經內科部部主任
  • 林口長庚紀念醫院神經內科教授級主治醫師
  • 台灣神經免疫醫學會 理事長
  • 台灣神經學會 監事

學歷

  • 英國倫敦大學醫學博士
  • 中山醫學院醫學系學士

經歷

  • 台灣神經學會 秘書長、理事及監事
  • 林口長庚紀念醫院神經內科系系主任
  • 林口長庚紀念醫院神經內科系副系主任
  • 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主治醫師

學會與認證

  • 台灣神經免疫醫學會
  • 台灣神經學學會
  • 臺灣醫學會
  • 神經科專科醫師證書
  • 神經重症專科醫師證書

論文及期刊發表

  • Correlations among disability, anti-AQP4 antibody status and prognosis in the spinal cord involved patients with NMOSD.
  • Epidemiology, treatment patterns and healthcare utilizations in multiple sclerosis in Taiwan.
  • The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.
  • Reappraisal of the Prognostic Factors of Outcome and Recovery Time in Patients with Idiopathic Bell's Palsy: A Retrospective Single-Center Analysis.
  • Reappraisal of the incidence, various types and risk factors of malignancies in patients with dermatomyositis and polymyositis in Taiwan.
  • Real-world evidence on the safety and effectiveness of fingolimod in patients with multiple sclerosis from Taiwan.
  • 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.
  • CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan.
  • Clinical and cytokine profile of adult acute necrotizing encephalopathy.
  • Development and validation of a Taiwan version of the DN4-T questionnaire.
  • Differences in Pain Intensity of Tumors Spread to the Anterior versus Anterolateral/Lateral Portions of the Vertebral Body Based on CT Scans.
  • A prospective, observational study on conversion of clinically isolated syndrome to multiple sclerosis during 4-year period (MS NEO study) in Taiwan.
  • A comparison between spinal cord infarction and neuromyelitis optica spectrum disorders: Clinical and MRI studies.
  • Genetic Analysis of Hereditary Transthyretin Ala97Ser Related Amyloidosis.
  • Validation and evaluation of two porphobilinogen deaminase activity assays for diagnosis of acute intermittent porphyria.
  • Development and validation of a Taiwan version of the ID Pain questionnaire (ID Pain-T).
  • Elevated serum levels of endothelin-1 in patients with chronic inflammatory demyelinating polyneuropathy.
  • A prospective, observational study of patients with uncommon distal symmetric painful small-fiber neuropathy.
  • 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
  • Increased serum concentrations of transforming growth factor-β1 (TGF-β1) in patients with Guillain-Barre syndrome
  • Correlations of clinical, neuroimaging, and electrophysiological features in Hirayama disease
  • An early granulocyte colony-stimulating factor treatment attenuates neuropathic pain through activation of mu opioid receptors on the injured nerve
  • Targeting the prodromal stage of spinocerebellar ataxia type 17 mice: G-CSF in the prevention of motor deficits via upregulating chaperone and autophagy levels
  • Porphyric neuropathies in an acute intermittent porphyria family
  • Wegener's Granulomatosis with Nervous System Involvement: A Hospital-Based Study
  • Clinical and radiological findings suggesting disorders other than tolosa-hunt syndrome among ophthalmoplegic patients: a retrospective analysis
  • Biomarkers for neuromyelitis optica
  • Comparison between the cranial magnetic resonance imaging features of neuromyelitis optica spectrum disorder versus multiple sclerosis in Taiwanese patients
  • Clinical correlations of motor and somatosensory evoked potentials in neuromyelitis optica
  • Deactivation of TBP contributes to SCA17 pathogenesis
  • The clinical presentation and electrophysiological findings of porphyric neuropathies: a follow-up study
  • Painful ophthalmoplegia with normal cranial imaging
  • Motor Conduction Findings in Fisher Syndrome
  • SLC1A2 Variant Is Associated with Essential Tremor in Taiwanese Population
  • Long-term follow-up of spinal and bulbar muscular atrophy in Taiwan
  • Association between PARK16 and Parkinson's disease in the Han Chinese population: a meta-analysis
  • Treatment of neuropathic pain in acute intermittent porphyria with gabapentin
  • Sensory Conduction Study in Fisher Syndrome: Patterns of Abnormalities and Their Clinical Correlation
  • A comparison of benign and inflammatory manifestations of Tolosa-Hunt syndrome
  • Analyses of haptoglobin level in the cerebrospinal fluid and serum of patients with neuromyelitis optica and multiple sclerosis
  • Pulmonary hypertension in a child with mitochondrial A3243G point mutation
  • Prognosis of symptomatic patients with the A3243G mutation of mitochondrial DNA
  • Early Systemic Granulocyte-Colony Stimulating Factor Treatment Attenuates Neuropathic Pain after Peripheral Nerve Injury
  • Distinct features between longitudinally extensive transverse myelitis presenting with and without anti-aquaporin 4 antibodies
  • Indomethacin protects rats from neuronal damage induced by traumatic brain injury and suppresses hippocampal IL-1β release through the inhibition of Nogo-A expression
  • Features of varicella zoster virus myelitis and dependence on immune status
  • Seizures and multiple sclerosis in Chinese patients: A clinical and magnetic resonance imaging study
  • Pulmonary hypertension in a child with mitochondrial A3243G point mutation
  • Identification of gene networks and pathways associated with Guillain-Barre syndrome
  • Peripheral Microcirculation Dysfunction evaluated by computed tomography perfusion study in Fabry patients