Dale J Lange

Summary

Affiliation: Mount Sinai School of Medicine
Country: USA

Publications

  1. pmc A ketogenic diet as a potential novel therapeutic intervention in amyotrophic lateral sclerosis
    Zhong Zhao
    Neuroinflammation Research Laboratories, Department of Psychiatry, USA
    BMC Neurosci 7:29. 2006
  2. ncbi request reprint Single-fiber electromyography shows terminal axon dysfunction in Miller Fisher syndrome: a case report
    Dale J Lange
    Department of Neurology, Mt Sinai School of Medicine, One Gustave L Levy Place, Box 1052, New York, New York 10029, USA
    Muscle Nerve 34:232-4. 2006
  3. ncbi request reprint High-frequency chest wall oscillation in ALS: an exploratory randomized, controlled trial
    D J Lange
    Department of Neurology, Mt Sinai School of Medicine, One Gustave L Levy Place, Box 1052, New York, NY 10029, USA
    Neurology 67:991-7. 2006
  4. ncbi request reprint Multifocal motor neuropathy with conduction block: slow but not benign
    Dale J Lange
    Department of Neurology, Mt Sinai School of Medicine, New York, NY 10029, USA
    Arch Neurol 63:1778-81. 2006
  5. doi request reprint Do A-waves help predict intravenous immunoglobulin response in multifocal motor neuropathy without block?
    Dale J Lange
    Department of Neurology, Division of Neuromuscular Disease, Mount Sinai School of Medicine, New York, New York, USA
    Muscle Nerve 43:537-42. 2011
  6. doi request reprint Pyrimethamine decreases levels of SOD1 in leukocytes and cerebrospinal fluid of ALS patients: a phase I pilot study
    Dale J Lange
    Department of Neurology, Hospital for Special Surgery, New York, NY 10021, USA
    Amyotroph Lateral Scler Frontotemporal Degener 14:199-204. 2013
  7. doi request reprint Diagnostic biopsy of the pronator teres and a motor branch of the median nerve: indications and technique
    Christopher J Dy
    Division of Hand and Upper Extremity Surgery, Department of Neurology, Hospital for Special Surgery, New York, NY, USA
    J Hand Surg Am 37:2570-5. 2012
  8. doi request reprint REM behavior disorder associated with familial amyotrophic lateral sclerosis
    Matthew R Ebben
    Weill Medical College of Cornell University, Hospital for Special Surgery, New York, NY 10065, USA
    Amyotroph Lateral Scler 13:473-4. 2012
  9. doi request reprint Differential gene expression in patients with amyotrophic lateral sclerosis
    Alexander Shtilbans
    Department of Neurology, Mount Sinai School of Medicine, New York, NY, USA
    Amyotroph Lateral Scler 12:250-6. 2011
  10. doi request reprint ALSFRS and appel ALS scores: discordance with disease progression
    Andrei Voustianiouk
    Department of Neurology and the MDA ALS Center, Mount Sinai School of Medicine, One Gustave L Levy Place, Box 1052, New York, New York 10029, USA
    Muscle Nerve 37:668-72. 2008

Collaborators

Detail Information

Publications13

  1. pmc A ketogenic diet as a potential novel therapeutic intervention in amyotrophic lateral sclerosis
    Zhong Zhao
    Neuroinflammation Research Laboratories, Department of Psychiatry, USA
    BMC Neurosci 7:29. 2006
    ..The cause of neuronal death in amyotrophic lateral sclerosis (ALS) is uncertain but mitochondrial dysfunction may play an important role. Ketones promote mitochondrial energy production and membrane stabilization...
  2. ncbi request reprint Single-fiber electromyography shows terminal axon dysfunction in Miller Fisher syndrome: a case report
    Dale J Lange
    Department of Neurology, Mt Sinai School of Medicine, One Gustave L Levy Place, Box 1052, New York, New York 10029, USA
    Muscle Nerve 34:232-4. 2006
    ..Clinical symptoms gradually resolved. SFEMG may help characterize neuropathies associated with antibodies to neuronal ganglioside and identify involvement of the terminal axon and neuromuscular junction...
  3. ncbi request reprint High-frequency chest wall oscillation in ALS: an exploratory randomized, controlled trial
    D J Lange
    Department of Neurology, Mt Sinai School of Medicine, One Gustave L Levy Place, Box 1052, New York, NY 10029, USA
    Neurology 67:991-7. 2006
    ..To evaluate changes in respiratory function in patients with ALS after using high-frequency chest wall oscillation (HFCWO)...
  4. ncbi request reprint Multifocal motor neuropathy with conduction block: slow but not benign
    Dale J Lange
    Department of Neurology, Mt Sinai School of Medicine, New York, NY 10029, USA
    Arch Neurol 63:1778-81. 2006
    ..To describe a patient with multifocal motor neuropathy with conduction block who had annual clinical and physiological examinations for 18 years but declined treatment for personal reasons...
  5. doi request reprint Do A-waves help predict intravenous immunoglobulin response in multifocal motor neuropathy without block?
    Dale J Lange
    Department of Neurology, Division of Neuromuscular Disease, Mount Sinai School of Medicine, New York, New York, USA
    Muscle Nerve 43:537-42. 2011
    ..Are there electrophysiological findings that predict response to intravenous immunoglobulin (IVIg) in patients with lower motor neuron (LMN) syndromes without multifocal conduction block (MCB)?..
  6. doi request reprint Pyrimethamine decreases levels of SOD1 in leukocytes and cerebrospinal fluid of ALS patients: a phase I pilot study
    Dale J Lange
    Department of Neurology, Hospital for Special Surgery, New York, NY 10021, USA
    Amyotroph Lateral Scler Frontotemporal Degener 14:199-204. 2013
    ..Thus, PYR use may be associated with a reduction in SOD1 in ALS patients. The significance is uncertain and further detailed study is required...
  7. doi request reprint Diagnostic biopsy of the pronator teres and a motor branch of the median nerve: indications and technique
    Christopher J Dy
    Division of Hand and Upper Extremity Surgery, Department of Neurology, Hospital for Special Surgery, New York, NY, USA
    J Hand Surg Am 37:2570-5. 2012
    ..We describe a surgical technique and clinical series of biopsy of the pronator teres muscle and a motor branch of the median nerve...
  8. doi request reprint REM behavior disorder associated with familial amyotrophic lateral sclerosis
    Matthew R Ebben
    Weill Medical College of Cornell University, Hospital for Special Surgery, New York, NY 10065, USA
    Amyotroph Lateral Scler 13:473-4. 2012
    ..We hope this case study will promote future studies on the prevalence of this association and will stimulate research in identifying the underlying pathogenic mechanism...
  9. doi request reprint Differential gene expression in patients with amyotrophic lateral sclerosis
    Alexander Shtilbans
    Department of Neurology, Mount Sinai School of Medicine, New York, NY, USA
    Amyotroph Lateral Scler 12:250-6. 2011
    ..In conclusion, there is differential tissue-specific gene expression in patients with ALS relative to MMN and controls. Further studies are necessary to evaluate the identified genes in larger patient groups and different tissues...
  10. doi request reprint ALSFRS and appel ALS scores: discordance with disease progression
    Andrei Voustianiouk
    Department of Neurology and the MDA ALS Center, Mount Sinai School of Medicine, One Gustave L Levy Place, Box 1052, New York, New York 10029, USA
    Muscle Nerve 37:668-72. 2008
    ..001). Questionnaire-based measurements should be compared against objective scales at all stages of disease severity before they are accepted as primary endpoint measures...
  11. pmc Vgf is a novel biomarker associated with muscle weakness in amyotrophic lateral sclerosis (ALS), with a potential role in disease pathogenesis
    Zhong Zhao
    James J Peters Veterans Affairs Medical Center, Bronx, NY 10468, USA
    Int J Med Sci 5:92-9. 2008
    ....
  12. ncbi request reprint Measures of dyspnea in patients with amyotrophic lateral sclerosis
    Noah Lechtzin
    Department of Medicine, Division of Pulmonary and Critical Care, Johns Hopkins University School of Medicine, 1830 E Monument Street, 5th Floor, Baltimore, Maryland 21205, USA
    Muscle Nerve 35:98-102. 2007
    ..The BDI and TDI thus appear to be useful measures in ALS and may have both clinical and research applications...
  13. pmc Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery
    Katrina Gwinn
    National Institute for Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America
    PLoS ONE 2:e1254. 2007
    ..This resource should facilitate genetic discoveries which we anticipate will ultimately provide a better understanding of the biological mechanisms of neurodegeneration in ALS...