402 top medical experts on Metabolic Brain Diseases across 54 countries and 33 U.S. states, including 237 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.

  1. Metabolic Brain Diseases: Acquired or inborn metabolic diseases that produce brain dysfunction or damage. These include primary (i.e., disorders intrinsic to the brain) and secondary (i.e., extracranial) metabolic conditions that adversely affect cerebral function.
  2. Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
  3. Broader Categories (#Experts): Metabolic Diseases (2,945), Brain Diseases (4,643) and Narrower Categories: Central Pontine Myelinolysis (764), Hepatic Encephalopathy (1,857), Inborn Metabolic Brain Diseases (1,358), Kernicterus (490), Marchiafava-Bignami Disease (243), Mitochondrial Encephalomyopathies (1,595), Reye Syndrome (125), Wernicke Encephalopathy (1,452).
  4. Clinical Trials ClinicalTrials.gov : at least 7 including 2 Completed, 4 Recruiting
  5. Synonyms: Central Nervous System Metabolic Disorders,  Metabolic Encephalopathies,  Brain Metabolic Disorders


  

        

                    


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  1. Frontera, Jennifer A   Neurocritical Care   Google Publications
    Department of Neurology, New York University Grossman School of Medicine, New York, NY, USA. .
    Physician 
    Relevant US NIH Grant Funding: $1,378,414 over the last 5 years
    Medical school: Johns Hopkins University School of Medicine (MD, 2000)
    Medicare Accepted; Medicare MIPS (Merit-based Incentive Payment System) rating: 86/100
    Disclosed payments from biomedical company (Alexion Pharmaceuticals, Inc.) in 2021 for $93.31
    Subjects: Brain Diseases, Metabolic; Brain Diseases; COVID-19; Critical Care
    Categories: Methods; Therapy
    Toxic Metabolic Encephalopathy in Hospitalized Patients with COVID-19. (2021)
    Metabolic encephalopathies in the critical care unit. (2012)

  2. Strauss, Kevin A   Pediatrics   Google Publications
    Clinic for Special Children, Strasburg, PA 17579, USA.
    Physician  Clinical Trial 
    Disclosed payments in 2021 from 22 biomedical companies, totalling $10,468.43, including $7,618.48 from  Novartis Gene Therapies, Inc. (fka AveXis, Inc.)
    Subjects: Amino Acid Metabolism, Inborn Errors; Arginine; Brain; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Corpus Striatum
    Categories: Genetics; Metabolism; Drug Therapy; Adverse Effects; Deficiency; Therapeutic Use
    Glutaric acidemia type 1: Treatment and outcome of 168 patients over three decades. (2020)
    Safety, efficacy and physiological actions of a lysine-free, arginine-rich formula to treat glutaryl-CoA dehydrogenase deficiency: focus on cerebral amino acid influx. (2011)

  3. Moritz, Michael L   Transplant Surgery   Google Publications
    Division of Nephrology, Department of Pediatrics, Childrens Hospital of Pittsburgh of UPMC, The University of Pittsburgh School of Medicine, One Childrens Hospital Drive, 4401 Penn Ave, Pittsburgh, PA 15224, USA.
    Physician 
    Medical school: University of Maryland School of Medicine (MD, 1980)
    Medicare Accepted; Medicare MIPS (Merit-based Incentive Payment System) rating: 86.4/100
    Disclosed payments from biomedical company (Alexion Pharmaceuticals, Inc.) in 2021 for $24.9
    Subjects: Brain Diseases, Metabolic; Hyponatremia; Sodium Chloride; Brain; Hypotonic Solutions; Iatrogenic Disease
    Categories: Prevention & Control; Administration & Dosage; Drug Therapy; Adverse Effects; Drug Effects
    New aspects in the pathogenesis, prevention, and treatment of hyponatremic encephalopathy in children. (2010)
    100 cc 3% sodium chloride bolus: a novel treatment for hyponatremic encephalopathy. (2010)

  4. Mullins, Mark E   Neuroradiology  Google Publications
    Department of Radiology and Imaging Sciences, Division of Neuroradiology, Emory University School of Medicine, Atlanta, GA. Top Hospital
    Physician 
    Medical school: Harvard Medical School (MD, 1997)
    Medicare Accepted; Medicare MIPS (Merit-based Incentive Payment System) rating: 85.6/100
    Subjects: Brain Diseases, Metabolic; Basal Ganglia Diseases; Leukoencephalopathies; Magnetic Resonance Imaging; Magnetic Resonance Spectroscopy; Neurotoxicity Syndromes
    Categories: Diagnosis; Methods
    Metabolic white matter diseases and the utility of MR spectroscopy. (2014)
    Imaging of acquired metabolic and toxic disorders of the basal ganglia. (2014)

  5. Kölker, Stefan     Google Publications
    Division of Child Neurology and Metabolic Medicine, Centre for Child and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany.
    Physician  Highly Cited  Highly Published  Clinical Trial  Case Reports 
    Subjects: Brain Diseases, Metabolic; Amino Acid Metabolism, Inborn Errors; Glutaryl-CoA Dehydrogenase; Brain; Lysine; Glutarates
    Categories: Diagnosis; Deficiency; Pathology; Metabolism; Therapy; Complications
    Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. (2017)
    The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. (2015)

  6. Fan, Ke-Qi  Google Publications
    MOE Laboratory of Biosystem Homeostasis and Protection and Life Sciences Institute, Zhejiang University, Hangzhou 310058, China.
    Scientist 
    Subjects: Anxiety; Behavior, Animal; Brain Diseases, Metabolic; Stress, Psychological
    Categories: Metabolism; Physiology
    Stress-Induced Metabolic Disorder in Peripheral CD4 (2019)

  7. Jin, Jin   Google Publications
    MOE Laboratory of Biosystem Homeostasis and Protection and Life Sciences Institute, Zhejiang University, Hangzhou 310058, China; Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou 310016, China. Electronic address: .
    Scientist 
    Subjects: Anxiety; Behavior, Animal; Brain Diseases, Metabolic; Stress, Psychological
    Categories: Metabolism; Physiology
    Stress-Induced Metabolic Disorder in Peripheral CD4 (2019)

  8. Ayus, Juan Carlos   Nephrology  Google Publications
    Physician  Highly Published 
    Subjects: Brain Diseases, Metabolic; Hyponatremia; Critical Illness; Sodium Chloride; Brain; Hypotonic Solutions
    Categories: Prevention & Control; Administration & Dosage; Drug Therapy; Adverse Effects; Complications; Drug Effects
    New aspects in the pathogenesis, prevention, and treatment of hyponatremic encephalopathy in children. (2010)
    100 cc 3% sodium chloride bolus: a novel treatment for hyponatremic encephalopathy. (2010)

  9. Chapman, Kimberly A   Family Medicine  Google Publications
    Childrens National Medical Center, 111 Michigan Avenue, N.W., Washington, DC, 20010, USA.
    Physician  Highly Cited  Highly Published 
    Medicare MIPS (Merit-based Incentive Payment System) rating: 73/100
    Disclosed payments in 2021 from 7 biomedical companies, totalling $266.68, including $104.62 from  AbbVie Inc.
    Subjects: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Ornithine Carbamoyltransferase Deficiency Disease; Urea Cycle Disorders, Inborn; Amino Acid Transport Disorders, Inborn
    Categories: Diagnosis; Pathology; Deficiency
    The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. (2015)
    The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 2: the evolving clinical phenotype. (2015)

  10. Vespa, Paul M   Neurology  Google Publications
    Physician  Highly Published 
    Medicare MIPS (Merit-based Incentive Payment System) rating: 59/100
    Disclosed payments in 2021 from 3 biomedical companies, totalling $3,390, including $2,415 from  UCB, Inc.
    Subjects: Brain Injuries; Brain Diseases, Metabolic; Brain; Cognition Disorders; Body Temperature; Cardiopulmonary Resuscitation
    Categories: Metabolism; Pathology; Physiopathology; Epidemiology; Methods; Physiology
    Early cerebral metabolic crisis after TBI influences outcome despite adequate hemodynamic resuscitation. (2012)
    Early metabolic crisis-related brain atrophy and cognition in traumatic brain injury. (2013)

  11. Mühlhausen, Chris  Google Publications
    Department of Pediatrics and Adolescent Medicine, University Medical Center, Göttingen, Germany.
    Scientist  Highly Cited  Highly Published  Clinical Trial 
    Subjects: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Glutarates; Ornithine Carbamoyltransferase Deficiency Disease; Urea Cycle Disorders, Inborn
    Categories: Diagnosis; Deficiency; Pathology; Therapy; Genetics; Metabolism
    Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. (2017)
    The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. (2015)

  12. Burgard, Peter   Google Publications
    Centre for Child and Adolescent Medicine, Department of General Paediatrics, Division of Neuropaediatrics and Metabolic Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, D-69120, Heidelberg, Germany.
    Scientist  Highly Cited  Highly Published  Clinical Trial 
    Subjects: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Lysine; Ornithine Carbamoyltransferase Deficiency Disease; Urea Cycle Disorders, Inborn
    Categories: Diagnosis; Deficiency; Pathology; Diet Therapy; Genetics; Psychology
    Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. (2017)
    The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. (2015)

  13. Achinger, Steven G   Nephrology  Google Publications
    Physician 
    Medical school: University of Miami, Lm Miller School of Medicine (MD, 2000)
    Medicare Accepted; Medicare MIPS (Merit-based Incentive Payment System) rating: 87/100
    Subjects: Brain Diseases, Metabolic; Critical Illness; Hyponatremia; Saline Solution, Hypertonic
    Categories: Complications; Etiology; Therapeutic Use; Therapy
    Treatment of Hyponatremic Encephalopathy in the Critically Ill. (2017)
    The authors reply. (2018)

  14. Chen, Wei    Google Publications
    Shanghai Key Laboratory of Regulatory Biology, Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, 500 Dongchuan Road, Shanghai 200241, China.
    Physician 
    Subjects: Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Anxiety; Asians; Behavior, Animal
    Categories: Metabolism; Enzymology; Genetics; Deficiency; Physiology
    Stress-Induced Metabolic Disorder in Peripheral CD4 (2019)

  15. Ferreira, Gustavo C   Pulmonary Disease  Google Publications
    Physician 
    Medical school: Other (MD, 1985)
    Medicare Accepted
    Disclosed payments in 2021 from 15 biomedical companies, totalling $445.1, including $262.5 from  Boehringer Ingelheim Pharmaceuticals, Inc.
    Subjects: Brain Diseases, Metabolic; Acute Kidney Injury; Brain; 3-Hydroxyacyl CoA Dehydrogenases; Energy Metabolism; Lipid Metabolism Disorders
    Categories: Metabolism; Toxicity; Chemically Induced; Deficiency; Complications; Drug Effects
    Long-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies induce oxidative stress in rat brain. (2010)
    Acute renal failure potentiates brain energy dysfunction elicited by methylmalonic acid. (2013)

  16. Lu, Wei    Google Publications
    Key Laboratory for Developmental Genes and Human Disease, Ministry of Education, Institute of Life Sciences, Jiangsu Province High-Tech Key Laboratory for Bio-Medical Research, Southeast University, Nanjing 210096, China.
    Physician 
    Subjects: Anxiety; Behavior, Animal; Brain Diseases, Metabolic; Stress, Psychological
    Categories: Metabolism; Physiology
    Stress-Induced Metabolic Disorder in Peripheral CD4 (2019)

  17. Heringer, Jana   Google Publications
    Centre for Child and Adolescent Medicine, Clinic I, Division of Neuropaediatrics and Metabolic Medicine, University Hospital Heidelberg, Im Neuenheimer Feld 430, 69120 Heidelberg, Germany.
    Scientist  Highly Cited  Highly Published  Clinical Trial 
    Subjects: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Amino Acid Transport Disorders, Inborn; Body Weights and Measures; Brain
    Categories: Pathology; Deficiency; Diagnosis; Diet Therapy; Psychology; Drug Therapy
    Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. (2017)
    Newborn screening: A disease-changing intervention for glutaric aciduria type 1. (2018)

  18. Burlina, Alberto B   Google Publications
    Division of Inherited Metabolic Diseases, Department of Paediatrics, University Hospital of Padua, Padua, Italy.
    Scientist  Highly Cited  Highly Published  Case Reports 
    Subjects: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Ornithine Carbamoyltransferase Deficiency Disease; Urea Cycle Disorders, Inborn; Amino Acid Transport Disorders, Inborn
    Categories: Diagnosis; Therapy; Deficiency; Pathology; Genetics; Metabolism
    The phenotypic spectrum of organic acidurias and urea cycle disorders. Part 1: the initial presentation. (2015)
    Diagnosis and management of glutaric aciduria type I--revised recommendations. (2011)

  19. Boy, Nikolas   Google Publications
    Division of Child Neurology and Metabolic Medicine, Centre for Child and Adolescent Medicine, University Hospital Heidelberg, Heidelberg, Germany. .
    Scientist  Highly Cited  Highly Published  Clinical Trial  Case Reports 
    Subjects: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Glutaryl-CoA Dehydrogenase; Brain; Hematoma, Subdural; Body Weights and Measures
    Categories: Deficiency; Complications; Diagnosis; Pathology; Etiology; Psychology
    Proposed recommendations for diagnosing and managing individuals with glutaric aciduria type I: second revision. (2017)
    Newborn screening: A disease-changing intervention for glutaric aciduria type 1. (2018)

  20. Cao, Qian  Google Publications
    Sir Run Run Shaw Hospital, College of Medicine, Zhejiang University, Hangzhou 310016, China.
    Scientist 
    Subjects: Anxiety; Behavior, Animal; Brain Diseases, Metabolic; Stress, Psychological
    Categories: Metabolism; Physiology
    Stress-Induced Metabolic Disorder in Peripheral CD4 (2019)

Note:
  1. These experts have limited publications on this topic in our database, so expertise assessment may not be accurate.
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These expert listings are for individual use without a fee. Biotechs, Pharmaceuticals, Recruiters, Consultants, Investors, Law firms, and other organizations may use this only for quick evaluations (no downloads or screen scraping) to identify the top medical experts for recruiting, advisory panels, boards, and consulting. Please contact us for licensing, customized queries, feedback and questions.

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