Lewis P. Rowland focuses on Pathology, Internal medicine, Mitochondrial DNA, Amyotrophic lateral sclerosis and Mitochondrial myopathy. His Internal medicine study combines topics from a wide range of disciplines, such as Endocrinology, Surgery and Cardiology. The study incorporates disciplines such as Leukoencephalopathy and Leukodystrophy in addition to Mitochondrial DNA.
His Amyotrophic lateral sclerosis research incorporates elements of Motor neuron, Dementia, Psychomotor learning and Paraproteinemia. He has included themes like Lactic acidosis, Mitochondrial encephalomyopathy, Heteroplasmy and Mitochondrial disease in his Mitochondrial myopathy study. His Multiple mitochondrial DNA deletions research is multidisciplinary, incorporating perspectives in Pearson syndrome and Kearns–Sayre syndrome.
Lewis P. Rowland mainly focuses on Pathology, Amyotrophic lateral sclerosis, Internal medicine, Disease and Neuroscience. His Pathology study often links to related topics such as Fasciculation. Lewis P. Rowland combines subjects such as Paraproteinemia, Motor neuron and Degenerative disease with his study of Amyotrophic lateral sclerosis.
His Internal medicine study incorporates themes from Endocrinology, Surgery, Weakness and Cardiology. The various areas that Lewis P. Rowland examines in his Endocrinology study include Duchenne muscular dystrophy and Myopathy.
His scientific interests lie mostly in Amyotrophic lateral sclerosis, Pathology, Psychiatry, Neuroscience and Internal medicine. His studies deal with areas such as Motor neuron, Physical medicine and rehabilitation and Degenerative disease as well as Amyotrophic lateral sclerosis. His work on Pathology is being expanded to include thematically relevant topics such as Mitochondrial DNA.
His Psychiatry study combines topics in areas such as Frontotemporal dementia and MEDLINE. His research in Internal medicine intersects with topics in Endocrinology, Surgery and Cardiology. His studies in Disease integrate themes in fields like Phenotype and Genetics.
Lewis P. Rowland mostly deals with Amyotrophic lateral sclerosis, Motor neuron, Pathology, Internal medicine and Neuroscience. His biological study spans a wide range of topics, including Dementia, Frontotemporal dementia and Health care. Lewis P. Rowland has researched Motor neuron in several fields, including Stem cell and Degenerative disease.
In the subject of general Pathology, his work in Spinal muscular atrophy, T-cell lymphoma and Polymyositis is often linked to Neoplastic transformation and Peripheral T-cell lymphoma, thereby combining diverse domains of study. In his research, Safety profile is intimately related to Surgery, which falls under the overarching field of Internal medicine. His Disease study integrates concerns from other disciplines, such as Phenotype and Genetics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome.
Steven G. Pavlakis;Peter C. Phillips;Salvatore DiMauro;Darryl C. De Vivo;Darryl C. De Vivo.
Annals of Neurology (1984)
Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
Carlos T. Moraes;Salvatore Dimauro;Massimo Zeviani;Anne Lombes.
The New England Journal of Medicine (1989)
Inclusion body myositis and myopathies.
Robert C. Griggs;Valerie Askanas;Salvatore DiMauro;Andrew Engel.
Annals of Neurology (1995)
Deletions of mitochondrial DNA in Kearns‐Sayre syndrome
M. Zeviani;C. T. Moraes;S. DiMauro;H. Nakase.
Duchenne muscular dystrophy: Deficiency of dystrophin at the muscle cell surface
Eduardo Bonilla;Craig E. Samitt;Armand F. Miranda;Armand F. Miranda;Arthur P. Hays;Arthur P. Hays.
Hashimoto encephalopathy: syndrome or myth?
Ji Y. Chong;Lewis P. Rowland;Robert D. Utiger.
JAMA Neurology (2003)
MELAS: Clinical features, biochemistry, and molecular genetics
E. Ciafaloni;E. Ricci;S. Shanske;C. T. Moraes.
Annals of Neurology (1992)
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder
Michio Hirano;G. Silvestri;D. M. Blake;A. Lombes.
Myasthenic crisis Clinical features, mortality, complications, and risk factors for prolonged intubation
C. E. Thomas;S. A. Mayer;Y. Gungor;R. Swarup.
MELAS: An original case and clinical criteria for diagnosis
Michio Hirano;Enzo Ricci;M. Richard Koenigsberger;Richard Defendini.
Neuromuscular Disorders (1992)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: