Lambert Eh
Impact in
- Neurology top 2%
- Myasthenia Gravis and Thymoma
- Peripheral Neuropathies and Disorders
- Botulinum Toxin and Related Neurological Disorders
- Autoimmune Neurological Disorders and Treatments
- Neurological diseases and metabolism
-
- Hereditary Neurological Disorders
Papers in
- Neurology 13
- Myasthenia Gravis and Thymoma 5
- Neurological diseases and metabolism 3
-
- Hereditary Neurological Disorders 4
- Neuroscience and Neural Engineering 2
- Co-authors
- Howard Fm (3 shared papers)D. Elmqvist (1 shared paper)Engel Ag (3 shared papers)O'Brien Pc (3 shared papers)Johnson Wj (4 shared papers)Dyck Pj (4 shared papers)Mulder Dw (3 shared papers)Winkelmann Rk (2 shared papers)
- Journals
- Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) (2 papers)PubMed (26 papers)
- Partner nations
- United States
In The Last Decade
Lambert Eh
27 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 79
- Neurology 751
- Cellular and Molecular Neuroscience 330
- Neurology 112
- Genetics 78
- Cell Biology 101
Countries citing papers authored by Lambert Eh
This map shows the geographic impact of Lambert Eh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Lambert Eh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lambert Eh more than expected).
Fields of papers citing papers by Lambert Eh
This network shows the impact of papers produced by Lambert Eh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Lambert Eh. The network helps show where Lambert Eh may publish in the future.
Co-authors
The 15 scholars most cited alongside Lambert Eh, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 28 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Immune complexes (IgG and C3) at the motor end-plate in myasthenia gravis: ultrastructural and light microscopic localization and electrophysiologic correlations. | 1977 | 252 |
| 2 | Segmental demyelination secondary to axonal degeneration in uremic neuropathy. | 1971 | 241 |
| 3 | Detailed analysis of neuromuscular transmission in a patient with the myasthenic syndrome sometimes associated with bronchogenic carcinoma. | 1968 | 182 |
| 4 | Prednisone-responsive hereditary motor and sensory neuropathy. | 1982 | 89 |
| 5 | Course of dermatomyositis-polymyositis: comparison of untreated and cortisone-treated patients. | 1968 | 72 |
| 6 | Electromyographic studies in amyotrophic lateral sclerosis. | 1957 | 66 |
| 7 | Severe hypomyelination and marked abnormality of conduction in Dejerine-Sottas hypertrophic neuropathy: myelin thickness and compound action potential of sural nerve in vitro. | 1971 | 51 |
| 8 | Linkage evidence for genetic heterogeneity among kinships with hereditary motor and sensory neuropathy, type I. | 1983 | 45 |
| 9 | Congenital myasthenia gravis in 13 smooth fox terriers. | 1983 | 36 |
| 10 | Electrical activity of muscle in polymyositis. | 1954 | 34 |
| 11 | Source of a type of insertion activity in electromyography with evaluation of a histologic method of localization. | 1955 | 32 |
| 12 | Facial myokymia affecting the electroencephalogram. | 1967 | 26 |
| 13 | Experience with a combined hemodialysis-renal transplantation program: neurologic aspects. | 1966 | 16 |
| 14 | Detection and evaluation of uremic peripheral neuropathy in patients on hemodialysis. | 1975 | 15 |
| 15 | Fast motor systems in man: physiopathology of the sonomotor response. | 1964 | 13 |
| 16 | Uremic neuropathy. III. Controlled study of restricted protein and fluid diet and infrequent hemodialysis versus conventional hemodialysis treatment. | 1975 | 12 |
| 17 | Compound action potentials of human sural nerve biopsies. | 1968 | 10 |
| 18 | Thymoma with myopathy. Report of a case. | 1969 | 4 |
| 19 | SYMPOSIUM ON MUSCLE DISEASE. | 1965 | 3 |
| 20 | A new myasthenic syndrome with end-plate acetyl cholinesterase (AChE) deficiency, small nerve terminals, and reduced acetylcholine release. | 1976 | 3 |
About Lambert Eh
Lambert Eh is a scholar working on Neurology, Cellular and Molecular Neuroscience, Endocrinology, Diabetes and Metabolism, Epidemiology and Molecular Biology, having authored 28 papers that have together received 1.2k indexed citations. Recurring topics across this work include Myasthenia Gravis and Thymoma (5 papers), Hereditary Neurological Disorders (4 papers), Neurological and metabolic disorders (4 papers), Inflammatory Myopathies and Dermatomyositis (3 papers), Dermatological and Skeletal Disorders (3 papers), Neurological diseases and metabolism (3 papers), Neuroscience and Neural Engineering (2 papers) and Cancer Treatment and Pharmacology (2 papers). The work is most often cited by research in Neurology (751 citations), Cellular and Molecular Neuroscience (330 citations), Neurology (112 citations), Genetics (78 citations) and Cell Biology (101 citations). Lambert Eh has collaborated with scholars based in United States. Frequent co-authors include Howard Fm, D. Elmqvist, Engel Ag, O'Brien Pc, Johnson Wj, Dyck Pj, Mulder Dw, Winkelmann Rk, Kerrie M. Sanders and Moore Sb. Their work appears in journals such as Munich Personal RePEc Archive (Ludwig Maximilian University of Munich) and PubMed.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.