| Year |
Citation |
Score |
| 1979 |
Askanas V, Engel WK, Reddy NB, Barth PG, Bethlem J, Krauss DR, Hibberd ME, Lawrence JV, Carter LS. X-linked recessive congenital muscle fiber hypotrophy with central nuclei: abnormalities of growth and adenylate cyclase in muscle tissue cultures. Archives of Neurology. 36: 604-9. PMID 573609 DOI: 10.1001/Archneur.1979.00500460038003 |
0.369 |
|
| 1978 |
Arts WF, Bethlem J, Dingemans KP, Eriksson AW. Investigations on the inheritance of nemaline myopathy. Archives of Neurology. 35: 72-7. PMID 623532 DOI: 10.1001/Archneur.1978.00500260010002 |
0.31 |
|
| 1978 |
Askanas V, Engel WK, Bethlem J. Leptomeres in cultured human muscle. Acta Neuropathologica. 42: 247-50. PMID 354307 DOI: 10.1007/Bf00690365 |
0.354 |
|
| 1978 |
Arts WF, Bethlem J, Volkers WS. Further investigations on benign myopathy with autosomal dominant inheritance. Journal of Neurology. 217: 201-6. PMID 75955 DOI: 10.1007/Bf00312962 |
0.308 |
|
| 1977 |
van Wijngaarden GK, Bethlem J, Dingemans KP, Coërs C, Telerman-Toppet N, Gérard JM. Familial focal loss of cross striations. Journal of Neurology. 216: 163-72. PMID 72134 DOI: 10.1007/Bf00313617 |
0.41 |
|
| 1976 |
Coërs C, Telerman-Toppet N, Gérard JM, Szliwowski H, Bethlem J, van Wijngaarden GK. Changes in motor innervation and histochemical pattern of muscle fibers in some congenital myopathies. Neurology. 26: 1046-53. PMID 988511 DOI: 10.1212/Wnl.26.11.1046 |
0.42 |
|
| 1976 |
Bethlem J, Wijngaarden GK. Benign myopathy, with autosomal dominant inheritance. A report on three pedigrees. Brain : a Journal of Neurology. 99: 91-100. PMID 963533 DOI: 10.1093/Brain/99.1.91 |
0.439 |
|
| 1975 |
Barth PG, Van Wijngaarden GK, Bethlem J. X-linked myotubular myopathy with fatal neonatal asphyxia. Neurology. 25: 531-6. PMID 1168872 DOI: 10.1212/Wnl.25.6.531 |
0.358 |
|
| 1974 |
Jennekens FG, Meijer AE, Bethlem J, Van Wijngaarden GK. Fibre hybrids in type groups. An investigation of human muscle biopsies. Journal of the Neurological Sciences. 23: 337-52. PMID 4154363 DOI: 10.1016/0022-510X(74)90152-X |
0.406 |
|
| 1973 |
Oosterhuis H, Bethlem J. Neurogenic muscle involvement in myasthenia gravis. A clinical and histopathological study. Journal of Neurology, Neurosurgery, and Psychiatry. 36: 244-54. PMID 4708458 DOI: 10.1136/Jnnp.36.2.244 |
0.624 |
|
| 1973 |
Bethlem J, van Wijngaarden GK, de Jong J. The incidence of lobulated fibres in the facioscapulo-humeral type of muscular dystrophy and the limb-girdle syndrome. Journal of the Neurological Sciences. 18: 351-8. PMID 4698315 DOI: 10.1016/0022-510X(73)90083-X |
0.636 |
|
| 1971 |
Bethlem J, van Wijngaarden GK, Meijer AE, Fleury P. Observations on central core disease. Journal of the Neurological Sciences. 14: 293-9. PMID 5135336 DOI: 10.1016/0022-510X(71)90218-8 |
0.469 |
|
| 1971 |
Meijer AE, Bethlem J, Van Wijngaarden GK. Diagnostic value of electrophoretical isoenzyme determination of L-lactate dehydrogenase in affected quadriceps muscle of patients with neuromuscular diseases. Clinica Chimica Acta; International Journal of Clinical Chemistry. 33: 247-52. PMID 5098006 DOI: 10.1016/0009-8981(71)90274-9 |
0.465 |
|
| 1970 |
Bethlem J, van Wijngaarden GK, Mumenthaler M, Meijer AE. Centronuclear myopathy with type I fiber atrophy and "myotubes". Archives of Neurology. 23: 70-3. PMID 4246348 DOI: 10.1001/Archneur.1970.00480250074010 |
0.423 |
|
| 1969 |
Bethlem J, van Wijngaarden GK, Meijer AE, Hülsmann WC. Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube-like structures. Neurology. 19: 705-10. PMID 5815134 DOI: 10.1212/Wnl.19.7.705 |
0.352 |
|
| 1968 |
van Wijngaarden GK, Hagen CJ, Bethlem J, Meijer AE. Myopathy of the quadriceps muscles. Journal of the Neurological Sciences. 7: 201-6. PMID 5707072 DOI: 10.1016/0022-510X(68)90142-1 |
0.448 |
|
| 1968 |
Oosterhuis HJ, Bethlem J, Feltkamp TE. Muscle pathology, thymoma, and immunological abnormalities in patients with myasthenia gravis. Journal of Neurology, Neurosurgery, and Psychiatry. 31: 460-3. PMID 4885252 |
0.59 |
|
| 1967 |
van Wijngaarden GK, Bethlem J, Meijer AE, Hülsmann WC, Feltkamp CA. Skeletal muscle disease with abnormal mitochondria. Brain : a Journal of Neurology. 90: 577-92. PMID 6058143 DOI: 10.1093/Brain/90.3.577 |
0.468 |
|
| 1967 |
Hulsmann WC, Bethlem J, Meijer AE, Fleury P, Schellens JP. Myopathy with abnormal structure and function of muscle mitochondria. Journal of Neurology, Neurosurgery, and Psychiatry. 30: 519-25. PMID 5583094 DOI: 10.1136/Jnnp.30.6.519 |
0.374 |
|
| 1966 |
Bethlem J, van Gool J, Hülsmann WC, Meijer AE. Familial non-progressive myopathy with muscle cramps after exercise. A new disease associated with cores in the muscle fibres. Brain : a Journal of Neurology. 89: 569-88. PMID 4224150 DOI: 10.1093/Brain/89.3.569 |
0.439 |
|
| 1964 |
BETHLEM J, VAN GOOL, DEN HARTOG JAGER WA. PROGRESSIVE MULTIFOCAL LEUCOENCEPHALOPATHY ASSOCIATED WITH MULTIPLE MYELOMA. Acta Neuropathologica. 3: 525-8. PMID 14192318 DOI: 10.1007/Bf00688461 |
0.631 |
|
| 1963 |
BETHLEM J, VANWIJNGAARDEN GK. THE INCIDENCE OF RINGED FIBRES AND SARCOPLASMIC MASSES IN NORMAL AND DISEASED MUSCLE. Journal of Neurology, Neurosurgery, and Psychiatry. 26: 326-32. PMID 14061015 DOI: 10.1136/Jnnp.26.4.326 |
0.451 |
|
| 1960 |
BETHLEM J, den HARTOG JAGER WA. [Study on the character of Lewy's corpuscles and their role in Parkinson's disease]. Nederlands Tijdschrift Voor Geneeskunde. 104: 809-12. PMID 13800155 |
0.627 |
|
| 1960 |
BETHLEM J, DEN HARTOG JAGER WA. The incidence and characteristics of Lewy bodies in idiopathic paralysis agitans (Parkinson's disease). Journal of Neurology, Neurosurgery, and Psychiatry. 23: 74-80. PMID 13800154 DOI: 10.1136/Jnnp.23.1.74 |
0.649 |
|
| 1960 |
den HARTOG JAGER WA, BETHLEM J. The distribution of Lewy bodies in the central and autonomic nervous systems in idiopathic paralysis agitans. Journal of Neurology, Neurosurgery, and Psychiatry. 23: 283-90. PMID 13711997 DOI: 10.1136/Jnnp.23.4.283 |
0.594 |
|
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