Výsledky vyhledávání - "A.E.J. de Jager"

Epidemiology of inclusion body myositis in the Netherlands: A nationwide study

Autor: S. G. Van Duinen, Umesh A. Badrising, B.G.M. van Engelen, C.J. Höweler, Axel R. Wintzen, Jan J.G.M. Verschuuren, P.A. van Doorn, Ferdinand C. Breedveld, Peter J. Koehler, Marion L.C. Maat-Schieman, A.E.J. De Jager, F.H.J. van den Hoogen, M. de Visser, Frans G. I. Jennekens, H. van der Leeuw, Jessica E. Hoogendijk

Publikováno v: Neurology, 55(9), 1385-1387. LIPPINCOTT WILLIAMS & WILKINS
Neurology, 55, 1385-1387. Lippincott Williams & Wilkins
Neurology, 55, 1385-1387
Neurology, 55, pp. 1385-1387
Neurology, 55(9), 1385-1387. Lippincott Williams and Wilkins

Epidemiologic data on inclusion body myositis (IBM) are scarce, and possibly biased, because they are derived from larger neuromuscular centers. The present nationwide collaborative cross-sectional study, which culminated on July 1, 1999, resulted in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::460ef24580166fa8dc6c0af3c1ec9176
https://doi.org/10.1212/wnl.55.9.1385

Zobrazit plný text záznamu

Determination of ammonia in cerebrospinal fluid using the indophenol direct method

Autor: A.E.J. de Jager, A Teelken, Albert Tangerman, J.R. Huizenga, C.H. Gips, Peter L.M. Jansen

Publikováno v: Molecular and chemical neuropathology / sponsored by the International Society for Neurochemistry and the World Federation of Neurology and research groups on neurochemistry and cerebrospinal fluid, 34(2-3), 169-177. Humana Press
Molecular and Chemical Neuropathology, 34, pp. 169-177
Molecular and Chemical Neuropathology, 34, 169-177

We have determined ammonia in cerebrospinal fluid (CSF) with the indophenol direct method. The results were compared with an enzymatic method. The method is very simple, and precision (coefficient of variation 1.6%) and linearity (r = 0.9999, p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d49673a2b5e512555839286eadc278
https://doi.org/10.1007/bf02815078

Zobrazit plný text záznamu

Ophthalmoplegic and lower cranial nerve variants merge into each other and into classical Guillain-Barr� syndrome

Autor: A.E.J. de Jager, C.H. Polman, J.P. ter Bruggen, F. G. A. Van Der Meche

Publikováno v: Muscle & Nerve. 21:239-242

We delineated the place of cranial nerve variants within the concept of clinically defined Guillain-Barre syndrome (GBS). In the ophthalmoplegic variant (n = 7) the oculomotor nerves were early involved. In a lower cranial nerve variant (n = 9) the c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dbedc5e7f2d560af159e9bf8c23cabac
https://doi.org/10.1002/(sici)1097-4598(199802)21:2<239::aid-mus13>3.0.co

Zobrazit plný text záznamu

Vocational perspectives and neuromuscular disorders

Autor: George W. Padberg, F. Andries, M. de Visser, C.W.J. Wevers, A.E.J. De Jager, Axel R. Wintzen, H.F.M. Busch, C.J. Höweler, J.H.J. Wokke

Publikováno v: International journal of rehabilitation research. Internationale Zeitschrift für Rehabilitationsforschung. Revue internationale de recherches de réadaptation, 20(3), 255-273. Lippincott Williams and Wilkins
International Journal of Rehabilitation Research, 20, 255-273
International Journal of Rehabilitation Research, 20, 3, pp. 255-273

The present study analyses the actual occupational situation, vocational handicaps and past labour career of a group of about 1000 Dutch patients suffering from a neuromuscular disorder (NMD). On the basis of the likelihood of a substantial employmen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b32e176563ef37f295fe7562932a3115
https://doi.org/10.1097/00004356-199709000-00003

Zobrazit plný text záznamu

Clinical signs in severe Guillain-Barré syndrome: analysis of 63 patients

Autor: A.E.J. de Jager, H. J. Sluiter

Publikováno v: Journal of the Neurological Sciences. 104:143-150

Clinical data are presented of 63 artificially ventilated Guillain-Barré patients. About half of them had an antecedent event. In 57% the disease was heralded by sensory symptoms. The mean progressive phase lasted 12 days, the plateau 12 days and th

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d856dac0ae9a097fe5bdfa99d44617bf
https://doi.org/10.1016/0022-510x(91)90303-o

Zobrazit plný text záznamu

Residual signs in severe Guillain-Barré syndrome

Autor: J.M. Minderhoud, A.E.J. de Jager

Publikováno v: JOURNAL OF THE NEUROLOGICAL SCIENCES, 104(2), 151-156. ELSEVIER SCIENCE BV

The residual signs in a group of seriously paralyzed Guillain-Barre patients are reported (follow-up 2-24 years) and the social effects of the illness are discussed. Thirty-five percent of the patients had recovered completely at the time of the foll

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdcadc726c05119cd9eca46a759db275
https://doi.org/10.1016/0022-510x(91)90304-p

Zobrazit plný text záznamu

Residual health status after Guillain-Barré syndrome

Autor: F. G. A. Van Der Meche, H. M. Jacobs, A.E.J. de Jager, R. A. J. A. M. Bernsen

Publikováno v: Journal of neurology, neurosurgery, and psychiatry. 62(6)

To study the extent to which patients experience residual problems in daily functioning several years after having Guillain-Barre syndrome (GBS) a survey of 123 patients who had had Guillain-Barre syndrome three to six years previously was performed,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de16b0983acb8999085a23cc3f33055e
https://pubmed.ncbi.nlm.nih.gov/9219755

Zobrazit plný text záznamu

Miyoshi-type distal muscular dystrophy: clinical spectrum in 24 Dutch patients

Autor: H.F.M. Busch, J.H.J. Wokke, M. de Visser, Y. van der Graaf, Nicolette C. Notermans, W. H. J. P. Linssen, A.E.J. De Jager, C.J. Höweler, P.A. van Doorn

Publikováno v: Brain, 120, 1989-1996. Oxford University Press
Brain, 120 ( Pt 11), 1989-1996. Oxford University Press

Miyoshi-type distal muscular dystrophy has now been found to be more frequent outside Japan than was previously thought. We studied 24 Dutch patients with Miyoshi-type distal muscular dystrophy and focused on its clinical expression and natural histo

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b706ff89886b05c245f70562a826c12e
https://dare.uva.nl/personal/pure/en/publications/miyoshitype-distal-muscular-dystrophy-clinical-spectrum-in-24-dutch-patients(4c181a5e-8fc7-48dd-80ac-ca92dc556aa5).html

Zobrazit plný text záznamu

Epidemiology of inclusion body myositis in the Netherlands

Autor: Frans G. I. Jennekens, S. G. Van Duinen, B.G.M. van Engelen, J.J.G. Verschuuren, H. van der Leeuw, C.J. Höweler, P.A. van Doorn, F. van den Hoogen, Marion L.C. Maat-Schieman, A.E.J. De Jager, Jessica E. Hoogendijk, U.A. Badrising, Peter J. Koehler, M. de Visser, Axel R. Wintzen

Publikováno v: Neuromuscular Disorders. 7:463-464

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4bb8bb5cd6c0764eb46cde46e44814dc
https://doi.org/10.1016/s0960-8966(97)87311-7

Zobrazit plný text záznamu

Residual physical outcome and daily living 3 to 6 years after Guillain-Barre syndrome

Autor: A.E.J. de Jager, R. A. J. A. M. Bernsen, P. I. M. Schmitz, F. G. A. Van Der Meche

Publikováno v: Neurology. 53:409-409

Three to six years after onset of Guillain-Barré syndrome, 63% of 122 patients showed one or more changes in their lifestyle, work, or leisure activities, or in the life of their partners. The changes were influenced by an impaired final functional

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f6afe38469703c1823d14c08e1b7cc3
https://doi.org/10.1212/wnl.53.2.409

Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání