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Your search keyword '"Wennekes, MJ"' showing total 4 results
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4 results on '"Wennekes, MJ"'

1. Adjunctive dexamethasone in adults with meningococcal meningitis

Author

Heckenberg, Sebastiaan G.B., primary, Brouwer, Matthijs C., additional, van der Ende, Arie, additional, van de Beek, Diederik, additional, Wennekes, MJ, additional, Esselink, RAJ, additional, de Graaf, RJ, additional, ten Houten, R, additional, Baart, JC, additional, Keunen, RWM, additional, Oerlemans, WGH, additional, Broere, D, additional, Straathof, CSM, additional, Verheul, GAM, additional, van de Vlasakker, CJW, additional, Enting, RH, additional, van Schaik, IN, additional, van der Plas, JPL, additional, Bienfait, HP, additional, Christiaans, MH, additional, Hoogerwaard, EM, additional, Reijneveld, JC, additional, Alting van Geusau, RB, additional, Berendes, JN, additional, Jacobs, BC, additional, van den Berg, JSP, additional, Witteveen, RJW, additional, Stevens, M, additional, Herderschee, D, additional, Struys, MA, additional, Jansen, C, additional, Anten, HWM, additional, Brekelmans, GFJ, additional, Fennis, TFM, additional, Prick, JJW, additional, Pop, PHM, additional, Wouda, EJ, additional, Bülens, C, additional, Lohman, HJMM, additional, Blankevoort, JP, additional, Visee, HF, additional, Smits, RCF, additional, Berntsen, PJIM, additional, Saxena, R, additional, Geelen, JAG, additional, Schiphof, PR, additional, Weisfelt, M, additional, Grosveld, WJHM, additional, van Zuilen, EV, additional, Kwa, IH, additional, van Domburg, PHMF, additional, Medaer, RHJ, additional, Koppenaal, A, additional, van der Kamp, W, additional, Holscher, RS, additional, Schipper, JP, additional, van Dijk, GW, additional, Kerkhoff, H, additional, Taphoorn, MJB, additional, Huisman, UW, additional, Kok, AJM, additional, van Spreeken, A, additional, Admiraal, P, additional, de Jong, PJ, additional, van Lieshout, HBM, additional, Zorgdrager, AN, additional, Gijsbers, CJ, additional, de Steen, Avan, additional, van Raak, EPM, additional, Gerrits, M, additional, Wieringa, EJ, additional, Leenders, EM, additional, Roebroek, RMJA, additional, Snoek, JW, additional, Vermeij, AJ, additional, Wessels, PH, additional, Boon, AM, additional, Vrooland, L, additional, Knibbeler, JGM, additional, ter Spill, HW, additional, Meijer, RJ, additional, Krooman, JP, additional, Heerema, J, additional, Oonk, JGW, additional, Molenaar, DSM, additional, Koeman, JP, additional, Hoefnagels, W, additional, Duyff, RF, additional, Don, JA, additional, Keuter, EJV, additional, Dunnewold, RJW, additional, Beintema, KD, additional, Zegerius, L, additional, Mauser, HW, additional, and Bollen, AE, additional

Published
2012
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2. [A child with peculiar movements: Sydenham chorea].

Author

Munts AG, Wennekes MJ, and Koehler PJ

Subjects
Child, Chorea drug therapy, Chorea physiopathology, Female, Humans, Pimozide therapeutic use, Rheumatic Fever microbiology, Treatment Outcome, Valproic Acid therapeutic use, Anti-Dyskinesia Agents therapeutic use, Chorea diagnosis, Rheumatic Fever complications
Abstract

An 11-year-old girl with Sydenham chorea presented with a rapid onset of serious restlessness of mainly the right side of the body. Additional laboratory investigations revealed no abnormalities, yet this is not unusual for such cases. Valproic acid and pimozide were then successively prescribed because of the chorea. For secondary prevention she received long-term oral penicillin. Sydenham chorea is a manifestation of rheumatic fever and occurs after a throat infection by group A streptococci. The disease is characteristic and consists of a combination of choreic movements, hypotonia and emotional lability. The clinical course is diverse. Improvement usually occurs over a period of several months, although a significant proportion of patients exhibit little recovery.

Published
2003

3. De novo translocation (2;18)(q21;q22) in a child with severe epilepsy, developmental delay and mild dysmorphism.

Author

Bal M, Schrander-Stumpel CT, Meers LE, Theunissen PM, Hamers AJ, Wennekes MJ, and Engelen JJ

Subjects
Chromosome Deletion, Cytogenetics methods, Fatal Outcome, Humans, In Situ Hybridization, Fluorescence, Infant, Male, Severity of Illness Index, Chromosomes, Human, Pair 18 genetics, Chromosomes, Human, Pair 2 genetics, Developmental Disabilities diagnosis, Developmental Disabilities genetics, Epilepsy diagnosis, Epilepsy genetics, Face abnormalities, Translocation, Genetic genetics
Abstract

De novo translocation (2;18)(q21;q22) in a patient with severe epilepsy developmental delay and mild dysmorphism: We report on a patient presenting with severe epilepsy, hypotonia, developmental delay, blepharophimosis, low-set ears, camptodactyly and tapering fingers, and cutaneous syndactyly of toes II and III of the right foot. The MRI showed some loss of volume of the white matter and delayed myelination, no other specific anomalies were present. Chromosome analysis revealed a translocation involving chromosomes 2 and 18, which was characterized further by FISH using band-specific probes. The possibility of a submicroscopic deletion is discussed and the patient is compared with patients reported in the literature with either 2q21 or 18q22 deletion.

Published
2000

4. Ossification of the posterior longitudinal ligament.

Author

Wennekes MJ, Anten HW, and Korten JJ

Subjects
Aged, Cervical Vertebrae surgery, Female, Humans, Laminectomy, Ligaments, Articular surgery, Male, Middle Aged, Ossification, Heterotopic surgery, Spinal Cord Compression diagnostic imaging, Spinal Diseases diagnostic imaging, Spinal Stenosis diagnostic imaging, Tomography, X-Ray Computed, Cervical Vertebrae diagnostic imaging, Ligaments, Articular diagnostic imaging, Ossification, Heterotopic diagnostic imaging
Abstract

Two non-Japanese patients with ossification of the cervical posterior longitudinal ligament were described. This abnormality is very common in Japan, but rare in non-Japanese people. The reason is unknown. Although the disease appears to be generally asymptomatic, it can cause a myelopathy. The clinical picture, the diagnostic important X-ray examinations and the histopathological findings are revealed. The similarity to the vascular pattern in the lumbar spine in cases of intermittent neurogenic claudication is noted.

Published
1985
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