[Trimethylaminuria: 'Help, my child smells of fish!']

Autor: T A, Stehmann, B, van Houten, J, van der Deure

Publikováno v: Nederlands tijdschrift voor geneeskunde. 162

Trimethylaminuria is caused by a functional enzyme defect and is usually congenital. This metabolic disease is characterised by body odour resembling fish.A 7-year-old boy was referred with abnormal body odour, which his mother described as resemblin

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a424d938b21b74e67d3b88debc011d0c
https://pubmed.ncbi.nlm.nih.gov/29600922

Pulmonary

Autor: M. Todorovič-Guid, L. Žic, Z. Kanič, S. Burja, K. Bračič, A. Piotrowski, P. Krajewski, P. Czech, P. Kawczyński, P. Stengert, J. van der Deure, G. C. Markhorst, K. Haasnoot, Fumimaro Hatori, Haruo Uchida, Masao Katayama, Rika Muto, H. M. Grubbauer, R. Kerbl, H. Litscher, G. Zobel, M. Trop, P. Jouvet, P. Hubert, D. Isabey, D. Pinquier, E. Dahan, M. Cloup, A. Harf, A. C. P. Ferreira, W. B. Carvalho, B. I. Kopelman, J. H. Lee, A. P. Kolesnichenko, O. B. Milenin, A. I. Gritsan, I. V. Kuznetsova, L. Albano, A. Panigazzi, L. Saligari, D. Capra, A. Reta, P. Engardt, M. Alderete, J. Fraser, A. Pengilly, Q. Mok, John Pope, David Birnkrant, James Martin, Anthony Repucci, J. F. Germain, B. Thebaud, C. Farnoux, A. Cortez, O. Sibony, F. Beaufils, V. Modesto, E. Ibiza, A. Abengochea, J. Arago, R. Sanchis, C. Ortola, R. Varas, E. Garcia, S. Kling, R. P. Gie, S. Amantéa, J. Piva, B. Palombini, Santamaría E. Ulloa, Navero J. L. Pérez, Rosa I. de la Ibarra, Hernández M. Espino, Jabalquinto M. J. Velasco, Pérez M. Frías, Rashid Mahmood, Sajid Maqbool, Waqar Hussain, Tariq Mahmood, Fauzia Shoukat, R. Bustos, O. Battisti, J. P. Langhendries, A. Francois, J. M. Bertrand, M. Fedora, R. Nekvasil, V. Vobruba, P. Srnsky, M. Zapadlo, Z. Zivkovic, S. Mihailovic

Publikováno v: Intensive Care Medicine. 22:S210-S214

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ea53fd87c842734aeae91f4a1267eea
https://doi.org/10.1007/bf03216394

The relationship between children with voiding problems and their parents

Autor: J. Labrie, J. van der Deure, A.J. Nieuwhof-Leppink, C. H. van der Vaart, T.P.V.M. de Jong, Marianne A.W. Vijverberg

Publikováno v: Journal of urology, 183(5), 1887-1891. Elsevier Inc.

We determined whether parents of children with overactive bladder and dysfunctional voiding had had similar symptoms in childhood. A case-control study was done in parents with and without children with overactive bladder or dysfunctional voiding. Al

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c0aa1c3ab910572fa90de6eaf02463cd
https://pubmed.ncbi.nlm.nih.gov/20303097

[Voiding difficulties in a child attributed to the use of ipratropium and salbutamol]

Autor: H L, Hooimeijer, J, van der Deure, J J, de Langen

Publikováno v: Nederlands tijdschrift voor geneeskunde. 151(49)

A 5-year-old child was referred to our clinic because of voiding difficulties. She had been continent for 2.5 years. She had a hesitation of the urinary flow and voided with variable residual volumes. She had been using ipratropium and salbutamol reg

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::6d43534ff58cc9f01877f14689004891
https://pubmed.ncbi.nlm.nih.gov/18225795

[Clinical reasoning and decision making in practice. A 9-year-old boy with isolated splenomegaly]

Autor: M M J W, Wijers-van Amelsfort, J, van der Deure, J, Bekker, H, Veeken, W, Hart

Publikováno v: Nederlands tijdschrift voor geneeskunde. 151(38)

Splenomegaly was discovered by chance in a 9-year-old boy who had no further complaints. Apart from splenomegaly and mild thrombocytopenia, no other pathological condition was found in the first instance. Ultrasound revealed a spleen with a median le

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::3847d4f218a803aa787bbdd0985a6f95
https://pubmed.ncbi.nlm.nih.gov/18265805