Zobrazeno 1 - 10
of 10
pro vyhledávání: '"P. C. J. de Laat"'
Autor:
Veroniek E. M. Harbers, Frédérique C. M. Bouwman, Ingrid M. P. van Rijnsoever, Bas H. Verhoeven, Carine J. M. van der Vleuten, Leo J. Schultze Kool, Peter C. J. de Laat, Chantal M. A. M. van der Horst, Wietske Kievit, D. Maroeska W. M. te Loo
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
IntroductionVascular malformations are rare congenital anomalies of the vascular system, which can involve the capillaries, veins, arteries, lymphatics, or a combination of vessel types. Patients with vascular malformations experience an impaired hea
Externí odkaz:
https://doaj.org/article/30adb709a8db488493df56d290cc0f8e
Autor:
Janne W. Bolt, Martine F. Raphael, Suzanne G. M. A. Pasmans, Hester Langeveld, Nanko de Graaf, Peter C. J. de Laat
Publikováno v:
Journal of Vascular Anomalies, Vol 4, Iss 1, p e057 (2023)
Objectives:. Diagnosing vascular anomalies can be difficult and incorrect diagnosis may result in diagnostic delay and suboptimal treatment. Adequate diagnosis and treatment of patients with vascular anomalies are best guaranteed by a multidisciplina
Externí odkaz:
https://doaj.org/article/da82b3daf55a4c9b92030890e228c3a2
Publikováno v:
Compendium kindergeneeskunde ISBN: 9789036817912
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4676bbea5c715291b02a3cc5e8e0395
https://doi.org/10.1007/978-90-368-1792-9_17
https://doi.org/10.1007/978-90-368-1792-9_17
Publikováno v:
Dermatologic therapy. 27(4)
Vascular autonomic dysregulation, in the most extreme presentation known as Harlequin phenomenon, is a rare condition. It manifests as a sudden and brief paroxystic change in skin color, resulting in two different colors on the body. It is supposed t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::210848334fe56cd643f39e9eea307ae1
https://pubmed.ncbi.nlm.nih.gov/24750208
https://pubmed.ncbi.nlm.nih.gov/24750208
Publikováno v:
The British journal of dermatology. 169(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6ab00ba9e8d654008fcb9065b553d62f
https://pubmed.ncbi.nlm.nih.gov/23421718
https://pubmed.ncbi.nlm.nih.gov/23421718
Autor:
S R, Janmohamed, F B, de Waard-van der Spek, G C, Madern, P C J, de Laat, W C J, Hop, A P, Oranje
Publikováno v:
Clinical and experimental dermatology. 38(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::26766fb96d32ccd5fc79d3b794970282
https://pubmed.ncbi.nlm.nih.gov/22369347
https://pubmed.ncbi.nlm.nih.gov/22369347
Autor:
S R, Janmohamed, F B, de Waard-van der Spek, G C, Madern, P C J, de Laat, W C J, Hop, A P, Oranje
Publikováno v:
Clinical and experimental dermatology. 36(7)
Haemangioma of infancy (HOI) is the most frequently occurring benign tumour of infancy. A good, reliable and objective scoring system for haemangioma activity is not yet available.We have developed a simple system called the Haemangioma Activity Scor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f1d38504889a6c7000ca41d94d597fb
https://pubmed.ncbi.nlm.nih.gov/23252756
https://pubmed.ncbi.nlm.nih.gov/23252756
Publikováno v:
Scandinavian journal of immunology. 35(6)
Longitudinal serum immunoglobulin levels were studied in 36 children with selective IgA deficiency during a median follow-up period of 5 years. Twenty-live children were "sporadic' cases, and 11 were "familiar. Serum and saliva IgA levels in 23 child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f73fbb5784cd6c12485c5e741fd5f9d
https://pubmed.ncbi.nlm.nih.gov/1604243
https://pubmed.ncbi.nlm.nih.gov/1604243
Autor:
Corry M.R. Weemaes, Jan A.J.M. Bakkeren, R. Gonera, G. B. A. Stoelinga, P. J. J. Van Munster, P. C. J. De Laat
Publikováno v:
Acta paediatrica Scandinavica. 80(8-9)
Clinical manifestations in 40 children with selective IgA deficiency were studied during a follow-up period of 2-10 years. The patients were divided into two groups: group I consisted of 25 children with "sporadic" IgA deficiency and group II of 15 c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a3499146f77ff6b1ddd0277fbc3d472
https://pubmed.ncbi.nlm.nih.gov/1957599
https://pubmed.ncbi.nlm.nih.gov/1957599
Autor:
G. B. A. Stoelinga, F. C. A. Van Den Brandt, P. C. J. De Laat, R.M. de Graaf, P. J. J. Van Munster, T. Van Lith, Jan A.J.M. Bakkeren, C.M.R. Weemes
Publikováno v:
Clinical immunology and immunopathology. 58(1)
Two families were investigated in which the mothers had selective IgA deficiency and circulating class-specific anti-IgA antibodies. Both gave birth to two children who were found to be IgA deficient. Three of these children developed anti-IgA antibo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddaf7d2a003762b531b608dc139e7d54
https://pubmed.ncbi.nlm.nih.gov/1983972
https://pubmed.ncbi.nlm.nih.gov/1983972