Zobrazeno 1 - 10
of 14
pro vyhledávání: '"J J, van der Harten"'
Publikováno v:
European Respiratory Journal. 10:504-507
A 49 year old man was referred to our hospital in 1994, because of intermittent fever and production of mucopurulent sputum. His complaints started at 43 yrs of age. The symptoms were mostly self-limiting, and occurred five times a year. Over the yea
Publikováno v:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 3(2)
Only incidental mention has been made to date of the combined occurrence of subependymal heterotopia and posterior encephalocele. We evaluated the presence of disseminated nodular subependymal heterotopia in two series of patients with posterior ence
Autor:
A. Rossi, William R. Wilcox, Daniel H. Cohn, David L. Rimoin, Andrea Superti-Furga, R. Gitzelmann, J. J. Van Der Harten, E. S. Lander, Beat Steinmann, J. Hästbacka
Publikováno v:
Annals of the New York Academy of Sciences. 785
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 137(26)
Publikováno v:
Tijdschrift voor kindergeneeskunde. 58(5)
A male neonate born after spontaneous labor during the 25 3/7 week of gestation, developed a fatal course of disseminated candidiasis. Disseminated candidiasis is seen in newborns undergoing intensive care and has a high mortality rate. Important eti
Autor:
W. Blom, Patricia A. Stewart, M. F. Niermeijer, F. G. A. Versteegh, J. W. Wladimiroff, J. J. Van Der Harten, J. G. M. Huijmans
Publikováno v:
Prenatal Diagnosis. 5:47-52
Congenital hypophosphatasia is an autosomal recessive disorder, which usually has a fatal outcome during the neonatal period. This report presents the prenatal diagnosis of hypophosphatasia at 16 weeks of gestation. The characteristic ultrasonic find
Publikováno v:
Tijdschrift voor kindergeneeskunde. 52(1)
Chondrodysplasia punctata congenita is an entity of genetic heterogeneity characterized by the presence of stippled epiphyseal and extra-epiphyseal calcifications in roentgenograms. There are at least three distinct types which differ in their mode o
Autor:
A, Talerman, J J, van der Harten
Publikováno v:
Cancer. 40(2)
A case of mixed germ cell-sex cord stroma tumor occurring in a normal 8-year-old girl with 46XX karyotype is reported. The child presented with evidence of isosexual precocious puberty 3 years prior to the excision of the tumor. Although the tumor wa
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 132(9)
Autor:
Peter G. Barth, J. J. van der Harten
Publikováno v:
Acta neuropathologica. 67(3-4)
A case of parabiotic twin pregnancy is described with early fetal co-twin loss and topical isocortical disruption and gastroschisis in the surviving twin. We conclude from this case that early fetal parabiotic twin syndrome (before 16 weeks of gestat