Zobrazeno 1 - 10
of 23
pro vyhledávání: '"A. M. Roodhooft"'
Publikováno v:
Clinical Genetics. 38:228-232
A patient who presented with most features of lacrimo-auriculo-dento-digital (LADD) syndrome, an autosomal dominant trait, is described. There was no deafness, and anomalies of the external ear and the upper limbs were discrete. Renal anomalies, cons
Autor:
Jan M. Roodhooft
The aim of this article is to report the findings of ocular examinations in a group of patients diagnosed with multiple sclerosis who were referred to the eye department of the Nationaal Multiple Sclerosis Centrum of Melsbroek, Belgium, from 2007 to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46fbfac90e3c0d97d8997e629b3b7932
https://europepmc.org/articles/PMC3882980/
https://europepmc.org/articles/PMC3882980/
Autor:
J M, Roodhooft
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. (313)
In its early course, multiple sclerosis (MS) manifests in a variety of symptoms so that ophthalmologists should know that the ocular problems are often the first sign of the disease and may predict additional demyelinating events.The author have revi
Autor:
J M, Roodhooft
Publikováno v:
Bulletin de la Societe belge d'ophtalmologie. (305)
A century ago Hess described how to map out ocular deviations on two pieces of paper in cases of diplopia. This paper discusses how to obtain useful information regarding ocular deviations from a chart that has been obtained from screen tests (Hess,
Publikováno v:
Pediatric Nephrology. 4:597-599
In a girl with recurrent haemolytic uraemic syndrome (HUS), persistently low serum levels of C3 were found. Analysis of complement phenotype revealed a hypomorphic variant of C3 Fast in the patient (C3fS) and a normal heterozygous pattern in both par
Autor:
S. E. Spitaels, K. Boven, A. M. Roodhooft, K. J. Van Acker, P. Van Reempts, E. L. J. Vercruyssen
Publikováno v:
Calcified tissue international
We describe two twin sisters in whom calcification of different arteries was detected in the first weeks of life. Transient renal insufficiency, arterial hypertension, and skeletal abnormalities were also observed. One child had anasarca and heart de
Publikováno v:
European journal of pediatrics. 149(8)
In a patient with methylmalonic acidaemia (MMAA), persistent neurological symptoms were observed in addition to the acute episodes of metabolic dysequilibrium. CT scan and magnetic resonance imaging revealed bilateral symmetrical necrosis of the glob
Publikováno v:
European journal of pediatrics. 149(5)
In a child who probably received an overdose of sodium valproate, progressive coma, intermittent tonic-clonic seizures and anuria developed. Laboratory investigations revealed coagulopathy, and anaemia and mildly disturbed liver function. Progressive
Autor:
Fadi P. Nasrallah, Jan M Roodhooft, Alex E. Jalkh, Arnaldo P. Cialdini, John J. Weiter, Clement L. Trempe
Publikováno v:
Ophthalmic Surgery, Lasers and Imaging Retina. 20:316-320
In age-related macular degeneration, communication between the retinal and choroidal circulations occurs spontaneously or following unsuccessful laser photocoagulation of subretinal new vessels. The resulting chorioretinal anastomotic complex, which
Publikováno v:
Clinical nephrology. 28(3)
In 7 children on chronic dialysis the correlation between serum aluminum, aluminum after desferrioxamine (DFO) challenge and bone aluminum was studied. In children the DFO challenge test is not superior to the serum aluminum level for the estimation