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pro vyhledávání: '"P G, Voorhoeve"'
Publikováno v:
Compendium kindergeneeskunde ISBN: 9789036817912
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d207568e7d7c1eac1e935a6178733d3
https://doi.org/10.1007/978-90-368-1792-9_41
https://doi.org/10.1007/978-90-368-1792-9_41
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 160
Three children presented with symptoms of an acute abdomen. In all three a diagnosis of pneumonia was subsequently established, and the patients made a full recovery following antibiotic therapy. When a paediatric patient presents with symptoms of an
Publikováno v:
Clinical Dysmorphology. 11:49-52
Accelerated growth and advanced bone age are consistent findings in Weaver-Smith syndrome (WSS). According to the rather scant reports in the literature, persons afflicted with WSS appear to achieve supranormal heights despite a significant bone age
Autor:
B.E. de Galan, J J G Hoorweg-Nijman, Cees Noordam, A. A. E. M. (Janielle) van Alfen-van der Velden, Ciska Westerlaken, P G Voorhoeve
Publikováno v:
Pediatric Diabetes, 11, 380-2
Pediatric Diabetes, 11, 6, pp. 380-2
Pediatric Diabetes, 11, 6, pp. 380-2
Contains fulltext : 89151.pdf (Publisher’s version ) (Closed access) The potential of inhaled insulin therapy for severe resistance to subcutaneous insulin was tested in a 7-yr old boy with type 1 diabetes mellitus. The efficiency of 1 mg inhaled i
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 152(31)
To evaluate the effects of frequent latching versus supplementary feeding of breastfed infants with hypoglycaemia on blood glucose concentrations and breastfeeding.Retrospective study of patient files.All breastfed infants born in the period of inves
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 150(43)
In two girls, aged 13 and 16 years, Cushing's syndrome was diagnosed. In addition, the first showed a decrease in linear growth and weight gain; a pituitary adenoma was found, which was surgically excised. The second girl was examined because of a ma
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(23)
Kallmann's syndrome is a genetic condition characterised by hypogonadotrophic hypogonadism and anosmia; additional neurological and non-neurological symptoms may also occur depending on the specific mode of inheritance. Mode of inheritance can be X-l
Publikováno v:
Nederlands tijdschrift voor geneeskunde. 148(3)
Persistent hyperinsulinemic hypoglycaemia in infancy (PHHI) presents a diagnostic and therapeutic challenge for the treating physician: increased glucose requirements, detectable insulin levels at the point of hypoglycaemia, inappropriately low blood