Zobrazeno 1 - 10
of 81
pro vyhledávání: '"B Brock Jacobsen"'
Publikováno v:
Acta Pathologica Microbiologica Scandinavica Section A Pathology. :751-755
A case of delivery complicated by extreme hyperlipaemia, probably of the Friederickson type IV, is reported. We found numerous foam cells in the placenta, mainly concentrated at the edge of the fibrin deposits in the intervillous space. In our opinio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39332890dafb68d2663d3337521f549b
https://doi.org/10.1111/j.1699-0463.1972.tb00346.x
https://doi.org/10.1111/j.1699-0463.1972.tb00346.x
Publikováno v:
Acta Paediatrica. 90:1116-1120
UNLABELLED In congenital hyperinsulinism (HI). the in vivo pancreatic beta-cell function is poorly described. Among 14 neonates with severe hyperinsulinaemic hypoglycaemia, 2 patients had very prolonged or persistent hypoglycaemia and mutation in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d96cdcc4811146b099ed8da965a30b7
https://doi.org/10.1111/j.1651-2227.2001.tb03239.x
https://doi.org/10.1111/j.1651-2227.2001.tb03239.x
Autor:
B Brock Jacobsen, H.A. Delemarre-van de Waal, U. Heinrich, N E Skakkebaek, J. Müller, Eberhard Keller, A.C.S. Hokken-Koelega, K. Hartmann
Publikováno v:
Hormone Research in Paediatrics. 51:109-112
Patient compliance is of vital importance for the outcome of any medical therapy. Compliance is especially a problem in long-term treatment of non-life threatening diseases, such as growth retardation in children. Until recently, all human growth hor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c80a0b7f354b47e76555fd9f31724799
https://doi.org/10.1159/000053171
https://doi.org/10.1159/000053171
Publikováno v:
Acta Paediatrica. 93:1192-1194
Aim: To ascertain the prevalence of germline mutations in the TSH receptor gene as a cause of juvenile thyrotoxicosis (JT) in non-autoimmune patients. TSH receptor gene mutations are not seen in autoimmune-active patients. Methods: In a nationwide st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4007132811562fbe887dc84fb59b5e54
https://doi.org/10.1111/j.1651-2227.2004.tb02747.x
https://doi.org/10.1111/j.1651-2227.2004.tb02747.x
Publikováno v:
Christesen, H T, Brusgaard, K, Beck-Nielsen, H & Brock-Jacobsen, B 2008, ' Non-insulinoma persistent hyperinsulinaemic hypoglycaemia caused by an activating glucokinase mutation : Hypoglycaemia unawareness and attacks ', Clinical Endocrinology, vol. 68, no. 5, pp. 747-755 . https://doi.org/10.1111/j.1365-2265.2008.03184.x
Summary Objective Adult-onset non-insulinoma persistent hyperinsulinaemic hypoglycaemia (NI-PHH) and the variant NI-pancreatogenous hypoglycaemia syndrome (NIPHS) are genetically unexplained diseases, without reports of hypoglycaemia unawareness or f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec47a7733787c51c5bd30c6517308fa
https://pubmed.ncbi.nlm.nih.gov/18208578
https://pubmed.ncbi.nlm.nih.gov/18208578
Publikováno v:
Acta Paediatrica. 79:20-27
Growth and endocrine status of 38 Nordic children surviving from medulloblastoma were reevaluated 5–15 years after the diagnosis. Group I included children treated before the age of 10, and group II were the patients > 10 years at onset of tumour t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::879910a845bcd6da9302f5d7393f8349
https://doi.org/10.1111/j.1651-2227.1990.tb17308.x
https://doi.org/10.1111/j.1651-2227.1990.tb17308.x
Publikováno v:
Tissue Antigens. 50:639-641
Previous studies have shown that HLA-DRB1*0301 and DQA1*0501 are associated with susceptibility to Graves' disease. Ninety Danish patients with early onset of Graves' disease and 102–192 controls were analyzed for HLA-DR and -DQ to investigate if t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2644f0126d50761aa067c9ae331380b4
https://doi.org/10.1111/j.1399-0039.1997.tb02922.x
https://doi.org/10.1111/j.1399-0039.1997.tb02922.x
Autor:
Mark J. Dunne, Khalid Hussain, Klaus Brusgaard, Mehul T. Dattani, John Gregory, RM Shepherd, E. A. Maher, H. T. Christesen, A. Luharia, Karen E. Cosgrove, Virpi V. Smith, Peter C. Hindmarsh, Benjamin Glaser, A. Sivaprasadarao, Sameer Kassem, Keith J. Lindley, B. Brock Jacobsen
Publikováno v:
The Journal of clinical endocrinology and metabolism. 90(7)
Background: Beckwith-Wiedemann syndrome (BWS) is a congenital overgrowth syndrome that is clinically and genetically heterogeneous. Hyperinsulinemic hypoglycemia occurs in about 50% of children with BWS and, in the majority of infants, it resolves sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c09b08915d27d1c85f8349d1986140d1
https://pubmed.ncbi.nlm.nih.gov/15811927
https://pubmed.ncbi.nlm.nih.gov/15811927
Publikováno v:
Rix, M, Laurberg, P, Hoejberg, A S & Brock-Jacobsen, B 2005, ' Pegvisomant therapy in pituitary gigantism: successful treatment in a 12-year-old girl ', European Journal of Endocrinology, vol. 153, no. 2, pp. 195-201 .
Objective: The use of a growth hormone (GH) receptor antagonist, pegvisomant has shown great promise in adults with acromegaly, but experience in paediatric patients is lacking. We aimed to describe the results of pegvisomant therapy in a 12-year-old
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1b285e82d2a3545be8ae33518f534d7
https://pure.au.dk/portal/da/publications/pegvisomant-therapy-in-pituitary-gigantism-successful-treatment-in-a-12yearold-girl(226a8480-bf3c-11da-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/pegvisomant-therapy-in-pituitary-gigantism-successful-treatment-in-a-12yearold-girl(226a8480-bf3c-11da-bee9-02004c4f4f50).html
Autor:
Niels Thomas Hertel, I. L. Pedersen, J. M. D. Hahnemann, N. Carlsen, Niels Clausen, B. Brock Jacobsen, Gitte Kerndrup
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 92(4)
UNLABELLED We report on a girl with an unusual Beckwith-Wiedemann syndrome (BWS) and hemihypertrophy, who developed an adrenocortical carcinoma with atypical clinical behaviour. At 4 y of age the girls was admitted to hospital with cushingoid feature
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5ba6f6f8e83425f8156da82c722fc7
https://pubmed.ncbi.nlm.nih.gov/12801110
https://pubmed.ncbi.nlm.nih.gov/12801110