Zobrazeno 1 - 7
of 7
pro vyhledávání: '"H. I. Aydin"'
Autor:
Matthias R. Baumgartner, Eva Morava, A. M. Das, S. Geb, J. B.C. deKlerk, Nathalie Guffon, Martin Lindner, Olaf Bodamer, E. Müller, Tamaris Zwickler, Stefan Kölker, Alberto Burlina, U. Wendel, E. M. Maier, Frits A. Wijburg, John H. Walter, Gülden Gökçay, Stephanie Grunewald, Friederike Hörster, Bernd Schwahn, H. I. Aydin
Publikováno v:
Journal of Inherited Metabolic Disease, 31, 3, pp. 361-7
Journal of inherited metabolic disease, 31(3), 361-367. Springer Netherlands
Journal of Inherited Metabolic Disease, 31, 361-7
Journal of Inherited Metabolic Disease, 31, 361-367. Springer Netherlands
Journal of inherited metabolic disease, 31(3), 361-367. Springer Netherlands
Journal of Inherited Metabolic Disease, 31, 361-7
Journal of Inherited Metabolic Disease, 31, 361-367. Springer Netherlands
Contains fulltext : 70060.pdf (Publisher’s version ) (Closed access) The long-term outcome of patients with methylmalonic aciduria (MMA) is still uncertain due to a high frequency of complications such as chronic renal failure and metabolic stroke.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f7483123521d31b63380cf513b08aa
https://doi.org/10.1007/s10545-008-0804-2
https://doi.org/10.1007/s10545-008-0804-2
Publikováno v:
Rheumatology International. 24:77-79
We propose that thrombosis in Behçet's syndrome may be due to disruption of the annexin V shield by antiphospholipid antibodies. Measurement of antiannexin V antibodies may be of value in confirming diagnosis and evaluating the risk of venous and ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53e75638d446bbcb07cc1a2fb882a7bc
https://doi.org/10.1007/s00296-002-0274-z
https://doi.org/10.1007/s00296-002-0274-z
Autor:
Matthias R. Baumgartner, Esther M. Maier, Carlo Dionisi-Vici, J. B. C. de Klerk, Stephanie Grunewald, Sven F. Garbade, Stefan Kölker, Frits A. Wijburg, Gülden Gökçay, Nathalie Guffon, Friederike Hörster, Bernd Schwahn, T. Zwickler, Angelo Burlina, John H. Walter, Anibh M. Das, Olaf Bodamer, H. I. Aydin, S. Geb, Martin Lindner, Eva Morava
Publikováno v:
Journal of Inherited Metabolic Disease, 32, 5, pp. 630-9
Journal of inherited metabolic disease, 32(5), 630-639. Springer Netherlands
Journal of Inherited Metabolic Disease, 32, 630-9
Journal of Inherited Metabolic Disease, 32, 630-639. Springer Netherlands
Journal of inherited metabolic disease, 32(5), 630-639. Springer Netherlands
Journal of Inherited Metabolic Disease, 32, 630-9
Journal of Inherited Metabolic Disease, 32, 630-639. Springer Netherlands
Contains fulltext : 80534.pdf (Publisher’s version ) (Closed access) Objectives Isolated methylmalonic acidurias (MMAurias) are caused by deficiency of methylmalonyl-CoA mutase or by defects in the synthesis of its cofactor 5'-deoxyadenosylcobalami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60e92f41935779007866db7f805082a2
https://hdl.handle.net/2066/80534
https://hdl.handle.net/2066/80534
Publikováno v:
International urology and nephrology. 32(3)
It is widely believed that nocturnal enuresis is caused by a hereditary delay in maturation of the various organ systems. In this study, growth and bone age were investigated in enuretic children. There was a significant bone age lag in the enuretic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93a0b1b3f21ca470d8abc5a1b9b1e239
https://pubmed.ncbi.nlm.nih.gov/11583358
https://pubmed.ncbi.nlm.nih.gov/11583358
Publikováno v:
International urology and nephrology. 32(3)
Although nocturnal enuresis is probably the most common developmental disorder in children, the pathogenesis and management remain unclear. Autonomic dysfunction is one of the proposed mechanisms for nocturnal enuresis in children. The objective of c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c5cb8209756ce800df71e25a330134b4
https://pubmed.ncbi.nlm.nih.gov/11583359
https://pubmed.ncbi.nlm.nih.gov/11583359
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 43(3)
Benzathine penicillin is the most widely used antibiotic in the prophylaxis of children with rheumatic fever. The aim of the present study was to evaluate the DNA damage in children receiving one dose of 1.2 million units benzathine penicillin every
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c631595b6810c0ab70095b6d5c401745
https://pubmed.ncbi.nlm.nih.gov/11380924
https://pubmed.ncbi.nlm.nih.gov/11380924
Publikováno v:
The Turkish journal of pediatrics. 42(3)
Congenital thoracic ectopic kidney is a very rare developmental anomaly and the rarest form of all ectopic kidneys. It is usually asymptomatic and discovered incidentally on a routine chest radiography. We report a thoracic ectopic kidney in a 19-mon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dce10675fab56d53c9ed6850ddd3475b
https://pubmed.ncbi.nlm.nih.gov/11105630
https://pubmed.ncbi.nlm.nih.gov/11105630