Zobrazeno 1 - 10
of 22
pro vyhledávání: '"S Geb"'
Publikováno v:
South African Medical Journal, Vol 114, Iss 5 (2024)
Background. The COVID‐19 pandemic had a profound effect on the health sector globally and in South Africa (SA). Objective. To review the effects of COVID‐19 on maternal, perinatal and reproductive health outcomes and service utilisation in SA.
Externí odkaz:
https://doaj.org/article/8ed17f2447c142ce805e03ed6d434495
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
Autor:
A Heitkamp, J Suh, S Gebhardt, J van Roosmalen, L R Murray, J I de Vries, T van den Akker, G Theron
Publikováno v:
South African Medical Journal, Vol 112, Iss 9 (2022)
Background. To improve maternal health, studies of maternal morbidity are increasingly being used to evaluate the quality of maternity care, in addition to studies of mortality. While South Africa (SA) has a well-established confidential enquiry into
Externí odkaz:
https://doaj.org/article/8b48738debc444588f4f203fc21bbae7
Autor:
M Qirshi, M Baz Bartels, S Dittrich, Matthias Kieslich, Franziska Hoche, M Selter, Stefan Vlaho, S Geb, M Laufs, J Althaus
Publikováno v:
Neuropediatrics. 41
Background information and Case report: CMT-Type 4E, or congenital hypomyelinating neuropathy (CHN) is an extremely rare disorder of myelin formation. Patients show early infantile hypotonia, distal muscle weakness, and areflexia. Complications are r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::645fd03d8d5bbc68a56405268fd12c2e
https://doi.org/10.1055/s-0030-1265563
https://doi.org/10.1055/s-0030-1265563
Autor:
Luciana Porto, J Althaus, Matthias Kieslich, M Laufs, Stefan Vlaho, M Qirshi, Franziska Hoche, M Baz Bartels, S Geb, S Dittrich
Publikováno v:
Neuropediatrics. 41
Pediatric multiple sclerosis (PMS), likely occurring in 0.2–0.6% of all MS cases, has been increasingly recognized in the past 10 years. PMS (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::56ddf99e4c1c7a73043ea5b1602cdf03
https://doi.org/10.1055/s-0030-1265582
https://doi.org/10.1055/s-0030-1265582
Autor:
S Geb, Franziska Hoche, R. Dresel, J Althaus, Matthias Kieslich, Stefan Vlaho, M Selter, S Dittrich, M Qirshi, Stefan Zielen, M Baz Bartels
Publikováno v:
Neuropediatrics. 41
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a74185fc364a154007ec1c7233953690
https://doi.org/10.1055/s-0030-1265602
https://doi.org/10.1055/s-0030-1265602
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
Autor:
S Dittrich, M Baz Bartels, M Qirshi, A Gal, Stefan Vlaho, V Boda, Matthias Kieslich, S Geb, U Orth
Publikováno v:
Neuropediatrics. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fabae6a78c5a6dae629ba7f1944ce1db
https://doi.org/10.1055/s-2008-1079552
https://doi.org/10.1055/s-2008-1079552
Autor:
M Baz Bartels, Luciana Porto, V Boda, R. Gerlach, J Althaus, Stefan Vlaho, M Laufs, Matthias Kieslich, S Geb
Publikováno v:
Neuropediatrics. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca8bcb416125739bb5ac02a0249b6faf
https://doi.org/10.1055/s-2008-1079570
https://doi.org/10.1055/s-2008-1079570
Autor:
V Boda, M Baz Bartels, Luciana Porto, S Geb, Matthias Kieslich, Stefan Vlaho, Thomas Klingebiel, J Althaus
Publikováno v:
Neuropediatrics. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab0ff24ebe3683988a60f9e2adfd6cdf
https://doi.org/10.1055/s-2008-1079542
https://doi.org/10.1055/s-2008-1079542