Magyari M - Search Results

1

Autologous hematopoietic stem cell transplantation of patients with aggressive relapsing-remitting multiple sclerosis: Danish nation-wide experience.

Jespersen F, Petersen SL, Andersen P, Sellebjerg F, Magyari M, Sørensen PS, Blinkenberg M. Jespersen F, et al. Among authors: magyari m. Mult Scler Relat Disord. 2023 Aug;76:104829. doi: 10.1016/j.msard.2023.104829. Epub 2023 Jun 13. Mult Scler Relat Disord. 2023. PMID: 37364374 Free article.

2

[Plasma factors influencing prostacyclin-like activity in diabetic microangiopathies].

Túri S, Magyari M, Csalánosiné NM. Túri S, et al. Among authors: magyari m. Orv Hetil. 1987 Jun 21;128(25):1311-5. Orv Hetil. 1987. PMID: 3302816 Hungarian. No abstract available.

3

[Iodine deficiency in cardiovascular diseases].

Molnár I, Magyari M, Stief L. Molnár I, et al. Among authors: magyari m. Orv Hetil. 1998 Aug 30;139(35):2071-3. Orv Hetil. 1998. PMID: 9755626 Hungarian.

4

Acute headache and persistent headache attributed to cervical artery dissection: Field testing of ICHD-III beta.

Schytz HW, Ashina M, Magyari M, Larsen VA, Olesen J, Iversen HK. Schytz HW, et al. Among authors: magyari m. Cephalalgia. 2014 Aug;34(9):712-716. doi: 10.1177/0333102414520767. Epub 2014 Feb 5. Cephalalgia. 2014. PMID: 24500814

5

[Prostacyclin-like activity modifying plasma factors in diabetic microangiopathy].

Magyari M, Túri S, Csanálosi-Németh M. Magyari M, et al. Fortschr Ophthalmol. 1990;87(3):269-73. Fortschr Ophthalmol. 1990. PMID: 2115854 German.

6

[Neurosarcoidosis--different manifestations].

Magyari M, Frederiksen J. Magyari M, et al. Ugeskr Laeger. 2010 Nov 29;172(48):3344-5. Ugeskr Laeger. 2010. PMID: 21118667 Danish.

7

Plasma factors influencing prostacyclin-like activity in patients with diabetic microangiopathy.

Turi S, Magyari M, Nemeth M, Bereczky C. Turi S, et al. Among authors: magyari m. Prostaglandins Leukot Essent Fatty Acids. 1988 Mar;31(3):107-11. doi: 10.1016/0952-3278(88)90105-6. Prostaglandins Leukot Essent Fatty Acids. 1988. PMID: 3287394

8

Novel heterozygous nonsense mutation of the OPTN gene segregating in a Danish family with ALS.

Tümer Z, Bertelsen B, Gredal O, Magyari M, Nielsen KC, Lucamp, Grønskov K, Brøndum-Nielsen K. Tümer Z, et al. Among authors: magyari m. Neurobiol Aging. 2012 Jan;33(1):208.e1-5. doi: 10.1016/j.neurobiolaging.2011.07.001. Epub 2011 Aug 26. Neurobiol Aging. 2012. PMID: 21852022

9

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis.

Zsurka G, Ormos J, Iványi B, Túri S, Endreffy E, Magyari M, Sonkodi S, Venetianer P. Zsurka G, et al. Among authors: magyari m. Hum Genet. 1997 Apr;99(4):484-7. doi: 10.1007/s004390050393. Hum Genet. 1997. PMID: 9099838

10

Reproduction and the risk of multiple sclerosis.

Magyari M, Koch-Henriksen N, Pfleger CC, Sørensen PS. Magyari M, et al. Mult Scler. 2013 Oct;19(12):1604-9. doi: 10.1177/1352458513481397. Epub 2013 Mar 18. Mult Scler. 2013. PMID: 23508651

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