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221 results

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Congenital disorders of glycosylation with defective fucosylation.
Hüllen A, Falkenstein K, Weigel C, Huidekoper H, Naumann-Bartsch N, Spenger J, Feichtinger RG, Schaefers J, Frenz S, Kotlarz D, Momen T, Khoshnevisan R, Riedhammer KM, Santer R, Herget T, Rennings A, Lefeber DJ, Mayr JA, Thiel C, Wortmann SB. Hüllen A, et al. Among authors: mayr ja. J Inherit Metab Dis. 2021 Nov;44(6):1441-1452. doi: 10.1002/jimd.12426. Epub 2021 Sep 15. J Inherit Metab Dis. 2021. PMID: 34389986
Loss of mitochondria in ganglioneuromas.
Feichtinger RG, Neureiter D, Mayr JA, Zimmermann FA, Berthold F, Jones N, Sperl W, Kofler B. Feichtinger RG, et al. Among authors: mayr ja. Front Biosci (Elite Ed). 2011 Jan 1;3(1):179-86. doi: 10.2741/e231. Front Biosci (Elite Ed). 2011. PMID: 21196296 Free article.
Alterations of respiratory chain complexes in sporadic pheochromocytoma.
Feichtinger RG, Zimmermann FA, Mayr JA, Neureiter D, Ratschek M, Jones N, Sperl W, Kofler B. Feichtinger RG, et al. Among authors: mayr ja. Front Biosci (Elite Ed). 2011 Jan 1;3(1):194-200. doi: 10.2741/e233. Front Biosci (Elite Ed). 2011. PMID: 21196298 Free article.
Respiratory chain complex I is a mitochondrial tumor suppressor of oncocytic tumors.
Zimmermann FA, Mayr JA, Feichtinger R, Neureiter D, Lechner R, Koegler C, Ratschek M, Rusmir H, Sargsyan K, Sperl W, Kofler B. Zimmermann FA, et al. Among authors: mayr ja. Front Biosci (Elite Ed). 2011 Jan 1;3(1):315-25. doi: 10.2741/e247. Front Biosci (Elite Ed). 2011. PMID: 21196312 Free article. Review.
Homozygous missense mutation in BOLA3 causes multiple mitochondrial dysfunctions syndrome in two siblings.
Haack TB, Rolinski B, Haberberger B, Zimmermann F, Schum J, Strecker V, Graf E, Athing U, Hoppen T, Wittig I, Sperl W, Freisinger P, Mayr JA, Strom TM, Meitinger T, Prokisch H. Haack TB, et al. Among authors: mayr ja. J Inherit Metab Dis. 2013 Jan;36(1):55-62. doi: 10.1007/s10545-012-9489-7. Epub 2012 May 5. J Inherit Metab Dis. 2013. PMID: 22562699
221 results