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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1992 1
1993 1
1994 1
1995 3
1996 2
1997 4
1998 2
1999 6
2000 5
2001 10
2002 4
2003 6
2004 6
2005 8
2006 1
2007 2
2008 2
2009 1
2012 1
2018 1
2023 0

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67 results

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Page 1
Neurologic phenotypes associated with COL4A1/2 mutations: Expanding the spectrum of disease.
Zagaglia S, Selch C, Nisevic JR, Mei D, Michalak Z, Hernandez-Hernandez L, Krithika S, Vezyroglou K, Varadkar SM, Pepler A, Biskup S, Leão M, Gärtner J, Merkenschlager A, Jaksch M, Møller RS, Gardella E, Kristiansen BS, Hansen LK, Vari MS, Helbig KL, Desai S, Smith-Hicks CL, Hino-Fukuyo N, Talvik T, Laugesaar R, Ilves P, Õunap K, Körber I, Hartlieb T, Kudernatsch M, Winkler P, Schimmel M, Hasse A, Knuf M, Heinemeyer J, Makowski C, Ghedia S, Subramanian GM, Striano P, Thomas RH, Micallef C, Thom M, Werring DJ, Kluger GJ, Cross JH, Guerrini R, Balestrini S, Sisodiya SM. Zagaglia S, et al. Among authors: jaksch m. Neurology. 2018 Nov 27;91(22):e2078-e2088. doi: 10.1212/WNL.0000000000006567. Epub 2018 Nov 9. Neurology. 2018. PMID: 30413629 Free PMC article.
Mitochondrial diabetes mellitus: a review.
Gerbitz KD, van den Ouweland JM, Maassen JA, Jaksch M. Gerbitz KD, et al. Among authors: jaksch m. Biochim Biophys Acta. 1995 May 24;1271(1):253-60. doi: 10.1016/0925-4439(95)00036-4. Biochim Biophys Acta. 1995. PMID: 7599217 Free article. Review.
DIDMOAD or Wolfram syndrome. A mitochondrial-mediated disorder.
Bezold R, Hofmann S, Jaksch M, Kaufhold P, Gerbitz KD. Bezold R, et al. Among authors: jaksch m. Diabetes Care. 1995 Apr;18(4):583-4. doi: 10.2337/diacare.18.4.583. Diabetes Care. 1995. PMID: 7497876 No abstract available.
MITOP, the mitochondrial proteome database: 2000 update.
Scharfe C, Zaccaria P, Hoertnagel K, Jaksch M, Klopstock T, Dembowski M, Lill R, Prokisch H, Gerbitz KD, Neupert W, Mewes HW, Meitinger T. Scharfe C, et al. Among authors: jaksch m. Nucleic Acids Res. 2000 Jan 1;28(1):155-8. doi: 10.1093/nar/28.1.155. Nucleic Acids Res. 2000. PMID: 10592209 Free PMC article.
MITOP: database for mitochondria-related proteins, genes and diseases.
Scharfe C, Zaccaria P, Hoertnagel K, Jaksch M, Klopstock T, Lill R, Prokisch H, Gerbitz KD, Mewes HW, Meitinger T. Scharfe C, et al. Among authors: jaksch m. Nucleic Acids Res. 1999 Jan 1;27(1):153-5. doi: 10.1093/nar/27.1.153. Nucleic Acids Res. 1999. PMID: 9847163 Free PMC article.
Risk of developing a mitochondrial DNA deletion disorder.
Chinnery PF, DiMauro S, Shanske S, Schon EA, Zeviani M, Mariotti C, Carrara F, Lombes A, Laforet P, Ogier H, Jaksch M, Lochmüller H, Horvath R, Deschauer M, Thorburn DR, Bindoff LA, Poulton J, Taylor RW, Matthews JN, Turnbull DM. Chinnery PF, et al. Among authors: jaksch m. Lancet. 2004 Aug 14-20;364(9434):592-6. doi: 10.1016/S0140-6736(04)16851-7. Lancet. 2004. PMID: 15313359
Characterization of cells in the developing human liver.
Nava S, Westgren M, Jaksch M, Tibell A, Broomé U, Ericzon BG, Sumitran-Holgersson S. Nava S, et al. Among authors: jaksch m. Differentiation. 2005 Jun;73(5):249-60. doi: 10.1111/j.1432-0436.2005.00019.x. Differentiation. 2005. PMID: 16026547
67 results