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

Year Number of Results
1979 1
1981 1
1982 4
1983 1
1984 1
1985 1
1987 4
1988 2
1989 1
1990 5
1991 1
1992 5
1993 5
1994 5
1995 2
1996 3
1997 2
1998 5
1999 1
2000 7
2001 4
2002 6
2003 9
2004 7
2005 10
2006 7
2007 5
2008 3
2009 2
2010 4
2011 2
2012 2
2013 4
2014 2
2015 1
2016 1
2017 1
2018 3
2019 2
2020 1
2021 4
2022 4
2023 1
2024 1

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131 results

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Page 1
[Dermatomyositis].
Stoltenburg-Didinger G, Genth E. Stoltenburg-Didinger G, et al. Z Rheumatol. 2009 Jun;68(4):287-94. doi: 10.1007/s00393-008-0398-y. Z Rheumatol. 2009. PMID: 19330338 Review. German.
Systematic Classification of Spina Bifida.
Schindelmann KH, Paschereit F, Steege A, Stoltenburg-Didinger G, Kaindl AM. Schindelmann KH, et al. Among authors: stoltenburg didinger g. J Neuropathol Exp Neurol. 2021 Mar 22;80(4):294-305. doi: 10.1093/jnen/nlab007. J Neuropathol Exp Neurol. 2021. PMID: 33576426
Congenital microcephaly-linked CDK5RAP2 affects eye development.
Zaqout S, Ravindran E, Stoltenburg-Didinger G, Kaindl AM. Zaqout S, et al. Among authors: stoltenburg didinger g. Ann Hum Genet. 2020 Jan;84(1):87-91. doi: 10.1111/ahg.12343. Epub 2019 Jul 29. Ann Hum Genet. 2020. PMID: 31355417
Cerebral Abnormalities in Spina Bifida: A Neuropathological Study.
Paschereit F, Schindelmann KH, Hummel M, Schneider J, Stoltenburg-Didinger G, Kaindl AM. Paschereit F, et al. Among authors: stoltenburg didinger g. Pediatr Dev Pathol. 2022 Mar-Apr;25(2):107-123. doi: 10.1177/10935266211040500. Epub 2021 Oct 6. Pediatr Dev Pathol. 2022. PMID: 34614376 Free PMC article.
Sudden infant death syndrome (SIDS)--standardised investigations and classification: recommendations.
Bajanowski T, Vege A, Byard RW, Krous HF, Arnestad M, Bachs L, Banner J, Blair PS, Borthne A, Dettmeyer R, Fleming P, Gaustad P, Gregersen M, Grøgaard J, Holter E, Isaksen CV, Jorgensen JV, de Lange C, Madea B, Moore I, Morland J, Opdal SH, Råsten-Almqvist P, Schlaud M, Sidebotham P, Skullerud K, Stoltenburg-Didinger G, Stray-Pedersen A, Sveum L, Rognum TO. Bajanowski T, et al. Among authors: stoltenburg didinger g. Forensic Sci Int. 2007 Jan 17;165(2-3):129-43. doi: 10.1016/j.forsciint.2006.05.028. Epub 2006 Jun 27. Forensic Sci Int. 2007. PMID: 16806765 Review.
Bi-allelic variants in CHKA cause a neurodevelopmental disorder with epilepsy and microcephaly.
Klöckner C, Fernández-Murray JP, Tavasoli M, Sticht H, Stoltenburg-Didinger G, Scholle LM, Bakhtiari S, Kruer MC, Darvish H, Firouzabadi SG, Pagnozzi A, Shukla A, Girisha KM, Narayanan DL, Kaur P, Maroofian R, Zaki MS, Noureldeen MM, Merkenschlager A, Gburek-Augustat J, Cali E, Banu S, Nahar K, Efthymiou S, Houlden H, Jamra RA, Williams J, McMaster CR, Platzer K. Klöckner C, et al. Among authors: stoltenburg didinger g. Brain. 2022 Jun 30;145(6):1916-1923. doi: 10.1093/brain/awac074. Brain. 2022. PMID: 35202461 Free PMC article.
Eosinophils in hereditary and inflammatory myopathies.
Schröder T, Fuchss J, Schneider I, Stoltenburg-Didinger G, Hanisch F. Schröder T, et al. Among authors: stoltenburg didinger g. Acta Myol. 2013 Dec;32(3):148-53. Acta Myol. 2013. PMID: 24803842 Free PMC article.
The p.S85C-mutation in MATR3 impairs stress granule formation in Matrin-3 myopathy.
Mensch A, Meinhardt B, Bley N, Hüttelmaier S, Schneider I, Stoltenburg-Didinger G, Kraya T, Müller T, Zierz S. Mensch A, et al. Among authors: stoltenburg didinger g. Exp Neurol. 2018 Aug;306:222-231. doi: 10.1016/j.expneurol.2018.05.012. Epub 2018 May 12. Exp Neurol. 2018. PMID: 29763601 No abstract available.
131 results