Coci EG - Search Results

1

Development of novel efficient SIN vectors with improved safety features for Wiskott-Aldrich syndrome stem cell based gene therapy.

Avedillo Díez I, Zychlinski D, Coci EG, Galla M, Modlich U, Dewey RA, Schwarzer A, Maetzig T, Mpofu N, Jaeckel E, Boztug K, Baum C, Klein C, Schambach A. Avedillo Díez I, et al. Among authors: coci eg. Mol Pharm. 2011 Oct 3;8(5):1525-37. doi: 10.1021/mp200132u. Epub 2011 Aug 31. Mol Pharm. 2011. PMID: 21851067

2

RETRACTED: Novel and safer self-inactivating vectors for gene therapy of Wiskott-Aldrich Syndrome.

Coci EG, Maetzig T, Zychlinski D, Rothe M, Suerth JD, Klein C, Schambach A. Coci EG, et al. Curr Gene Ther. 2015 Apr 9;15(3):245 - 254. doi: 10.2174/1566523215666150126120327. Curr Gene Ther. 2015. Retraction in: Curr Gene Ther. 2015;15(3):245 - 254.. PMID: 25963902 Retracted.

3

WITHDRAWN: Assessment of hematopoietic and neurologic pathophysiology of HCLS1-associated protein X-1 deficiency in a Hax1-knockout mouse model.

Coci EG, Thau-Habermann N, Maetzig T, Li Z, Klein C, Petri S, Schambach A. Coci EG, et al. Exp Hematol. 2014 Oct 28:S0301-472X(14)00716-4. doi: 10.1016/j.exphem.2014.10.010. Online ahead of print. Exp Hematol. 2014. PMID: 25448489

4

CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NIFA genes.

Coci EG, Koehler U, Liehr T, Stelzner A, Fink C, Langen H, Riedel J. Coci EG, et al. Mol Cytogenet. 2016 Feb 3;9:10. doi: 10.1186/s13039-016-0219-y. eCollection 2016. Mol Cytogenet. 2016. PMID: 26848311 Free PMC article.

5

Novel homozygous missense mutation in ALDH7A1 causes neonatal pyridoxine dependent epilepsy.

Coci EG, Codutti L, Fink C, Bartsch S, Grüning G, Lücke T, Kurth I, Riedel J. Coci EG, et al. Mol Cell Probes. 2017 Apr;32:18-23. doi: 10.1016/j.mcp.2016.11.002. Epub 2016 Nov 14. Mol Cell Probes. 2017. PMID: 27856333

6

Correction to: CANPMR syndrome and chromosome 1p32-p31 deletion syndrome coexist in two related individuals affected by simultaneous haplo-insufficiency of CAMTA1 and NFIA genes.

Coci EG, Koehler U, Liehr T, Stelzner A, Fink C, Langen H, Riedel J. Coci EG, et al. Mol Cytogenet. 2021 Mar 9;14(1):17. doi: 10.1186/s13039-021-00534-5. Mol Cytogenet. 2021. PMID: 33750428 Free PMC article. No abstract available.

7

Exploring two novel cases of suspected ictal epileptic headache, a rare form of paediatric epilepsy.

Coci EG, Riedel J. Coci EG, et al. Acta Paediatr. 2017 May;106(5):786-790. doi: 10.1111/apa.13713. Epub 2017 Feb 7. Acta Paediatr. 2017. PMID: 27992068

8

Novel Unbalanced Translocations Affecting the Long Arms of Chromosomes 10 and 22 Cause Complex Syndromes with Very Severe Neurodevelopmental Delay, Speech Impairment, Autistic Behavior, and Epilepsy.

Coci EG, Auhuber A, Langenbach A, Mrasek K, Riedel J, Leenen A, Lücke T, Liehr T. Coci EG, et al. Cytogenet Genome Res. 2017;151(4):171-178. doi: 10.1159/000471501. Epub 2017 May 10. Cytogenet Genome Res. 2017. PMID: 28486223

9

7q11.23 microduplication syndrome: neurophysiological and neuroradiological insights into a rare chromosomal disorder.

Castiglia L, Husain RA, Marquardt I, Fink C, Liehr T, Serino D, Elia M, Coci EG. Castiglia L, et al. Among authors: coci eg. J Intellect Disabil Res. 2018 May;62(5):359-370. doi: 10.1111/jir.12457. Epub 2017 Dec 20. J Intellect Disabil Res. 2018. PMID: 29266505

10

De-novo interstitial 2.33 Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome.

Akbaroghli S, Tonekaboni SH, Kariminejad R, Liehr T, Coci EG. Akbaroghli S, et al. Among authors: coci eg. Clin Dysmorphol. 2018 Jul;27(3):97-100. doi: 10.1097/MCD.0000000000000224. Clin Dysmorphol. 2018. PMID: 29738340 No abstract available.

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