Author/Creator: Zeitz, C. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Zeitz, C.

1. A novel nonsense variant in REEP6 is involved in a sporadic rod‐cone dystrophy case. Issue 3 (27th February 2018)

Authors:: Méjécase, C.; Mohand‐Saïd, S.; El Shamieh, S.; Antonio, A.; Condroyer, C.; Blanchard, S.; Letexier, M.; Saraiva, J.‐P.; Sahel, J.‐A.; Audo, I.; Zeitz, C.
Journal:: Clinical genetics
Issue:: Volume 93:Issue 3(2018)
Page Start:: 707
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

2. Aetiology of resuscitated out-of-hospital cardiac arrest treated at hospital. (January 2022)

Authors:: Wittwer, M.R.; Zeitz, C.; Beltrame, J.F.; Arstall, M.A.
Journal:: Resuscitation
Issue:: Volume 170(2022)
Page Start:: 178
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. ARL2BP mutations account for 0.1% of autosomal recessive rod‐cone dystrophies with the report of a novel splice variant. Issue 1 (6th February 2017)

Authors:: Audo, I.; El Shamieh, S.; Méjécase, C.; Michiels, C.; Demontant, V.; Antonio, A.; Condroyer, C.; Boyard, F.; Letexier, M.; Saraiva, J.‐P.; Blanchard, S.; Mohand‐Saïd, S.; Sahel, J.‐A.; Zeitz, C.
Journal:: Clinical genetics
Issue:: Volume 92:Issue 1(2017)
Page Start:: 109
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

4. Congenital stationary night blindness in a patient with mild learning disability due to a compound heterozygous microdeletion of 15q13 and a missense mutation in TRPM1. (4th May 2021)

Authors:: Delle Fave, M.; Cordonnier, M.; Vallee, l.; Condroyer, C.; Zeitz, C.; Balikova, I.
Journal:: Ophthalmic genetics
Issue:: Volume 42:Number 3(2021)
Page Start:: 296
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

5. Management of Indigenous patients presenting with non ST‐segment elevation acute coronary syndrome in South Australia: a retrospective cohort study. Issue 2 (February 2016)

Authors:: Roe, Y. L.; Esterman, A.; McDermott, R.; Zeitz, C.
Journal:: Internal medicine journal
Issue:: Volume 46:Issue 2(2016)
Page Start:: 202
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

6. Next‐generation sequencing confirms the implication of SLC24A1 in autosomal‐recessive congenital stationary night blindness. Issue 6 (4th March 2016)

Authors:: Neuillé, M.; Malaichamy, S.; Vadalà, M.; Michiels, C.; Condroyer, C.; Sachidanandam, R.; Srilekha, S.; Arokiasamy, T.; Letexier, M.; Démontant, V.; Sahel, J.‐A.; Sen, P.; Audo, I.; Soumittra, N.; Zeitz, C.
Journal:: Clinical genetics
Issue:: Volume 89:Issue 6(2016)
Page Start:: 690
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗