Scientific paper - Original scientific paper
Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association
Collegium Antropologicum, 35 (2011), S. 1; 333-338. urn:nbn:hr:105:894773


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Šarac, H., Telarović, S., Markeljević, J., Perić, B., Pavliša, G. & Radoš, M. (2011). Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association . Collegium Antropologicum, 35. (S. 1), 333-338. Retrieved from https://urn.nsk.hr/urn:nbn:hr:105:894773

Šarac, Helena, et al. "Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ." Collegium Antropologicum, vol. 35, no. S. 1, 2011, pp. 333-338. https://urn.nsk.hr/urn:nbn:hr:105:894773

Šarac, Helena, Srđana Telarović, Jasenka Markeljević, Berislav Perić, Goran Pavliša and Marko Radoš. "Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ." Collegium Antropologicum 35, no. S. 1 (2011): 333-338. https://urn.nsk.hr/urn:nbn:hr:105:894773

Šarac, H., et al. (2011) 'Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ', Collegium Antropologicum, 35(S. 1), pp. 333-338. Available at: https://urn.nsk.hr/urn:nbn:hr:105:894773 (Accessed 27 April 2024)

Šarac H, Telarović S, Markeljević J, Perić B, Pavliša G, Radoš M. Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association . Collegium Antropologicum [Internet]. 2011 January [cited 2024 April 27];35(S. 1):333-338. Available at: https://urn.nsk.hr/urn:nbn:hr:105:894773

H. Šarac, S. Telarović, J. Markeljević, B. Perić, G. Pavliša and M. Radoš, "Symptomatic capillary telangiectasia of the pons and intracerebral developmental venous anomaly – a rare association ", Collegium Antropologicum, vol. 35, no. S. 1, pp. 333-338, January 2011. [Online]. Available at: https://urn.nsk.hr/urn:nbn:hr:105:894773. [Accessed: 27 April 2024]