Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Nesat, Cullu"'
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 7, Iss 1, Pp 65-66 (2020)
Externí odkaz:
https://doaj.org/article/5ac7cd0a0b604ed08892f61bd759bbe4
Autor:
Kenan Sakar, Anil Ugurlu, Mehmet Kapan, Gulhan Akbaba, Nesat Cullu, Onder Ozcan, Ozcan Dere, Ozan Kandemir, Yelda Dere, Nese Cinar
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::419690e6cf292c3c01a9abd712c23b8c
https://doi.org/10.1530/endoabs.90.p582
https://doi.org/10.1530/endoabs.90.p582
Autor:
Kenan Sakar, Anil Ugurlu, Uyar Irmak Taskiran, Gulhan Akbaba, Ismail Kirli, Nesat Cullu, Onder Ozcan, Ozcan Dere, Ozan Kandemir, Yelda Dere, Nese Cinar
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::df514c53a620deae720aa2baab4fb970
https://doi.org/10.1530/endoabs.90.p592
https://doi.org/10.1530/endoabs.90.p592
Publikováno v:
Anatolian Journal of Cardiology, Vol 23, Iss 5, Pp 5013-5013 (2020)
Externí odkaz:
https://doaj.org/article/68d13a6906a5484a8eba30be02824d9e
Autor:
Ozkan Ilhan, Evren Gumus, Nilay Hakan, Hande Istar, Bugra Harmandar, Hasim Olgun, Suleyman Cuneyt Karakus, Nesat Cullu, Juergen Kohlhase, James D. Sutherland, Rosa Barrio
Publikováno v:
Journal of Pediatric Genetics.
Townes–Brocks syndrome (TBS) is a rare syndrome characterized by triad of anal, ear, and thumb anomalies. Further malformations/anomalies include congenital heart diseases, foot malformations, sensorineural and/or conductive hearing impairment, gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11494661cd5b09b40bcd6e140117442d
https://doi.org/10.1055/s-0041-1740371
https://doi.org/10.1055/s-0041-1740371
Townes–Brocks syndrome (TBS) is a rare syndrome characterized by triad of anal, ear, and thumb anomalies. Further malformations/anomalies include congenital heart diseases, foot malformations, sensorineural and/or conductive hearing impairment, gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2659::7051790c293c76b270fd8139479c132e
https://zenodo.org/record/7125671
https://zenodo.org/record/7125671
Publikováno v:
Case Reports in Cardiology, Vol 2015 (2015)
Giant hiatal hernias, generally seen at advanced ages, can rarely cause cardiac symptoms such as dyspnea and chest pain. Here, we aimed to present a case with a large hiatal hernia that largely protruded to intrathoracic cavity and caused dyspnea, pa
Externí odkaz:
https://doaj.org/article/00d68c8f4415402e9cdaccb4cd2d9d23
Publikováno v:
Case Reports in Radiology, Vol 2015 (2015)
Background. Spontaneous orbital haemorrhage is a very rare condition and vision-threatening event. It may occur due to trauma, orbital surgery/injections, orbital vascular anomalies, and a variety of systemic predisposing factors. Signs of retrobulba
Externí odkaz:
https://doaj.org/article/2fa42b6bc60c4185a3595fb3ac829cd0
Publikováno v:
Quantitative imaging in medicine and surgery. 5(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::99fc40a9876d2b63c94bba014129852c
https://pubmed.ncbi.nlm.nih.gov/26435927
https://pubmed.ncbi.nlm.nih.gov/26435927
Autor:
Ekrem, Karakas, Nesat, Cullu, Omer, Karakas, Mustafa, Calik, Fatima Nurefsan, Boyaci, Sema, Yildiz, Hasan, Cece, Ali, Akal
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 64(1)
Joubert syndrome is a rare disease characterised by clinical and radiological findings. Among the classic clinical findings of JS are hypotonia, ataxia, mental-motor retardation, respiratory and opthalmological findings. The paediatric cases included
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b9d35be8880a7b779ab380557fb6740
https://pubmed.ncbi.nlm.nih.gov/24605724
https://pubmed.ncbi.nlm.nih.gov/24605724