Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Adina Zamfir"'
Autor:
Ileana Alexandra Sanda, Razvan Hainarosie, Irina Gabriela Ionita, Catalina Voiosu, Marius Razvan Ristea, Adina Zamfir Chiru Anton
Publikováno v:
Medicina, Vol 60, Iss 8, p 1205 (2024)
Background: Narrow-band imaging is an advanced endoscopic technology used to detect changes on the laryngeal tissue surface, employing a comparative approach alongside white-light endoscopy to facilitate histopathological examination. Objective: This
Externí odkaz:
https://doaj.org/article/84fb14f62c1a45ecae2beefcd0aff6bf
Autor:
Dragos Octavian Palade, Razvan Hainarosie, Adina Zamfir, Daniela Vrinceanu, Mihaela Pertea, Mihail Tusaliu, Florin Mocanu, Catalina Voiosu
Publikováno v:
Medicina, Vol 60, Iss 6, p 914 (2024)
Background and objectives: Paragangliomas of the head and neck are rare, slow-growing neuroendocrine tumors, benign in their vast majority, but with a possibility of developing distant metastases. They show great inheritable character, and their beha
Externí odkaz:
https://doaj.org/article/6b6e37c3bc234ebf801a6151cf76624d
Autor:
Dan Cristian Gheorghe, Augustina Enculescu, Adina Elena Stanciu, Veronica Epure, Adina Zamfir-Chiru-Anton
Publikováno v:
Clinical Pathology, Vol 16 (2023)
Introduction: Teratomas, tumors derived from all 3 fetal germ cell layers, are rarely located in the head and neck region and extremely rare in the Eustachian tube area. Case report: The authors present the case of a 2 years old child with chronic ea
Externí odkaz:
https://doaj.org/article/c0133a7af08e4f94955099ec3881e976
Autor:
Dan Cristian Gheorghe, Adina E. Stanciu, Adina Zamfir‐Chiru‐Anton, Oprea Doru, Veronica Epure
Publikováno v:
Clinical Case Reports, Vol 10, Iss 12, Pp n/a-n/a (2022)
Abstract Moebius Syndrome is a rare multifactorial condition defined by congenital complete or partial VII and VIth cranial nerves palsy and other physical abnormalities. We present the case of a 3 months old infant with Moebius sequence and breathin
Externí odkaz:
https://doaj.org/article/5b2efbfc72fa47d7a4a8e302e6730134
Publikováno v:
Medicina, Vol 59, Iss 3, p 461 (2023)
Background: The persistent stapedial artery (PSA) is a rare congenital vascular malformation involving the middle ear. It is usually associated with pulsatile tinnitus and/or conductive hearing loss and can account for multiple risks during middle ea
Externí odkaz:
https://doaj.org/article/4d094b80008848379ee8c0fd5540e1fb
Publikováno v:
Romanian Journal of Medical Practice, Vol 15, Iss 1, Pp 112-114 (2020)
Hairy polyps are tumors that have been described in the literature as congenital masses usually found in the nasopharynx. Clinical symptoms are a consequence of disease dimensions and anatomical positioning. Although rare, this kind of tumors can be
Externí odkaz:
https://doaj.org/article/3d18afe2af754e99ae0e83db52278303
Publikováno v:
Romanian Medical Journal, Vol 67, Iss 1, Pp 87-89 (2020)
Hunter syndrome is the type II of mucopolysaccharidose. With impaired glycosaminoglycan catabolism, heparan and dermatan sulfate accumulate in lysosomes. Multiple organ dysfunction is a consequence of this effect. We present the case of a a 9 year-ol
Externí odkaz:
https://doaj.org/article/a480ef512eca4dfa9170e29144918662
Publikováno v:
Romanian Medical Journal, Vol 67, Iss 1, Pp 99-101 (2020)
Branchial anomalies are a group of malformations resulting from incomplete closure of the pharyngeal pouches and clefts. They manifest as cysts, fistulae and sinus tracts located in the neck. We present the case of a 3 years-old girl admitted to the
Externí odkaz:
https://doaj.org/article/5ee995ecf2794b9d8fa8ad3acd9db7d8
Publikováno v:
Romanian Journal of Medical Practice, Vol 13, Iss 4, Pp 289-292 (2018)
Bacterial meningitis is a severe disease, accompanied by high risk of death or long term neurological morbidity. With modern day medicine, patients expect complete control of the disease. Objective. Disease pathogeny is hardly obvious in each bacte
Externí odkaz:
https://doaj.org/article/3dd4805dfe004ae28f5a693367d9b379
Publikováno v:
Romanian Journal of Medical Practice, Vol 13, Iss 1, Pp 58-61 (2018)
Congenital high airways obstruction syndrome (CHAOS) is a rare condition consisting of malformations of the larynx (diaphragm, stenosis, atresia) or trachea possibly associated with other organ congenital anomalies. Diagnosis can be established by
Externí odkaz:
https://doaj.org/article/acae6cf790304406ab50e301887bd723