Zobrazeno 1 - 10 of 15 pro vyhledávání: '"HALDUN BARIS DIREN"'
1
A Rare Cause of Pulmonary Emboli in a Patient with Deep Vein Thrombosis: Doppler Ultrasonographic Compressibility Maneuver
Autor: Haldun Baris Diren, Hakan Karamustafa, Muzaffer Bahçivan, Serdar Aslan, Muzaffer Elmali
Publikováno v: CardioVascular and Interventional Radiology. 30:803-805
Deep vein thrombosis (DVT) often begins in the calf veins or around the venous valves in the solar plexus in the lower extremities. Thrombus formation does not organize before 5–10 days and the risk of proximal progress and pulmonary thromboembolus
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddb11a00a5b7fa608ad534fcb53d26b5
https://doi.org/10.1007/s00270-007-9075-9
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2
Proton magnetic resonance spectroscopy of the anterior cingulate gyrus and caudate nucleus in schizophrenia patients versus healthy controls
Autor: Incesu, L., Baydin, M., Aslan, K., HALDUN BARIS DIREN, Sahin, H., Boke, O., Dane, S.
Publikováno v: Scopus-Elsevier
DANE, SENOL/0000-0001-5572-9454; DANE, SENOL/0000-0001-5572-9454; DIREN, HALDUN BARIS/0000-0001-8958-2040 WOS: 000288931100012 Proton magnetic resonance spectroscopy (H-1-MRS) permits the assessment of cerebral neurometabolites, such as N-acetylaspar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cf124017d254df55dc88366ef460da04
https://hdl.handle.net/20.500.12712/17340
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4
Bilateral split-hand with bilateral tibial aplasia
Autor: R. N. Sener, B. S. Sayli, F. Sener, Haldun Baris Diren, E. Isikan
Publikováno v: Pediatric radiology. 19(4)
PubMed: 2748235 The familial type of congenital split-hand associated with aplasia of the tibia is a very rare anomaly. Moreover, bilateral involvement of the hands and legs of the individual case is much rarer. In this paper, a case showing bilatera
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26efbdd316f415684eca7e5f20da595b
https://pubmed.ncbi.nlm.nih.gov/2748235
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5
Kozlowski type spondylometaphyseal dysplasia: A case report with literature review
Autor: Ms, Nural, HALDUN BARIS DIREN, Sakarya O, Yalin T, Dağdemir A
Publikováno v: Scopus-Elsevier
Europe PubMed Central
PubMed: 16752352 Spondylometaphyseal dysplasia is a type of bone dysplasia characterized by vertebral and metaphyseal changes of varying severity. Diagnosis of the disease is difficult because the severity of bone involvement differs and symptoms cha
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cc1585b3b2eb5363221aab0b61a4cdef
http://www.scopus.com/inward/record.url?eid=2-s2.0-33745016480&partnerID=MN8TOARS
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6
Computed tomography in agenesis of the right lobe of the liver
Autor: Demirci A, HALDUN BARIS DIREN, Mb, Selcuk
Publikováno v: Europe PubMed Central
Congenital agenesis of the right lobe of the liver is a rare anomaly. In a case report the diagnosis was made by computed tomography. A retro- or suprahepatic location of the gallbladder and compensatory hypertrophy of the left liver lobe and/or caud
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::e1b1cde4707d80a388bdbb46da2a8c72
http://europepmc.org/abstract/med/2340215
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8
Joubert syndrome with atrial septal defect and persistent left superior vena cava
Autor: Elmali M, Ozmen Z, Ceyhun M, Tokatlioğlu O, Incesu L, HALDUN BARIS DIREN
Publikováno v: Scopus-Elsevier
Europe PubMed Central
DIREN, HALDUN BARIS/0000-0001-8958-2040 WOS: 000254343000010 PubMed: 17562515 Joubert syndrome is a rare disorder characterized by hypotonia, ataxia, episodic hyperpnoea, psychomotor delay, abnormal ocular movements, and molar tooth sign on magnetic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::d2a5746927e38e81b08b3783a390f3e6
http://www.scopus.com/inward/record.url?eid=2-s2.0-34249984174&partnerID=MN8TOARS
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9
Dyggve-Melchior-Clausen syndrome without mental retardation (Smith-McCort dysplasia)
Autor: Bayrak, I. K., Nural, M. S., HALDUN BARIS DIREN
Publikováno v: Scopus-Elsevier
PubMed: 16206059 Radiographic features of a 15-year-old boy with Smith-McCort dysplasia are presented. Dyggve-Melchior-Clausen syndrome without mental retardation has clinical and radiographic findings similar to those of Smith-McCort dysplasia. Both
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::45c5adc32ee678553927bb69e270794e
http://www.scopus.com/inward/record.url?eid=2-s2.0-23844476277&partnerID=MN8TOARS
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10
The effectiveness of magnetization transfer technique in the evaluation of acute plaques in the central nervous system of multiple sclerosis patients and its correlation with the clinical findings
Autor: Atalay K, HALDUN BARIS DIREN, Gelmez S, Incesu L, Terzi M
Publikováno v: Scopus-Elsevier
Europe PubMed Central
PubMed: 16206053 Purpose: To determine the value of magnetization transfer (MT) imaging in the evaluation of acute plaques, which cause clinical findings in the brain magnetic resonance (MR) images of patients with relapsing-remitting multiple sclero
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8e574b80e3bc234f430f0db7e8014b3f
http://www.scopus.com/inward/record.url?eid=2-s2.0-23844452537&partnerID=MN8TOARS
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