scholarly journals Clinical, diagnostic and therapeutic management of patients with breast tuberculosis: Analysis of 46 Cases

2016 ◽  
Vol 32 (1) ◽  
pp. 27-31 ◽  
Author(s):  
Murat Ozgur Kilic ◽  
Cemile Sağlam ◽  
Filiz D. Ağca ◽  
Serdar G. Terzioğlu
2014 ◽  
Vol 26 (4) ◽  
pp. 338-342
Author(s):  
Roberto Di Vito ◽  
Cosima Posari ◽  
Silvia Bucco ◽  
Martina Camplese ◽  
Federica Giunta ◽  
...  

2009 ◽  
Vol 19 (2) ◽  
pp. 49-57
Author(s):  
Brian E. Petty ◽  
Seth H. Dailey

Abstract Chronic cough is the most frequent reason cited by patients for seeking medical care in an ambulatory setting and may account for 10% to 38% of a pulmonologist's practice. Because chronic cough can be caused by or correlated with a wide array of disorders and behaviors, the diagnosis of etiologic factors and determination of appropriate therapeutic management in these cases can prove to be daunting for the physician and speech-language pathologist alike. This article will describe the phenomenon of chronic cough, discuss the many etiologic factors to consider, and review some of the more common ways in which speech-language pathologists and physicians collaborate to treat this challenging condition.


Skull Base ◽  
2007 ◽  
Vol 17 (S 2) ◽  
Author(s):  
Sung Kim ◽  
Jong Lee ◽  
Ho-Ki Lee ◽  
In-Seok Moon

Author(s):  
А.Ю. Рудник ◽  
М.А. Федяков ◽  
О.С. Глотов

На сегодняшний день в базе данных Online Mendelian Inheritance in Man (OMIM) описано более 6613 заболеваний и фенотипов, 4241 имеют доказанную генетическую основу, не менее 45% вкючают офтальмологические проявления. В статье приведен ряд клинический примеров пациентов с офтальмологическими симптомами различных генетических заболеваний (алкаптонурия, болезнь Штаргардта, синдром микроцефалии с или без хориоретинопатии; астроцитарная гамартома) с целью демонстрации эффективного клинико-диагностического скрининга генетической патологии у пациентов. So far, the Online Mendelian Inheritance in Man (OMIM) database describes more than 6613 diseases and phenotypes, 4241 have a proven genetic basis, 45% of which are combined with ophthalmological manifestations. The article provides a number of clinical examples of patients with ophthalmological manifestations of various genetic diseases (alcaptonuria, Stadgart ‘s disease, microcephaly syndrome with or without choriretinopathy; Astrocytic gamartoma) to demonstrate effective clinical-diagnostic screening of genetic pathology in patients.


2020 ◽  
Vol 4 (30) ◽  
pp. 26
Author(s):  
Boris Marinov Krâstev ◽  
Mihai Brăila ◽  
Cristina Maria Pucă ◽  
Anca Daniela Brăila

2020 ◽  
Vol 3 (68) ◽  
pp. 147
Author(s):  
Ioniţă Ducu ◽  
Roxana-Elena Bohîlţea ◽  
Dan Teleanu ◽  
Natalia Ţurcan ◽  
Monica Mihaela Cîrstoiu

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