Results 71 to 80 of about 3,727 (171)
Swiss Medical Weekly: Quo vadis? [PDF]
, 2022 No abstract ...
Aguzzi, Adriano, Waeber, Gérard
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Mounier-Kuhn syndrome: A case study
South African Journal of Radiology, 2002 No abstract available.
M. J. Trollip
doaj +1 more source
Incidental Finding of Mounier-Kuhn Syndrome
Scholars Journal of Medical Case Reports, 2023 Tracheobronchomegaly (TBM) or Mounier - Kuhn syndrome is a rare disorder of uncertain etiology characterized by marked dilatation of the trachea and bronchi and recurrent lower respiratory tract infection.
H. J, A. J
semanticscholar +1 more source
Mounier Kuhn syndrome in adult: a case report [PDF]
, 2017 Mounier-Kuhn syndrome or tracheobronchomegaly is a rare congenital abnormality of the trachea and main bronchi characterized by marked cystic dilatation of the tracheobronchial tree, associated with tracheal diverticulosis, bronchiectasis and recurrent ...
Deka, Nabanita +2 more
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Acute respiratory symptoms in mounier-kuhn syndrome
Journal of the Belgian Society of Radiology, 2010 Background: A 73-year-old female patient presented at the emergency room with cough and dyspnea. There was green sputum production and she had fever. She had given up smoking 15 years before.
P A de Jong, J K Vette, L Meiss
doaj +1 more source
Lung India, 2012 Lower respiratory tract infection is one of the common causes of morbidity in India which is occasionally undiagnosed. In this regard tracheobronchomegaly is one of those conditions which masquerade as chronic bronchitis and bronchiectasis and are ...
Ashish K Jaiswal +4 more
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Infratentorial Abnormalities in Vascular Dementia [PDF]
, 2006 Background and Purpose—Infratentorial abnormalities may cause cognitive deficits, but current research criteria for vascular dementia (VaD) do not consider them.
Barkhof, F. +4 more
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Traqueobroncomegalia (Síndrome de Mournier-Kuhn) en una mujer de 75 años: reporte de un caso [PDF]
Tracheobronchomegaly, or Mounier-Kuhn syndrome, is a little-known disease characterized by dilation of the trachea and main bronchi, associated with recurrent respiratory infections, bronchiectasis, tracheomalacia, and tracheal diverticula.
Aparicio, Madonna, Carrasco, Nicolás
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A rare cause of recurrent respiratory infections [PDF]
, 2015 Universitatea de Stat de Medicină și Farmacie „Nicolae Testemiţanu”, Departamentul de medicină internă, Disciplina pneumologie și alergologie, Chișinău, Republica Moldova; Centrul de Diagnostic German, Chișinău, Republica ...
Botnaru, Victor +2 more
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William Campbell Syndrome as a Cause of Asymmetrical Bronchiectasis In a 10-Year-Old Child: A Case Report [PDF]
Background: William Campbell Syndrome is a rare congenital disease of the bronchial cartilages involving the 4th to 6th generation of bronchial divisions with involvement of bilateral lungs.
Asim Rehman +5 more
core +2 more sources