Search Results - "Balliu, Pere Ramon"

Listeria monocytogenes: generalised maculopapular rash may be the clue by Benitez-Segura, Ignacio, Fiol-Jaume, Miguel, Balliu, Pere Ramon, Tejedor, Maria

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Multiple congenital vascular lesions in a newborn: a diagnostic challenge by Tejedor, Maria, Gracia-Darder, Inés, Balliu, Pere Ramon, Ramos Asensio, Rafael Félix, Jarque, Pilar, Martin-Santiago, Ana

“…The CT scan (figure 1D,E) revealed a large right thoracic mass with an extensive cerebral bleeding, signs of hypoxaemic encephalopathy, that led to brain death…”
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Digestive tract symptoms in congenital langerhans cell histiocytosis: a fatal condition in an illness usually considered benign by Vetter-Laracy, Susanne, Salinas, Jose Antonio, Martin-Santiago, Ana, Guibelalde, Mercedes, Balliu, Pere-Ramon

“…Congenital Langerhans cell histiocytosis is usually limited to cutaneous lesions and has a good prognosis. In rare cases of gut involvement, mortality is high…”
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Neonatal Listeriosis and The Importance of Body Surface Cultures by Sailer, Sebastian, Badia, Pere Ramon Balliu, Vetter-Laracy, Susanne Irene Christa, Benítez-Segura, Ignacio, de Gopegui Bordes, Enrique Ruiz

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Dacryocystocele: a rare cause of neonatal respiratory distress by Moreno-Calero, Clara, Benítez-Segura, Ignacio, Ramis, Laia Ferrés, Ferré, Consuelo Galiana, Busto, Jordi Roldan, Balliu-Badia, Pere Ramon

“…Abstract Dacryocystocele consist in congenital dilatation of the tear duct. It is a benign anomaly with a good prognosis that is caused by blockage of the…”
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Splenic haemorrhage in a newborn as the first manifestation of wandering spleen syndrome by Balliu, Pere-Ramon, Bregante, Juan, Pérez-Velasco, Maria-Carmen, Fiol, Miguel, Galiana, Consuelo, Herrera, Manuel, Mulet, Jaime

“…Wandering spleen is an unusual condition in children and is even more rarely diagnosed in the neonatal period. A case of splenic haemorrhage after dystocic…”
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Presentation, clinical course, and outcome of the congenital form of myotonic dystrophy by Roig, M, Balliu, P R, Navarro, C, Brugera, R, Losada, M

“…We report the clinical experience of 18 patients with the congenital form of myotonic dystrophy, the majority of whom were diagnosed during the neonatal period…”
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Diagnostic Difficulties Reveal Rare form of Membranous Esophageal Atresia by Arasa, Eva Beltran, Vetter-Laracy, Susanne, Benítez-Segura, Ignacio, Montero, Ana Moreno, Irastorza, Claudia Marhuenda, Badia, Pere Ramon Balliu

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Estudio retrospectivo sobre las características clínicas de las patologías respiratorias agudas asociadas al aislamiento de citomegalovirus (1995-2006) by Figuerola Mulet, Joan, Reina Prieto, Jordi, Balliu Badia, Pere Ramon

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