Results 71 to 80 of about 6,261,021 (148)

Co-initiation of continuous renal replacement therapy, peritoneal dialysis, and extracorporeal membrane oxygenation in neonatal life-threatening hyaline membrane disease: A case report. [PDF]

Medicine (Baltimore), 2019
Li G, Zhang L, Sun Y, Chen J, Zhou C.
europepmc   +1 more source

Castleman′s disease: Hyaline vascular type

, 2014
Castleman′s disease is a rare disease of lymph node with two identified forms, the hyaline vascular type and plasma cell type. It presents as localized or systemic lymphadenopathy or even as extranodal mass and may give rise to several differential ...
Srikanth Shastry, Anandam Gadda
core   +1 more source

Risk factors for Pulmonary Interstitial Emphysema(PIE) in Mechanically Ventilated Neonates with Hyaline Membrane Diseas

, 1997
Purpose : Pulmonary interstitial emphysema(PIE) is a common and serious complication of mechanical ventilation in infants with hyaline membrane disease.
이철, 남궁란, 김명준
core  

Respiratory distress syndrome [Sikintili solunum sendromu]

, 2005
Respiratory distress caused by surfactant deficiency and global immaturity of lungs is called "respiratory distress syndrome". Hyaline membrane disease is a pathologic diagnosis characterized by hyaline membrane formation due to alveolar injury and ...
Erbey F., Tutak E., Özcan K., Özlü F.
core   +1 more source

Morphology of pulmonary extralobar sequestration in neonatal death by hyaline membrane disease

, 1994
Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Departamento de Anatomia Patológica. Rio de Janeiro, RJ, Brasil.Fundação Oswaldo Cruz. Instituto Fernandes Figueira. Departamento de Anatomia Patológica.
Garcia, Aparecida Gomes Pinto, Pegado, Claudia Schwartz   +1 more
core  

A case report of Lipoid Proteinosis

Majallah-i Dānishgāh-i ̒Ulūm-i Pizishkī-i Bābul, 1999
Objective: Lipoid proteinosis is a rare, autosomal recessive disease, characterized by persistent non-inflammatory popular lesions in the skin and mucous membranes.
S Tirgar Tabari
doaj  

Development of a calcifying fibrous pseudotumour within a lesion of Castleman disease, hyaline-vascular subtype

, 1999
A nine year old boy with localised Castleman disease of the hyaline- vascular subtype developed a calcifying fibrous pseudotumour. This pathological association does not appear to have been described before.
Roufosse, Candice, Laget, J.P., Dargent, Jean-Louis, Delplace, Jérôme, Lespagnard, Laurence   +4 more
core  

Trop-1/EpCAM Thr115 is a driver of hyperproliferative cell repair and of severe lung damage in COVID-19. [PDF]

iScience
Baldassarri M, Trerotola M, Brunelli G, La Francesca N, Bergantini L, Tella B, Rollo G, Altemura C, Giacomazzi V, Guerra E, Ceci M, Pantalone L, Minetto S, Bargagli E, Pomara C, Lattanzio R, Moschella A, Previtera FM, Bellan C, Network for Italian Genomes, GEN-COVID Multicenter Study, Renieri A, Fallerini C, Alberti S.   +23 more
europepmc   +1 more source

Lipoid Proteinosis with Homozygous ECM1 c.507del Variant and Functionally Significant Eyelid Involvement: A Case Report. [PDF]

Clin Cosmet Investig Dermatol
Hu L, Xu Y, Zhao W.
europepmc   +1 more source

Extra-articular Synovial Chondromatosis of the Subacromial-Subdeltoid Bursa Mimicking Rice Body Synovitis: A Case Report. [PDF]

Cureus
Megharaj R, Kammar SF, Pawar V, Naik CG.
europepmc   +1 more source