Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Katri Vuopala"'
Autor:
Pentti Nieminen, Katri Vuopala, Witold Mazur, Hideo Kobayashi, Vuokko L. Kinnula, Steffen Ohlmeier, Tuula Toljamo
Publikováno v:
European Respiratory Journal. 38:277-284
Serum surfactant protein (SP)-A has been postulated to associate with pulmonary fibrosis, but its role in cigarette smoking-related lung diseases is undefined. SP-A levels in plasma and induced sputum in nonsmokers, smokers with respiratory symptoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df7bbfaabe40337a87032522b8f228c3
https://doi.org/10.1183/09031936.00110510
https://doi.org/10.1183/09031936.00110510
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 131(6)
Autoimmune enteropathy (AIE) is characterized by protracted diarrhea, malabsorption, immunomediated damage to the intestinal mucosa, and unresponsiveness to changes in diet. The disease is mainly manifested in the small intestine. Lymphocyte deposits
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::86a95499ed4c012a73e4eeae7c4338c1
https://pubmed.ncbi.nlm.nih.gov/26237896
https://pubmed.ncbi.nlm.nih.gov/26237896
Publikováno v:
Pediatric Pulmonology. 35:8-16
Inhaled nitric oxide (NO) is a selective vasodilator in pulmonary hypertension. However, the safety of inhaled NO (iNO) has not been established. Using an immunohistochemical technique, we studied the expression of NO synthase (NOS) isoforms NOS1, NO
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f903d4a8883107463c4df4a3203dd91
https://doi.org/10.1002/ppul.10222
https://doi.org/10.1002/ppul.10222
Autor:
Olli, Säynäjäkangas, Ulpu, Tervashonka, Annika, Olli, Merja, Kurkinen, Airi, Jartti, Katri, Vuopala, Katriina, Kahlos
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 130(16)
Hepatopulmonary syndrome (HPS) is characterized by the triad of liver disease, intrapulmonary vascular dilatation and arterial deoxygenation. Mediating factors are tumor necrosis factor a, endothelin 1 and nitric oxide. Typical symptom is an increase
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2b8d34c158bb1c58d22392668fabb815
https://pubmed.ncbi.nlm.nih.gov/25269369
https://pubmed.ncbi.nlm.nih.gov/25269369
Publikováno v:
Pediatrics. 105:1013-1019
Objective.Fulminant early-onset neonatal pneumonia is associated with ascending intrauterine infection (IUI), prematurity, persistent pulmonary hypertension (PPHN), and septicemia. Nitric oxide (NO) as an inflammatory mediator is included in antimicr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98a1c560bd8564febe1a35b9699a0ab2
https://doi.org/10.1542/peds.105.5.1013
https://doi.org/10.1542/peds.105.5.1013
Autor:
Johanna Uusimaa, Riitta Herva, Ilmo E. Hassinen, Heikki Rantala, Katri Vuopala, Kari Majamaa, Leena Vainionpää, Anne M. Remes, Matti Nuutinen
Publikováno v:
Pediatrics. 105:598-603
Objectives. To assess the frequency of mitochondrial abnormalities in muscle histology, defects in respiratory chain enzyme activities, and mutations in mitochondrial DNA (mtDNA) in children with unexplained psychomotor retardation in the population
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fb6f3562da96f81625832a397ff2cf4
https://doi.org/10.1542/peds.105.3.598
https://doi.org/10.1542/peds.105.3.598
Autor:
Leena Peltonen, Marjo Kestilä, Riitta Herva, Jaakko Ignatius, Satu Kuure, Heli Honkala, Niklas Pakkasjärvi, Heidi O. Nousiainen, Katri Vuopala, Jonna Tallila
Publikováno v:
Nature Genetics. 40:155-157
The most severe forms of motoneuron disease manifest in utero are characterized by marked atrophy of spinal cord motoneurons and fetal immobility. Here, we report that the defective gene underlying lethal motoneuron syndrome LCCS1 is the mRNA export
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::731c2dc370a65f586a675cf66f29227b
https://doi.org/10.1038/ng.2007.65
https://doi.org/10.1038/ng.2007.65
Publikováno v:
Acta Neuropathologica. 90:176-183
Two female siblings with the fetal akinesia deformation sequence (FADS) are described. Both showed facial anomalies, arthrogrypotic extremities, hypoplastic lungs, and fetal growth retardation. The central nervous system of the second sibling, includ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::261870b79496c72c3fd4f929f6df8739
https://doi.org/10.1007/bf00294318
https://doi.org/10.1007/bf00294318
Publikováno v:
Human Pathology. 26:12-19
Fifteen infants (11 families) with lethal arthrogryposis and anterior horn motor neuron loss are described. The clinical presentation was the fetal akinesia deformation sequence (FADS) with multiple contractures and facial anomalies. At autopsy neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c40a68309826ad0457694c8280d24686
https://doi.org/10.1016/0046-8177(95)90109-4
https://doi.org/10.1016/0046-8177(95)90109-4
Publikováno v:
Neuropediatrics. 25:308-315
Eighty-three cases of multiple congenital joint contractures, i.e., arthrogryposis, which were related with either a stillborn fetus, a termination of pregnancy following prenatal diagnosis or death within 28 days postnatally, were studied. Sixty-sev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59d69416099515327b2cd236f54af6de
https://doi.org/10.1055/s-2008-1073045
https://doi.org/10.1055/s-2008-1073045