Search Results - "Paavola, P"

Overall survival after stereotactic radiotherapy or surgical metastasectomy in oligometastatic renal cell carcinoma patients treated at two Swedish centres 2005–2014 by Stenman, M., Sinclair, G., Paavola, P., Wersäll, P., Harmenberg, U., Lindskog, M.

“…Investigate effects of stereotactic radiotherapy (SRT) or surgical metastasectomy (SM) on overall survival (OS) in metastatic renal cell carcinoma (mRCC) in…”
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A simple score to predict severe leptospirosis by Smith, Simon, Kennedy, Brendan J, Dermedgoglou, Alexis, Poulgrain, Suzanne S, Paavola, Matthew P, Minto, Tarryn L, Luc, Michael, Liu, Yu-Hsuan, Hanson, Josh

“…The case-fatality rate of severe leptospirosis can exceed 50%. While prompt supportive care can improve survival, predicting those at risk of developing severe…”
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Severe leptospirosis in tropical Australia: Optimising intensive care unit management to reduce mortality by Smith, Simon, Liu, Yu-Hsuan, Carter, Angus, Kennedy, Brendan J, Dermedgoglou, Alexis, Poulgrain, Suzanne S, Paavola, Matthew P, Minto, Tarryn L, Luc, Michael, Hanson, Josh

“…Severe leptospirosis can have a case-fatality rate of over 50%, even with intensive care unit (ICU) support. Multiple strategies-including protective…”
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Characteristics and circumstances of homicidal acts committed by offenders with schizophrenia by Joyal, C C, Putkonen, A, Paavola, P, Tiihonen, J

“…While men with schizophrenia are at higher risk of displaying homicidal behaviours compared with the general population, very little is known about the…”
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Functional polymorphism in IL12B promoter site is associated with ulcerative colitis by Szperl, A., Saavalainen, P., Weersma, R.K., Lappalainen, M., Paavola‐Sakki, P., Halme, L., Färkkilä, M., Turunen, U., Kontula, K., Ponsioen, C.Y., Wijmenga, C., van Diemen, C.C.

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Standardised photographic documentation of the auricle by Mäkitie, A.A., Paavola, P., Klockars, T.

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Operative and nonoperative treatment of clavicle fractures in adults by Virtanen, Kaisa J, Malmivaara, Antti O V, Remes, Ville M, Paavola, Mika P

“…Background and purpose Traditionally, clavicle fractures have been treated nonoperatively. However, many recent studies have concentrated on the results of…”
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Familial and Sporadic Inflammatory Bowel Disease: Comparison of Clinical Features and Serological Markers in a Genetically Homogeneous Population by Halme, L., Turunen, U., Heliö, T., Paavola, P., Walle, T., Miettinen, A., Järvinen, H., Kontula, K., Färkkilä, M.

“…Background: The familial occurrence of inflammatory bowel disease (IBD) and the clinical features of familial and sporadic IBD in the genetically homogeneous…”
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CARD15/NOD2 gene variants are associated with familially occurring and complicated forms of Crohn’s disease by Heliö, T, Halme, L, Lappalainen, M, Fodstad, H, Paavola-Sakki, P, Turunen, U, Färkkilä, M, Krusius, T, Kontula, K

“…Background: Variants of the caspase activating recruitment domain 15/nucleotide oligomerisation domain 2 (CARD15/NOD2) gene have been associated with…”
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Operative and nonoperative treatment of clavicle fractures in adults: A systematic review of 1,190 patients from the literature by Virtanen, Kaisa J, Malmivaara, Antti O V, Remes, Ville M, Paavola, Mika P

“…Background and purpose Traditionally, clavicle fractures have been treated nonoperatively. However, many recent studies have concentrated on the results of…”
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Surgical treatment of Rockwood grade-V acromioclavicular joint dislocations: 50 patients followed for 15-22 years by Virtanen, Kaisa J, Remes, Ville M, Tulikoura, Ilkka T A, Pajarinen, Jarkko T, Savolainen, Vesa T, Björkenheim, Jan-Magnus G, Paavola, Mika P

“…Background and purpose Long-term outcome after surgery for grade-V acromioclavicular joint dislocation has not been reported. We performed a retrospective…”
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CARD15 frameshift mutation in patients with Crohn disease is associated with immune dysregulation by Halme, L., Turunen, U., Paavola-Sakki, P., Heliö, T., Lappalainen, M., Färkkilä, M., Kontula, K., Repo, H.

“…Background: Mutations in the caspase-activating recruitment domain 15 (CARD15) gene are associated with Crohn disease (CD). CARD15 is an intracellular receptor…”
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Association study of FUT2 (rs601338) with celiac disease and inflammatory bowel disease in the Finnish population by Parmar, A. S., Alakulppi, N., Paavola-Sakki, P., Kurppa, K., Halme, L., Färkkilä, M., Turunen, U., Lappalainen, M., Kontula, K., Kaukinen, K., Mäki, M., Lindfors, K., Partanen, J., Sistonen, P., Mättö, J., Wacklin, P., Saavalainen, P., Einarsdottir, E.

“…Homozygosity for a nonsense mutation in the fucosyltransferase 2 (FUT2) gene (rs601338G>A) leads to the absence of ABH blood groups (FUT2 non‐secretor status)…”
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Association of celiac disease genes with inflammatory bowel disease in Finnish and Swedish patients by Parmar, A S, Lappalainen, M, Paavola-Sakki, P, Halme, L, Färkkilä, M, Turunen, U, Kontula, K, Aromaa, A, Salomaa, V, Peltonen, L, Halfvarson, J, Törkvist, L, D'Amato, M, Saavalainen, P, Einarsdottir, E

“…Some genetic loci may affect susceptibility to multiple immune system-related diseases. In the current study, we investigated whether the known susceptibility…”
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Molecular cytogenetic mapping of 24 CEPH YACs and 24 gene-specific large insert probes to chromosome 17 by Bärlund, M, Nupponen, N N, Karhu, R, Tanner, M M, Paavola, P, Kallioniemi, O P, Kallioniemi, A

“…Defining boundaries of chromosomal rearrangements at the molecular level would benefit from landmarks that link the cytogenetic map to physical, genetic, and…”
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Comprehensive Copy Number and Gene Expression Profiling of the 17q23 Amplicon in Human Breast Cancer by Monni, Outi, Bärlund, Maarit, Mousses, Spyro, Kononen, Juha, Sauter, Guido, Heiskanen, Mervi, Paavola, Paulina, Avela, Kristiina, Chen, Yidong, Bittner, Michael L., Kallioniemi, Anne

“…The biological significance of DNA amplification in cancer is thought to be due to the selection of increased expression of a single or few important genes…”
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Meckel syndrome by Salonen, R, Paavola, P

“…Meckel syndrome (MKS) is a lethal syndrome with a central nervous system malformation, usually occipital meningoencephalocele, bilaterally large multicystic…”
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International Collaboration Provides Convincing Linkage Replication in Complex Disease through Analysis of a Large Pooled Data Set: Crohn Disease and Chromosome 16 by Cavanaugh, Juleen

“…Numerous familial, non-Mendelian (i.e., complex) diseases have been screened by linkage analysis for regions harboring susceptibility genes. Except for rare,…”
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MKS1 , encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome by Peltonen, Leena, Kyttälä, Mira, Tallila, Jonna, Salonen, Riitta, Kopra, Outi, Kohlschmidt, Nicolai, Paavola-Sakki, Paulina, Kestilä, Marjo

“…Meckel syndrome (MKS) is a severe fetal developmental disorder reported in most populations. The clinical hallmarks are occipital meningoencephalocele, cystic…”
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The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24 by Peltonen, Leena, Paavola, Paulina, Weissenbach, Jean, Salonen, Riitta

“…Autosomal recessive Meckel syndrome (OMIM 249000) (MES), first described in 1822 by Johann F. Meckel, is a major monogenic malformation syndrome with a neural…”
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