Zobrazeno 1 - 10
of 96
pro vyhledávání: '"Toivo T. Salmi"'
Autor:
Anu Usvasalo, Riikka Räty, Sakari Knuutila, Kim Vettenranta, Arja Harila-Saari, Esa Jantunen, Marjut Kauppila, Pirjo Koistinen, Katriina Parto, Pekka Riikonen, Toivo T. Salmi, Raija Silvennoinen, Erkki Elonen, Ulla M. Saarinen-Pihkala
Publikováno v:
Haematologica, Vol 93, Iss 8 (2008)
Background Interest has recently been paid to adolescents and young adults with acute lymphoblastic leukemia, particularly because all reports so far published indicate that these patients have a better outcome when treated with pediatric rather than
Externí odkaz:
https://doaj.org/article/68767df05d8543a6af6d5a5c6c3b3c96
Autor:
Tore Stokland, Magnus Sabel, Benedicte Bang, Henrik Hasle, Steen Rosthøj, Miriam Entesarian, Edvard Nordenskjöld, Samuel C. C. Chiang, Magnus Nordenskjöld, Toivo T. Salmi, Caroline Björklund, Britt-Marie Holmqvist, Ljubica Rajić, Hans-Gustaf Ljunggren, Marie Meeths, Janez Jazbec, Jacek Winiarski, Yenan T. Bryceson, Susan Pfeifer, Bengt Fadeel, Stephanie M. Wood, Heinrich Schlums, Gordana Jakovljević, Jan-Inge Henter
Publikováno v:
Meeths, M, Chiang, S C C, Wood, S M, Entesarian, M, Schlums, H, Bang, B, Nordenskjöld, E, Björklund, C, Jakovljevic, G, Jazbec, J, Hasle, H, Holmqvist, B-M, Rajic, L, Pfeifer, S, Rosthøj, S, Sabel, M, Salmi, T T, Stokland, T, Winiarski, J, Ljunggren, H-G, Fadeel, B, Nordenskjöld, M, Henter, J-I & Bryceson, Y T 2011, ' Familial hemophagocytic lymphohistiocytosis type 3 (FHL3) caused by deep intronic mutation and inversion in UNC13D ', Blood, vol. 118, no. 22, pp. 5783-93 . https://doi.org/10.1182/blood-2011-07-369090
Familial hemophagocytic lymphohistiocytosis (FHL) is an autosomal recessive, often-fatal hyperinflammatory disorder. Mutations in PRF1, UNC13D, STX11, and STXBP2 are causative of FHL2, 3, 4, and 5, respectively. In a majority of suspected FHL patient
Publikováno v:
Cancer Epidemiology. 35(2):202-210
The aims: The aims of this Finnish total cohort survey were to compare the health related quality of life (HRQL) of childhood cancer survivors with for age, gender and place of residence matched controls, to analyse whether the disease-related factor
Autor:
Saija Hurme, Anne-Mari Hatanpää, Toivo T. Salmi, Irma E. Holopainen, Päivi M. Lähteenmäki, T. Karki, Hannu Mikola, Maria Leino, Liisa S. Järvelä
Publikováno v:
Clinical Neurophysiology. 122:62-72
Objective The purpose of this study was to analyze event related potentials mismatch negativity (MMN) and P3a in childhood cancer patients at the time of diagnosis (Study 1) and after treatment (Study 2) to evaluate their clinical usefulness in scree
Publikováno v:
Acta Pathologica Microbiologica Scandinavica Section A Pathology. :223-226
We describe an 8-year-old girl who presented a massive mediastinal tumour of thymic origin. Surgical excision was unsuccessful. Irradiation treatment (4,500 rad) together with intensive combination chemotherapy resulted in regression of the tumour. A
Autor:
Markku Kallajoki, Toivo T. Salmi, Victoria Keros, Päivi M. Lähteenmäki, Kirsi Jahnukainen, Mirja Nurmio
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 94:2119-2122
Isolation of spermatogonial stem cells before potentially sterilizing cancer therapy, followed by transplantation of these cells into the testis after such treatment, may be an effective approach to prevent infertility among prepubertal boys sufferin
Autor:
Katriina Parto, Marjut Kauppila, Toivo T. Salmi, Pirjo Koistinen, Erkki Elonen, Anu Usvasalo, Esa Jantunen, Riikka Räty, Arja Harila-Saari, Raija Silvennoinen, Ulla M. Saarinen-Pihkala, Sakari Knuutila, Pekka Riikonen, Kim Vettenranta
Publikováno v:
Haematologica. 93:1161-1168
Background Interest has recently been paid to adolescents and young adults with acute lymphoblastic leukemia, particularly because all reports so far published indicate that these patients have a better outcome when treated with pediatric rather than
Autor:
Timo Jahnukainen, Marika Grönroos, Toivo T. Salmi, Kerttu Irjala, Merja Möttönen, Mikko Perkkiö
Publikováno v:
Pediatric Blood & Cancer. 51:535-539
Background High-dose methotrexate (HD-MTX) is commonly used in treatment of pediatric leukemias and lymphomas. Transient deterioration in renal function is frequently noted during HD-MTX treatment, but possible long-term changes are less well known.
Autor:
Timo Jahnukainen, Marika Grönroos, Kerttu Irjala, Risto Härkönen, Merja Möttönen, Saija Hurme, Toivo T. Salmi
Publikováno v:
Pediatric Nephrology. 23:797-803
Evaluation of renal function should be performed as part of the follow-up during and after chemotherapy in pediatric cancer patients. The aim of this study was to compare an isotope clearance method [isotope glomerular filtration rate (iGFR)] with al
Autor:
Veli Kairisto, Tarja-Terttu Pelliniemi, Toivo T. Salmi, Janita Johansson, Hans Helenius, Kati Kohonen, Mauri M. Hämäläinen, Kari Remes, Jukka Aurén, Vesa Juvonen
Publikováno v:
European Journal of Haematology. 80:201-207
Objectives: Wilms tumour gene 1 (WT1) is overexpressed in leucocytes of most acute myeloid leukaemia (AML) patients. However, the clinical relevance of WT1 gene expression as minimal residual disease (MRD) marker in AML has been questioned. Methods: