Zobrazeno 1 - 10
of 24
pro vyhledávání: '"L A, Aaltonen"'
Publikováno v:
Rhinology.
Studies assaying morbidity related to sinonasal inverted papilloma (SNIP) and its treatment are lacking. We evaluated how operative treatment of SNIP affects patients' health-related quality of life (HRQoL) and symptoms.We prospectively recruited con
Autor:
L-M Aaltonen, Saku T. Sinkkonen, Leif Bäck, Johanna Ruohoalho, Paavo Pietarinen, Antti Mäkitie
Publikováno v:
Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-LaryngologyCervico-Facial Surgery. 42(2)
Publikováno v:
Clinical Otolaryngology. 37:305-308
Publikováno v:
Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-LaryngologyCervico-Facial Surgery. 37(4)
Publikováno v:
Methods in molecular medicine. 50
Cowden syndrome is a rare dominantly inherited condition with predisposition to benign hamartomatous polyposis of the intestine, as well as malignant tumors of the breast and thyroid, and possibly some other cancer types. Other features include macro
Autor:
L A, Aaltonen, S, Roth
Publikováno v:
Methods in molecular medicine. 50
Juvenile polyposis (JP) is a rare dominantly inherited tumor predisposition syndrome, the typical lesion being a benign hamartomatous intestinal polyp with dilated crypts. Solitary juvenile polyps are relatively common in childhood, and appear not to
Autor:
L A, Aaltonen, E, Avizienyte
Publikováno v:
Methods in molecular medicine. 50
While Peutz-Jeghers syndrome (PJS) has been acknowledged as a clinical entity for decades (1,2), the molecular background for the disease has been unraveled only very recently. PJS has two cardinal features: First, many but not all patients display m
Autor:
H, Nakagawa, G J, Nuovo, E E, Zervos, E W, Martin, R, Salovaara, L A, Aaltonen, A, de la Chapelle
Publikováno v:
Cancer research. 61(19)
Hypermethylation of the MLH1 promoter underlies most sporadic colorectal cancers with microsatellite instability (MSI). To investigate the role of hypermethylation in the normal colonic mucosa as a possible precursor lesion, we studied 700 bp upstrea
Autor:
A, Hemminki, E, Avizienyte, S, Roth, A, Loukola, L A, Aaltonen, H, Järvinen, A, de la Chapelle
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 114(7)
Autor:
A, Loukola, K, Eklin, P, Laiho, R, Salovaara, P, Kristo, H, Järvinen, J P, Mecklin, V, Launonen, L A, Aaltonen
Publikováno v:
Cancer research. 61(11)
Hereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant cancer predisposition syndrome caused by germ-line mutations in DNA mismatch repair genes. It is relevant to identify HNPCC patients because colonoscopic screening of individu