Pierre van Ostade Spreekstalmeester (uncredited) 1 Kunt u me de weg naar Hamelen vertellen, meneer? (1972) Noraly Beyer Nieuwslezer (uncredited) 1 A Life in Suitcases (2005)MOVIEmeter Members only Become a member to access additional data Try IMDbPro Premium for free Ratings...
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we never got paid more than a few dollars in a year. It was too much work keeping up with the companies who change their code so often, I had to constantly update, so have given up getting any help with costs of maintaining this domain for more than 20 years, all by myself. Since...
“It was a blessing to have had the tutelage, support and friendship of the late great Carmen Carrozza. Through the years, Carmen and his wife Jean made a ‘home away from home’ for me in New York. His brothers and their wives, Pat and Connie, and Tony and Mimma welcomed me like ...
风が吹き抜けてく 少しの距离さえ （close to your heart）もどかしく感じる程 溢れる想い （stay with me）モノクロのまま见过ごした景色 すべてがここから辉き出すよ （Light up your day!）We can sing a song! 太阳浴びて 一つになろう あの空にClap your hands!どんな未来だって どん...
“This is the best of times for people like me,” Miller said. “When I got into comics, there was quite literally nothing [other than superheroes] being published. As much as I love superheroes, it seemed silly that an entire story form should be trapped in one genre.” ...
The apartment host, Bruce, loves to answer all the questions for us, and I can feel that Bruce does want us to have a REALLY GOOD trip in Japan. I am so touched, and this is why I give this apartment & Bruce this highly recommendation. Believe me, if you are a well-educated ...
cTehoevceerlelsxpwreersesisopno.t(tded) on SD-ura as well as on plates containing Different DRG1 alleles were overexpressed from were spplaostmtedidosnunYdPeDr,tShDe -cuornatraonldofSDth-euirnad +uc 0i.b5l me CMUcPo1pppreormsuoltfearte(PtoCUinP1d)uincethoveewreilxdp-rte...
Homozygous mutations in YME1L were found to cause a mitochondriopathy with optic at- rophy in a consanguineous pedigree [15] but it remains to be seen whether mutations in YME1L are of broader pathogenic relevance. Recessive mutations in SPG7 coding for the m-AAA protease subunit paraple...