Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Mutations in the ENG, ACVRL1, and SMAD4 genes and clinical manifestations of hereditary haemorrhagic telangiectasia: experience from the Center for Osler's Disease, Uppsala University HospitalKarlsson, Torbjörn ; Cherif, HonarUpsala journal of medical sciences, 2018-09, Vol.123 (3), p.153-157 [Periódico revisado por pares]England: Taylor & FrancisTexto completo disponível |
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2 |
Material Type: Artigo
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Endoglin in HIV-associated preeclamptic placentaeGovender, Nalini ; Naicker, Thajasvarie ; Moodley, JagidesaHypertension in pregnancy, 2015-07, Vol.34 (3), p.342-354 [Periódico revisado por pares]England: Informa HealthcareTexto completo disponível |
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3 |
Material Type: Artigo
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Impact of genotype and mutation type on health-related quality of life in patients with hereditary hemorrhagic telangiectasiaPfister, Markus ; Zalaman, Ilse M. ; Blumenstock, Gunnar ; Mauz, Paul-Stefan ; Baumann, IngoActa oto-laryngologica, 2009-01, Vol.129 (8), p.862-866 [Periódico revisado por pares]Stockholm: Informa UK LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Whole-genome microarray and targeted analysis of angiogenesis-regulating gene expression (ENG, FLT1, VEGF, PlGF) in placentas from pre-eclamptic and small-for-gestational-age pregnanciesToft, Johanne Holm ; Lian, Ingrid Alsos ; Tarca, Adi Laurentiu ; Erez, Offer ; Espinoza, Jimmy ; Eide, Irina Poliakova ; Bjørge, Line ; Chen-Sun ; Draghici, Sorin ; Romero, Roberto ; Austgulen, RigmorThe journal of maternal-fetal & neonatal medicine, 2008-01, Vol.21 (4), p.267-273 [Periódico revisado por pares]England: Informa UK LtdSem texto completo |