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dai: 125373627
scopus: 36788432100

Stegmann, A.P.A.

(Sander Stegmann)


mutation patient ang i ang ii ndufa genet angiotensin paang i holoprosencephaly chymase study mitochondrial ang ii levels paang organ analysis fluid level figure leigh syndrome organ bath fluid genetic deletion cause disease angiotensin ii protein inhibitor ndufa 9 ficiency family application organ bath captopril heart schalekamp madh danser ahj subunit leigh j med genet table chymostatin fi broblasts semilobar brain adventitial syndrome fetus generation release artery picture broblast netherland holoprosencephaly adc paulussen ang ii release identi semilobar hpe department tissue vasoconstriction angiotensin i identi fied alobar luminal inhibition danser paang i application region ang ii generation patient fi broblasts segment cleft alobar hpe i activity control saxena pr dubourg c receptor article




3 Most Recent Publications

Defective NDUFA9 as a novel cause of neonatally fatal complex I disease (Article)
van den Bosch, B.J.C. Gerards, M. Schoonderwoerd, K. Coo, I.F.M. de Smeets, H.J. Sluiter, W. Stegmann, A.P.A. Jongen, E.L.C. Hellebrekers, D.M.E.I. Oegema, R. Lambrichs, E.H. Prokisch, H. Danhauser, K.
2012-01-01
The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes (Article)
Paulussen, A.D.C. Schrander-Stumpel, C.T.R.M. Bever, Y. van Stolte-Dijkstra, I. Kerstjense-Frederikse, W.S. Herkert, J.C. Essen, J.A. van Lichtenbelt, K.D. Haeringen, A. van Kwee, M.L. Lachmeijer, A.M.A. Tan-Sindhunata, G.M.B. Tserpelis, D.C.J. Maarle, M.C. Arens, Y.H.J.M. Smeets, E.E.J.G.L. Die-Smulders, C. de Engelen, J.J.M. Smeets, H. Herbergs, J. Spee, M.K.M. Stegmann, A.P.A. Mancini, G.M. Brooks, A.S. Colée, M. Maat-Kievit, A.A. Simon, M.E.H.
2010-09-01
ACE-versus chymase-dependent angiotensin II generation in human coronary arteries: a matter of efficiency? (Article)
Tom, B. Garrelds, I.M. Scalbert, E. Stegmann, A.P.A. Boomsma, F. Saxena, P.R. Danser, A.H.J.
2003-01-01