Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol von Knoblauch, Hans, Bauerfeind, Anja, Toliat, Mohammad Reza, Becker, Christian, Luganskaja, Tatjana, Günther, Ulf Peter, Rohde, Klaus, Schuster, Herbert, Junghans, Christine, Luft, Friedrich C., Nürnberg, Peter, Reich, Jens Georg

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Schizophrenia, human genetics and genetic counselling. Human genetic counselling as part of the psychiatric/psychotherapeutic treatment concept von Knoblauch, H

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Expansion of the Phenotypic Spectrum of the CACNA1A T666M Mutation: A Family with Familial Hemiplegic Migraine Type 1, Cerebellar Atrophy and Mental Retardation von Freilinger, T, Bohe, M, Wegener, B, Müller-Myhsok, B, Dichgans, M, Knoblauch, H

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From self psychology to selves in relationship: a radical process of micro and macro expansion in conceptual experience von Knoblauch, Steven H

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From Self Psychology to Selves in Relationship von Knoblauch, Steven H.

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Common haplotypes in five genes influence genetic variance of LDL and HDL cholesterol in the general population von Knoblauch, Hans, Bauerfeind, Anja, Krähenbühl, Christine, Daury, Aurelie, Rohde, Klaus, Bejanin, Stéphane, Essioux, Laurent, Schuster, Herbert, Luft, Friedrich C., Georg Reich, Jens

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P1.32 A genetic variant within caveolin-3 protects against statin-induced myopathy von Knoblauch, H, Giannakidou-Jordan, E, Busjahn, A, Rosada, A, Carl, M, Kassner, U, Wenzel, K, Steinhagen-Thiessen, E, Spuler, S

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Technology and social interaction: the emergence of 'workplace studies' von Heath, Christian, Knoblauch, Hubert, Luff, Paul

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Uridine nucleotide receptors and their ligands : Structural, physiological, and pathophysiological aspects, with special emphasis on the nervous system von HEILBRONN, E, KNOBLAUCH, B. H. A, MÜLLER, C. E

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Physikalische und numerische Modellierung des Strömungsverhaltens im Stauraum des KW Feistritz-Ludmannsdorf an der Drau von Dorfmann, C., Knoblauch, H., Moser, A.

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Sudden death and Wegener's granulomatosis of the pituitary von WOYWODT, A, KNOBLAUCH, H, KETTRITZ, R, SCHNEIDER, W, GÖBEL, U

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Europe and Invisible Religion von Knoblauch, Hubert

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A new mutation in the elastin gene causing supravalvular aortic stenosis von Boeckel, Thomas, Dierks, Astrid, Vergopoulos, Athanasios, Bähring, Sylvia, Knoblauch, Hans, Müller-Myhsok, Bertram, Baron, Heike, Aydin, Atakan, Bein, Georg, Luft, Friedrich C, Schuster, Herbert

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Clinical and molecular cytogenetic studies of a large de novo interstitial deletion 16q11.2-16q21 including the putative transcription factor gene SALL1 von Knoblauch, H, Thiel, G, Tinschert, S, Körner, H, Tennstedt, C, Chaoui, R, Kohlhase, J, Dixkens, C, Blanck, C

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Sudden death and Wegener's granulomatosis of the pituitary: Case Report von Woywodt, A, Knoblauch, H, Kettritz, R, Schneider, W, Goebel, U

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Gestational diabetes von Knoblauch, H, Luft, F

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Wasserwirtschaftliche Optimierung der Stauraumspülungen an der Oberen Mur von BADURA, H, KNOBLAUCH, H, SCHNEIDER, J, HARREITER, H, DEMEL, S

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Increased Parental Ages and Uniparental Disomy 15: A Paternal Age Effect? von Robinson, W.P., Lorda-Sanchez, I., Malcolm, S., Langlois, S., Schuffenhauer, S., Knoblauch, H., Horsthemke, B., Schinzel, A.A.

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A Brief Note on a New Beginning von Knoblauch, Steven H

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Fetal trisomy 10 mosaicism: ultrasound, cytogenetic and morphologic findings in early pregnancy von Knoblauch, H., Sommer, D., Zimmer, C., Tennstedt, C., Heling, K., Bollmann, R., Bommer, C., Tinschert, S., Körner, H.

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