MYBPH acts as modifier of cardiac hypertrophy in hypertrophic cardiomyopathy (HCM) patients von Mouton, J. M., van der Merwe, L., Goosen, A., Revera, M., Brink, P. A., Moolman-Smook, J. C., Kinnear, C.

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Ascribing novel functions to the sarcomeric protein, myosin binding protein H (MyBPH) in cardiac sarcomere contraction von Mouton, Jomien, Loos, Ben, Moolman-Smook, Johanna C, Kinnear, Craig J

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Mitochondrial haplogroups modify the risk of developing hypertrophic cardiomyopathy in a Danish population von Hagen, Christian M, Aidt, Frederik H, Hedley, Paula L, Jensen, Morten K, Havndrup, Ole, Kanters, Jørgen K, Moolman-Smook, Johanna C, Larsen, Severin O, Bundgaard, Henning, Christiansen, Michael

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Sudden Death due to Troponin T Mutations von Moolman, Johanna C, Corfield, Valerie A, Posen, Berthold, Ngumbela, Kholiswa, Seidman, Christine, Brink, Paul A, Watkins, Hugh

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Outcomes of outpatient ureteral stenting without fluoroscopy at Groote Schuur Hospital, Cape Town, South Africa von Jaumdally, S.Z., Kowlessur, B., Wicht, J., Lazarus, J., Kaestner, L., Cassim, F., Van den Heever, A.P., Moolman, C., Kolia, M.E., Sinha, S., Pinto, G., Govender, P., Salukazana, S., Panackal, A., Dewar, M., De Wet, E., De Jager, S., Jehle, C.H.

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Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy von REDWOOD, C. S, MOOLMAN-SMOOK, J. C, WATKINS, H

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MT‐CYB mutations in hypertrophic cardiomyopathy von Hagen, Christian M., Aidt, Frederik H., Havndrup, Ole, Hedley, Paula L., Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K., Moolman‐Smook, Johanna C., Møller, Daniel V., Bundgaard, Henning, Christiansen, Michael

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RBBP6 Interacts with Multifunctional Protein YB-1 through Its RING Finger Domain, Leading to Ubiquitination and Proteosomal Degradation of YB-1 von Chibi, Moredreck, Meyer, Mervin, Skepu, Amanda, G. Rees, D. Jasper, Moolman-Smook, Johanna C., Pugh, David J.R.

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The Origins of Hypertrophic Cardiomyopathy–Causing Mutations in Two South African Subpopulations: A Unique Profile of Both Independent and Founder Events von Moolman-Smook, Johanna C., De Lange, Willem J., Bruwer, Eduard C.D., Brink, Paul A., Corfield, Valerie A.

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Mutations of the Light Meromyosin Domain of the β-Myosin Heavy Chain Rod in Hypertrophic Cardiomyopathy von Blair, Edward, Redwood, Charles, de Jesus Oliveira, Marisa, Moolman-Smook, J C, Brink, Paul, Corfield, V A, Östman-Smith, Ingegerd, Watkins, Hugh

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The role of the brain-derived neurotrophic factor (BDNF) val66met variant in the phenotypic expression of obsessive-compulsive disorder (OCD) von Katerberg, Hilga, Lochner, Christine, Cath, Danielle C., de Jonge, Peter, Bochdanovits, Zoltán, Moolman-Smook, Johanna C., Hemmings, Sîan M.J., Carey, Paul D., Stein, Dan J., Sondervan, David, Boer, Johan A. den, van Balkom, Anton J.L.M., Polman, Annemiek, Heutink, Peter

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Gene for progressive familial heart block type I maps to chromosome 19q13 von BRINK, P. A, FERREIRA, A, MOOLMAN, J. C, WEYMAR, H. W, VAN DER MERWE, P.-L, CORFIELD, V. A

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Clinical features, survival experience, and profile of plakophylin-2 gene mutations in participants of the Arrhythmogenic Right Ventricular Cardiomyopathy Registry of South Africa von Watkins, David A., BSc, Hendricks, Neil, MBChB, Shaboodien, Gasnat, PhD, Mbele, Mzwandile, Msc, Parker, Michelle, Msc, Vezi, Brian Z., MBChB, Latib, Azeem, MBBCh, Chin, Ashley, MBChB, Little, Francesca, PhD, Badri, Motasim, PhD, Moolman-Smook, Johanna C., PhD, Okreglicki, Andrzej, MBChB, MMed, Mayosi, Bongani M., MBChB, DPhil

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Cardiac myosin binding protein C, adrenergic stimulation and cardiac contractility von Ramburan, Amsha, Korkie, Lundi, Moolman-Smook, Johanna C.

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MT‐CYB mutations in hypertrophic cardiomyopathy von Hagen, Christian M., Aidt, Frederik H., Havndrup, Ole, Hedley, Paula L., Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K., Moolman‐Smook, Johanna C., Møller, Daniel V., Bundgaard, Henning, Christiansen, Michael

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Association between a catechol- o-methyltransferase polymorphism and obsessive–compulsive disorder in the Afrikaner population von Niehaus, D.J.H, Kinnear, C.J, Corfield, V.A, du Toit, P.L, van Kradenburg, J, Moolman-Smook, J.C, Weyers, J.B, Potgieter, A, Seedat, S, Emsley, R.A, Knowles, J.A, Brink, P.A, Stein, D.J

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Cluster analysis of obsessive-compulsive spectrum disorders in patients with obsessive-compulsive disorder: clinical and genetic correlates von Lochner, Christine, Hemmings, Sian M.J., Kinnear, Craig J., Niehaus, Dana J.H., Nel, Daniel G., Corfield, Valerie A., Moolman-Smook, Johanna C., Seedat, Soraya, Stein, Dan J.

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Gender in obsessive–compulsive disorder: clinical and genetic findings von Lochner, Christine, Hemmings, Sian M.J., Kinnear, Craig J., Moolman-Smook, Johanna C., Corfield, Valerie A., Knowles, James A., Niehaus, Dana J.H., Stein, Dan J.

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Violence in Male Patients with Schizophrenia: Risk Markers in a South African Population von Koen, L., Kinnear, C. J., Corfield, V. A., Emsley, R. A., Jordaan, E., Keyter, N., Moolman-Smook, J. C., Stein, D. J., Niehaus, D. J. H.

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Early- versus late-onset obsessive–compulsive disorder: investigating genetic and clinical correlates von Hemmings, Sı̂an M.J., Kinnear, Craig J., Lochner, Christine, Niehaus, Dana J.H., Knowles, James A., Moolman-Smook, Johanna C., Corfield, Valerie A., Stein, Dan J.

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