Clinical and cardiovascular magnetic resonance profile of cardiomyopathy patients from South Africa: Pilot of the IMHOTEP study
Kraus, S.M., Samuels, P., Jermy, S., Laing, N., Van der Wall, M., September, U., Ntsekhe, M., Chin, A., Moosa, S., Sliwa, K., Ntusi, N.A.B.
Published in International journal of cardiology (15.03.2024)
Published in International journal of cardiology (15.03.2024)
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Heterozygous CAPN3 missense variants causing autosomal‐dominant calpainopathy in seven unrelated families
González‐Mera, L., Ravenscroft, G., Cabrera‐Serrano, M., Ermolova, N., Domínguez‐González, C., Arteche‐López, A., Soltanzadeh, P., Evesson, F., Navas, C., Mavillard, F., Clayton, J., Rodrigo, P., Servián‐Morilla, E., Cooper, S. T, Waddell, L., Reardon, K., Corbett, A., Hernandez‐Laín, A., Sanchez, A., Esteban Perez, J., Paradas‐Lopez, C., Rivas‐Infante, E., Spencer, M., Laing, N., Olivé, M.
Published in Neuropathology and applied neurobiology (01.02.2021)
Published in Neuropathology and applied neurobiology (01.02.2021)
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Antimicrobial susceptibility of clinical isolates of Neisseria gonorrhoeae to alternative antimicrobials with therapeutic potential
Lagacé-Wiens, P R S, Adam, H J, Laing, N M, Baxter, M R, Martin, I, Mulvey, M R, Karlowsky, J A, Hoban, D J, Zhanel, G G
Published in Journal of antimicrobial chemotherapy (01.08.2017)
Published in Journal of antimicrobial chemotherapy (01.08.2017)
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Ryanodine receptor type 3 (RYR3) as a novel gene associated with a myopathy with nemaline bodies
Nilipour, Y., Nafissi, S., Tjust, A. E., Ravenscroft, G., Hossein Nejad Nedai, H., Taylor, R. L., Varasteh, V., Pedrosa Domellöf, F., Zangi, M., Tonekaboni, S. H., Olivé, M., Kiiski, K., Sagath, L., Davis, M. R., Laing, N. G., Tajsharghi, H.
Published in European journal of neurology (01.06.2018)
Published in European journal of neurology (01.06.2018)
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Journal Article
Core-rod myopathy caused by mutations in the nebulin gene
Romero, N B, Lehtokari, V-L, Quijano-Roy, S, Monnier, N, Claeys, K G, Carlier, R Y, Pellegrini, N, Orlikowski, D, Barois, A, Laing, N G, Lunardi, J, Fardeau, M, Pelin, K, Wallgren-Pettersson, C
Published in Neurology (06.10.2009)
Published in Neurology (06.10.2009)
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Journal Article
Altered myogenesis and premature senescence underlie human TRIM32-related myopathy
Servián-Morilla, E, Cabrera-Serrano, M, Rivas-Infante, E, Carvajal, A, Lamont, P J, Pelayo-Negro, A L, Ravenscroft, G, Junckerstorff, R, Dyke, J M, Fletcher, S, Adams, A M, Mavillard, F, Fernández-García, M A, Nieto-González, J L, Laing, N G, Paradas, C
Published in Acta neuropathologica communications (01.03.2019)
Published in Acta neuropathologica communications (01.03.2019)
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Journal Article
Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation
Jain, R K, Jayawant, S, Squier, W, Muntoni, F, Sewry, C A, Manzur, A, Quinlivan, R, Lillis, S, Jungbluth, H, Sparrow, J C, Ravenscroft, G, Nowak, K J, Memo, M, Marston, S B, Laing, N G
Published in Neurology (03.04.2012)
Published in Neurology (03.04.2012)
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Journal Article
Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement
Cullup, T, Lamont, P.J, Cirak, S, Damian, M.S, Wallefeld, W, Gooding, R, Tan, S.V, Sheehan, J, Muntoni, F, Abbs, S, Sewry, C.A, Dubowitz, V, Laing, N.G, Jungbluth, H
Published in Neuromuscular disorders : NMD (01.12.2012)
Published in Neuromuscular disorders : NMD (01.12.2012)
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Journal Article
An overview of the genetic basis of cardiovascular disease
Laing, N., Shaboodien, G., Kraus, S.M., Ntusi, N.A.B.
Published in South African medical journal (01.06.2019)
Published in South African medical journal (01.06.2019)
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Journal Article
Variants in ACTG2 underlie a substantial number of Australasian patients with primary chronic intestinal pseudo‐obstruction
Ravenscroft, G., Pannell, S., O'Grady, G., Ong, R., Ee, H. C., Faiz, F., Marns, L., Goel, H., Kumarasinghe, P., Sollis, E., Sivadorai, P., Wilson, M., Magoffin, A., Nightingale, S., Freckmann, M.‐L., Kirk, E. P., Sachdev, R., Lemberg, D. A., Delatycki, M. B., Kamm, M. A., Basnayake, C., Lamont, P. J., Amor, D. J., Jones, K., Schilperoort, J., Davis, M. R., Laing, N. G.
Published in Neurogastroenterology and motility (01.09.2018)
Published in Neurogastroenterology and motility (01.09.2018)
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Journal Article
Adult onset distal and proximal myopathy with complete ophthalmoplegia associated with a novel de novo p.(Leu1877Pro) mutation in MYH2
Cabrera-Serrano, M., Fabian, V.A., Boutilier, J., Wise, C., Faiz, F., Lamont, P.J., Laing, N.G.
Published in Clinical genetics (01.12.2015)
Published in Clinical genetics (01.12.2015)
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Journal Article
Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy
Lamont, P J, Udd, B, Mastaglia, F L, de Visser, M, Hedera, P, Voit, T, Bridges, L R, Fabian, V, Rozemuller, A, Laing, N G
Published in Journal of neurology, neurosurgery and psychiatry (01.02.2006)
Published in Journal of neurology, neurosurgery and psychiatry (01.02.2006)
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Journal Article
Production impact of a targeted selective treatment system based on liveweight gain in a commercial flock
Busin, V., Kenyon, F., Parkin, T., McBean, D., Laing, N., Sargison, N.D., Ellis, K.
Published in The veterinary journal (1997) (01.05.2014)
Published in The veterinary journal (1997) (01.05.2014)
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Journal Article
A novel MYH7 founder mutation causing Laing distal myopathy in Southern Spain
Carbonell-Corvillo, P., Tristán-Clavijo, E., Cabrera-Serrano, M., Servián-Morilla, E., García-Martín, G., Villarreal-Pérez, L., Rivas-Infante, E., Area-Gómez, E., Chamorro-Muñoz, M.I., Gil-Gálvez, A., Miranda-Vizuete, A., Martinez-Mir, A., Laing, N., Paradas, C.
Published in Neuromuscular disorders : NMD (01.10.2018)
Published in Neuromuscular disorders : NMD (01.10.2018)
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Journal Article
Hemifacial microsomia: progress in understanding the genetic basis of a complex malformation syndrome
KELBERMAN, D, TYSON, J, HAAN, E. A, LAING, N. G, LIM, J, MALCOLM, S, SINGER, S. L, WINTER, R. M, BITNER-GLINDZICZ, M, CHANDLER, D. C, MCINERNEY, A. M, SLEE, J, ALBERT, D, AYMAT, A, BOTMA, M, CALVERT, M, GOLDBLATT, J
Published in Human genetics (01.12.2001)
Published in Human genetics (01.12.2001)
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Antibiotic resistance in Escherichia coli outpatient urinary isolates: final results from the North American Urinary Tract Infection Collaborative Alliance (NAUTICA)
Zhanel, George G., Hisanaga, Tamiko L., Laing, Nancy M., DeCorby, Melanie R., Nichol, Kim A., Weshnoweski, Barb, Johnson, Jack, Noreddin, Ayman, Low, Don E., Karlowsky, James A., Hoban, Daryl J.
Published in International journal of antimicrobial agents (01.06.2006)
Published in International journal of antimicrobial agents (01.06.2006)
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Central core disease: clinical, pathological, and genetic features
Quinlivan, R M, Muller, C R, Davis, M, Laing, N G, Evans, G A, Dwyer, J, Dove, J, Roberts, A P, Sewry, C A
Published in Archives of disease in childhood (01.12.2003)
Published in Archives of disease in childhood (01.12.2003)
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Journal Article
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores
Jungbluth, H, Müller, C R, Halliger-Keller, B, Brockington, M, Brown, S C, Feng, L, Chattopadhyay, A, Mercuri, E, Manzur, A Y, Ferreiro, A, Laing, N G, Davis, M R, Roper, H P, Dubowitz, V, Bydder, G, Sewry, C A, Muntoni, F
Published in Neurology (23.07.2002)
Published in Neurology (23.07.2002)
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Journal Article
Clinical course correlates poorly with muscle pathology in nemaline myopathy
Ryan, M M, Ilkovski, B, Strickland, C D, Schnell, C, Sanoudou, D, Midgett, C, Houston, R, Muirhead, D, Dennett, X, Shield, L K, De Girolami, U, Iannaccone, S T, Laing, N G, North, K N, Beggs, A H
Published in Neurology (25.02.2003)
Published in Neurology (25.02.2003)
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