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Methods of modifying through-thickness electrical conductivity of CFRP for use in structural health monitoring, and its effect on mechanical properties – A review

Composites. Part A, Applied science and manufacturing, 2020-06, Vol.133, p.105885, Article 105885

2020

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Percutaneous closure of the patent foramen ovale: A cardiological perspective

SA heart journal, 2017-04, Vol.7 (4), p.264-271

Brown, S.C.

2017

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Chronic pulmonary arterial hypertension in children

SA heart journal, 2017-04, Vol.4 (1), p.18-25

2017

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Transapical left ventricular access for difficult to reach interventional targets in the left heart

Catheterization and cardiovascular interventions, 2009-07, Vol.74 (1), p.137-142

2009

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Percutaneous closure of ventricular septal defects in childhood

SA heart journal, 2017-04, Vol.4 (1), p.26-31

2017

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Stenting the arterial duct: Practical aspects and review of outcomes

SA heart journal, 2017-03, Vol.10 (3), p.514-519

2017

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P.8.7 Assessment of neuromuscular junction abnormalities induced by α -dystroglycan glycosylation defects

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.781-782

2013

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P.8.8 Basement membrane deposition during muscle development in the FKRP Deficient Mouse

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.782-782

2013

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Flow cytometry analysis: A quantitative method for collagen VI deficiency screening

Neuromuscular disorders : NMD, 2012-02, Vol.22 (2), p.139-148

2012

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P19 Structural brain defects associated with a knock-down in fukutin related protein in the mouse

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S12-S12

2012

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P.8.9 Progressive muscular dystrophy in a mouse model of FKRP deficiency

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.782-782

2013

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P2.16 Deposition of the inner limiting membrane in the eye of a mouse model for Muscle Eye Brain disease

Neuromuscular disorders : NMD, 2011-10, Vol.21 (9), p.665-665

2011

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P59 Transcriptome analysis in a mouse model of FKRP-deficient muscular dystrophy

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S22-S23

2014

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P21 Basement membrane deposition in the skeletal muscle of the FKRPknock-down mouse

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S12-S13

2012

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G.P.10 Basement membrane deposition in the skeletal muscle of the FKRP knock-down mouse

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.814-815

2012

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G.P.4 A comparison of the structural brain defects in dystroglycanopathy mouse models

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.813-813

2012

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P11 A reduction in the expression of Fukutin-related protein leads to the altered deposition of multiple laminin alpha chains in a mouse model for Muscle Eye Brain disease

Neuromuscular disorders : NMD, 2011, Vol.21, p.S9-S10

2011

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P17 Deposition of the inner limiting membrane in the eye of a mouse model for Muscle Eye Brain disease

Neuromuscular disorders : NMD, 2011, Vol.21, p.S11-S11

2011

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G.P.321

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.918-918

2014

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Early experience with cervical endoscopic spinal surgery (CESS): a potential adjunct to ACDF/disc arthroplasty

The spine journal, 2015-03, Vol.15 (3), p.S74-S74

2015

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G.P.6 Assessing the long term expression of LARGE as a potential therapy in a mouse model of LGMD2I

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.813-814

2012

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P.1.17 Immunostaining of the sarcolemma with a new monoclonal antibody against alpha-dystroglycan core and its relevance to diagnosis

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.746-747

2013

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Optimal paediatric cardiac services in South Africa – what do we need?

SA heart journal, 2017-04, Vol.7 (1), p.10-16

2017

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Audit of paediatric cardiac services in South Africa

SA heart journal, 2017-04, Vol.7 (1), p.4-9

2017

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P12 Generation of a new mouse model for therapeutic testing in the dystroglycanopathies

Neuromuscular disorders : NMD, 2011, Vol.21, p.S10-S10

2011

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Methods of modifying through-thickness electrical conductivity of CFRP for use in structural health monitoring, and its effect on mechanical properties – A review

Percutaneous closure of the patent foramen ovale: A cardiological perspective

Chronic pulmonary arterial hypertension in children

Transapical left ventricular access for difficult to reach interventional targets in the left heart

Percutaneous closure of ventricular septal defects in childhood

Stenting the arterial duct: Practical aspects and review of outcomes

P.8.7 Assessment of neuromuscular junction abnormalities induced by α -dystroglycan glycosylation defects

P.8.8 Basement membrane deposition during muscle development in the FKRP Deficient Mouse

Flow cytometry analysis: A quantitative method for collagen VI deficiency screening

P19 Structural brain defects associated with a knock-down in fukutin related protein in the mouse

P.8.9 Progressive muscular dystrophy in a mouse model of FKRP deficiency

P2.16 Deposition of the inner limiting membrane in the eye of a mouse model for Muscle Eye Brain disease

P59 Transcriptome analysis in a mouse model of FKRP-deficient muscular dystrophy

P21 Basement membrane deposition in the skeletal muscle of the FKRPknock-down mouse

G.P.10 Basement membrane deposition in the skeletal muscle of the FKRP knock-down mouse

G.P.4 A comparison of the structural brain defects in dystroglycanopathy mouse models

P11 A reduction in the expression of Fukutin-related protein leads to the altered deposition of multiple laminin alpha chains in a mouse model for Muscle Eye Brain disease

P17 Deposition of the inner limiting membrane in the eye of a mouse model for Muscle Eye Brain disease

G.P.321

Early experience with cervical endoscopic spinal surgery (CESS): a potential adjunct to ACDF/disc arthroplasty

G.P.6 Assessing the long term expression of LARGE as a potential therapy in a mouse model of LGMD2I

P.1.17 Immunostaining of the sarcolemma with a new monoclonal antibody against alpha-dystroglycan core and its relevance to diagnosis

Optimal paediatric cardiac services in South Africa – what do we need?

Audit of paediatric cardiac services in South Africa

P12 Generation of a new mouse model for therapeutic testing in the dystroglycanopathies

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