Surita Meldau (S Meldau)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 11

Top Venues

Orphanet journal of rare diseases

African journal of laboratory medicine

Human mutation

Journal of clinical pathology

University of Cape Town

University of Cape Town (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Cape Town May 01 2016

South Africa

Lecturer / Medical Scientist :: Chemical Pathology

National Health Laboratory Service Sep 01 2007

South Africa

Medical Scientist :: Chemical Pathology

Education History

University of Cape Town

South Africa

MSC

Publications

Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend Christiaan Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, null null, Ronald J A Wanders, Francois Hendrikus van der Westhuizen
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 19 (1) (2024)
Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend Christiaan Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, null null, Ronald J A Wanders, Francois Hendrikus van der Westhuizen
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 19 (1) (2024)
Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend Christiaan Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, null null, Ronald J A Wanders, Francois Hendrikus van der Westhuizen
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 19 (1) (2024)
Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend Christiaan Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, null null, Ronald J A Wanders, Francois Hendrikus van der Westhuizen
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 19 (1) (2024)
Herbert Makgopa, Tanja Kemp, Surita Meldau, Engela M Honey, Bettina Chale-Matsau
Maternally inherited diabetes and deafness with a variable presentation across three generations within a pedigree, South Africa. African journal of laboratory medicine 13 (1) (2024)
Michelle Bisschoff, Izelle Smuts, Marli Dercksen, Maryke Schoonen, Barend Christiaan Vorster, George van der Watt, Careni Spencer, Kireshnee Naidu, Franclo Henning, Surita Meldau, Robert McFarland, Robert W Taylor, Krutik Patel, Mahmoud R Fassad, Jana Vandrovcova, null null, Ronald J A Wanders, Francois Hendrikus van der Westhuizen
Clinical, biochemical, and genetic spectrum of MADD in a South African cohort: an ICGNMD study. Orphanet journal of rare diseases 19 (1) (2024)
Herbert Makgopa, Tanja Kemp, Surita Meldau, Engela M Honey, Bettina Chale-Matsau
Maternally inherited diabetes and deafness with a variable presentation across three generations within a pedigree, South Africa. African journal of laboratory medicine 13 (1) (2024)
Lisa Roberts, Stephanie Julius, Shrinav Dawlat, Safiye Yildiz, George Rebello, Surita Meldau, Komala Pillay, Alina Esterhuizen, Alvera Vorster, Gameda Benefeld, Jorge Emanuel Batista da Rocha, Peter Beighton, Sean L Sellars, Kebashni Thandrayen, John M Pettifor, Raj S Ramesar
Renal dysfunction, rod-cone dystrophy, and sensorineural hearing loss caused by a mutation in RRM2B. Human mutation 41 (11) (2020)
Surita Meldau, Elizabeth Patricia Owen, Kashief Khan, Gillian Tracy Riordan
Mitochondrial molecular genetic results in a South African cohort: divergent mitochondrial and nuclear DNA findings. Journal of clinical pathology (2020)
Celeste Swart, Surita Meldau, Chad M Centner, Adrian David Marais, Fierdoz Omar
Validation of PHASE for deriving N-acetyltransferase 2 haplotypes in the Western Cape mixed ancestry population. African journal of laboratory medicine 9 (1) (2020)
Surita Meldau, R J De Lacy, G T M Riordan, E A Goddard, K Pillay, K J Fieggen, A D Marais, G F Van der Watt
Identification of a single MPV17 nonsense-associated altered splice variant in 24 South African infants with mitochondrial neurohepatopathy. Clinical genetics 93 (5) (2018)

Surita Meldau.css-eqlu8i{font-size:small;padding-left:4px;} (S Meldau)

Publication Activity (10 Years)

Top Topics

Top Venues

Surita Meldau (S Meldau)