Ronald J A Wanders (Ronald Wanders)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Topics

Spectrum Disorder

Endoplasmic Reticulum

Top Venues

Orphanet journal of rare diseases

Journal of inherited metabolic disease

EMBO molecular medicine

Physiological reviews

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

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)
Frederic M Vaz, Sacha Ferdinandusse, Gajja S Salomons, Ronald J A Wanders
Disorders of fatty acid homeostasis. Journal of inherited metabolic disease (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)
Frederic M Vaz, Sacha Ferdinandusse, Gajja S Salomons, Ronald J A Wanders
Disorders of fatty acid homeostasis. Journal of inherited metabolic disease (2024)
Ingeborg Hauth, Hans R Waterham, Ronald J A Wanders, Saskia N van der Crabben, Clara D M van Karnebeek
A mild case of sodium-dependent multivitamin transporter (SMVT) deficiency illustrating the importance of treatment response in variant classification. Cold Spring Harbor molecular case studies 8 (2) (2022)
Ronald J A Wanders, Myriam Baes, Daniela Ribeiro, Sacha Ferdinandusse, Hans R Waterham
The physiological functions of human peroxisomes. Physiological reviews 103 (1) (2022)
Ruben Zapata Perez, Ronald J A Wanders, Clara D M van Karnebeek, Riekelt H L Houtkooper
NAD+ homeostasis in human health and disease. EMBO molecular medicine 13 (7) (2021)
Frederic M Vaz, Henk van Lenthe, Martin A T Vervaart, Femke S Stet, Johanne H Klinkspoor, Hilary J Vernon, Susan M I Goorden, Riekelt H L Houtkooper, Willem Kulik, Ronald J A Wanders
An improved functional assay in blood spot to diagnose Barth syndrome using the monolysocardiolipin/cardiolipin ratio. Journal of inherited metabolic disease (2021)
Tanguy Demaret, Sharat Varma, Xavier Stephenne, Françoise Smets, Isabelle Scheers, Ronald J A Wanders, Lionel Van Maldergem, Raymond Reding, Etienne M Sokal
Living-donor liver transplantation for mild Zellweger spectrum disorder: Up to 17 years follow-up. Pediatric transplantation 22 (3) (2018)