Franclo Henning (F Henning)

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 17

Top Topics

Clinical Practice

Top Venues

Orphanet journal of rare diseases

Clinical genetics

European journal of neurology

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)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Franclo Henning, Kireshnee Naidu, Christopher J Record, Natalia Dominik, Jana Vandrovcova, Frans Lubbe, Marli Dercksen, null null, Lindsay A Wilson, Francois Van Der Westhuizen, Mary M Reilly, Henry Houlden, Michael G Hanna, Jonathan A Carr
Extended Phenotype of PEX11B Pathogenic Variants: Ataxia, Tremor, and Dystonia Due to a Novel C.2T > G Variant. Movement disorders clinical practice (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics (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)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (1) (2024)
Emiliano Giardina, Pilar Camaño, Sarah Burton-Jones, Gianina Ravenscroft, Franclo Henning, Frédérique Magdinier, Nienke van der Stoep, Patrick J van der Vliet, Rafaëlle Bernard, Pedro José Tomaselli, Mark R Davis, Ichizo Nishino, Zehra Piraye Oflazer, Valerie Race, Venugopalan Yamuna Vishnu, Victoria Williams, Claudia Ferreira Da Rosa Sobreira, Silvère M van der Maarel, Steven A Moore, Nicol C Voermans, Richard J L F Lemmers
Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: Update of the 2012 guidelines. Clinical genetics 106 (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)
Lindsay A Wilson, William L Macken, Luke D Perry, Christopher J Record, Katherine R Schon, Rodrigo Siqueira Soares Frezatti, Sharika V Raga, Kireshnee Naidu, Özlem Yayıcı Köken, Ipek Polat, Musambo M Kapapa, Natalia Dominik, Stephanie Efthymiou, Heba Morsy, Melissa Nel, Mahmoud R Fassad, Fei Gao, Krutik Patel, Maryke Schoonen, Michelle Bisschoff, Armand Vorster, Hallgeir Jonvik, Ronel Human, Elsa Lubbe, Malebo Nonyane, Seena Vengalil, Saraswati Nashi, Kosha Srivastava, Richard J L F Lemmers, Alisha Reyaz, Rinkle Mishra, Ana Töpf, Christina I Trainor, Elizabeth C Steyn, Amokelani C Mahungu, Patrick J van der Vliet, Ahmet Cevdet Ceylan, A Semra Hiz, Büşranur Çavdarlı, C Nur Semerci Gündüz, Gülay Güleç Ceylan, Madhu Nagappa, Karthik B Tallapaka, Periyasamy Govindaraj, Silvère M van der Maarel, Gayathri Narayanappa, Bevinahalli N Nandeesh, Somwe Wa Somwe, David R Bearden, Michelle P Kvalsund, Gita M Ramdharry, Yavuz Oktay, Uluç Yiş, Haluk Topaloğlu, Anna Sarkozy, Enrico Bugiardini, Franclo Henning, Jo M Wilmshurst, Jeannine M Heckmann, Robert McFarland, Robert W Taylor, Izelle Smuts, Francois Hendrikus van der Westhuizen, Claudia Ferreira Da Rosa Sobreira, Pedro José Tomaselli, Wilson Marques, Rohit Bhatia, Ashwin B Dalal, M V Padma Srivastava, Sireesha Yareeda, Atchayaram Nalini, Venugopalan Yamuna Vishnu, Kumarasamy Thangaraj, Volker Straub, Rita Horvath, Patrick F Chinnery, Robert D S Pitceathly, Francesco Muntoni, Henry Houlden, Jana Vandrovcova, Mary M Reilly, Michael G Hanna
Neuromuscular disease genetics in underrepresented populations: increasing data diversity. Brain : a journal of neurology (2023)
Franclo Henning, Tertius Abraham Kohn
Preservation of shortening velocity and power output in single muscle fibres from patients with idiopathic inflammatory myopathies. Journal of muscle research and cell motility (2022)
Jaime Luna, Jeremy Jost, Mouhamadou Diagana, Leila Ait Aissa, Meriem Tazir, Lamia Ali Pacha, Imen Kacem, Riadh Gouider, Franclo Henning, Anna Basse, Ousmane Cisse, Aa Koffi Balogou, Damelan Kombate, Mendinatou Agbetou, Dismand Houinato, Dieu Donné Gnonlonfoun, Athanase Millogo, Thierry Agba, Mouftao Belo, Noudy Sengxeu, Bello Hamidou, Pierre-Marie Preux, Marin Benoit, Philippe Couratier, null null
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS study. Amyotrophic lateral sclerosis & frontotemporal degeneration (2021)
Franclo Henning, Tertius Abraham Kohn
An exploratory study of contractile force production in muscle fibers from patients with inflammatory myopathies. Muscle & nerve 62 (2) (2020)
Franclo Henning, J M Heckmann, K Naidu, L Vlok, H M Cross, B Marin
Incidence of motor neuron disease/amyotrophic lateral sclerosis in South Africa: a 4-year prospective study. European journal of neurology 28 (1) (2020)
Ludo Van Hillegondsberg, Jonathan Carr, Naeem Brey, Franclo Henning
Using Eulerian video magnification to enhance detection of fasciculations in people with amyotrophic lateral sclerosis. Muscle & nerve 56 (6) (2017)