“Next generation sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease”

por Arowolo, Afolake T., Adeola, Henry A., Khumalo, Nonhlanhla P.
Publicado 2017

Androgenetic alopecia: An update

por Ntshingila, Sincengile, Oputu, Ogheneochuko, Arowolo, Afolake T., Khumalo, Nonhlanhla P.
Publicado 2023

Systems Approach to Human Hair Fibers: Interdependence Between Physical, Mechanical, Biochemical and Geometric Properties of Natural Healthy Hair

por Cloete, Elsabe, Khumalo, Nonhlanhla P., Van Wyk, Jennifer C., Ngoepe, Malebogo N.
Publicado 2019

Human T cell lymphotropic virus type 1- associated infective dermatitis in KwaZulu Natal, South Africa

por Hlela, Carol, Graham, Natalie, Bhigjee, Ahmed I, Taylor, Graham P, Khumalo, Nonhlanhla P, Mosam, Anisa
Publicado 2013

Correction: Advances in surface modifications of the silicone breast implant and impact on its biocompatibility and biointegration

por Foroushani, Fatemeh Tavakoli, Dzobo, Kevin, Khumalo, Nonhlanhla P, Mora, Vanessa Zamora, Mezerville, Roberto de, Bayat, Ardeshir
Publicado 2023

Pathologic grooming (acne excoriee, trichotillomania, and nail biting) in 4 generations of a single family

por Khumalo, Nonhlanhla P., Shaboodien, Gasnat, Hemmings, Sian M.J., Moolman-Smook, Johanna C., Stein, Dan J.
Publicado 2016

Advances in surface modifications of the silicone breast implant and impact on its biocompatibility and biointegration

por Foroushani, Fatemeh Tavakoli, Dzobo, Kevin, Khumalo, Nonhlanhla P, Mora, Vanessa Zamora, de Mezerville, Roberto, Bayat, Ardeshir
Publicado 2022

Reliability of Histopathology for the Early Recognition of Fibrosis in Traction Alopecia: Correlation with Clinical Severity

por Ngwanya, Reginald Mzudumile, Adeola, Henry Ademola, Beach, Renée A., Gantsho, Nomphelo, Walker, Christopher L., Pillay, Komala, Prokopetz, Robert, Gumedze, Freedom, Khumalo, Nonhlanhla P.
Publicado 2019

National suicide management guidelines recommending family-based prevention, intervention and postvention and their association with suicide mortality rates: systematic review

por Panesar, Balpreet, Soni, Divya, Khan, Mohammed I., Bdair, Faris, Holek, Matthew, Tahir, Talha, Woo, Julia, Sanger, Nitika, Khumalo, Nonhlanhla P., Minuzzi, Luciano, Thabane, Lehana, Samaan, Zainab
Publicado 2022

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

por Mercier, Sandra, Küry, Sébastien, Salort-Campana, Emmanuelle, Magot, Armelle, Agbim, Uchenna, Besnard, Thomas, Bodak, Nathalie, Bou-Hanna, Chantal, Bréhéret, Flora, Brunelle, Perrine, Caillon, Florence, Chabrol, Brigitte, Cormier-Daire, Valérie, David, Albert, Eymard, Bruno, Faivre, Laurence, Figarella-Branger, Dominique, Fleurence, Emmanuelle, Ganapathi, Mythily, Gherardi, Romain, Goldenberg, Alice, Hamel, Antoine, Igual, Jeanine, Irvine, Alan D., Israël-Biet, Dominique, Kannengiesser, Caroline, Laboisse, Christian, Le Caignec, Cédric, Mahé, Jean-Yves, Mallet, Stéphanie, MacGowan, Stuart, McAleer, Maeve A., McLean, Irwin, Méni, Cécile, Munnich, Arnold, Mussini, Jean-Marie, Nagy, Peter L., Odel, Jeffrey, O’Regan, Grainne M., Péréon, Yann, Perrier, Julie, Piard, Juliette, Puzenat, Eve, Sampson, Jacinda B., Smith, Frances, Soufir, Nadem, Tanji, Kurenai, Thauvin, Christel, Ulane, Christina, Watson, Rosemarie M., Khumalo, Nonhlanhla P., Mayosi, Bongani M., Barbarot, Sébastien, Bézieau, Stéphane
Publicado 2015